Canonical Allele Identifier: CA2187816854

Gene: CYP1A1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74724874A= , CM000677.2:g.74724874A=	GRCh38
NC_000015.9:g.75017215A= , CM000677.1:g.75017215A=	GRCh37
NC_000015.8:g.72804268A=	NCBI36
NG_008431.1:g.7333A=
NG_008431.2:g.7333A=
NG_061374.1:g.5655T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000379727.8:c.-30+567T= MANE Select	ENSP00000369050.3:n.-30+567T=
ENST00000379727.7:c.-30+567T=	ENSP00000369050.3:n.-30+567T=
ENST00000395048.6:c.-27+567T=	ENSP00000378488.2:n.-27+567T=
ENST00000395049.8:c.-30+567T=	ENSP00000378489.4:n.-30+567T=
ENST00000562201.5:c.-27+567T=	ENSP00000455340.1:n.-27+567T=
ENST00000564596.5:c.-221+567T=	ENSP00000457668.1:n.-221+567T=
ENST00000566503.1:c.-221+567T=	ENSP00000455846.1:n.-221+567T=
ENST00000567032.5:c.-30+291T=	ENSP00000456585.1:n.-30+291T=
ENST00000569630.5:c.-27+567T=	ENSP00000455051.1:n.-27+567T=
ENST00000617691.4:c.-27+567T=	ENSP00000482863.1:n.-27+567T=
NM_000499.3:c.-27+567T=	NP_000490.1:n.-27+567T=
XM_005254185.1:c.-30+567T=	XP_005254242.1:n.-30+567T=
NM_000499.5:c.-27+567T=	NP_000490.1:n.-27+567T=
NM_001319216.2:c.-30+567T=	NP_001306145.1:n.-30+567T=
NM_001319217.2:c.-30+567T= MANE Select	NP_001306146.1:n.-30+567T=