Canonical Allele Identifier: CA1929374934

Gene: CYP2C8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037037G= , CM000672.2:g.95037037G=	GRCh38
NC_000010.10:g.96796794G= , CM000672.1:g.96796794G=	GRCh37
NC_000010.9:g.96786784G=	NCBI36
NG_007972.1:g.37461C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.*91C= MANE Select	ENSP00000360317.3:n.*91C=
ENST00000371270.5:c.*91C=	ENSP00000360317.3:n.*91C=
ENST00000490994.6:c.*1350C=	ENSP00000433314.1:n.*1350C=
ENST00000525991.5:c.*1139C=	ENSP00000433842.1:n.*1139C=
ENST00000526814.5:n.1819C=
ENST00000527420.5:c.*421C=	ENSP00000433191.1:n.*421C=
ENST00000527953.5:n.1858C=
ENST00000533320.5:n.1798C=
ENST00000535898.5:c.*91C=	ENSP00000445062.1:n.*91C=
ENST00000539050.5:c.*91C=	ENSP00000442343.2:n.*91C=
ENST00000623108.3:c.*91C=	ENSP00000485110.1:n.*91C=
NM_000770.3:c.*91C= MANE Select	NP_000761.3:n.*91C=
NM_001198853.1:c.*91C=	NP_001185782.1:n.*91C=
NM_001198854.1:c.*91C=	NP_001185783.1:n.*91C=
NM_001198855.1:c.*91C=	NP_001185784.1:n.*91C=