Canonical Allele Identifier: CA1929375039

Gene: CYP2C8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037096A= , CM000672.2:g.95037096A=	GRCh38
NC_000010.10:g.96796853A= , CM000672.1:g.96796853A=	GRCh37
NC_000010.9:g.96786843A=	NCBI36
NG_007972.1:g.37402T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.*32T= MANE Select	ENSP00000360317.3:n.*32T=
ENST00000371270.5:c.*32T=	ENSP00000360317.3:n.*32T=
ENST00000490994.6:c.*1291T=	ENSP00000433314.1:n.*1291T=
ENST00000525991.5:c.*1080T=	ENSP00000433842.1:n.*1080T=
ENST00000526814.5:n.1760T=
ENST00000527420.5:c.*362T=	ENSP00000433191.1:n.*362T=
ENST00000527953.5:n.1799T=
ENST00000533320.5:n.1739T=
ENST00000535898.5:c.*32T=	ENSP00000445062.1:n.*32T=
ENST00000539050.5:c.*32T=	ENSP00000442343.2:n.*32T=
ENST00000623108.3:c.*32T=	ENSP00000485110.1:n.*32T=
NM_000770.3:c.*32T= MANE Select	NP_000761.3:n.*32T=
NM_001198853.1:c.*32T=	NP_001185782.1:n.*32T=
NM_001198854.1:c.*32T=	NP_001185783.1:n.*32T=
NM_001198855.1:c.*32T=	NP_001185784.1:n.*32T=