Canonical Allele Identifier: CA470843727

Gene: CYP2C8

Linked Data

• MyVariant Identifiers: chr10:g.96827062G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95067305G>T , CM000672.2:g.95067305G>T	GRCh38
NC_000010.10:g.96827062G>T , CM000672.1:g.96827062G>T	GRCh37
NC_000010.9:g.96817052G>T	NCBI36
NG_007972.1:g.7193C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.384C>A MANE Select	ENSP00000360317.3:p.Leu128=
ENST00000371270.5:c.384C>A	ENSP00000360317.3:p.Leu128=
ENST00000479946.2:n.688C>A
ENST00000490994.6:c.*170C>A	ENSP00000433314.1:n.*170C>A
ENST00000525991.5:c.259C>A	ENSP00000433842.1:p.His87Asn
ENST00000526814.5:n.639C>A
ENST00000527420.5:c.384C>A	ENSP00000433191.1:p.Leu128=
ENST00000527953.5:n.639C>A
ENST00000533320.5:n.618C>A
ENST00000535898.5:c.78C>A	ENSP00000445062.1:p.Leu26=
ENST00000539050.5:c.174C>A	ENSP00000442343.2:p.Leu58=
ENST00000623108.3:c.174C>A	ENSP00000485110.1:p.Leu58=
ENST00000628935.1:c.126C>A	ENSP00000487145.1:p.Leu42=
NM_000770.3:c.384C>A MANE Select	NP_000761.3:p.Leu128=
NM_001198853.1:c.174C>A	NP_001185782.1:p.Leu58=
NM_001198854.1:c.78C>A	NP_001185783.1:p.Leu26=
NM_001198855.1:c.174C>A	NP_001185784.1:p.Leu58=
XR_945610.1:n.480C>A