Canonical Allele Identifier: CA377682780

Gene: CYP2C8

Linked Data

• MyVariant Identifiers: chr10:g.96827001C>T (hg19) ; chr10:g.95067244C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95067244C>T , CM000672.2:g.95067244C>T	GRCh38
NC_000010.10:g.96827001C>T , CM000672.1:g.96827001C>T	GRCh37
NC_000010.9:g.96816991C>T	NCBI36
NG_007972.1:g.7254G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.445G>A MANE Select	ENSP00000360317.3:p.Ala149Thr
ENST00000371270.5:c.445G>A	ENSP00000360317.3:p.Ala149Thr
ENST00000479946.2:n.749G>A
ENST00000490994.6:c.*231G>A	ENSP00000433314.1:n.*231G>A
ENST00000525991.5:c.*20G>A	ENSP00000433842.1:n.*20G>A
ENST00000526814.5:n.700G>A
ENST00000527420.5:c.445G>A	ENSP00000433191.1:p.Ala149Thr
ENST00000527953.5:n.700G>A
ENST00000533320.5:n.679G>A
ENST00000535898.5:c.139G>A	ENSP00000445062.1:p.Ala47Thr
ENST00000539050.5:c.235G>A	ENSP00000442343.2:p.Ala79Thr
ENST00000623108.3:c.235G>A	ENSP00000485110.1:p.Ala79Thr
ENST00000628935.1:c.187G>A	ENSP00000487145.1:p.Ala63Thr
NM_000770.3:c.445G>A MANE Select	NP_000761.3:p.Ala149Thr
NM_001198853.1:c.235G>A	NP_001185782.1:p.Ala79Thr
NM_001198854.1:c.139G>A	NP_001185783.1:p.Ala47Thr
NM_001198855.1:c.235G>A	NP_001185784.1:p.Ala79Thr
XR_945610.1:n.541G>A