Canonical Allele Identifier: CA1146915341
Gene: TRIT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.39847547C= , CM000663.2:g.39847547C= GRCh38
NC_000001.10:g.40313219C= , CM000663.1:g.40313219C= GRCh37
NC_000001.9:g.40085806C= NCBI36
NG_042822.1:g.40965G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000316891.10:c.928+1G= MANE Select ENSP00000321810.5:n.928+1G=
ENST00000648678.1:c.1820+1G= ENSP00000497805.1:n.1820+1G=
ENST00000316891.9:c.928+1G= ENSP00000321810.5:n.928+1G=
ENST00000372818.5:c.928+1G= ENSP00000361905.1:n.928+1G=
ENST00000441669.6:c.682+1G= ENSP00000388333.2:n.682+1G=
ENST00000462797.5:c.928+1G= ENSP00000473773.1:n.928+1G=
ENST00000465417.5:n.113-250G=
ENST00000467774.1:n.210+1G=
ENST00000486825.6:c.833+1G=
ENST00000489945.5:c.*346+1G= ENSP00000473745.1:n.*346+1G=
ENST00000491865.5:n.164-250G=
ENST00000492612.6:c.772+1G=
ENST00000495175.6:c.*350+1G= ENSP00000474264.1:n.*350+1G=
ENST00000537440.5:c.17-250G= ENSP00000437700.1:n.17-250G=
ENST00000541099.5:c.-140-2907G= ENSP00000437896.1:n.-140-2907G=
NM_001312691.1:c.928+1G= NP_001299620.1:n.928+1G=
NM_001312692.1:c.682+1G= NP_001299621.1:n.682+1G=
NM_017646.4:c.928+1G= NP_060116.2:n.928+1G=
NM_017646.5:c.928+1G= NP_060116.2:n.928+1G=
NR_132401.1:n.944+1G=
NR_132402.1:n.802+1G=
NR_132403.1:n.798+1G=
NR_132404.1:n.798+1G=
NR_132405.1:n.794+1G=
NR_132406.1:n.686-250G=
NR_132407.1:n.562+1G=
NR_132408.1:n.558+1G=
NR_132409.1:n.419+1G=
NR_132410.1:n.446-250G=
NR_132412.1:n.307-250G=
NR_132413.1:n.195-2907G=
NR_132414.1:n.195-5634G=
NR_132415.1:n.1035+1G=
XM_005270954.1:c.685+1G= XP_005271011.1:n.685+1G=
XM_006710706.1:c.505+1G= XP_006710769.1:n.505+1G=
XM_005270954.2:c.685+1G= XP_005271011.1:n.685+1G=
XR_946672.2:n.1028+1G=
NM_017646.6:c.928+1G= MANE Select NP_060116.2:n.928+1G=