Canonical Allele Identifier: CA2187827313
Gene: CYP1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755361_74755362delinsAC , CM000677.2:g.74755361_74755362delinsAC GRCh38
NC_000015.9:g.75047702_75047703delinsAC , CM000677.1:g.75047702_75047703delinsAC GRCh37
NC_000015.8:g.72834755_72834756delinsAC NCBI36
NG_008431.1:g.37820_37821delinsAC
NG_008431.2:g.37820_37821delinsAC
NG_061543.1:g.11517_11518delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.*273_*274delinsAC MANE Select ENSP00000342007.4:n.*273_*274delinsAC
ENST00000343932.4:c.*273_*274delinsAC ENSP00000342007.4:n.*273_*274delinsAC
NM_000761.4:c.*273_*274delinsAC NP_000752.2:n.*273_*274delinsAC
NM_000761.5:c.*273_*274delinsAC MANE Select NP_000752.2:n.*273_*274delinsAC