Canonical Allele Identifier: CA1929375528

Gene: CYP2C8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037309C= , CM000672.2:g.95037309C=	GRCh38
NC_000010.10:g.96797066C= , CM000672.1:g.96797066C=	GRCh37
NC_000010.9:g.96787056C=	NCBI36
NG_007972.1:g.37189G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1292G= MANE Select	ENSP00000360317.3:p.Gly431=
ENST00000371270.5:c.1292G=	ENSP00000360317.3:p.Gly431=
ENST00000490994.6:c.*1078G=	ENSP00000433314.1:n.*1078G=
ENST00000525991.5:c.*867G=	ENSP00000433842.1:n.*867G=
ENST00000526814.5:n.1547G=
ENST00000527420.5:c.*149G=	ENSP00000433191.1:n.*149G=
ENST00000527953.5:n.1586G=
ENST00000531714.1:n.480G=
ENST00000533320.5:n.1526G=
ENST00000535898.5:c.986G=	ENSP00000445062.1:p.Gly329=
ENST00000539050.5:c.1082G=	ENSP00000442343.2:p.Gly361=
ENST00000623108.3:c.1082G=	ENSP00000485110.1:p.Gly361=
NM_000770.3:c.1292G= MANE Select	NP_000761.3:p.Gly431=
NM_001198853.1:c.1082G=	NP_001185782.1:p.Gly361=
NM_001198854.1:c.986G=	NP_001185783.1:p.Gly329=
NM_001198855.1:c.1082G=	NP_001185784.1:p.Gly361=
XR_945610.1:n.1427G=