Canonical Allele Identifier: CA2408701049
Gene: TRMU HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.46352590_46352607delinsCTGTGAGTTACGTATCAA , CM000684.2:g.46352590_46352607delinsCTGTGAGTTACGTATCAA GRCh38
NC_000022.10:g.46748487_46748504delinsCTGTGAGTTACGTATCAA , CM000684.1:g.46748487_46748504delinsCTGTGAGTTACGTATCAA GRCh37
NC_000022.9:g.45127151_45127168delinsCTGTGAGTTACGTATCAA NCBI36
NG_012173.1:g.22190_22207delinsCTGTGAGTTACGTATCAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000465378.6:n.1080_1097delinsCTGTGAGTTACGTATCAA
ENST00000642923.1:c.667+260_667+277delinsCTGTGAGTTACGTATCAA ENSP00000494255.1:n.667+260_667+277delinsCTGTGAGTTACGTATCAA
ENST00000643137.1:c.667+260_667+277delinsCTGTGAGTTACGTATCAA ENSP00000495331.1:n.667+260_667+277delinsCTGTGAGTTACGTATCAA
ENST00000644006.1:c.*216+260_*216+277delinsCTGTGAGTTACGTATCAA ENSP00000493778.1:n.*216+260_*216+277delinsCTGTGAGTTACGTATCAA...
ENST00000645026.1:n.823+260_823+277delinsCTGTGAGTTACGTATCAA
ENST00000645190.1:c.772+260_772+277delinsCTGTGAGTTACGTATCAA MANE Select ENSP00000496496.1:n.772+260_772+277delinsCTGTGAGTTACGTATCAA
ENST00000647301.1:c.*216+260_*216+277delinsCTGTGAGTTACGTATCAA ENSP00000496641.1:n.*216+260_*216+277delinsCTGTGAGTTACGTATCAA...
ENST00000290846.8:c.772+260_772+277delinsCTGTGAGTTACGTATCAA ENSP00000290846.4:n.772+260_772+277delinsCTGTGAGTTACGTATCAA
ENST00000381019.3:c.772+260_772+277delinsCTGTGAGTTACGTATCAA ENSP00000370407.3:n.772+260_772+277delinsCTGTGAGTTACGTATCAA
ENST00000381021.7:c.*365+260_*365+277delinsCTGTGAGTTACGTATCAA ENSP00000370409.3:n.*365+260_*365+277delinsCTGTGAGTTACGTATCAA...
ENST00000441818.5:c.*306+260_*306+277delinsCTGTGAGTTACGTATCAA ENSP00000393014.1:n.*306+260_*306+277delinsCTGTGAGTTACGTATCAA...
ENST00000453630.5:c.*310+260_*310+277delinsCTGTGAGTTACGTATCAA ENSP00000398488.1:n.*310+260_*310+277delinsCTGTGAGTTACGTATCAA...
ENST00000456595.5:c.*306+260_*306+277delinsCTGTGAGTTACGTATCAA ENSP00000413880.1:n.*306+260_*306+277delinsCTGTGAGTTACGTATCAA...
ENST00000457572.5:c.*216+260_*216+277delinsCTGTGAGTTACGTATCAA ENSP00000407700.1:n.*216+260_*216+277delinsCTGTGAGTTACGTATCAA...
