Canonical Allele Identifier: CA2187814969

Gene: CYP1A1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74720721T= , CM000677.2:g.74720721T=	GRCh38
NC_000015.9:g.75013062T= , CM000677.1:g.75013062T=	GRCh37
NC_000015.8:g.72800115T=	NCBI36
NG_008431.1:g.3180T=
NG_008431.2:g.3180T=
NG_061374.1:g.9808A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379727.8:c.1307A= MANE Select	ENSP00000369050.3:p.Asp436=
ENST00000379727.7:c.1307A=	ENSP00000369050.3:p.Asp436=
ENST00000395048.6:c.1307A=	ENSP00000378488.2:p.Asp436=
ENST00000395049.8:c.1220A=	ENSP00000378489.4:p.Asp407=
ENST00000562201.5:c.*544A=	ENSP00000455340.1:n.*544A=
ENST00000564596.5:c.*242A=	ENSP00000457668.1:n.*242A=
ENST00000566503.1:c.524A=	ENSP00000455846.1:p.Asp175=
ENST00000567032.5:c.1307A=	ENSP00000456585.1:p.Asp436=
ENST00000569630.5:c.*896A=	ENSP00000455051.1:n.*896A=
ENST00000612821.4:c.1223A=	ENSP00000479744.1:p.Asp408=
ENST00000617691.4:c.1220A=	ENSP00000482863.1:p.Asp407=
NM_000499.3:c.1307A=	NP_000490.1:p.Asp436=
XM_005254185.1:c.1307A=	XP_005254242.1:p.Asp436=
NM_000499.5:c.1307A=	NP_000490.1:p.Asp436=
NM_001319216.2:c.1220A=	NP_001306145.1:p.Asp407=
NM_001319217.2:c.1307A= MANE Select	NP_001306146.1:p.Asp436=