Canonical Allele Identifier: CA377682710

Gene: CYP2C8

Linked Data

• MyVariant Identifiers: chr10:g.96826988A>T (hg19) ; chr10:g.95067231A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95067231A>T , CM000672.2:g.95067231A>T	GRCh38
NC_000010.10:g.96826988A>T , CM000672.1:g.96826988A>T	GRCh37
NC_000010.9:g.96816978A>T	NCBI36
NG_007972.1:g.7267T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.458T>A MANE Select	ENSP00000360317.3:p.Val153Glu
ENST00000371270.5:c.458T>A	ENSP00000360317.3:p.Val153Glu
ENST00000479946.2:n.762T>A
ENST00000490994.6:c.*244T>A	ENSP00000433314.1:n.*244T>A
ENST00000525991.5:c.*33T>A	ENSP00000433842.1:n.*33T>A
ENST00000526814.5:n.713T>A
ENST00000527420.5:c.458T>A	ENSP00000433191.1:p.Val153Glu
ENST00000527953.5:n.713T>A
ENST00000533320.5:n.692T>A
ENST00000535898.5:c.152T>A	ENSP00000445062.1:p.Val51Glu
ENST00000539050.5:c.248T>A	ENSP00000442343.2:p.Val83Glu
ENST00000623108.3:c.248T>A	ENSP00000485110.1:p.Val83Glu
ENST00000628935.1:c.200T>A	ENSP00000487145.1:p.Val67Glu
NM_000770.3:c.458T>A MANE Select	NP_000761.3:p.Val153Glu
NM_001198853.1:c.248T>A	NP_001185782.1:p.Val83Glu
NM_001198854.1:c.152T>A	NP_001185783.1:p.Val51Glu
NM_001198855.1:c.248T>A	NP_001185784.1:p.Val83Glu
XR_945610.1:n.554T>A