Canonical Allele Identifier: CA377677544

Gene: CYP2C8

Linked Data

• MyVariant Identifiers: chr10:g.96797034G>T (hg19) ; chr10:g.95037277G>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1324C>A MANE Select	ENSP00000360317.3:p.Arg442Ser
ENST00000371270.5:c.1324C>A	ENSP00000360317.3:p.Arg442Ser
ENST00000490994.6:c.*1110C>A	ENSP00000433314.1:n.*1110C>A
ENST00000525991.5:c.*899C>A	ENSP00000433842.1:n.*899C>A
ENST00000526814.5:n.1579C>A
ENST00000527420.5:c.*181C>A	ENSP00000433191.1:n.*181C>A
ENST00000527953.5:n.1618C>A
ENST00000531714.1:n.512C>A
ENST00000533320.5:n.1558C>A
ENST00000535898.5:c.1018C>A	ENSP00000445062.1:p.Arg340Ser
ENST00000539050.5:c.1114C>A	ENSP00000442343.2:p.Arg372Ser
ENST00000623108.3:c.1114C>A	ENSP00000485110.1:p.Arg372Ser
NM_000770.3:c.1324C>A MANE Select	NP_000761.3:p.Arg442Ser
NM_001198853.1:c.1114C>A	NP_001185782.1:p.Arg372Ser
NM_001198854.1:c.1018C>A	NP_001185783.1:p.Arg340Ser
NM_001198855.1:c.1114C>A	NP_001185784.1:p.Arg372Ser
XR_945610.1:n.1459C>A