Canonical Allele Identifier: CA1164144302
Gene: TRIT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.39847296A= , CM000663.2:g.39847296A= GRCh38
NC_000001.10:g.40312968A= , CM000663.1:g.40312968A= GRCh37
NC_000001.9:g.40085555A= NCBI36
NG_042822.1:g.41216T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000316891.10:c.930T= MANE Select ENSP00000321810.5:p.Gly310=
ENST00000648678.1:c.1822T= ENSP00000497805.1:n.1822T=
ENST00000316891.9:c.930T= ENSP00000321810.5:p.Gly310=
ENST00000372818.5:c.928+252T= ENSP00000361905.1:n.928+252T=
ENST00000441669.6:c.684T= ENSP00000388333.2:p.Gly228=
ENST00000462797.5:c.930T= ENSP00000473773.1:p.Gly310=
ENST00000465417.5:n.114T=
ENST00000467774.1:n.212T=
ENST00000486825.6:c.835T=
ENST00000489945.5:c.*348T= ENSP00000473745.1:n.*348T=
ENST00000491865.5:n.165T=
ENST00000492612.6:c.774T=
ENST00000495175.6:c.*352T= ENSP00000474264.1:n.*352T=
ENST00000537440.5:c.18T= ENSP00000437700.1:p.Gly6=
ENST00000541099.5:c.-140-2656T= ENSP00000437896.1:n.-140-2656T=
NM_001312691.1:c.928+252T= NP_001299620.1:n.928+252T=
NM_001312692.1:c.684T= NP_001299621.1:p.Gly228=
NM_017646.4:c.930T= NP_060116.2:p.Gly310=
NM_017646.5:c.930T= NP_060116.2:p.Gly310=
NR_132401.1:n.946T=
NR_132402.1:n.804T=
NR_132403.1:n.800T=
NR_132404.1:n.800T=
NR_132405.1:n.796T=
NR_132406.1:n.687T=
NR_132407.1:n.564T=
NR_132408.1:n.560T=
NR_132409.1:n.421T=
NR_132410.1:n.447T=
NR_132412.1:n.308T=
NR_132413.1:n.195-2656T=
NR_132414.1:n.195-5383T=
NR_132415.1:n.1037T=
XM_005270954.1:c.687T= XP_005271011.1:p.Gly229=
XM_006710706.1:c.507T= XP_006710769.1:p.Gly169=
XM_005270954.2:c.687T= XP_005271011.1:p.Gly229=
XR_946672.2:n.1030T=
NM_017646.6:c.930T= MANE Select NP_060116.2:p.Gly310=