Canonical Allele Identifier: CA1929375247

Gene: CYP2C8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037184T= , CM000672.2:g.95037184T=	GRCh38
NC_000010.10:g.96796941T= , CM000672.1:g.96796941T=	GRCh37
NC_000010.9:g.96786931T=	NCBI36
NG_007972.1:g.37314A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1417A= MANE Select	ENSP00000360317.3:p.Thr473=
ENST00000371270.5:c.1417A=	ENSP00000360317.3:p.Thr473=
ENST00000490994.6:c.*1203A=	ENSP00000433314.1:n.*1203A=
ENST00000525991.5:c.*992A=	ENSP00000433842.1:n.*992A=
ENST00000526814.5:n.1672A=
ENST00000527420.5:c.*274A=	ENSP00000433191.1:n.*274A=
ENST00000527953.5:n.1711A=
ENST00000531714.1:n.605A=
ENST00000533320.5:n.1651A=
ENST00000535898.5:c.1111A=	ENSP00000445062.1:p.Thr371=
ENST00000539050.5:c.1207A=	ENSP00000442343.2:p.Thr403=
ENST00000623108.3:c.1207A=	ENSP00000485110.1:p.Thr403=
NM_000770.3:c.1417A= MANE Select	NP_000761.3:p.Thr473=
NM_001198853.1:c.1207A=	NP_001185782.1:p.Thr403=
NM_001198854.1:c.1111A=	NP_001185783.1:p.Thr371=
NM_001198855.1:c.1207A=	NP_001185784.1:p.Thr403=
XR_945610.1:n.1552A=