Canonical Allele Identifier: CA1929375032

Gene: CYP2C8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037092T= , CM000672.2:g.95037092T=	GRCh38
NC_000010.10:g.96796849T= , CM000672.1:g.96796849T=	GRCh37
NC_000010.9:g.96786839T=	NCBI36
NG_007972.1:g.37406A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.*36A= MANE Select	ENSP00000360317.3:n.*36A=
ENST00000371270.5:c.*36A=	ENSP00000360317.3:n.*36A=
ENST00000490994.6:c.*1295A=	ENSP00000433314.1:n.*1295A=
ENST00000525991.5:c.*1084A=	ENSP00000433842.1:n.*1084A=
ENST00000526814.5:n.1764A=
ENST00000527420.5:c.*366A=	ENSP00000433191.1:n.*366A=
ENST00000527953.5:n.1803A=
ENST00000533320.5:n.1743A=
ENST00000535898.5:c.*36A=	ENSP00000445062.1:n.*36A=
ENST00000539050.5:c.*36A=	ENSP00000442343.2:n.*36A=
ENST00000623108.3:c.*36A=	ENSP00000485110.1:n.*36A=
NM_000770.3:c.*36A= MANE Select	NP_000761.3:n.*36A=
NM_001198853.1:c.*36A=	NP_001185782.1:n.*36A=
NM_001198854.1:c.*36A=	NP_001185783.1:n.*36A=
NM_001198855.1:c.*36A=	NP_001185784.1:n.*36A=