Canonical Allele Identifier: CA377682733

Gene: CYP2C8

Linked Data

• MyVariant Identifiers: chr10:g.96826993G>C (hg19) ; chr10:g.95067236G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95067236G>C , CM000672.2:g.95067236G>C	GRCh38
NC_000010.10:g.96826993G>C , CM000672.1:g.96826993G>C	GRCh37
NC_000010.9:g.96816983G>C	NCBI36
NG_007972.1:g.7262C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.453C>G MANE Select	ENSP00000360317.3:p.Cys151Trp
ENST00000371270.5:c.453C>G	ENSP00000360317.3:p.Cys151Trp
ENST00000479946.2:n.757C>G
ENST00000490994.6:c.*239C>G	ENSP00000433314.1:n.*239C>G
ENST00000525991.5:c.*28C>G	ENSP00000433842.1:n.*28C>G
ENST00000526814.5:n.708C>G
ENST00000527420.5:c.453C>G	ENSP00000433191.1:p.Cys151Trp
ENST00000527953.5:n.708C>G
ENST00000533320.5:n.687C>G
ENST00000535898.5:c.147C>G	ENSP00000445062.1:p.Cys49Trp
ENST00000539050.5:c.243C>G	ENSP00000442343.2:p.Cys81Trp
ENST00000623108.3:c.243C>G	ENSP00000485110.1:p.Cys81Trp
ENST00000628935.1:c.195C>G	ENSP00000487145.1:p.Cys65Trp
NM_000770.3:c.453C>G MANE Select	NP_000761.3:p.Cys151Trp
NM_001198853.1:c.243C>G	NP_001185782.1:p.Cys81Trp
NM_001198854.1:c.147C>G	NP_001185783.1:p.Cys49Trp
NM_001198855.1:c.243C>G	NP_001185784.1:p.Cys81Trp
XR_945610.1:n.549C>G