Canonical Allele Identifier: CA1929374996

Gene: CYP2C8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037081A= , CM000672.2:g.95037081A=	GRCh38
NC_000010.10:g.96796838A= , CM000672.1:g.96796838A=	GRCh37
NC_000010.9:g.96786828A=	NCBI36
NG_007972.1:g.37417T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.*47T= MANE Select	ENSP00000360317.3:n.*47T=
ENST00000371270.5:c.*47T=	ENSP00000360317.3:n.*47T=
ENST00000490994.6:c.*1306T=	ENSP00000433314.1:n.*1306T=
ENST00000525991.5:c.*1095T=	ENSP00000433842.1:n.*1095T=
ENST00000526814.5:n.1775T=
ENST00000527420.5:c.*377T=	ENSP00000433191.1:n.*377T=
ENST00000527953.5:n.1814T=
ENST00000533320.5:n.1754T=
ENST00000535898.5:c.*47T=	ENSP00000445062.1:n.*47T=
ENST00000539050.5:c.*47T=	ENSP00000442343.2:n.*47T=
ENST00000623108.3:c.*47T=	ENSP00000485110.1:n.*47T=
NM_000770.3:c.*47T= MANE Select	NP_000761.3:n.*47T=
NM_001198853.1:c.*47T=	NP_001185782.1:n.*47T=
NM_001198854.1:c.*47T=	NP_001185783.1:n.*47T=
NM_001198855.1:c.*47T=	NP_001185784.1:n.*47T=