Canonical Allele Identifier: CA2187814540

Gene: CYP1A1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74719722A= , CM000677.2:g.74719722A=	GRCh38
NC_000015.9:g.75012063A= , CM000677.1:g.75012063A=	GRCh37
NC_000015.8:g.72799116A=	NCBI36
NG_008431.1:g.2181A=
NG_008431.2:g.2181A=
NG_061374.1:g.10807T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379727.8:c.*767T= MANE Select	ENSP00000369050.3:n.*767T=
ENST00000379727.7:c.*767T=	ENSP00000369050.3:n.*767T=
ENST00000395048.6:c.*767T=	ENSP00000378488.2:n.*767T=
ENST00000612821.4:c.2222T=	ENSP00000479744.1:n.2222T=
ENST00000617691.4:c.*767T=	ENSP00000482863.1:n.*767T=
NM_000499.3:c.*767T=	NP_000490.1:n.*767T=
XM_005254185.1:c.*767T=	XP_005254242.1:n.*767T=
NM_000499.5:c.*767T=	NP_000490.1:n.*767T=
NM_001319216.2:c.*767T=	NP_001306145.1:n.*767T=
NM_001319217.2:c.*767T= MANE Select	NP_001306146.1:n.*767T=