Canonical Allele Identifier: CA2408700849
Gene: TRMU HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.46352262A= , CM000684.2:g.46352262A= GRCh38
NC_000022.10:g.46748159A= , CM000684.1:g.46748159A= GRCh37
NC_000022.9:g.45126823A= NCBI36
NG_012173.1:g.21862A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000465378.6:n.754-2A=
ENST00000642923.1:c.601-2A= ENSP00000494255.1:n.601-2A=
ENST00000643137.1:c.601-2A= ENSP00000495331.1:n.601-2A=
ENST00000644006.1:c.*150-2A= ENSP00000493778.1:n.*150-2A=
ENST00000645026.1:n.757-2A=
ENST00000645190.1:c.706-2A= MANE Select ENSP00000496496.1:n.706-2A=
ENST00000647301.1:c.*150-2A= ENSP00000496641.1:n.*150-2A=
ENST00000290846.8:c.706-2A= ENSP00000290846.4:n.706-2A=
ENST00000381019.3:c.706-2A= ENSP00000370407.3:n.706-2A=
ENST00000381021.7:c.*299-2A= ENSP00000370409.3:n.*299-2A=
ENST00000441818.5:c.*240-2A= ENSP00000393014.1:n.*240-2A=
ENST00000453630.5:c.*244-2A= ENSP00000398488.1:n.*244-2A=
ENST00000456595.5:c.*240-2A= ENSP00000413880.1:n.*240-2A=
ENST00000457572.5:c.*150-2A= ENSP00000407700.1:n.*150-2A=
ENST00000463785.1:n.174-2A=
ENST00000479648.1:n.526-2A=
ENST00000485175.5:n.666-2A=
ENST00000486620.5:n.748-2A=
NM_001282782.1:c.364-2A= NP_001269711.1:n.364-2A=
NM_001282783.1:c.286-2A= NP_001269712.1:n.286-2A=
NM_001282784.1:c.286-2A= NP_001269713.1:n.286-2A=
NM_001282785.1:c.706-2A= NP_001269714.1:n.706-2A=
NM_018006.4:c.706-2A= NP_060476.2:n.706-2A=
NR_104240.1:n.1015-2A=
NR_104241.1:n.908-2A=
XM_005261678.1:c.310-2A= XP_005261735.1:n.310-2A=
XM_005261681.1:c.310-2A= XP_005261738.1:n.310-2A=
XM_011530271.1:c.601-2A= XP_011528573.1:n.601-2A=
XM_011530272.1:c.706-2A= XP_011528574.1:n.706-2A=
XM_011530273.1:c.706-2A= XP_011528575.1:n.706-2A=
XM_011530274.1:c.364-2A= XP_011528576.1:n.364-2A=
XM_011530275.1:c.310-2A= XP_011528577.1:n.310-2A=
XM_011530271.2:c.601-2A= XP_011528573.1:n.601-2A=
XM_011530272.2:c.706-2A= XP_011528574.1:n.706-2A=
XM_011530273.2:c.706-2A= XP_011528575.1:n.706-2A=
XM_011530274.2:c.364-2A= XP_011528576.1:n.364-2A=
XM_024452260.1:c.601-2A= XP_024308028.1:n.601-2A=
XR_001755261.2:n.752-2A=
XR_001755262.2:n.752-2A=
NM_018006.5:c.706-2A= MANE Select NP_060476.2:n.706-2A=
NM_001282782.2:c.364-2A= NP_001269711.1:n.364-2A=
NM_001282783.2:c.286-2A= NP_001269712.1:n.286-2A=
NM_001282784.2:c.286-2A= NP_001269713.1:n.286-2A=
NM_001282785.2:c.706-2A= NP_001269714.1:n.706-2A=
NR_104240.2:n.702-2A=
NR_104241.2:n.595-2A=