Canonical Allele Identifier: CA377677349

Gene: CYP2C8

Linked Data

• MyVariant Identifiers: chr10:g.96796946G>A (hg19) ; chr10:g.95037189G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037189G>A , CM000672.2:g.95037189G>A	GRCh38
NC_000010.10:g.96796946G>A , CM000672.1:g.96796946G>A	GRCh37
NC_000010.9:g.96786936G>A	NCBI36
NG_007972.1:g.37309C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1412C>T MANE Select	ENSP00000360317.3:p.Ala471Val
ENST00000371270.5:c.1412C>T	ENSP00000360317.3:p.Ala471Val
ENST00000490994.6:c.*1198C>T	ENSP00000433314.1:n.*1198C>T
ENST00000525991.5:c.*987C>T	ENSP00000433842.1:n.*987C>T
ENST00000526814.5:n.1667C>T
ENST00000527420.5:c.*269C>T	ENSP00000433191.1:n.*269C>T
ENST00000527953.5:n.1706C>T
ENST00000531714.1:n.600C>T
ENST00000533320.5:n.1646C>T
ENST00000535898.5:c.1106C>T	ENSP00000445062.1:p.Ala369Val
ENST00000539050.5:c.1202C>T	ENSP00000442343.2:p.Ala401Val
ENST00000623108.3:c.1202C>T	ENSP00000485110.1:p.Ala401Val
NM_000770.3:c.1412C>T MANE Select	NP_000761.3:p.Ala471Val
NM_001198853.1:c.1202C>T	NP_001185782.1:p.Ala401Val
NM_001198854.1:c.1106C>T	NP_001185783.1:p.Ala369Val
NM_001198855.1:c.1202C>T	NP_001185784.1:p.Ala401Val
XR_945610.1:n.1547C>T