Canonical Allele Identifier: CA1929374944

Gene: CYP2C8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037047A= , CM000672.2:g.95037047A=	GRCh38
NC_000010.10:g.96796804A= , CM000672.1:g.96796804A=	GRCh37
NC_000010.9:g.96786794A=	NCBI36
NG_007972.1:g.37451T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.*81T= MANE Select	ENSP00000360317.3:n.*81T=
ENST00000371270.5:c.*81T=	ENSP00000360317.3:n.*81T=
ENST00000490994.6:c.*1340T=	ENSP00000433314.1:n.*1340T=
ENST00000525991.5:c.*1129T=	ENSP00000433842.1:n.*1129T=
ENST00000526814.5:n.1809T=
ENST00000527420.5:c.*411T=	ENSP00000433191.1:n.*411T=
ENST00000527953.5:n.1848T=
ENST00000533320.5:n.1788T=
ENST00000535898.5:c.*81T=	ENSP00000445062.1:n.*81T=
ENST00000539050.5:c.*81T=	ENSP00000442343.2:n.*81T=
ENST00000623108.3:c.*81T=	ENSP00000485110.1:n.*81T=
NM_000770.3:c.*81T= MANE Select	NP_000761.3:n.*81T=
NM_001198853.1:c.*81T=	NP_001185782.1:n.*81T=
NM_001198854.1:c.*81T=	NP_001185783.1:n.*81T=
NM_001198855.1:c.*81T=	NP_001185784.1:n.*81T=