Canonical Allele Identifier: CA1929375113

Gene: CYP2C8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037135G= , CM000672.2:g.95037135G=	GRCh38
NC_000010.10:g.96796892G= , CM000672.1:g.96796892G=	GRCh37
NC_000010.9:g.96786882G=	NCBI36
NG_007972.1:g.37363C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1466C= MANE Select	ENSP00000360317.3:p.Pro489=
ENST00000371270.5:c.1466C=	ENSP00000360317.3:p.Pro489=
ENST00000490994.6:c.*1252C=	ENSP00000433314.1:n.*1252C=
ENST00000525991.5:c.*1041C=	ENSP00000433842.1:n.*1041C=
ENST00000526814.5:n.1721C=
ENST00000527420.5:c.*323C=	ENSP00000433191.1:n.*323C=
ENST00000527953.5:n.1760C=
ENST00000533320.5:n.1700C=
ENST00000535898.5:c.1160C=	ENSP00000445062.1:p.Pro387=
ENST00000539050.5:c.1256C=	ENSP00000442343.2:p.Pro419=
ENST00000623108.3:c.1256C=	ENSP00000485110.1:p.Pro419=
NM_000770.3:c.1466C= MANE Select	NP_000761.3:p.Pro489=
NM_001198853.1:c.1256C=	NP_001185782.1:p.Pro419=
NM_001198854.1:c.1160C=	NP_001185783.1:p.Pro387=
NM_001198855.1:c.1256C=	NP_001185784.1:p.Pro419=