Canonical Allele Identifier: CA2187827293

Gene: CYP1A2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74755349_74755350delinsTC , CM000677.2:g.74755349_74755350delinsTC	GRCh38
NC_000015.9:g.75047690_75047691delinsTC , CM000677.1:g.75047690_75047691delinsTC	GRCh37
NC_000015.8:g.72834743_72834744delinsTC	NCBI36
NG_008431.1:g.37808_37809delinsTC
NG_008431.2:g.37808_37809delinsTC
NG_061543.1:g.11505_11506delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343932.5:c.*261_*262delinsTC MANE Select	ENSP00000342007.4:n.*261_*262delinsTC
ENST00000343932.4:c.*261_*262delinsTC	ENSP00000342007.4:n.*261_*262delinsTC
NM_000761.4:c.*261_*262delinsTC	NP_000752.2:n.*261_*262delinsTC
NM_000761.5:c.*261_*262delinsTC MANE Select	NP_000752.2:n.*261_*262delinsTC