Canonical Allele Identifier: CA2187814987

Gene: CYP1A1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74720762G= , CM000677.2:g.74720762G=	GRCh38
NC_000015.9:g.75013103G= , CM000677.1:g.75013103G=	GRCh37
NC_000015.8:g.72800156G=	NCBI36
NG_008431.1:g.3221G=
NG_008431.2:g.3221G=
NG_061374.1:g.9767C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379727.8:c.1266C= MANE Select	ENSP00000369050.3:p.Val422=
ENST00000379727.7:c.1266C=	ENSP00000369050.3:p.Val422=
ENST00000395048.6:c.1266C=	ENSP00000378488.2:p.Val422=
ENST00000395049.8:c.1179C=	ENSP00000378489.4:p.Val393=
ENST00000562201.5:c.*503C=	ENSP00000455340.1:n.*503C=
ENST00000564596.5:c.*201C=	ENSP00000457668.1:n.*201C=
ENST00000566503.1:c.483C=	ENSP00000455846.1:p.Val161=
ENST00000567032.5:c.1266C=	ENSP00000456585.1:p.Val422=
ENST00000569630.5:c.*855C=	ENSP00000455051.1:n.*855C=
ENST00000612821.4:c.1182C=	ENSP00000479744.1:p.Val394=
ENST00000617691.4:c.1179C=	ENSP00000482863.1:p.Val393=
NM_000499.3:c.1266C=	NP_000490.1:p.Val422=
XM_005254185.1:c.1266C=	XP_005254242.1:p.Val422=
NM_000499.5:c.1266C=	NP_000490.1:p.Val422=
NM_001319216.2:c.1179C=	NP_001306145.1:p.Val393=
NM_001319217.2:c.1266C= MANE Select	NP_001306146.1:p.Val422=