Canonical Allele Identifier: CA1929375217

Gene: CYP2C8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037174A= , CM000672.2:g.95037174A=	GRCh38
NC_000010.10:g.96796931A= , CM000672.1:g.96796931A=	GRCh37
NC_000010.9:g.96786921A=	NCBI36
NG_007972.1:g.37324T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1427T= MANE Select	ENSP00000360317.3:p.Ile476=
ENST00000371270.5:c.1427T=	ENSP00000360317.3:p.Ile476=
ENST00000490994.6:c.*1213T=	ENSP00000433314.1:n.*1213T=
ENST00000525991.5:c.*1002T=	ENSP00000433842.1:n.*1002T=
ENST00000526814.5:n.1682T=
ENST00000527420.5:c.*284T=	ENSP00000433191.1:n.*284T=
ENST00000527953.5:n.1721T=
ENST00000533320.5:n.1661T=
ENST00000535898.5:c.1121T=	ENSP00000445062.1:p.Ile374=
ENST00000539050.5:c.1217T=	ENSP00000442343.2:p.Ile406=
ENST00000623108.3:c.1217T=	ENSP00000485110.1:p.Ile406=
NM_000770.3:c.1427T= MANE Select	NP_000761.3:p.Ile476=
NM_001198853.1:c.1217T=	NP_001185782.1:p.Ile406=
NM_001198854.1:c.1121T=	NP_001185783.1:p.Ile374=
NM_001198855.1:c.1217T=	NP_001185784.1:p.Ile406=
XR_945610.1:n.1562T=