Canonical Allele Identifier: CA2187814980

Gene: CYP1A1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74720747G= , CM000677.2:g.74720747G=	GRCh38
NC_000015.9:g.75013088G= , CM000677.1:g.75013088G=	GRCh37
NC_000015.8:g.72800141G=	NCBI36
NG_008431.1:g.3206G=
NG_008431.2:g.3206G=
NG_061374.1:g.9782C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379727.8:c.1281C= MANE Select	ENSP00000369050.3:p.Phe427=
ENST00000379727.7:c.1281C=	ENSP00000369050.3:p.Phe427=
ENST00000395048.6:c.1281C=	ENSP00000378488.2:p.Phe427=
ENST00000395049.8:c.1194C=	ENSP00000378489.4:p.Phe398=
ENST00000562201.5:c.*518C=	ENSP00000455340.1:n.*518C=
ENST00000564596.5:c.*216C=	ENSP00000457668.1:n.*216C=
ENST00000566503.1:c.498C=	ENSP00000455846.1:p.Phe166=
ENST00000567032.5:c.1281C=	ENSP00000456585.1:p.Phe427=
ENST00000569630.5:c.*870C=	ENSP00000455051.1:n.*870C=
ENST00000612821.4:c.1197C=	ENSP00000479744.1:p.Phe399=
ENST00000617691.4:c.1194C=	ENSP00000482863.1:p.Phe398=
NM_000499.3:c.1281C=	NP_000490.1:p.Phe427=
XM_005254185.1:c.1281C=	XP_005254242.1:p.Phe427=
NM_000499.5:c.1281C=	NP_000490.1:p.Phe427=
NM_001319216.2:c.1194C=	NP_001306145.1:p.Phe398=
NM_001319217.2:c.1281C= MANE Select	NP_001306146.1:p.Phe427=