Canonical Allele Identifier: CA2187814532

Gene: CYP1A1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74719700T= , CM000677.2:g.74719700T=	GRCh38
NC_000015.9:g.75012041T= , CM000677.1:g.75012041T=	GRCh37
NC_000015.8:g.72799094T=	NCBI36
NG_008431.1:g.2159T=
NG_008431.2:g.2159T=
NG_061374.1:g.10829A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379727.8:c.*789A= MANE Select	ENSP00000369050.3:n.*789A=
ENST00000379727.7:c.*789A=	ENSP00000369050.3:n.*789A=
ENST00000395048.6:c.*789A=	ENSP00000378488.2:n.*789A=
ENST00000612821.4:c.2244A=	ENSP00000479744.1:n.2244A=
ENST00000617691.4:c.*789A=	ENSP00000482863.1:n.*789A=
NM_000499.3:c.*789A=	NP_000490.1:n.*789A=
XM_005254185.1:c.*789A=	XP_005254242.1:n.*789A=
NM_000499.5:c.*789A=	NP_000490.1:n.*789A=
NM_001319216.2:c.*789A=	NP_001306145.1:n.*789A=
NM_001319217.2:c.*789A= MANE Select	NP_001306146.1:n.*789A=