Canonical Allele Identifier: CA377677834

Gene: CYP2C8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95038992T>G , CM000672.2:g.95038992T>G	GRCh38
NC_000010.10:g.96798749T>G , CM000672.1:g.96798749T>G	GRCh37
NC_000010.9:g.96788739T>G	NCBI36
NG_007972.1:g.35506A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1196A>C MANE Select	ENSP00000360317.3:p.Lys399Thr
ENST00000371270.5:c.1196A>C	ENSP00000360317.3:p.Lys399Thr
ENST00000479946.2:n.1539A>C
ENST00000490994.6:c.*982A>C	ENSP00000433314.1:n.*982A>C
ENST00000525991.5:c.*771A>C	ENSP00000433842.1:n.*771A>C
ENST00000526814.5:n.1451A>C
ENST00000527420.5:c.*53A>C	ENSP00000433191.1:n.*53A>C
ENST00000527953.5:n.1490A>C
ENST00000531714.1:n.384A>C
ENST00000533320.5:n.1430A>C
ENST00000535898.5:c.890A>C	ENSP00000445062.1:p.Lys297Thr
ENST00000539050.5:c.986A>C	ENSP00000442343.2:p.Lys329Thr
ENST00000623108.3:c.986A>C	ENSP00000485110.1:p.Lys329Thr
NM_000770.3:c.1196A>C MANE Select	NP_000761.3:p.Lys399Thr
NM_001198853.1:c.986A>C	NP_001185782.1:p.Lys329Thr
NM_001198854.1:c.890A>C	NP_001185783.1:p.Lys297Thr
NM_001198855.1:c.986A>C	NP_001185784.1:p.Lys329Thr
XR_945610.1:n.1331A>C