Gene entry
ALK
ALK receptor tyrosine kinase
- Chromosome
- 2
- Cytoband
- 2p23.2-p23.1
- Variants (rsID)
- 213
ALK is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 2 (region 2p23.2-p23.1). Its official name is “ALK receptor tyrosine kinase”. The reference table lists 213 variants (rsID) for this gene.
Clinically classified variants
22 reference-table entries with clinical significance.
- rs12151564Benignsingle nucleotide variant
- rs13419205Benignsingle nucleotide variant
- rs143916398Benignsingle nucleotide variantNeuroblastoma, susceptibility to, 3|Hereditary cancer-predisposing syndrome
- rs146074150Benignsingle nucleotide variantNeuroblastoma, susceptibility to, 3|Hereditary cancer-predisposing syndrome
- rs17007666Benignsingle nucleotide variant
- rs1881420Benignsingle nucleotide variantHereditary cancer-predisposing syndrome|Neuroblastoma, susceptibility to, 3|Squamous cell lung carcinoma
- rs200868013Benignsingle nucleotide variantNeuroblastoma, susceptibility to, 3|Hereditary cancer-predisposing syndrome
- rs2256740Benignsingle nucleotide variantHereditary cancer-predisposing syndrome|Neuroblastoma, susceptibility to, 3
- rs35073634Benignsingle nucleotide variantHereditary cancer-predisposing syndrome|Neuroblastoma, susceptibility to, 3
- rs35093491Benignsingle nucleotide variantNeuroblastoma, susceptibility to, 3|Hereditary cancer-predisposing syndrome
- rs35228363Benignsingle nucleotide variantNeuroblastoma, susceptibility to, 3|Hereditary cancer-predisposing syndrome
- rs113994091Conflicting interpretationssingle nucleotide variantNeuroblastoma, susceptibility to, 3|Neuroblastoma|Hereditary cancer-predisposing syndrome
- rs147858673Conflicting interpretationssingle nucleotide variantNeuroblastoma, susceptibility to, 3|Hereditary cancer-predisposing syndrome
- rs56181542Conflicting interpretationssingle nucleotide variantNeuroblastoma, susceptibility to, 3|Hereditary cancer-predisposing syndrome
- rs61754865Conflicting interpretationssingle nucleotide variantNeuroblastoma, susceptibility to, 3|Hereditary cancer-predisposing syndrome
- rs74716434Conflicting interpretationssingle nucleotide variantNeuroblastoma Susceptibility|Neuroblastoma, susceptibility to, 3|Hereditary cancer-predisposing syndrome
- rs79339096Conflicting interpretationssingle nucleotide variantNeuroblastoma Susceptibility|Neuroblastoma, susceptibility to, 3|Hereditary cancer-predisposing syndrome
- rs144437923Likely benignsingle nucleotide variantNeuroblastoma, susceptibility to, 3|Hereditary cancer-predisposing syndrome
- rs140928266Uncertain significancesingle nucleotide variantNeuroblastoma, susceptibility to, 3
- rs199691702Uncertain significancesingle nucleotide variantNeuroblastoma, susceptibility to, 3
- rs200641396Uncertain significancesingle nucleotide variantNeuroblastoma, susceptibility to, 3
- rs80227749Uncertain significancesingle nucleotide variantNeuroblastoma, susceptibility to, 3
Other listed variants
- rs952455
- rs1528424
- rs1881419
- rs1881425
- rs2257135
- rs2541178
- rs2631941
- rs2631949
- rs2631950
- rs2631958
- rs2879502
- rs3884503
- rs3927337
- rs3936219
- rs4074943
- rs4132594
- rs4233750
- rs4265970
- rs4340463
- rs4381747
- rs4458170
- rs4630725
- rs4635489
- rs4665463
- rs4666183
- rs4666184
- rs4666195
- rs4666200
- rs4666234
- rs4666243
- rs4666247
- rs4666251
- rs5011189
- rs6547926
- rs6547928
- rs6547930
- rs6547945
- rs6547972
- rs6709634
- rs6711746
- rs6726799
- rs6735933
- rs6737999
- rs6740703
- rs6740714
- rs6744445
- rs6754181
- rs6757945
- rs7425108
- rs7567152
- rs7568229
- rs7568708
- rs7569431
- rs7571379
- rs7572957
- rs7576748
- rs7583871
- rs7589120
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.