Canonical Allele Identifier: CA1929388240

Gene: CYP2C8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95067259G= , CM000672.2:g.95067259G=	GRCh38
NC_000010.10:g.96827016G= , CM000672.1:g.96827016G=	GRCh37
NC_000010.9:g.96817006G=	NCBI36
NG_007972.1:g.7239C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.430C= MANE Select	ENSP00000360317.3:p.Arg144=
ENST00000371270.5:c.430C=	ENSP00000360317.3:p.Arg144=
ENST00000479946.2:n.734C=
ENST00000490994.6:c.*216C=	ENSP00000433314.1:n.*216C=
ENST00000525991.5:c.*5C=	ENSP00000433842.1:n.*5C=
ENST00000526814.5:n.685C=
ENST00000527420.5:c.430C=	ENSP00000433191.1:p.Arg144=
ENST00000527953.5:n.685C=
ENST00000533320.5:n.664C=
ENST00000535898.5:c.124C=	ENSP00000445062.1:p.Arg42=
ENST00000539050.5:c.220C=	ENSP00000442343.2:p.Arg74=
ENST00000623108.3:c.220C=	ENSP00000485110.1:p.Arg74=
ENST00000628935.1:c.172C=	ENSP00000487145.1:p.Arg58=
NM_000770.3:c.430C= MANE Select	NP_000761.3:p.Arg144=
NM_001198853.1:c.220C=	NP_001185782.1:p.Arg74=
NM_001198854.1:c.124C=	NP_001185783.1:p.Arg42=
NM_001198855.1:c.220C=	NP_001185784.1:p.Arg74=
XR_945610.1:n.526C=