Canonical Allele Identifier: CA2629512232
Gene: CYP1A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755025dup , CM000677.2:g.74755025dup GRCh38
NC_000015.9:g.75047366dup , CM000677.1:g.75047366dup GRCh37
NC_000015.8:g.72834419dup NCBI36
NG_008431.1:g.37484dup
NG_008431.2:g.37484dup
NG_061543.1:g.11181dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.1488dup MANE Select ENSP00000342007.4:p.Leu497AlafsTer9
ENST00000343932.4:c.1488dup ENSP00000342007.4:p.Leu497AlafsTer9
NM_000761.4:c.1488dup NP_000752.2:p.Leu497AlafsTer9
NM_000761.5:c.1488dup MANE Select NP_000752.2:p.Leu497AlafsTer9