ENST00000463785.1:n.306_323delinsCTGTGAGTTACGTATCAA
NM_001282782.1:c.430+260_430+277delinsCTGTGAGTTACGTATCAA NP_001269711.1:n.430+260_430+277delinsCTGTGAGTTACGTATCAA
NM_001282783.1:c.352+260_352+277delinsCTGTGAGTTACGTATCAA NP_001269712.1:n.352+260_352+277delinsCTGTGAGTTACGTATCAA
NM_001282784.1:c.352+260_352+277delinsCTGTGAGTTACGTATCAA NP_001269713.1:n.352+260_352+277delinsCTGTGAGTTACGTATCAA
NM_001282785.1:c.772+260_772+277delinsCTGTGAGTTACGTATCAA NP_001269714.1:n.772+260_772+277delinsCTGTGAGTTACGTATCAA
NM_018006.4:c.772+260_772+277delinsCTGTGAGTTACGTATCAA NP_060476.2:n.772+260_772+277delinsCTGTGAGTTACGTATCAA
NR_104240.1:n.1081+260_1081+277delinsCTGTGAGTTACGTATCAA
NR_104241.1:n.974+260_974+277delinsCTGTGAGTTACGTATCAA
XM_005261678.1:c.376+260_376+277delinsCTGTGAGTTACGTATCAA XP_005261735.1:n.376+260_376+277delinsCTGTGAGTTACGTATCAA
XM_005261681.1:c.376+260_376+277delinsCTGTGAGTTACGTATCAA XP_005261738.1:n.376+260_376+277delinsCTGTGAGTTACGTATCAA
XM_011530271.1:c.667+260_667+277delinsCTGTGAGTTACGTATCAA XP_011528573.1:n.667+260_667+277delinsCTGTGAGTTACGTATCAA
XM_011530272.1:c.772+260_772+277delinsCTGTGAGTTACGTATCAA XP_011528574.1:n.772+260_772+277delinsCTGTGAGTTACGTATCAA
XM_011530273.1:c.772+260_772+277delinsCTGTGAGTTACGTATCAA XP_011528575.1:n.772+260_772+277delinsCTGTGAGTTACGTATCAA
XM_011530274.1:c.430+260_430+277delinsCTGTGAGTTACGTATCAA XP_011528576.1:n.430+260_430+277delinsCTGTGAGTTACGTATCAA
XM_011530275.1:c.376+260_376+277delinsCTGTGAGTTACGTATCAA XP_011528577.1:n.376+260_376+277delinsCTGTGAGTTACGTATCAA
XM_011530271.2:c.667+260_667+277delinsCTGTGAGTTACGTATCAA XP_011528573.1:n.667+260_667+277delinsCTGTGAGTTACGTATCAA
XM_011530272.2:c.772+260_772+277delinsCTGTGAGTTACGTATCAA XP_011528574.1:n.772+260_772+277delinsCTGTGAGTTACGTATCAA
XM_011530273.2:c.772+260_772+277delinsCTGTGAGTTACGTATCAA XP_011528575.1:n.772+260_772+277delinsCTGTGAGTTACGTATCAA
XM_011530274.2:c.430+260_430+277delinsCTGTGAGTTACGTATCAA XP_011528576.1:n.430+260_430+277delinsCTGTGAGTTACGTATCAA
XM_024452260.1:c.667+260_667+277delinsCTGTGAGTTACGTATCAA XP_024308028.1:n.667+260_667+277delinsCTGTGAGTTACGTATCAA
XR_001755261.2:n.884_901delinsCTGTGAGTTACGTATCAA
XR_001755262.2:n.884_901delinsCTGTGAGTTACGTATCAA
NM_018006.5:c.772+260_772+277delinsCTGTGAGTTACGTATCAA MANE Select NP_060476.2:n.772+260_772+277delinsCTGTGAGTTACGTATCAA
NM_001282782.2:c.430+260_430+277delinsCTGTGAGTTACGTATCAA NP_001269711.1:n.430+260_430+277delinsCTGTGAGTTACGTATCAA
NM_001282783.2:c.352+260_352+277delinsCTGTGAGTTACGTATCAA NP_001269712.1:n.352+260_352+277delinsCTGTGAGTTACGTATCAA
NM_001282784.2:c.352+260_352+277delinsCTGTGAGTTACGTATCAA NP_001269713.1:n.352+260_352+277delinsCTGTGAGTTACGTATCAA
NM_001282785.2:c.772+260_772+277delinsCTGTGAGTTACGTATCAA NP_001269714.1:n.772+260_772+277delinsCTGTGAGTTACGTATCAA
NR_104240.2:n.768+260_768+277delinsCTGTGAGTTACGTATCAA
NR_104241.2:n.661+260_661+277delinsCTGTGAGTTACGTATCAA