Canonical Allele Identifier: CA352863787
Gene: TRAIP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49840354T>A , CM000665.2:g.49840354T>A GRCh38
NC_000003.11:g.49877787T>A , CM000665.1:g.49877787T>A GRCh37
NC_000003.10:g.49852791T>A NCBI36
NG_046695.1:g.21206A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000331456.7:c.725A>T MANE Select ENSP00000328203.2:p.Glu242Val
ENST00000331456.6:c.725A>T ENSP00000328203.2:p.Glu242Val
ENST00000469027.5:c.260A>T ENSP00000420085.1:p.Glu87Val
ENST00000473195.5:c.300A>T ENSP00000419556.1:p.Ter100Cys
ENST00000475495.1:n.199A>T
ENST00000482582.5:c.677A>T ENSP00000418544.1:p.Glu226Val
NM_005879.2:c.725A>T NP_005870.2:p.Glu242Val
XM_011533264.1:c.494A>T XP_011531566.1:p.Glu165Val
XR_940361.1:n.835A>T
XM_017005526.1:c.428A>T XP_016861015.1:p.Glu143Val
XR_001739979.1:n.835A>T
NM_005879.3:c.725A>T MANE Select NP_005870.2:p.Glu242Val