Canonical Allele Identifier: CA1929389891

Gene: CYP2C8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95068581A= , CM000672.2:g.95068581A=	GRCh38
NC_000010.10:g.96828338A= , CM000672.1:g.96828338A=	GRCh37
NC_000010.9:g.96818328A=	NCBI36
NG_007972.1:g.5917T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000371270.6:c.168+654T= MANE Select	ENSP00000360317.3:n.168+654T=
ENST00000371270.5:c.168+654T=	ENSP00000360317.3:n.168+654T=
ENST00000479946.2:n.301+616T=
ENST00000490994.6:c.206+616T=	ENSP00000433314.1:n.206+616T=
ENST00000525991.5:c.206+616T=	ENSP00000433842.1:n.206+616T=
ENST00000526814.5:n.252+654T=
ENST00000527420.5:c.168+654T=	ENSP00000433191.1:n.168+654T=
ENST00000527953.5:n.252+654T=
ENST00000533320.5:n.231+616T=
ENST00000535898.5:c.25+616T=	ENSP00000445062.1:n.25+616T=
ENST00000539050.5:c.-57T=	ENSP00000442343.2:n.-57T=
ENST00000623108.3:c.-43+616T=	ENSP00000485110.1:n.-43+616T=
NM_000770.3:c.168+654T= MANE Select	NP_000761.3:n.168+654T=
NM_001198853.1:c.-43+616T=	NP_001185782.1:n.-43+616T=
NM_001198854.1:c.25+616T=	NP_001185783.1:n.25+616T=
NM_001198855.1:c.-57T=	NP_001185784.1:n.-57T=
XR_945610.1:n.264+654T=