Canonical Allele Identifier: CA2187816438

Gene: CYP1A1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74723851G= , CM000677.2:g.74723851G=	GRCh38
NC_000015.9:g.75016192G= , CM000677.1:g.75016192G=	GRCh37
NC_000015.8:g.72803245G=	NCBI36
NG_008431.1:g.6310G=
NG_008431.2:g.6310G=
NG_061374.1:g.6678C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001319217.2:c.-29-725C= MANE Select	NP_001306146.1:n.-29-725C=
ENST00000379727.8:c.-29-725C= MANE Select	ENSP00000369050.3:n.-29-725C=
NM_000499.3:c.-26-728C=	NP_000490.1:n.-26-728C=
NM_000499.5:c.-26-728C=	NP_000490.1:n.-26-728C=
NM_001319216.2:c.-29-725C=	NP_001306145.1:n.-29-725C=
ENST00000379727.7:c.-29-725C=	ENSP00000369050.3:n.-29-725C=
ENST00000395048.6:c.-26-728C=	ENSP00000378488.2:n.-26-728C=
ENST00000395049.8:c.-29-725C=	ENSP00000378489.4:n.-29-725C=
ENST00000562201.5:c.-26-728C=	ENSP00000455340.1:n.-26-728C=
ENST00000564596.5:c.-220-1317C=	ENSP00000457668.1:n.-220-1317C=
ENST00000566503.1:c.-220-1317C=	ENSP00000455846.1:n.-220-1317C=
ENST00000567032.5:c.-29-725C=	ENSP00000456585.1:n.-29-725C=
ENST00000569630.5:c.-26-728C=	ENSP00000455051.1:n.-26-728C=
ENST00000617691.4:c.-26-728C=	ENSP00000482863.1:n.-26-728C=
XM_005254185.1:c.-29-725C=	XP_005254242.1:n.-29-725C=