Canonical Allele Identifier: CA2839024182

Gene: CYP2C8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95067218dup , CM000672.2:g.95067218dup	GRCh38
NC_000010.10:g.96826975dup , CM000672.1:g.96826975dup	GRCh37
NC_000010.9:g.96816965dup	NCBI36
NG_007972.1:g.7284dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.475dup MANE Select	ENSP00000360317.3:p.Thr159AsnfsTer7
ENST00000371270.5:c.475dup	ENSP00000360317.3:p.Thr159AsnfsTer7
ENST00000479946.2:n.779dup
ENST00000490994.6:c.*261dup	ENSP00000433314.1:n.*261dup
ENST00000525991.5:c.*50dup	ENSP00000433842.1:n.*50dup
ENST00000526814.5:n.730dup
ENST00000527420.5:c.475dup	ENSP00000433191.1:p.Thr159AsnfsTer7
ENST00000527953.5:n.730dup
ENST00000533320.5:n.709dup
ENST00000535898.5:c.169dup	ENSP00000445062.1:p.Thr57AsnfsTer7
ENST00000539050.5:c.265dup	ENSP00000442343.2:p.Thr89AsnfsTer7
ENST00000623108.3:c.265dup	ENSP00000485110.1:p.Thr89AsnfsTer7
ENST00000628935.1:c.217dup	ENSP00000487145.1:p.Thr73AsnfsTer7
NM_000770.3:c.475dup MANE Select	NP_000761.3:p.Thr159AsnfsTer7
NM_001198853.1:c.265dup	NP_001185782.1:p.Thr89AsnfsTer7
NM_001198854.1:c.169dup	NP_001185783.1:p.Thr57AsnfsTer7
NM_001198855.1:c.265dup	NP_001185784.1:p.Thr89AsnfsTer7
XR_945610.1:n.571dup