Canonical Allele Identifier: CA411946187
Gene: TRMU HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.46352157G>T , CM000684.2:g.46352157G>T GRCh38
NC_000022.10:g.46748054G>T , CM000684.1:g.46748054G>T GRCh37
NC_000022.9:g.45126718G>T NCBI36
NG_012173.1:g.21757G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000465378.6:n.736G>T
ENST00000642923.1:c.583G>T ENSP00000494255.1:p.Glu195Ter
ENST00000643137.1:c.583G>T ENSP00000495331.1:p.Glu195Ter
ENST00000644006.1:c.*132G>T ENSP00000493778.1:n.*132G>T
ENST00000645026.1:n.739G>T
ENST00000645190.1:c.688G>T MANE Select ENSP00000496496.1:p.Glu230Ter
ENST00000647301.1:c.*132G>T ENSP00000496641.1:n.*132G>T
ENST00000290846.8:c.688G>T ENSP00000290846.4:p.Glu230Ter
ENST00000381019.3:c.688G>T ENSP00000370407.3:p.Glu230Ter
ENST00000381021.7:c.*281G>T ENSP00000370409.3:n.*281G>T
ENST00000441818.5:c.*222G>T ENSP00000393014.1:n.*222G>T
ENST00000453630.5:c.*226G>T ENSP00000398488.1:n.*226G>T
ENST00000456595.5:c.*222G>T ENSP00000413880.1:n.*222G>T
ENST00000457572.5:c.*132G>T ENSP00000407700.1:n.*132G>T
ENST00000463785.1:n.156G>T
ENST00000479648.1:n.508G>T
ENST00000485175.5:n.648G>T
ENST00000486620.5:n.730G>T
NM_001282782.1:c.346G>T NP_001269711.1:p.Glu116Ter
NM_001282783.1:c.268G>T NP_001269712.1:p.Glu90Ter
NM_001282784.1:c.268G>T NP_001269713.1:p.Glu90Ter
NM_001282785.1:c.688G>T NP_001269714.1:p.Glu230Ter
NM_018006.4:c.688G>T NP_060476.2:p.Glu230Ter
NR_104240.1:n.997G>T
NR_104241.1:n.890G>T
XM_005261678.1:c.292G>T XP_005261735.1:p.Glu98Ter
XM_005261681.1:c.292G>T XP_005261738.1:p.Glu98Ter
XM_011530271.1:c.583G>T XP_011528573.1:p.Glu195Ter
XM_011530272.1:c.688G>T XP_011528574.1:p.Glu230Ter
XM_011530273.1:c.688G>T XP_011528575.1:p.Glu230Ter
XM_011530274.1:c.346G>T XP_011528576.1:p.Glu116Ter
XM_011530275.1:c.292G>T XP_011528577.1:p.Glu98Ter
XM_011530271.2:c.583G>T XP_011528573.1:p.Glu195Ter
XM_011530272.2:c.688G>T XP_011528574.1:p.Glu230Ter
XM_011530273.2:c.688G>T XP_011528575.1:p.Glu230Ter
XM_011530274.2:c.346G>T XP_011528576.1:p.Glu116Ter
XM_024452260.1:c.583G>T XP_024308028.1:p.Glu195Ter
XR_001755261.2:n.734G>T
XR_001755262.2:n.734G>T
NM_018006.5:c.688G>T MANE Select NP_060476.2:p.Glu230Ter
NM_001282782.2:c.346G>T NP_001269711.1:p.Glu116Ter
NM_001282783.2:c.268G>T NP_001269712.1:p.Glu90Ter
NM_001282784.2:c.268G>T NP_001269713.1:p.Glu90Ter
NM_001282785.2:c.688G>T NP_001269714.1:p.Glu230Ter
NR_104240.2:n.684G>T
NR_104241.2:n.577G>T