Canonical Allele Identifier: CA2408700697
Gene: TRMU HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.46352018T= , CM000684.2:g.46352018T= GRCh38
NC_000022.10:g.46747915T= , CM000684.1:g.46747915T= GRCh37
NC_000022.9:g.45126579T= NCBI36
NG_012173.1:g.21618T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000465378.6:n.700-103T=
ENST00000642923.1:c.547-103T= ENSP00000494255.1:n.547-103T=
ENST00000643137.1:c.547-103T= ENSP00000495331.1:n.547-103T=
ENST00000644006.1:c.*96-103T= ENSP00000493778.1:n.*96-103T=
ENST00000645026.1:n.703-103T=
ENST00000645190.1:c.652-103T= MANE Select ENSP00000496496.1:n.652-103T=
ENST00000647301.1:c.*96-103T= ENSP00000496641.1:n.*96-103T=
ENST00000290846.8:c.652-103T= ENSP00000290846.4:n.652-103T=
ENST00000381019.3:c.652-103T= ENSP00000370407.3:n.652-103T=
ENST00000381021.7:c.*245-103T= ENSP00000370409.3:n.*245-103T=
ENST00000441818.5:c.*186-103T= ENSP00000393014.1:n.*186-103T=
ENST00000453630.5:c.*190-103T= ENSP00000398488.1:n.*190-103T=
ENST00000456595.5:c.*186-103T= ENSP00000413880.1:n.*186-103T=
ENST00000457572.5:c.*96-103T= ENSP00000407700.1:n.*96-103T=
ENST00000463785.1:n.120-103T=
ENST00000479648.1:n.369T=
ENST00000485175.5:n.612-103T=
ENST00000486620.5:n.694-103T=
NM_001282782.1:c.310-103T= NP_001269711.1:n.310-103T=
NM_001282783.1:c.232-103T= NP_001269712.1:n.232-103T=
NM_001282784.1:c.232-103T= NP_001269713.1:n.232-103T=
NM_001282785.1:c.652-103T= NP_001269714.1:n.652-103T=
NM_018006.4:c.652-103T= NP_060476.2:n.652-103T=
NR_104240.1:n.961-103T=
NR_104241.1:n.854-103T=
XM_005261678.1:c.256-103T= XP_005261735.1:n.256-103T=
XM_005261681.1:c.256-103T= XP_005261738.1:n.256-103T=
XM_011530271.1:c.547-103T= XP_011528573.1:n.547-103T=
XM_011530272.1:c.652-103T= XP_011528574.1:n.652-103T=
XM_011530273.1:c.652-103T= XP_011528575.1:n.652-103T=
XM_011530274.1:c.310-103T= XP_011528576.1:n.310-103T=
XM_011530275.1:c.256-103T= XP_011528577.1:n.256-103T=
XM_011530271.2:c.547-103T= XP_011528573.1:n.547-103T=
XM_011530272.2:c.652-103T= XP_011528574.1:n.652-103T=
XM_011530273.2:c.652-103T= XP_011528575.1:n.652-103T=
XM_011530274.2:c.310-103T= XP_011528576.1:n.310-103T=
XM_024452260.1:c.547-103T= XP_024308028.1:n.547-103T=
XR_001755261.2:n.698-103T=
XR_001755262.2:n.698-103T=
NM_018006.5:c.652-103T= MANE Select NP_060476.2:n.652-103T=
NM_001282782.2:c.310-103T= NP_001269711.1:n.310-103T=
NM_001282783.2:c.232-103T= NP_001269712.1:n.232-103T=
NM_001282784.2:c.232-103T= NP_001269713.1:n.232-103T=
NM_001282785.2:c.652-103T= NP_001269714.1:n.652-103T=
NR_104240.2:n.648-103T=
NR_104241.2:n.541-103T=