Canonical Allele Identifier: CA2574328564
Gene: TRIT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.39847566del , CM000663.2:g.39847566del GRCh38
NC_000001.10:g.40313238del , CM000663.1:g.40313238del GRCh37
NC_000001.9:g.40085825del NCBI36
NG_042822.1:g.40947del

Transcript Alleles

HGVS Amino-acid Change
ENST00000316891.10:c.911del MANE Select ENSP00000321810.5:p.Asn304ThrfsTer4
ENST00000648678.1:c.1803del ENSP00000497805.1:n.1803del
ENST00000316891.9:c.911del ENSP00000321810.5:p.Asn304ThrfsTer4
ENST00000372818.5:c.911del ENSP00000361905.1:p.Asn304ThrfsTer4
ENST00000441669.6:c.665del ENSP00000388333.2:p.Asn222ThrfsTer4
ENST00000462797.5:c.911del ENSP00000473773.1:p.Asn304ThrfsTer4
ENST00000465417.5:n.113-268del
ENST00000467774.1:n.193del
ENST00000486825.6:c.816del
ENST00000489945.5:c.*329del ENSP00000473745.1:n.*329del
ENST00000491865.5:n.164-268del
ENST00000492612.6:c.755del
ENST00000495175.6:c.*333del ENSP00000474264.1:n.*333del
ENST00000537440.5:c.17-268del ENSP00000437700.1:n.17-268del
ENST00000541099.5:c.-140-2925del ENSP00000437896.1:n.-140-2925del
NM_001312691.1:c.911del NP_001299620.1:p.Asn304ThrfsTer4
NM_001312692.1:c.665del NP_001299621.1:p.Asn222ThrfsTer4
NM_017646.4:c.911del NP_060116.2:p.Asn304ThrfsTer4
NM_017646.5:c.911del NP_060116.2:p.Asn304ThrfsTer4
NR_132401.1:n.927del
NR_132402.1:n.785del
NR_132403.1:n.781del
NR_132404.1:n.781del
NR_132405.1:n.777del
NR_132406.1:n.686-268del
NR_132407.1:n.545del
NR_132408.1:n.541del
NR_132409.1:n.402del
NR_132410.1:n.446-268del
NR_132412.1:n.307-268del
NR_132413.1:n.195-2925del
NR_132414.1:n.195-5652del
NR_132415.1:n.1018del
XM_005270954.1:c.668del XP_005271011.1:p.Asn223ThrfsTer4
XM_006710706.1:c.488del XP_006710769.1:p.Asn163ThrfsTer4
XM_005270954.2:c.668del XP_005271011.1:p.Asn223ThrfsTer4
XR_946672.2:n.1011del
NM_017646.6:c.911del MANE Select NP_060116.2:p.Asn304ThrfsTer4