Canonical Allele Identifier: CA1929375141

Gene: CYP2C8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037147A= , CM000672.2:g.95037147A=	GRCh38
NC_000010.10:g.96796904A= , CM000672.1:g.96796904A=	GRCh37
NC_000010.9:g.96786894A=	NCBI36
NG_007972.1:g.37351T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1454T= MANE Select	ENSP00000360317.3:p.Ile485=
ENST00000371270.5:c.1454T=	ENSP00000360317.3:p.Ile485=
ENST00000490994.6:c.*1240T=	ENSP00000433314.1:n.*1240T=
ENST00000525991.5:c.*1029T=	ENSP00000433842.1:n.*1029T=
ENST00000526814.5:n.1709T=
ENST00000527420.5:c.*311T=	ENSP00000433191.1:n.*311T=
ENST00000527953.5:n.1748T=
ENST00000533320.5:n.1688T=
ENST00000535898.5:c.1148T=	ENSP00000445062.1:p.Ile383=
ENST00000539050.5:c.1244T=	ENSP00000442343.2:p.Ile415=
ENST00000623108.3:c.1244T=	ENSP00000485110.1:p.Ile415=
NM_000770.3:c.1454T= MANE Select	NP_000761.3:p.Ile485=
NM_001198853.1:c.1244T=	NP_001185782.1:p.Ile415=
NM_001198854.1:c.1148T=	NP_001185783.1:p.Ile383=
NM_001198855.1:c.1244T=	NP_001185784.1:p.Ile415=