Canonical Allele Identifier: CA2408700880
Gene: TRMU HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.46352305_46352308delinsCAAT , CM000684.2:g.46352305_46352308delinsCAAT GRCh38
NC_000022.10:g.46748202_46748205delinsCAAT , CM000684.1:g.46748202_46748205delinsCAAT GRCh37
NC_000022.9:g.45126866_45126869delinsCAAT NCBI36
NG_012173.1:g.21905_21908delinsCAAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000465378.6:n.795_798delinsCAAT
ENST00000642923.1:c.642_645delinsCAAT ENSP00000494255.1:p.Asp214=
ENST00000643137.1:c.642_645delinsCAAT ENSP00000495331.1:p.Asp214=
ENST00000644006.1:c.*191_*194delinsCAAT ENSP00000493778.1:n.*191_*194delinsCAAT
ENST00000645026.1:n.798_801delinsCAAT
ENST00000645190.1:c.747_750delinsCAAT MANE Select ENSP00000496496.1:p.Asp249=
ENST00000647301.1:c.*191_*194delinsCAAT ENSP00000496641.1:n.*191_*194delinsCAAT
ENST00000290846.8:c.747_750delinsCAAT ENSP00000290846.4:p.Asp249=
ENST00000381019.3:c.747_750delinsCAAT ENSP00000370407.3:p.Asp249=
ENST00000381021.7:c.*340_*343delinsCAAT ENSP00000370409.3:n.*340_*343delinsCAAT
ENST00000441818.5:c.*281_*284delinsCAAT ENSP00000393014.1:n.*281_*284delinsCAAT
ENST00000453630.5:c.*285_*288delinsCAAT ENSP00000398488.1:n.*285_*288delinsCAAT
ENST00000456595.5:c.*281_*284delinsCAAT ENSP00000413880.1:n.*281_*284delinsCAAT
ENST00000457572.5:c.*191_*194delinsCAAT ENSP00000407700.1:n.*191_*194delinsCAAT
ENST00000463785.1:n.215_218delinsCAAT
ENST00000479648.1:n.567_570delinsCAAT
ENST00000485175.5:n.707_710delinsCAAT
ENST00000486620.5:n.789_792delinsCAAT
NM_001282782.1:c.405_408delinsCAAT NP_001269711.1:p.Asp135=
NM_001282783.1:c.327_330delinsCAAT NP_001269712.1:p.Asp109=
NM_001282784.1:c.327_330delinsCAAT NP_001269713.1:p.Asp109=
NM_001282785.1:c.747_750delinsCAAT NP_001269714.1:p.Asp249=
NM_018006.4:c.747_750delinsCAAT NP_060476.2:p.Asp249=
NR_104240.1:n.1056_1059delinsCAAT
NR_104241.1:n.949_952delinsCAAT
XM_005261678.1:c.351_354delinsCAAT XP_005261735.1:p.Asp117=
XM_005261681.1:c.351_354delinsCAAT XP_005261738.1:p.Asp117=
XM_011530271.1:c.642_645delinsCAAT XP_011528573.1:p.Asp214=
XM_011530272.1:c.747_750delinsCAAT XP_011528574.1:p.Asp249=
XM_011530273.1:c.747_750delinsCAAT XP_011528575.1:p.Asp249=
XM_011530274.1:c.405_408delinsCAAT XP_011528576.1:p.Asp135=
XM_011530275.1:c.351_354delinsCAAT XP_011528577.1:p.Asp117=
XM_011530271.2:c.642_645delinsCAAT XP_011528573.1:p.Asp214=
XM_011530272.2:c.747_750delinsCAAT XP_011528574.1:p.Asp249=
XM_011530273.2:c.747_750delinsCAAT XP_011528575.1:p.Asp249=
XM_011530274.2:c.405_408delinsCAAT XP_011528576.1:p.Asp135=
XM_024452260.1:c.642_645delinsCAAT XP_024308028.1:p.Asp214=
XR_001755261.2:n.793_796delinsCAAT
XR_001755262.2:n.793_796delinsCAAT
NM_018006.5:c.747_750delinsCAAT MANE Select NP_060476.2:p.Asp249=
NM_001282782.2:c.405_408delinsCAAT NP_001269711.1:p.Asp135=
NM_001282783.2:c.327_330delinsCAAT NP_001269712.1:p.Asp109=
NM_001282784.2:c.327_330delinsCAAT NP_001269713.1:p.Asp109=
NM_001282785.2:c.747_750delinsCAAT NP_001269714.1:p.Asp249=
NR_104240.2:n.743_746delinsCAAT
NR_104241.2:n.636_639delinsCAAT