Canonical Allele Identifier: CA470843335

Gene: CYP2C8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95058362G>T , CM000672.2:g.95058362G>T	GRCh38
NC_000010.10:g.96818119G>T , CM000672.1:g.96818119G>T	GRCh37
NC_000010.9:g.96808109G>T	NCBI36
NG_007972.1:g.16136C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000770.3:c.792C>A MANE Select	NP_000761.3:p.Ile264=
ENST00000371270.6:c.792C>A MANE Select	ENSP00000360317.3:p.Ile264=
NM_001198853.1:c.582C>A	NP_001185782.1:p.Ile194=
NM_001198854.1:c.486C>A	NP_001185783.1:p.Ile162=
NM_001198855.1:c.582C>A	NP_001185784.1:p.Ile194=
ENST00000371270.5:c.792C>A	ENSP00000360317.3:p.Ile264=
ENST00000479946.2:n.1096C>A
ENST00000490994.6:c.*578C>A	ENSP00000433314.1:n.*578C>A
ENST00000525991.5:c.*367C>A	ENSP00000433842.1:n.*367C>A
ENST00000526814.5:n.1047C>A
ENST00000527420.5:c.792C>A	ENSP00000433191.1:p.Ile264=
ENST00000527953.5:n.1047C>A
ENST00000533320.5:n.1026C>A
ENST00000535898.5:c.486C>A	ENSP00000445062.1:p.Ile162=
ENST00000539050.5:c.582C>A	ENSP00000442343.2:p.Ile194=
ENST00000623108.3:c.582C>A	ENSP00000485110.1:p.Ile194=
ENST00000628935.1:c.534C>A	ENSP00000487145.1:p.Ile178=
XR_945610.1:n.888C>A