Canonical Allele Identifier: CA2629509226
Gene: CYP1A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74751834_74751845del , CM000677.2:g.74751834_74751845del GRCh38
NC_000015.9:g.75044175_75044186del , CM000677.1:g.75044175_75044186del GRCh37
NC_000015.8:g.72831228_72831239del NCBI36
NG_008431.1:g.34293_34304del
NG_008431.2:g.34293_34304del
NG_061543.1:g.7990_8001del

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.1022_1033del MANE Select ENSP00000342007.4:p.Arg341_Gln344del
ENST00000343932.4:c.1022_1033del ENSP00000342007.4:p.Arg341_Gln344del
NM_000761.4:c.1022_1033del NP_000752.2:p.Arg341_Gln344del
NM_000761.5:c.1022_1033del MANE Select NP_000752.2:p.Arg341_Gln344del