Canonical Allele Identifier: CA1929375481

Gene: CYP2C8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037295C= , CM000672.2:g.95037295C=	GRCh38
NC_000010.10:g.96797052C= , CM000672.1:g.96797052C=	GRCh37
NC_000010.9:g.96787042C=	NCBI36
NG_007972.1:g.37203G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1306G= MANE Select	ENSP00000360317.3:p.Ala436=
ENST00000371270.5:c.1306G=	ENSP00000360317.3:p.Ala436=
ENST00000490994.6:c.*1092G=	ENSP00000433314.1:n.*1092G=
ENST00000525991.5:c.*881G=	ENSP00000433842.1:n.*881G=
ENST00000526814.5:n.1561G=
ENST00000527420.5:c.*163G=	ENSP00000433191.1:n.*163G=
ENST00000527953.5:n.1600G=
ENST00000531714.1:n.494G=
ENST00000533320.5:n.1540G=
ENST00000535898.5:c.1000G=	ENSP00000445062.1:p.Ala334=
ENST00000539050.5:c.1096G=	ENSP00000442343.2:p.Ala366=
ENST00000623108.3:c.1096G=	ENSP00000485110.1:p.Ala366=
NM_000770.3:c.1306G= MANE Select	NP_000761.3:p.Ala436=
NM_001198853.1:c.1096G=	NP_001185782.1:p.Ala366=
NM_001198854.1:c.1000G=	NP_001185783.1:p.Ala334=
NM_001198855.1:c.1096G=	NP_001185784.1:p.Ala366=
XR_945610.1:n.1441G=