Canonical Allele Identifier: CA2408701017
Gene: TRMU HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.46352527_46352557delinsGTGGCCTCAGCTGAGATGCTGGAGTTCATGA , CM000684.2:g.46352527_46352557delinsGTGGCCTCAGCTGAGATGCTGGAGTTCATGA GRCh38
NC_000022.10:g.46748424_46748454delinsGTGGCCTCAGCTGAGATGCTGGAGTTCATGA , CM000684.1:g.46748424_46748454delinsGTGGCCTCAGCTGAGATGCTGGAGTTCATGA GRCh37
NC_000022.9:g.45127088_45127118delinsGTGGCCTCAGCTGAGATGCTGGAGTTCATGA NCBI36
NG_012173.1:g.22127_22157delinsGTGGCCTCAGCTGAGATGCTGGAGTTCATGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000465378.6:n.1017_1047delinsGTGGCCTCAGCTGAGATGCTGGAGTTCATGA
ENST00000642923.1:c.667+197_667+227delinsGTGGCCTCAGCTGAGATGCTGGAGTTCATGA ENSP00000494255.1:n.667+197_667+227delinsGTGGCCTCAGCTGAGATGCT...
ENST00000643137.1:c.667+197_667+227delinsGTGGCCTCAGCTGAGATGCTGGAGTTCATGA ENSP00000495331.1:n.667+197_667+227delinsGTGGCCTCAGCTGAGATGCT...
ENST00000644006.1:c.*216+197_*216+227delinsGTGGCCTCAGCTGAGATGCTGGAGTTCATGA ENSP00000493778.1:n.*216+197_*216+227delinsGTGGCCTCAGCTGAGATG...
ENST00000645026.1:n.823+197_823+227delinsGTGGCCTCAGCTGAGATGCTGGAGTTCATGA
ENST00000645190.1:c.772+197_772+227delinsGTGGCCTCAGCTGAGATGCTGGAGTTCATGA MANE Select ENSP00000496496.1:n.772+197_772+227delinsGTGGCCTCAGCTGAGATGCT...
ENST00000647301.1:c.*216+197_*216+227delinsGTGGCCTCAGCTGAGATGCTGGAGTTCATGA ENSP00000496641.1:n.*216+197_*216+227delinsGTGGCCTCAGCTGAGATG...
ENST00000290846.8:c.772+197_772+227delinsGTGGCCTCAGCTGAGATGCTGGAGTTCATGA ENSP00000290846.4:n.772+197_772+227delinsGTGGCCTCAGCTGAGATGCT...
ENST00000381019.3:c.772+197_772+227delinsGTGGCCTCAGCTGAGATGCTGGAGTTCATGA ENSP00000370407.3:n.772+197_772+227delinsGTGGCCTCAGCTGAGATGCT...
ENST00000381021.7:c.*365+197_*365+227delinsGTGGCCTCAGCTGAGATGCTGGAGTTCATGA ENSP00000370409.3:n.*365+197_*365+227delinsGTGGCCTCAGCTGAGATG...
ENST00000441818.5:c.*306+197_*306+227delinsGTGGCCTCAGCTGAGATGCTGGAGTTCATGA ENSP00000393014.1:n.*306+197_*306+227delinsGTGGCCTCAGCTGAGATG...
ENST00000453630.5:c.*310+197_*310+227delinsGTGGCCTCAGCTGAGATGCTGGAGTTCATGA ENSP00000398488.1:n.*310+197_*310+227delinsGTGGCCTCAGCTGAGATG...
ENST00000456595.5:c.*306+197_*306+227delinsGTGGCCTCAGCTGAGATGCTGGAGTTCATGA ENSP00000413880.1:n.*306+197_*306+227delinsGTGGCCTCAGCTGAGATG...
ENST00000457572.5:c.*216+197_*216+227delinsGTGGCCTCAGCTGAGATGCTGGAGTTCATGA ENSP00000407700.1:n.*216+197_*216+227delinsGTGGCCTCAGCTGAGATG...
ENST00000463785.1:n.243_273delinsGTGGCCTCAGCTGAGATGCTGGAGTTCATGA
NM_001282782.1:c.430+197_430+227delinsGTGGCCTCAGCTGAGATGCTGGAGTTCATGA NP_001269711.1:n.430+197_430+227delinsGTGGCCTCAGCTGAGATGCTGGA...
NM_001282783.1:c.352+197_352+227delinsGTGGCCTCAGCTGAGATGCTGGAGTTCATGA NP_001269712.1:n.352+197_352+227delinsGTGGCCTCAGCTGAGATGCTGGA...
NM_001282784.1:c.352+197_352+227delinsGTGGCCTCAGCTGAGATGCTGGAGTTCATGA NP_001269713.1:n.352+197_352+227delinsGTGGCCTCAGCTGAGATGCTGGA...
NM_001282785.1:c.772+197_772+227delinsGTGGCCTCAGCTGAGATGCTGGAGTTCATGA NP_001269714.1:n.772+197_772+227delinsGTGGCCTCAGCTGAGATGCTGGA...
