Canonical Allele Identifier: CA1929375151

Gene: CYP2C8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037149C= , CM000672.2:g.95037149C=	GRCh38
NC_000010.10:g.96796906C= , CM000672.1:g.96796906C=	GRCh37
NC_000010.9:g.96786896C=	NCBI36
NG_007972.1:g.37349G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1452G= MANE Select	ENSP00000360317.3:p.Gln484=
ENST00000371270.5:c.1452G=	ENSP00000360317.3:p.Gln484=
ENST00000490994.6:c.*1238G=	ENSP00000433314.1:n.*1238G=
ENST00000525991.5:c.*1027G=	ENSP00000433842.1:n.*1027G=
ENST00000526814.5:n.1707G=
ENST00000527420.5:c.*309G=	ENSP00000433191.1:n.*309G=
ENST00000527953.5:n.1746G=
ENST00000533320.5:n.1686G=
ENST00000535898.5:c.1146G=	ENSP00000445062.1:p.Gln382=
ENST00000539050.5:c.1242G=	ENSP00000442343.2:p.Gln414=
ENST00000623108.3:c.1242G=	ENSP00000485110.1:p.Gln414=
NM_000770.3:c.1452G= MANE Select	NP_000761.3:p.Gln484=
NM_001198853.1:c.1242G=	NP_001185782.1:p.Gln414=
NM_001198854.1:c.1146G=	NP_001185783.1:p.Gln382=
NM_001198855.1:c.1242G=	NP_001185784.1:p.Gln414=