Canonical Allele Identifier: CA1929375431

Gene: CYP2C8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037268G= , CM000672.2:g.95037268G=	GRCh38
NC_000010.10:g.96797025G= , CM000672.1:g.96797025G=	GRCh37
NC_000010.9:g.96787015G=	NCBI36
NG_007972.1:g.37230C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1333C= MANE Select	ENSP00000360317.3:p.Leu445=
ENST00000371270.5:c.1333C=	ENSP00000360317.3:p.Leu445=
ENST00000490994.6:c.*1119C=	ENSP00000433314.1:n.*1119C=
ENST00000525991.5:c.*908C=	ENSP00000433842.1:n.*908C=
ENST00000526814.5:n.1588C=
ENST00000527420.5:c.*190C=	ENSP00000433191.1:n.*190C=
ENST00000527953.5:n.1627C=
ENST00000531714.1:n.521C=
ENST00000533320.5:n.1567C=
ENST00000535898.5:c.1027C=	ENSP00000445062.1:p.Leu343=
ENST00000539050.5:c.1123C=	ENSP00000442343.2:p.Leu375=
ENST00000623108.3:c.1123C=	ENSP00000485110.1:p.Leu375=
NM_000770.3:c.1333C= MANE Select	NP_000761.3:p.Leu445=
NM_001198853.1:c.1123C=	NP_001185782.1:p.Leu375=
NM_001198854.1:c.1027C=	NP_001185783.1:p.Leu343=
NM_001198855.1:c.1123C=	NP_001185784.1:p.Leu375=
XR_945610.1:n.1468C=