Canonical Allele Identifier: CA377682774

Gene: CYP2C8

Linked Data

• MyVariant Identifiers: chr10:g.96827000G>A (hg19) ; chr10:g.95067243G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95067243G>A , CM000672.2:g.95067243G>A	GRCh38
NC_000010.10:g.96827000G>A , CM000672.1:g.96827000G>A	GRCh37
NC_000010.9:g.96816990G>A	NCBI36
NG_007972.1:g.7255C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.446C>T MANE Select	ENSP00000360317.3:p.Ala149Val
ENST00000371270.5:c.446C>T	ENSP00000360317.3:p.Ala149Val
ENST00000479946.2:n.750C>T
ENST00000490994.6:c.*232C>T	ENSP00000433314.1:n.*232C>T
ENST00000525991.5:c.*21C>T	ENSP00000433842.1:n.*21C>T
ENST00000526814.5:n.701C>T
ENST00000527420.5:c.446C>T	ENSP00000433191.1:p.Ala149Val
ENST00000527953.5:n.701C>T
ENST00000533320.5:n.680C>T
ENST00000535898.5:c.140C>T	ENSP00000445062.1:p.Ala47Val
ENST00000539050.5:c.236C>T	ENSP00000442343.2:p.Ala79Val
ENST00000623108.3:c.236C>T	ENSP00000485110.1:p.Ala79Val
ENST00000628935.1:c.188C>T	ENSP00000487145.1:p.Ala63Val
NM_000770.3:c.446C>T MANE Select	NP_000761.3:p.Ala149Val
NM_001198853.1:c.236C>T	NP_001185782.1:p.Ala79Val
NM_001198854.1:c.140C>T	NP_001185783.1:p.Ala47Val
NM_001198855.1:c.236C>T	NP_001185784.1:p.Ala79Val
XR_945610.1:n.542C>T