NM_018006.4:c.772+197_772+227delinsGTGGCCTCAGCTGAGATGCTGGAGTTCATGA NP_060476.2:n.772+197_772+227delinsGTGGCCTCAGCTGAGATGCTGGAGTT...
NR_104240.1:n.1081+197_1081+227delinsGTGGCCTCAGCTGAGATGCTGGAGTTCATGA
NR_104241.1:n.974+197_974+227delinsGTGGCCTCAGCTGAGATGCTGGAGTTCATGA
XM_005261678.1:c.376+197_376+227delinsGTGGCCTCAGCTGAGATGCTGGAGTTCATGA XP_005261735.1:n.376+197_376+227delinsGTGGCCTCAGCTGAGATGCTGGA...
XM_005261681.1:c.376+197_376+227delinsGTGGCCTCAGCTGAGATGCTGGAGTTCATGA XP_005261738.1:n.376+197_376+227delinsGTGGCCTCAGCTGAGATGCTGGA...
XM_011530271.1:c.667+197_667+227delinsGTGGCCTCAGCTGAGATGCTGGAGTTCATGA XP_011528573.1:n.667+197_667+227delinsGTGGCCTCAGCTGAGATGCTGGA...
XM_011530272.1:c.772+197_772+227delinsGTGGCCTCAGCTGAGATGCTGGAGTTCATGA XP_011528574.1:n.772+197_772+227delinsGTGGCCTCAGCTGAGATGCTGGA...
XM_011530273.1:c.772+197_772+227delinsGTGGCCTCAGCTGAGATGCTGGAGTTCATGA XP_011528575.1:n.772+197_772+227delinsGTGGCCTCAGCTGAGATGCTGGA...
XM_011530274.1:c.430+197_430+227delinsGTGGCCTCAGCTGAGATGCTGGAGTTCATGA XP_011528576.1:n.430+197_430+227delinsGTGGCCTCAGCTGAGATGCTGGA...
XM_011530275.1:c.376+197_376+227delinsGTGGCCTCAGCTGAGATGCTGGAGTTCATGA XP_011528577.1:n.376+197_376+227delinsGTGGCCTCAGCTGAGATGCTGGA...
XM_011530271.2:c.667+197_667+227delinsGTGGCCTCAGCTGAGATGCTGGAGTTCATGA XP_011528573.1:n.667+197_667+227delinsGTGGCCTCAGCTGAGATGCTGGA...
XM_011530272.2:c.772+197_772+227delinsGTGGCCTCAGCTGAGATGCTGGAGTTCATGA XP_011528574.1:n.772+197_772+227delinsGTGGCCTCAGCTGAGATGCTGGA...
XM_011530273.2:c.772+197_772+227delinsGTGGCCTCAGCTGAGATGCTGGAGTTCATGA XP_011528575.1:n.772+197_772+227delinsGTGGCCTCAGCTGAGATGCTGGA...
XM_011530274.2:c.430+197_430+227delinsGTGGCCTCAGCTGAGATGCTGGAGTTCATGA XP_011528576.1:n.430+197_430+227delinsGTGGCCTCAGCTGAGATGCTGGA...
XM_024452260.1:c.667+197_667+227delinsGTGGCCTCAGCTGAGATGCTGGAGTTCATGA XP_024308028.1:n.667+197_667+227delinsGTGGCCTCAGCTGAGATGCTGGA...
XR_001755261.2:n.821_851delinsGTGGCCTCAGCTGAGATGCTGGAGTTCATGA
XR_001755262.2:n.821_851delinsGTGGCCTCAGCTGAGATGCTGGAGTTCATGA
NM_018006.5:c.772+197_772+227delinsGTGGCCTCAGCTGAGATGCTGGAGTTCATGA MANE Select NP_060476.2:n.772+197_772+227delinsGTGGCCTCAGCTGAGATGCTGGAGTT...
NM_001282782.2:c.430+197_430+227delinsGTGGCCTCAGCTGAGATGCTGGAGTTCATGA NP_001269711.1:n.430+197_430+227delinsGTGGCCTCAGCTGAGATGCTGGA...
NM_001282783.2:c.352+197_352+227delinsGTGGCCTCAGCTGAGATGCTGGAGTTCATGA NP_001269712.1:n.352+197_352+227delinsGTGGCCTCAGCTGAGATGCTGGA...
NM_001282784.2:c.352+197_352+227delinsGTGGCCTCAGCTGAGATGCTGGAGTTCATGA NP_001269713.1:n.352+197_352+227delinsGTGGCCTCAGCTGAGATGCTGGA...
NM_001282785.2:c.772+197_772+227delinsGTGGCCTCAGCTGAGATGCTGGAGTTCATGA NP_001269714.1:n.772+197_772+227delinsGTGGCCTCAGCTGAGATGCTGGA...
NR_104240.2:n.768+197_768+227delinsGTGGCCTCAGCTGAGATGCTGGAGTTCATGA
NR_104241.2:n.661+197_661+227delinsGTGGCCTCAGCTGAGATGCTGGAGTTCATGA