Canonical Allele Identifier: CA1929388283

Gene: CYP2C8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95067281C= , CM000672.2:g.95067281C=	GRCh38
NC_000010.10:g.96827038C= , CM000672.1:g.96827038C=	GRCh37
NC_000010.9:g.96817028C=	NCBI36
NG_007972.1:g.7217G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.408G= MANE Select	ENSP00000360317.3:p.Met136=
ENST00000371270.5:c.408G=	ENSP00000360317.3:p.Met136=
ENST00000479946.2:n.712G=
ENST00000490994.6:c.*194G=	ENSP00000433314.1:n.*194G=
ENST00000525991.5:c.283G=	ENSP00000433842.1:p.Gly95=
ENST00000526814.5:n.663G=
ENST00000527420.5:c.408G=	ENSP00000433191.1:p.Met136=
ENST00000527953.5:n.663G=
ENST00000533320.5:n.642G=
ENST00000535898.5:c.102G=	ENSP00000445062.1:p.Met34=
ENST00000539050.5:c.198G=	ENSP00000442343.2:p.Met66=
ENST00000623108.3:c.198G=	ENSP00000485110.1:p.Met66=
ENST00000628935.1:c.150G=	ENSP00000487145.1:p.Met50=
NM_000770.3:c.408G= MANE Select	NP_000761.3:p.Met136=
NM_001198853.1:c.198G=	NP_001185782.1:p.Met66=
NM_001198854.1:c.102G=	NP_001185783.1:p.Met34=
NM_001198855.1:c.198G=	NP_001185784.1:p.Met66=
XR_945610.1:n.504G=