Canonical Allele Identifier: CA411946126
Gene: TRMU HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.46352130A>T , CM000684.2:g.46352130A>T GRCh38
NC_000022.10:g.46748027A>T , CM000684.1:g.46748027A>T GRCh37
NC_000022.9:g.45126691A>T NCBI36
NG_012173.1:g.21730A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000465378.6:n.709A>T
ENST00000642923.1:c.556A>T ENSP00000494255.1:p.Met186Leu
ENST00000643137.1:c.556A>T ENSP00000495331.1:p.Met186Leu
ENST00000644006.1:c.*105A>T ENSP00000493778.1:n.*105A>T
ENST00000645026.1:n.712A>T
ENST00000645190.1:c.661A>T MANE Select ENSP00000496496.1:p.Met221Leu
ENST00000647301.1:c.*105A>T ENSP00000496641.1:n.*105A>T
ENST00000290846.8:c.661A>T ENSP00000290846.4:p.Met221Leu
ENST00000381019.3:c.661A>T ENSP00000370407.3:p.Met221Leu
ENST00000381021.7:c.*254A>T ENSP00000370409.3:n.*254A>T
ENST00000441818.5:c.*195A>T ENSP00000393014.1:n.*195A>T
ENST00000453630.5:c.*199A>T ENSP00000398488.1:n.*199A>T
ENST00000456595.5:c.*195A>T ENSP00000413880.1:n.*195A>T
ENST00000457572.5:c.*105A>T ENSP00000407700.1:n.*105A>T
ENST00000463785.1:n.129A>T
ENST00000479648.1:n.481A>T
ENST00000485175.5:n.621A>T
ENST00000486620.5:n.703A>T
NM_001282782.1:c.319A>T NP_001269711.1:p.Met107Leu
NM_001282783.1:c.241A>T NP_001269712.1:p.Met81Leu
NM_001282784.1:c.241A>T NP_001269713.1:p.Met81Leu
NM_001282785.1:c.661A>T NP_001269714.1:p.Met221Leu
NM_018006.4:c.661A>T NP_060476.2:p.Met221Leu
NR_104240.1:n.970A>T
NR_104241.1:n.863A>T
XM_005261678.1:c.265A>T XP_005261735.1:p.Met89Leu
XM_005261681.1:c.265A>T XP_005261738.1:p.Met89Leu
XM_011530271.1:c.556A>T XP_011528573.1:p.Met186Leu
XM_011530272.1:c.661A>T XP_011528574.1:p.Met221Leu
XM_011530273.1:c.661A>T XP_011528575.1:p.Met221Leu
XM_011530274.1:c.319A>T XP_011528576.1:p.Met107Leu
XM_011530275.1:c.265A>T XP_011528577.1:p.Met89Leu
XM_011530271.2:c.556A>T XP_011528573.1:p.Met186Leu
XM_011530272.2:c.661A>T XP_011528574.1:p.Met221Leu
XM_011530273.2:c.661A>T XP_011528575.1:p.Met221Leu
XM_011530274.2:c.319A>T XP_011528576.1:p.Met107Leu
XM_024452260.1:c.556A>T XP_024308028.1:p.Met186Leu
XR_001755261.2:n.707A>T
XR_001755262.2:n.707A>T
NM_018006.5:c.661A>T MANE Select NP_060476.2:p.Met221Leu
NM_001282782.2:c.319A>T NP_001269711.1:p.Met107Leu
NM_001282783.2:c.241A>T NP_001269712.1:p.Met81Leu
NM_001282784.2:c.241A>T NP_001269713.1:p.Met81Leu
NM_001282785.2:c.661A>T NP_001269714.1:p.Met221Leu
NR_104240.2:n.657A>T
NR_104241.2:n.550A>T