Canonical Allele Identifier: CA470843701

Gene: CYP2C8

Linked Data

• MyVariant Identifiers: chr10:g.96827017G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95067260G>A , CM000672.2:g.95067260G>A	GRCh38
NC_000010.10:g.96827017G>A , CM000672.1:g.96827017G>A	GRCh37
NC_000010.9:g.96817007G>A	NCBI36
NG_007972.1:g.7238C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.429C>T MANE Select	ENSP00000360317.3:p.Asp143=
ENST00000371270.5:c.429C>T	ENSP00000360317.3:p.Asp143=
ENST00000479946.2:n.733C>T
ENST00000490994.6:c.*215C>T	ENSP00000433314.1:n.*215C>T
ENST00000525991.5:c.*4C>T	ENSP00000433842.1:n.*4C>T
ENST00000526814.5:n.684C>T
ENST00000527420.5:c.429C>T	ENSP00000433191.1:p.Asp143=
ENST00000527953.5:n.684C>T
ENST00000533320.5:n.663C>T
ENST00000535898.5:c.123C>T	ENSP00000445062.1:p.Asp41=
ENST00000539050.5:c.219C>T	ENSP00000442343.2:p.Asp73=
ENST00000623108.3:c.219C>T	ENSP00000485110.1:p.Asp73=
ENST00000628935.1:c.171C>T	ENSP00000487145.1:p.Asp57=
NM_000770.3:c.429C>T MANE Select	NP_000761.3:p.Asp143=
NM_001198853.1:c.219C>T	NP_001185782.1:p.Asp73=
NM_001198854.1:c.123C>T	NP_001185783.1:p.Asp41=
NM_001198855.1:c.219C>T	NP_001185784.1:p.Asp73=
XR_945610.1:n.525C>T