Canonical Allele Identifier: CA1929375189

Gene: CYP2C8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037161T= , CM000672.2:g.95037161T=	GRCh38
NC_000010.10:g.96796918T= , CM000672.1:g.96796918T=	GRCh37
NC_000010.9:g.96786908T=	NCBI36
NG_007972.1:g.37337A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1440A= MANE Select	ENSP00000360317.3:p.Pro480=
ENST00000371270.5:c.1440A=	ENSP00000360317.3:p.Pro480=
ENST00000490994.6:c.*1226A=	ENSP00000433314.1:n.*1226A=
ENST00000525991.5:c.*1015A=	ENSP00000433842.1:n.*1015A=
ENST00000526814.5:n.1695A=
ENST00000527420.5:c.*297A=	ENSP00000433191.1:n.*297A=
ENST00000527953.5:n.1734A=
ENST00000533320.5:n.1674A=
ENST00000535898.5:c.1134A=	ENSP00000445062.1:p.Pro378=
ENST00000539050.5:c.1230A=	ENSP00000442343.2:p.Pro410=
ENST00000623108.3:c.1230A=	ENSP00000485110.1:p.Pro410=
NM_000770.3:c.1440A= MANE Select	NP_000761.3:p.Pro480=
NM_001198853.1:c.1230A=	NP_001185782.1:p.Pro410=
NM_001198854.1:c.1134A=	NP_001185783.1:p.Pro378=
NM_001198855.1:c.1230A=	NP_001185784.1:p.Pro410=