Canonical Allele Identifier: CA2187814622

Gene: CYP1A1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74719894A= , CM000677.2:g.74719894A=	GRCh38
NC_000015.9:g.75012235A= , CM000677.1:g.75012235A=	GRCh37
NC_000015.8:g.72799288A=	NCBI36
NG_008431.1:g.2353A=
NG_008431.2:g.2353A=
NG_061374.1:g.10635T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000379727.8:c.*595T= MANE Select	ENSP00000369050.3:n.*595T=
ENST00000379727.7:c.*595T=	ENSP00000369050.3:n.*595T=
ENST00000395048.6:c.*595T=	ENSP00000378488.2:n.*595T=
ENST00000612821.4:c.2050T=	ENSP00000479744.1:n.2050T=
ENST00000617691.4:c.*595T=	ENSP00000482863.1:n.*595T=
NM_000499.3:c.*595T=	NP_000490.1:n.*595T=
XM_005254185.1:c.*595T=	XP_005254242.1:n.*595T=
NM_000499.5:c.*595T=	NP_000490.1:n.*595T=
NM_001319216.2:c.*595T=	NP_001306145.1:n.*595T=
NM_001319217.2:c.*595T= MANE Select	NP_001306146.1:n.*595T=