Canonical Allele Identifier: CA1929375118

Gene: CYP2C8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037137G= , CM000672.2:g.95037137G=	GRCh38
NC_000010.10:g.96796894G= , CM000672.1:g.96796894G=	GRCh37
NC_000010.9:g.96786884G=	NCBI36
NG_007972.1:g.37361C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1464C= MANE Select	ENSP00000360317.3:p.Ile488=
ENST00000371270.5:c.1464C=	ENSP00000360317.3:p.Ile488=
ENST00000490994.6:c.*1250C=	ENSP00000433314.1:n.*1250C=
ENST00000525991.5:c.*1039C=	ENSP00000433842.1:n.*1039C=
ENST00000526814.5:n.1719C=
ENST00000527420.5:c.*321C=	ENSP00000433191.1:n.*321C=
ENST00000527953.5:n.1758C=
ENST00000533320.5:n.1698C=
ENST00000535898.5:c.1158C=	ENSP00000445062.1:p.Ile386=
ENST00000539050.5:c.1254C=	ENSP00000442343.2:p.Ile418=
ENST00000623108.3:c.1254C=	ENSP00000485110.1:p.Ile418=
NM_000770.3:c.1464C= MANE Select	NP_000761.3:p.Ile488=
NM_001198853.1:c.1254C=	NP_001185782.1:p.Ile418=
NM_001198854.1:c.1158C=	NP_001185783.1:p.Ile386=
NM_001198855.1:c.1254C=	NP_001185784.1:p.Ile418=