Canonical Allele Identifier: CA470843708

Gene: CYP2C8

Linked Data

• MyVariant Identifiers: chr10:g.96827032C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95067275C>T , CM000672.2:g.95067275C>T	GRCh38
NC_000010.10:g.96827032C>T , CM000672.1:g.96827032C>T	GRCh37
NC_000010.9:g.96817022C>T	NCBI36
NG_007972.1:g.7223G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000371270.6:c.414G>A MANE Select	ENSP00000360317.3:p.Lys138=
ENST00000371270.5:c.414G>A	ENSP00000360317.3:p.Lys138=
ENST00000479946.2:n.718G>A
ENST00000490994.6:c.*200G>A	ENSP00000433314.1:n.*200G>A
ENST00000525991.5:c.289G>A	ENSP00000433842.1:p.Glu97Lys
ENST00000526814.5:n.669G>A
ENST00000527420.5:c.414G>A	ENSP00000433191.1:p.Lys138=
ENST00000527953.5:n.669G>A
ENST00000533320.5:n.648G>A
ENST00000535898.5:c.108G>A	ENSP00000445062.1:p.Lys36=
ENST00000539050.5:c.204G>A	ENSP00000442343.2:p.Lys68=
ENST00000623108.3:c.204G>A	ENSP00000485110.1:p.Lys68=
ENST00000628935.1:c.156G>A	ENSP00000487145.1:p.Lys52=
NM_000770.3:c.414G>A MANE Select	NP_000761.3:p.Lys138=
NM_001198853.1:c.204G>A	NP_001185782.1:p.Lys68=
NM_001198854.1:c.108G>A	NP_001185783.1:p.Lys36=
NM_001198855.1:c.204G>A	NP_001185784.1:p.Lys68=
XR_945610.1:n.510G>A