Canonical Allele Identifier: CA377682906

Gene: CYP2C8

Linked Data

• MyVariant Identifiers: chr10:g.96827021T>C (hg19) ; chr10:g.95067264T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95067264T>C , CM000672.2:g.95067264T>C	GRCh38
NC_000010.10:g.96827021T>C , CM000672.1:g.96827021T>C	GRCh37
NC_000010.9:g.96817011T>C	NCBI36
NG_007972.1:g.7234A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.425A>G MANE Select	ENSP00000360317.3:p.Glu142Gly
ENST00000371270.5:c.425A>G	ENSP00000360317.3:p.Glu142Gly
ENST00000479946.2:n.729A>G
ENST00000490994.6:c.*211A>G	ENSP00000433314.1:n.*211A>G
ENST00000525991.5:c.300A>G	ENSP00000433842.1:p.Ter100Trp
ENST00000526814.5:n.680A>G
ENST00000527420.5:c.425A>G	ENSP00000433191.1:p.Glu142Gly
ENST00000527953.5:n.680A>G
ENST00000533320.5:n.659A>G
ENST00000535898.5:c.119A>G	ENSP00000445062.1:p.Glu40Gly
ENST00000539050.5:c.215A>G	ENSP00000442343.2:p.Glu72Gly
ENST00000623108.3:c.215A>G	ENSP00000485110.1:p.Glu72Gly
ENST00000628935.1:c.167A>G	ENSP00000487145.1:p.Glu56Gly
NM_000770.3:c.425A>G MANE Select	NP_000761.3:p.Glu142Gly
NM_001198853.1:c.215A>G	NP_001185782.1:p.Glu72Gly
NM_001198854.1:c.119A>G	NP_001185783.1:p.Glu40Gly
NM_001198855.1:c.215A>G	NP_001185784.1:p.Glu72Gly
XR_945610.1:n.521A>G