Canonical Allele Identifier: CA1929366556

Gene: CYP2C8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95048941G= , CM000672.2:g.95048941G=	GRCh38
NC_000010.10:g.96808698G= , CM000672.1:g.96808698G=	GRCh37
NC_000010.9:g.96798688G=	NCBI36
NG_007972.1:g.25557C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.820-2990C= MANE Select	ENSP00000360317.3:n.820-2990C=
ENST00000371270.5:c.820-2990C=	ENSP00000360317.3:n.820-2990C=
ENST00000479946.2:n.1124-2990C=
ENST00000490994.6:c.*606-2990C=	ENSP00000433314.1:n.*606-2990C=
ENST00000525991.5:c.*395-2990C=	ENSP00000433842.1:n.*395-2990C=
ENST00000526814.5:n.1075-2990C=
ENST00000527420.5:c.820-2990C=	ENSP00000433191.1:n.820-2990C=
ENST00000527953.5:n.1075-2990C=
ENST00000533320.5:n.1054-2990C=
ENST00000535898.5:c.514-2990C=	ENSP00000445062.1:n.514-2990C=
ENST00000539050.5:c.610-2990C=	ENSP00000442343.2:n.610-2990C=
ENST00000623108.3:c.610-2990C=	ENSP00000485110.1:n.610-2990C=
ENST00000628935.1:c.562-2990C=	ENSP00000487145.1:n.562-2990C=
NM_000770.3:c.820-2990C= MANE Select	NP_000761.3:n.820-2990C=
NM_001198853.1:c.610-2990C=	NP_001185782.1:n.610-2990C=
NM_001198854.1:c.514-2990C=	NP_001185783.1:n.514-2990C=
NM_001198855.1:c.610-2990C=	NP_001185784.1:n.610-2990C=
XR_945610.1:n.916-2990C=