Canonical Allele Identifier: CA1929375434

Gene: CYP2C8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037269C= , CM000672.2:g.95037269C=	GRCh38
NC_000010.10:g.96797026C= , CM000672.1:g.96797026C=	GRCh37
NC_000010.9:g.96787016C=	NCBI36
NG_007972.1:g.37229G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1332G= MANE Select	ENSP00000360317.3:p.Glu444=
ENST00000371270.5:c.1332G=	ENSP00000360317.3:p.Glu444=
ENST00000490994.6:c.*1118G=	ENSP00000433314.1:n.*1118G=
ENST00000525991.5:c.*907G=	ENSP00000433842.1:n.*907G=
ENST00000526814.5:n.1587G=
ENST00000527420.5:c.*189G=	ENSP00000433191.1:n.*189G=
ENST00000527953.5:n.1626G=
ENST00000531714.1:n.520G=
ENST00000533320.5:n.1566G=
ENST00000535898.5:c.1026G=	ENSP00000445062.1:p.Glu342=
ENST00000539050.5:c.1122G=	ENSP00000442343.2:p.Glu374=
ENST00000623108.3:c.1122G=	ENSP00000485110.1:p.Glu374=
NM_000770.3:c.1332G= MANE Select	NP_000761.3:p.Glu444=
NM_001198853.1:c.1122G=	NP_001185782.1:p.Glu374=
NM_001198854.1:c.1026G=	NP_001185783.1:p.Glu342=
NM_001198855.1:c.1122G=	NP_001185784.1:p.Glu374=
XR_945610.1:n.1467G=