Canonical Allele Identifier: CA377683241

Gene: CYP2C8

Linked Data

• MyVariant Identifiers: chr10:g.96827097C>A (hg19) ; chr10:g.95067340C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95067340C>A , CM000672.2:g.95067340C>A	GRCh38
NC_000010.10:g.96827097C>A , CM000672.1:g.96827097C>A	GRCh37
NC_000010.9:g.96817087C>A	NCBI36
NG_007972.1:g.7158G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.349G>T MANE Select	ENSP00000360317.3:p.Gly117Ter
ENST00000371270.5:c.349G>T	ENSP00000360317.3:p.Gly117Ter
ENST00000479946.2:n.653G>T
ENST00000490994.6:c.*135G>T	ENSP00000433314.1:n.*135G>T
ENST00000525991.5:c.224G>T	ENSP00000433842.1:p.Trp75Leu
ENST00000526814.5:n.604G>T
ENST00000527420.5:c.349G>T	ENSP00000433191.1:p.Gly117Ter
ENST00000527953.5:n.604G>T
ENST00000533320.5:n.583G>T
ENST00000535898.5:c.43G>T	ENSP00000445062.1:p.Gly15Ter
ENST00000539050.5:c.139G>T	ENSP00000442343.2:p.Gly47Ter
ENST00000623108.3:c.139G>T	ENSP00000485110.1:p.Gly47Ter
ENST00000628935.1:c.91G>T	ENSP00000487145.1:p.Gly31Ter
NM_000770.3:c.349G>T MANE Select	NP_000761.3:p.Gly117Ter
NM_001198853.1:c.139G>T	NP_001185782.1:p.Gly47Ter
NM_001198854.1:c.43G>T	NP_001185783.1:p.Gly15Ter
NM_001198855.1:c.139G>T	NP_001185784.1:p.Gly47Ter
XR_945610.1:n.445G>T