Canonical Allele Identifier: CA658832940

Gene: CYP2C8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.[95038992T>C;95067273C>T] , CM000672.2:g.[95038992T>C;95067273C>T]	GRCh38
NC_000010.10:g.[96798749T>C;96827030C>T] , CM000672.1:g.[96798749T>C;96827030C>T]	GRCh37
NC_000010.9:g.[96788739T>C;96817020C>T]	NCBI36
NG_007972.1:g.[7225G>A;35506A>G]

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.[416G>A;1196A>G] MANE Select	ENSP00000360317.3:p.[Arg139Lys;Lys399Arg]
ENST00000371270.5:c.[416G>A;1196A>G]	ENSP00000360317.3:p.[Arg139Lys;Lys399Arg]
ENST00000479946.2:n.[720G>A;1539A>G]
ENST00000490994.6:c.[*202G>A;*982A>G]	ENSP00000433314.1:n.[*202G>A;*982A>G]
ENST00000525991.5:c.[291G>A;*771A>G]	ENSP00000433842.1:[p.Glu97=;n.*771A>G]
ENST00000526814.5:n.[671G>A;1451A>G]
ENST00000527420.5:c.[416G>A;*53A>G]	ENSP00000433191.1:[p.Arg139Lys;n.*53A>G]
ENST00000527953.5:n.[671G>A;1490A>G]
ENST00000533320.5:n.[650G>A;1430A>G]
ENST00000535898.5:c.[110G>A;890A>G]	ENSP00000445062.1:p.[Arg37Lys;Lys297Arg]
ENST00000539050.5:c.[206G>A;986A>G]	ENSP00000442343.2:p.[Arg69Lys;Lys329Arg]
ENST00000623108.3:c.[206G>A;986A>G]	ENSP00000485110.1:p.[Arg69Lys;Lys329Arg]
NM_000770.3:c.[416G>A;1196A>G] MANE Select	NP_000761.3:p.[Arg139Lys;Lys399Arg]
NM_001198853.1:c.[206G>A;986A>G]	NP_001185782.1:p.[Arg69Lys;Lys329Arg]
NM_001198854.1:c.[110G>A;890A>G]	NP_001185783.1:p.[Arg37Lys;Lys297Arg]
NM_001198855.1:c.[206G>A;986A>G]	NP_001185784.1:p.[Arg69Lys;Lys329Arg]
XR_945610.1:n.[512G>A;1331A>G]