Canonical Allele Identifier: CA2187814522

Gene: CYP1A1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74719674T= , CM000677.2:g.74719674T=	GRCh38
NC_000015.9:g.75012015T= , CM000677.1:g.75012015T=	GRCh37
NC_000015.8:g.72799068T=	NCBI36
NG_008431.1:g.2133T=
NG_008431.2:g.2133T=
NG_061374.1:g.10855A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379727.8:c.*815A= MANE Select	ENSP00000369050.3:n.*815A=
ENST00000379727.7:c.*815A=	ENSP00000369050.3:n.*815A=
ENST00000395048.6:c.*815A=	ENSP00000378488.2:n.*815A=
ENST00000612821.4:c.2270A=	ENSP00000479744.1:n.2270A=
ENST00000617691.4:c.*815A=	ENSP00000482863.1:n.*815A=
NM_000499.3:c.*815A=	NP_000490.1:n.*815A=
XM_005254185.1:c.*815A=	XP_005254242.1:n.*815A=
NM_000499.5:c.*815A=	NP_000490.1:n.*815A=
NM_001319216.2:c.*815A=	NP_001306145.1:n.*815A=
NM_001319217.2:c.*815A= MANE Select	NP_001306146.1:n.*815A=