Canonical Allele Identifier: CA7609593
Gene: TRIP4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.64418562G>A , CM000677.2:g.64418562G>A GRCh38
NC_000015.9:g.64710761G>A , CM000677.1:g.64710761G>A GRCh37
NC_000015.8:g.62497814G>A NCBI36
NG_046848.1:g.35759G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261884.8:c.1192G>A MANE Select ENSP00000261884.3:p.Ala398Thr
ENST00000261884.7:c.1192G>A ENSP00000261884.3:p.Ala398Thr
ENST00000560475.1:c.111+8734G>A
ENST00000560567.5:c.1065G>A ENSP00000453106.1:p.Gln355=
NM_016213.4:c.1192G>A NP_057297.2:p.Ala398Thr
XM_005254789.1:c.502G>A XP_005254846.1:p.Ala168Thr
XR_243130.1:n.1123G>A
NM_001321924.1:c.502G>A NP_001308853.1:p.Ala168Thr
NR_135855.1:n.1125G>A
NM_001321924.2:c.502G>A NP_001308853.1:p.Ala168Thr
NM_016213.5:c.1192G>A MANE Select NP_057297.2:p.Ala398Thr
NR_135855.2:n.1093G>A