Canonical Allele Identifier: CA377677543

Gene: CYP2C8

Linked Data

• gnomAD v4: 10-95037277-G-C
• COSMIC: COSM5758169 ; COSM5758170
• MyVariant Identifiers: chr10:g.96797034G>C (hg19) ; chr10:g.95037277G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037277G>C , CM000672.2:g.95037277G>C	GRCh38
NC_000010.10:g.96797034G>C , CM000672.1:g.96797034G>C	GRCh37
NC_000010.9:g.96787024G>C	NCBI36
NG_007972.1:g.37221C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1324C>G MANE Select	ENSP00000360317.3:p.Arg442Gly
ENST00000371270.5:c.1324C>G	ENSP00000360317.3:p.Arg442Gly
ENST00000490994.6:c.*1110C>G	ENSP00000433314.1:n.*1110C>G
ENST00000525991.5:c.*899C>G	ENSP00000433842.1:n.*899C>G
ENST00000526814.5:n.1579C>G
ENST00000527420.5:c.*181C>G	ENSP00000433191.1:n.*181C>G
ENST00000527953.5:n.1618C>G
ENST00000531714.1:n.512C>G
ENST00000533320.5:n.1558C>G
ENST00000535898.5:c.1018C>G	ENSP00000445062.1:p.Arg340Gly
ENST00000539050.5:c.1114C>G	ENSP00000442343.2:p.Arg372Gly
ENST00000623108.3:c.1114C>G	ENSP00000485110.1:p.Arg372Gly
NM_000770.3:c.1324C>G MANE Select	NP_000761.3:p.Arg442Gly
NM_001198853.1:c.1114C>G	NP_001185782.1:p.Arg372Gly
NM_001198854.1:c.1018C>G	NP_001185783.1:p.Arg340Gly
NM_001198855.1:c.1114C>G	NP_001185784.1:p.Arg372Gly
XR_945610.1:n.1459C>G