Canonical Allele Identifier: CA470841229

Gene: CYP2C8

Linked Data

• MyVariant Identifiers: chr10:g.96797032G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037275G>T , CM000672.2:g.95037275G>T	GRCh38
NC_000010.10:g.96797032G>T , CM000672.1:g.96797032G>T	GRCh37
NC_000010.9:g.96787022G>T	NCBI36
NG_007972.1:g.37223C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1326C>A MANE Select	ENSP00000360317.3:p.Arg442=
ENST00000371270.5:c.1326C>A	ENSP00000360317.3:p.Arg442=
ENST00000490994.6:c.*1112C>A	ENSP00000433314.1:n.*1112C>A
ENST00000525991.5:c.*901C>A	ENSP00000433842.1:n.*901C>A
ENST00000526814.5:n.1581C>A
ENST00000527420.5:c.*183C>A	ENSP00000433191.1:n.*183C>A
ENST00000527953.5:n.1620C>A
ENST00000531714.1:n.514C>A
ENST00000533320.5:n.1560C>A
ENST00000535898.5:c.1020C>A	ENSP00000445062.1:p.Arg340=
ENST00000539050.5:c.1116C>A	ENSP00000442343.2:p.Arg372=
ENST00000623108.3:c.1116C>A	ENSP00000485110.1:p.Arg372=
NM_000770.3:c.1326C>A MANE Select	NP_000761.3:p.Arg442=
NM_001198853.1:c.1116C>A	NP_001185782.1:p.Arg372=
NM_001198854.1:c.1020C>A	NP_001185783.1:p.Arg340=
NM_001198855.1:c.1116C>A	NP_001185784.1:p.Arg372=
XR_945610.1:n.1461C>A