Canonical Allele Identifier: CA377683199

Gene: CYP2C8

Linked Data

• MyVariant Identifiers: chr10:g.96827087C>G (hg19) ; chr10:g.95067330C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95067330C>G , CM000672.2:g.95067330C>G	GRCh38
NC_000010.10:g.96827087C>G , CM000672.1:g.96827087C>G	GRCh37
NC_000010.9:g.96817077C>G	NCBI36
NG_007972.1:g.7168G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.359G>C MANE Select	ENSP00000360317.3:p.Trp120Ser
ENST00000371270.5:c.359G>C	ENSP00000360317.3:p.Trp120Ser
ENST00000479946.2:n.663G>C
ENST00000490994.6:c.*145G>C	ENSP00000433314.1:n.*145G>C
ENST00000525991.5:c.234G>C	ENSP00000433842.1:p.Met78Ile
ENST00000526814.5:n.614G>C
ENST00000527420.5:c.359G>C	ENSP00000433191.1:p.Trp120Ser
ENST00000527953.5:n.614G>C
ENST00000533320.5:n.593G>C
ENST00000535898.5:c.53G>C	ENSP00000445062.1:p.Trp18Ser
ENST00000539050.5:c.149G>C	ENSP00000442343.2:p.Trp50Ser
ENST00000623108.3:c.149G>C	ENSP00000485110.1:p.Trp50Ser
ENST00000628935.1:c.101G>C	ENSP00000487145.1:p.Trp34Ser
NM_000770.3:c.359G>C MANE Select	NP_000761.3:p.Trp120Ser
NM_001198853.1:c.149G>C	NP_001185782.1:p.Trp50Ser
NM_001198854.1:c.53G>C	NP_001185783.1:p.Trp18Ser
NM_001198855.1:c.149G>C	NP_001185784.1:p.Trp50Ser
XR_945610.1:n.455G>C