Canonical Allele Identifier: CA753655777
Gene: TRMU HGNC NCBI

Linked Data

dbSNP Id: rs1489643441

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.46352045_46352048dup , CM000684.2:g.46352045_46352048dup GRCh38
NC_000022.10:g.46747942_46747945dup , CM000684.1:g.46747942_46747945dup GRCh37
NC_000022.9:g.45126606_45126609dup NCBI36
NG_012173.1:g.21645_21648dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000465378.6:n.700-76_700-73dup
ENST00000642923.1:c.547-76_547-73dup ENSP00000494255.1:n.547-76_547-73dup
ENST00000643137.1:c.547-76_547-73dup ENSP00000495331.1:n.547-76_547-73dup
ENST00000644006.1:c.*96-76_*96-73dup ENSP00000493778.1:n.*96-76_*96-73dup
ENST00000645026.1:n.703-76_703-73dup
ENST00000645190.1:c.652-76_652-73dup MANE Select ENSP00000496496.1:n.652-76_652-73dup
ENST00000647301.1:c.*96-76_*96-73dup ENSP00000496641.1:n.*96-76_*96-73dup
ENST00000290846.8:c.652-76_652-73dup ENSP00000290846.4:n.652-76_652-73dup
ENST00000381019.3:c.652-76_652-73dup ENSP00000370407.3:n.652-76_652-73dup
ENST00000381021.7:c.*245-76_*245-73dup ENSP00000370409.3:n.*245-76_*245-73dup
ENST00000441818.5:c.*186-76_*186-73dup ENSP00000393014.1:n.*186-76_*186-73dup
ENST00000453630.5:c.*190-76_*190-73dup ENSP00000398488.1:n.*190-76_*190-73dup
ENST00000456595.5:c.*186-76_*186-73dup ENSP00000413880.1:n.*186-76_*186-73dup
ENST00000457572.5:c.*96-76_*96-73dup ENSP00000407700.1:n.*96-76_*96-73dup
ENST00000463785.1:n.120-76_120-73dup
ENST00000479648.1:n.396_399dup
ENST00000485175.5:n.612-76_612-73dup
ENST00000486620.5:n.694-76_694-73dup
NM_001282782.1:c.310-76_310-73dup NP_001269711.1:n.310-76_310-73dup
NM_001282783.1:c.232-76_232-73dup NP_001269712.1:n.232-76_232-73dup
NM_001282784.1:c.232-76_232-73dup NP_001269713.1:n.232-76_232-73dup
NM_001282785.1:c.652-76_652-73dup NP_001269714.1:n.652-76_652-73dup
NM_018006.4:c.652-76_652-73dup NP_060476.2:n.652-76_652-73dup
NR_104240.1:n.961-76_961-73dup
NR_104241.1:n.854-76_854-73dup
XM_005261678.1:c.256-76_256-73dup XP_005261735.1:n.256-76_256-73dup
XM_005261681.1:c.256-76_256-73dup XP_005261738.1:n.256-76_256-73dup
XM_011530271.1:c.547-76_547-73dup XP_011528573.1:n.547-76_547-73dup
XM_011530272.1:c.652-76_652-73dup XP_011528574.1:n.652-76_652-73dup
XM_011530273.1:c.652-76_652-73dup XP_011528575.1:n.652-76_652-73dup
XM_011530274.1:c.310-76_310-73dup XP_011528576.1:n.310-76_310-73dup
XM_011530275.1:c.256-76_256-73dup XP_011528577.1:n.256-76_256-73dup
XM_011530271.2:c.547-76_547-73dup XP_011528573.1:n.547-76_547-73dup
XM_011530272.2:c.652-76_652-73dup XP_011528574.1:n.652-76_652-73dup
XM_011530273.2:c.652-76_652-73dup XP_011528575.1:n.652-76_652-73dup
XM_011530274.2:c.310-76_310-73dup XP_011528576.1:n.310-76_310-73dup
XM_024452260.1:c.547-76_547-73dup XP_024308028.1:n.547-76_547-73dup
XR_001755261.2:n.698-76_698-73dup
XR_001755262.2:n.698-76_698-73dup
NM_018006.5:c.652-76_652-73dup MANE Select NP_060476.2:n.652-76_652-73dup
NM_001282782.2:c.310-76_310-73dup NP_001269711.1:n.310-76_310-73dup
NM_001282783.2:c.232-76_232-73dup NP_001269712.1:n.232-76_232-73dup
NM_001282784.2:c.232-76_232-73dup NP_001269713.1:n.232-76_232-73dup
NM_001282785.2:c.652-76_652-73dup NP_001269714.1:n.652-76_652-73dup
NR_104240.2:n.648-76_648-73dup
NR_104241.2:n.541-76_541-73dup