Canonical Allele Identifier: CA1929357795

Gene: CYP2C8

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1196A= MANE Select	ENSP00000360317.3:p.Lys399=
ENST00000371270.5:c.1196A=	ENSP00000360317.3:p.Lys399=
ENST00000479946.2:n.1539A=
ENST00000490994.6:c.*982A=	ENSP00000433314.1:n.*982A=
ENST00000525991.5:c.*771A=	ENSP00000433842.1:n.*771A=
ENST00000526814.5:n.1451A=
ENST00000527420.5:c.*53A=	ENSP00000433191.1:n.*53A=
ENST00000527953.5:n.1490A=
ENST00000531714.1:n.384A=
ENST00000533320.5:n.1430A=
ENST00000535898.5:c.890A=	ENSP00000445062.1:p.Lys297=
ENST00000539050.5:c.986A=	ENSP00000442343.2:p.Lys329=
ENST00000623108.3:c.986A=	ENSP00000485110.1:p.Lys329=
NM_000770.3:c.1196A= MANE Select	NP_000761.3:p.Lys399=
NM_001198853.1:c.986A=	NP_001185782.1:p.Lys329=
NM_001198854.1:c.890A=	NP_001185783.1:p.Lys297=
NM_001198855.1:c.986A=	NP_001185784.1:p.Lys329=
XR_945610.1:n.1331A=