Canonical Allele Identifier: CA2408700783
Gene: TRMU HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.46352138C= , CM000684.2:g.46352138C= GRCh38
NC_000022.10:g.46748035C= , CM000684.1:g.46748035C= GRCh37
NC_000022.9:g.45126699C= NCBI36
NG_012173.1:g.21738C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000465378.6:n.717C=
ENST00000642923.1:c.564C= ENSP00000494255.1:p.Phe188=
ENST00000643137.1:c.564C= ENSP00000495331.1:p.Phe188=
ENST00000644006.1:c.*113C= ENSP00000493778.1:n.*113C=
ENST00000645026.1:n.720C=
ENST00000645190.1:c.669C= MANE Select ENSP00000496496.1:p.Phe223=
ENST00000647301.1:c.*113C= ENSP00000496641.1:n.*113C=
ENST00000290846.8:c.669C= ENSP00000290846.4:p.Phe223=
ENST00000381019.3:c.669C= ENSP00000370407.3:p.Phe223=
ENST00000381021.7:c.*262C= ENSP00000370409.3:n.*262C=
ENST00000441818.5:c.*203C= ENSP00000393014.1:n.*203C=
ENST00000453630.5:c.*207C= ENSP00000398488.1:n.*207C=
ENST00000456595.5:c.*203C= ENSP00000413880.1:n.*203C=
ENST00000457572.5:c.*113C= ENSP00000407700.1:n.*113C=
ENST00000463785.1:n.137C=
ENST00000479648.1:n.489C=
ENST00000485175.5:n.629C=
ENST00000486620.5:n.711C=
NM_001282782.1:c.327C= NP_001269711.1:p.Phe109=
NM_001282783.1:c.249C= NP_001269712.1:p.Phe83=
NM_001282784.1:c.249C= NP_001269713.1:p.Phe83=
NM_001282785.1:c.669C= NP_001269714.1:p.Phe223=
NM_018006.4:c.669C= NP_060476.2:p.Phe223=
NR_104240.1:n.978C=
NR_104241.1:n.871C=
XM_005261678.1:c.273C= XP_005261735.1:p.Phe91=
XM_005261681.1:c.273C= XP_005261738.1:p.Phe91=
XM_011530271.1:c.564C= XP_011528573.1:p.Phe188=
XM_011530272.1:c.669C= XP_011528574.1:p.Phe223=
XM_011530273.1:c.669C= XP_011528575.1:p.Phe223=
XM_011530274.1:c.327C= XP_011528576.1:p.Phe109=
XM_011530275.1:c.273C= XP_011528577.1:p.Phe91=
XM_011530271.2:c.564C= XP_011528573.1:p.Phe188=
XM_011530272.2:c.669C= XP_011528574.1:p.Phe223=
XM_011530273.2:c.669C= XP_011528575.1:p.Phe223=
XM_011530274.2:c.327C= XP_011528576.1:p.Phe109=
XM_024452260.1:c.564C= XP_024308028.1:p.Phe188=
XR_001755261.2:n.715C=
XR_001755262.2:n.715C=
NM_018006.5:c.669C= MANE Select NP_060476.2:p.Phe223=
NM_001282782.2:c.327C= NP_001269711.1:p.Phe109=
NM_001282783.2:c.249C= NP_001269712.1:p.Phe83=
NM_001282784.2:c.249C= NP_001269713.1:p.Phe83=
NM_001282785.2:c.669C= NP_001269714.1:p.Phe223=
NR_104240.2:n.665C=
NR_104241.2:n.558C=