Canonical Allele Identifier: CA377682893

Gene: CYP2C8

Linked Data

• MyVariant Identifiers: chr10:g.96827020C>G (hg19) ; chr10:g.95067263C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95067263C>G , CM000672.2:g.95067263C>G	GRCh38
NC_000010.10:g.96827020C>G , CM000672.1:g.96827020C>G	GRCh37
NC_000010.9:g.96817010C>G	NCBI36
NG_007972.1:g.7235G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.426G>C MANE Select	ENSP00000360317.3:p.Glu142Asp
ENST00000371270.5:c.426G>C	ENSP00000360317.3:p.Glu142Asp
ENST00000479946.2:n.730G>C
ENST00000490994.6:c.*212G>C	ENSP00000433314.1:n.*212G>C
ENST00000525991.5:c.*1G>C	ENSP00000433842.1:n.*1G>C
ENST00000526814.5:n.681G>C
ENST00000527420.5:c.426G>C	ENSP00000433191.1:p.Glu142Asp
ENST00000527953.5:n.681G>C
ENST00000533320.5:n.660G>C
ENST00000535898.5:c.120G>C	ENSP00000445062.1:p.Glu40Asp
ENST00000539050.5:c.216G>C	ENSP00000442343.2:p.Glu72Asp
ENST00000623108.3:c.216G>C	ENSP00000485110.1:p.Glu72Asp
ENST00000628935.1:c.168G>C	ENSP00000487145.1:p.Glu56Asp
NM_000770.3:c.426G>C MANE Select	NP_000761.3:p.Glu142Asp
NM_001198853.1:c.216G>C	NP_001185782.1:p.Glu72Asp
NM_001198854.1:c.120G>C	NP_001185783.1:p.Glu40Asp
NM_001198855.1:c.216G>C	NP_001185784.1:p.Glu72Asp
XR_945610.1:n.522G>C