Canonical Allele Identifier: CA2187816815

Gene: CYP1A1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74724752A= , CM000677.2:g.74724752A=	GRCh38
NC_000015.9:g.75017093A= , CM000677.1:g.75017093A=	GRCh37
NC_000015.8:g.72804146A=	NCBI36
NG_008431.1:g.7211A=
NG_008431.2:g.7211A=
NG_061374.1:g.5777T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379727.8:c.-30+689T= MANE Select	ENSP00000369050.3:n.-30+689T=
ENST00000379727.7:c.-30+689T=	ENSP00000369050.3:n.-30+689T=
ENST00000395048.6:c.-27+689T=	ENSP00000378488.2:n.-27+689T=
ENST00000395049.8:c.-30+689T=	ENSP00000378489.4:n.-30+689T=
ENST00000562201.5:c.-27+689T=	ENSP00000455340.1:n.-27+689T=
ENST00000564596.5:c.-221+689T=	ENSP00000457668.1:n.-221+689T=
ENST00000566503.1:c.-221+689T=	ENSP00000455846.1:n.-221+689T=
ENST00000567032.5:c.-30+413T=	ENSP00000456585.1:n.-30+413T=
ENST00000569630.5:c.-27+689T=	ENSP00000455051.1:n.-27+689T=
ENST00000617691.4:c.-27+689T=	ENSP00000482863.1:n.-27+689T=
NM_000499.3:c.-27+689T=	NP_000490.1:n.-27+689T=
XM_005254185.1:c.-30+689T=	XP_005254242.1:n.-30+689T=
NM_000499.5:c.-27+689T=	NP_000490.1:n.-27+689T=
NM_001319216.2:c.-30+689T=	NP_001306145.1:n.-30+689T=
NM_001319217.2:c.-30+689T= MANE Select	NP_001306146.1:n.-30+689T=