Canonical Allele Identifier: CA2187814770

Gene: CYP1A1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74720319A= , CM000677.2:g.74720319A=	GRCh38
NC_000015.9:g.75012660A= , CM000677.1:g.75012660A=	GRCh37
NC_000015.8:g.72799713A=	NCBI36
NG_008431.1:g.2778A=
NG_008431.2:g.2778A=
NG_061374.1:g.10210T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379727.8:c.*170T= MANE Select	ENSP00000369050.3:n.*170T=
ENST00000379727.7:c.*170T=	ENSP00000369050.3:n.*170T=
ENST00000395048.6:c.*170T=	ENSP00000378488.2:n.*170T=
ENST00000567032.5:c.*170T=	ENSP00000456585.1:n.*170T=
ENST00000612821.4:c.1625T=	ENSP00000479744.1:n.1625T=
ENST00000617691.4:c.*170T=	ENSP00000482863.1:n.*170T=
NM_000499.3:c.*170T=	NP_000490.1:n.*170T=
XM_005254185.1:c.*170T=	XP_005254242.1:n.*170T=
NM_000499.5:c.*170T=	NP_000490.1:n.*170T=
NM_001319216.2:c.*170T=	NP_001306145.1:n.*170T=
NM_001319217.2:c.*170T= MANE Select	NP_001306146.1:n.*170T=