Canonical Allele Identifier: CA1929375315

Gene: CYP2C8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037215A= , CM000672.2:g.95037215A=	GRCh38
NC_000010.10:g.96796972A= , CM000672.1:g.96796972A=	GRCh37
NC_000010.9:g.96786962A=	NCBI36
NG_007972.1:g.37283T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1386T= MANE Select	ENSP00000360317.3:p.Asp462=
ENST00000371270.5:c.1386T=	ENSP00000360317.3:p.Asp462=
ENST00000490994.6:c.*1172T=	ENSP00000433314.1:n.*1172T=
ENST00000525991.5:c.*961T=	ENSP00000433842.1:n.*961T=
ENST00000526814.5:n.1641T=
ENST00000527420.5:c.*243T=	ENSP00000433191.1:n.*243T=
ENST00000527953.5:n.1680T=
ENST00000531714.1:n.574T=
ENST00000533320.5:n.1620T=
ENST00000535898.5:c.1080T=	ENSP00000445062.1:p.Asp360=
ENST00000539050.5:c.1176T=	ENSP00000442343.2:p.Asp392=
ENST00000623108.3:c.1176T=	ENSP00000485110.1:p.Asp392=
NM_000770.3:c.1386T= MANE Select	NP_000761.3:p.Asp462=
NM_001198853.1:c.1176T=	NP_001185782.1:p.Asp392=
NM_001198854.1:c.1080T=	NP_001185783.1:p.Asp360=
NM_001198855.1:c.1176T=	NP_001185784.1:p.Asp392=
XR_945610.1:n.1521T=