Canonical Allele Identifier: CA2408700820
Gene: TRMU HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.46352152A= , CM000684.2:g.46352152A= GRCh38
NC_000022.10:g.46748049A= , CM000684.1:g.46748049A= GRCh37
NC_000022.9:g.45126713A= NCBI36
NG_012173.1:g.21752A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000465378.6:n.731A=
ENST00000642923.1:c.578A= ENSP00000494255.1:p.Asn193=
ENST00000643137.1:c.578A= ENSP00000495331.1:p.Asn193=
ENST00000644006.1:c.*127A= ENSP00000493778.1:n.*127A=
ENST00000645026.1:n.734A=
ENST00000645190.1:c.683A= MANE Select ENSP00000496496.1:p.Asn228=
ENST00000647301.1:c.*127A= ENSP00000496641.1:n.*127A=
ENST00000290846.8:c.683A= ENSP00000290846.4:p.Asn228=
ENST00000381019.3:c.683A= ENSP00000370407.3:p.Asn228=
ENST00000381021.7:c.*276A= ENSP00000370409.3:n.*276A=
ENST00000441818.5:c.*217A= ENSP00000393014.1:n.*217A=
ENST00000453630.5:c.*221A= ENSP00000398488.1:n.*221A=
ENST00000456595.5:c.*217A= ENSP00000413880.1:n.*217A=
ENST00000457572.5:c.*127A= ENSP00000407700.1:n.*127A=
ENST00000463785.1:n.151A=
ENST00000479648.1:n.503A=
ENST00000485175.5:n.643A=
ENST00000486620.5:n.725A=
NM_001282782.1:c.341A= NP_001269711.1:p.Asn114=
NM_001282783.1:c.263A= NP_001269712.1:p.Asn88=
NM_001282784.1:c.263A= NP_001269713.1:p.Asn88=
NM_001282785.1:c.683A= NP_001269714.1:p.Asn228=
NM_018006.4:c.683A= NP_060476.2:p.Asn228=
NR_104240.1:n.992A=
NR_104241.1:n.885A=
XM_005261678.1:c.287A= XP_005261735.1:p.Asn96=
XM_005261681.1:c.287A= XP_005261738.1:p.Asn96=
XM_011530271.1:c.578A= XP_011528573.1:p.Asn193=
XM_011530272.1:c.683A= XP_011528574.1:p.Asn228=
XM_011530273.1:c.683A= XP_011528575.1:p.Asn228=
XM_011530274.1:c.341A= XP_011528576.1:p.Asn114=
XM_011530275.1:c.287A= XP_011528577.1:p.Asn96=
XM_011530271.2:c.578A= XP_011528573.1:p.Asn193=
XM_011530272.2:c.683A= XP_011528574.1:p.Asn228=
XM_011530273.2:c.683A= XP_011528575.1:p.Asn228=
XM_011530274.2:c.341A= XP_011528576.1:p.Asn114=
XM_024452260.1:c.578A= XP_024308028.1:p.Asn193=
XR_001755261.2:n.729A=
XR_001755262.2:n.729A=
NM_018006.5:c.683A= MANE Select NP_060476.2:p.Asn228=
NM_001282782.2:c.341A= NP_001269711.1:p.Asn114=
NM_001282783.2:c.263A= NP_001269712.1:p.Asn88=
NM_001282784.2:c.263A= NP_001269713.1:p.Asn88=
NM_001282785.2:c.683A= NP_001269714.1:p.Asn228=
NR_104240.2:n.679A=
NR_104241.2:n.572A=