Canonical Allele Identifier: CA1929375376

Gene: CYP2C8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037239C= , CM000672.2:g.95037239C=	GRCh38
NC_000010.10:g.96796996C= , CM000672.1:g.96796996C=	GRCh37
NC_000010.9:g.96786986C=	NCBI36
NG_007972.1:g.37259G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1362G= MANE Select	ENSP00000360317.3:p.Gln454=
ENST00000371270.5:c.1362G=	ENSP00000360317.3:p.Gln454=
ENST00000490994.6:c.*1148G=	ENSP00000433314.1:n.*1148G=
ENST00000525991.5:c.*937G=	ENSP00000433842.1:n.*937G=
ENST00000526814.5:n.1617G=
ENST00000527420.5:c.*219G=	ENSP00000433191.1:n.*219G=
ENST00000527953.5:n.1656G=
ENST00000531714.1:n.550G=
ENST00000533320.5:n.1596G=
ENST00000535898.5:c.1056G=	ENSP00000445062.1:p.Gln352=
ENST00000539050.5:c.1152G=	ENSP00000442343.2:p.Gln384=
ENST00000623108.3:c.1152G=	ENSP00000485110.1:p.Gln384=
NM_000770.3:c.1362G= MANE Select	NP_000761.3:p.Gln454=
NM_001198853.1:c.1152G=	NP_001185782.1:p.Gln384=
NM_001198854.1:c.1056G=	NP_001185783.1:p.Gln352=
NM_001198855.1:c.1152G=	NP_001185784.1:p.Gln384=
XR_945610.1:n.1497G=