Canonical Allele Identifier: CA1929388234

Gene: CYP2C8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95067257A= , CM000672.2:g.95067257A=	GRCh38
NC_000010.10:g.96827014A= , CM000672.1:g.96827014A=	GRCh37
NC_000010.9:g.96817004A=	NCBI36
NG_007972.1:g.7241T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.432T= MANE Select	ENSP00000360317.3:p.Arg144=
ENST00000371270.5:c.432T=	ENSP00000360317.3:p.Arg144=
ENST00000479946.2:n.736T=
ENST00000490994.6:c.*218T=	ENSP00000433314.1:n.*218T=
ENST00000525991.5:c.*7T=	ENSP00000433842.1:n.*7T=
ENST00000526814.5:n.687T=
ENST00000527420.5:c.432T=	ENSP00000433191.1:p.Arg144=
ENST00000527953.5:n.687T=
ENST00000533320.5:n.666T=
ENST00000535898.5:c.126T=	ENSP00000445062.1:p.Arg42=
ENST00000539050.5:c.222T=	ENSP00000442343.2:p.Arg74=
ENST00000623108.3:c.222T=	ENSP00000485110.1:p.Arg74=
ENST00000628935.1:c.174T=	ENSP00000487145.1:p.Arg58=
NM_000770.3:c.432T= MANE Select	NP_000761.3:p.Arg144=
NM_001198853.1:c.222T=	NP_001185782.1:p.Arg74=
NM_001198854.1:c.126T=	NP_001185783.1:p.Arg42=
NM_001198855.1:c.222T=	NP_001185784.1:p.Arg74=
XR_945610.1:n.528T=