Canonical Allele Identifier: CA2527239122
Gene: TRMT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.13109989del , CM000681.2:g.13109989del GRCh38
NC_000019.9:g.13220803del , CM000681.1:g.13220803del GRCh37
NC_000019.8:g.13081803del NCBI36
NG_054900.1:g.12580del

Transcript Alleles

HGVS Amino-acid Change
ENST00000357720.9:c.1033del MANE Select ENSP00000350352.4:p.Val345CysfsTer?
ENST00000221504.12:c.1020-150del ENSP00000221504.7:n.1020-150del
ENST00000357720.8:c.1033del ENSP00000350352.4:p.Val345CysfsTer?
ENST00000437766.5:c.1033del ENSP00000416149.1:p.Val345CysfsTer?
ENST00000587487.5:c.391del ENSP00000465370.1:p.Val131CysfsTer?
ENST00000588511.5:n.1218del
ENST00000592062.5:c.1033del ENSP00000466967.1:p.Val345CysfsTer?
ENST00000593157.5:n.1062del
NM_001136035.2:c.1033del NP_001129507.1:p.Val345CysfsTer?
NM_001142554.1:c.1020-150del NP_001136026.1:n.1020-150del
NM_017722.3:c.1033del NP_060192.1:p.Val345CysfsTer?
XM_005259983.1:c.1020-150del XP_005260040.1:n.1020-150del
XM_006722793.2:c.391del XP_006722856.1:p.Val131CysfsTer?
XM_011528124.1:c.925del XP_011526426.1:p.Val309CysfsTer?
XM_011528125.1:c.391del XP_011526427.1:p.Val131CysfsTer?
XM_011528126.1:c.250del XP_011526428.1:p.Val84CysfsTer?
NM_001136035.3:c.1033del NP_001129507.1:p.Val345CysfsTer?
NM_001142554.2:c.1020-150del NP_001136026.1:n.1020-150del
NM_001351760.1:c.1020-150del NP_001338689.1:n.1020-150del
NM_001351761.1:c.925del NP_001338690.1:p.Val309CysfsTer?
NM_001351762.1:c.250del NP_001338691.1:p.Val84CysfsTer?
NM_017722.4:c.1033del NP_060192.1:p.Val345CysfsTer?
XM_024451587.1:c.391del XP_024307355.1:p.Val131CysfsTer?
XM_024451588.1:c.391del XP_024307356.1:p.Val131CysfsTer?
XM_024451589.1:c.391del XP_024307357.1:p.Val131CysfsTer?
XM_024451590.1:c.378-150del XP_024307358.1:n.378-150del
XM_024451591.1:c.250del XP_024307359.1:p.Val84CysfsTer?
XM_024451592.1:c.250del XP_024307360.1:p.Val84CysfsTer?
XM_024451593.1:c.250del XP_024307361.1:p.Val84CysfsTer?
XR_002958328.1:n.1146-150del
XR_002958329.1:n.845-150del
NM_001136035.4:c.1033del MANE Select NP_001129507.1:p.Val345CysfsTer?
NM_001142554.3:c.1020-150del NP_001136026.1:n.1020-150del
NM_001351760.2:c.1020-150del NP_001338689.1:n.1020-150del
NM_001351761.2:c.925del NP_001338690.1:p.Val309CysfsTer?
NM_001351762.2:c.250del NP_001338691.1:p.Val84CysfsTer?
NM_017722.5:c.1033del NP_060192.1:p.Val345CysfsTer?