Gene entry
ASL
argininosuccinate lyase
- Chromosome
- 7
- Cytoband
- 7q11.21
- Variants (rsID)
- 13
ASL is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 7 (region 7q11.21). Its official name is “argininosuccinate lyase”. The reference table lists 13 variants (rsID) for this gene.
Clinically classified variants
13 reference-table entries with clinical significance.
- rs374304304Conflicting interpretationssingle nucleotide variantArgininosuccinate lyase deficiency
- rs766867890Conflicting interpretationssingle nucleotide variantArgininosuccinate lyase deficiency
- rs201523601Likely pathogenicsingle nucleotide variantArgininosuccinate lyase deficiency
- rs142637046Pathogenicsingle nucleotide variantArgininosuccinate lyase deficiency
- rs145138923Pathogenicsingle nucleotide variantArgininosuccinate lyase deficiency
- rs199938613Pathogenicsingle nucleotide variantArgininosuccinate lyase deficiency
- rs28940286Pathogenicsingle nucleotide variantArgininosuccinate lyase deficiency
- rs28940287Pathogenicsingle nucleotide variantArgininosuccinate lyase deficiency
- rs28941472Pathogenicsingle nucleotide variantArgininosuccinate lyase deficiency
- rs28941473Pathogenicsingle nucleotide variantArgininosuccinate lyase deficiency
- rs367543005Pathogenicsingle nucleotide variantArgininosuccinate lyase deficiency
- rs369879957Pathogenicsingle nucleotide variantArgininosuccinate lyase deficiency
- rs367543006Not classifiedsingle nucleotide variantArgininosuccinate lyase deficiency
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.