Canonical Allele Identifier: CA2657374844
Gene: TRMU HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.46352209_46352219del , CM000684.2:g.46352209_46352219del GRCh38
NC_000022.10:g.46748106_46748116del , CM000684.1:g.46748106_46748116del GRCh37
NC_000022.9:g.45126770_45126780del NCBI36
NG_012173.1:g.21809_21819del

Transcript Alleles

HGVS Amino-acid Change
ENST00000465378.6:n.753+35_754-45del
ENST00000642923.1:c.600+35_601-45del ENSP00000494255.1:n.600+35_601-45del
ENST00000643137.1:c.600+35_601-45del ENSP00000495331.1:n.600+35_601-45del
ENST00000644006.1:c.*149+35_*150-45del ENSP00000493778.1:n.*149+35_*150-45del
ENST00000645026.1:n.756+35_757-45del
ENST00000645190.1:c.705+35_706-45del MANE Select ENSP00000496496.1:n.705+35_706-45del
ENST00000647301.1:c.*149+35_*150-45del ENSP00000496641.1:n.*149+35_*150-45del
ENST00000290846.8:c.705+35_706-45del ENSP00000290846.4:n.705+35_706-45del
ENST00000381019.3:c.705+35_706-45del ENSP00000370407.3:n.705+35_706-45del
ENST00000381021.7:c.*298+35_*299-45del ENSP00000370409.3:n.*298+35_*299-45del
ENST00000441818.5:c.*239+35_*240-45del ENSP00000393014.1:n.*239+35_*240-45del
ENST00000453630.5:c.*243+35_*244-45del ENSP00000398488.1:n.*243+35_*244-45del
ENST00000456595.5:c.*239+35_*240-45del ENSP00000413880.1:n.*239+35_*240-45del
ENST00000457572.5:c.*149+35_*150-45del ENSP00000407700.1:n.*149+35_*150-45del
ENST00000463785.1:n.173+35_174-45del
ENST00000479648.1:n.525+35_526-45del
ENST00000485175.5:n.665+35_666-45del
ENST00000486620.5:n.747+35_748-45del
NM_001282782.1:c.363+35_364-45del NP_001269711.1:n.363+35_364-45del
NM_001282783.1:c.285+35_286-45del NP_001269712.1:n.285+35_286-45del
NM_001282784.1:c.285+35_286-45del NP_001269713.1:n.285+35_286-45del
NM_001282785.1:c.705+35_706-45del NP_001269714.1:n.705+35_706-45del
NM_018006.4:c.705+35_706-45del NP_060476.2:n.705+35_706-45del
NR_104240.1:n.1014+35_1015-45del
NR_104241.1:n.907+35_908-45del
XM_005261678.1:c.309+35_310-45del XP_005261735.1:n.309+35_310-45del
XM_005261681.1:c.309+35_310-45del XP_005261738.1:n.309+35_310-45del
XM_011530271.1:c.600+35_601-45del XP_011528573.1:n.600+35_601-45del
XM_011530272.1:c.705+35_706-45del XP_011528574.1:n.705+35_706-45del
XM_011530273.1:c.705+35_706-45del XP_011528575.1:n.705+35_706-45del
XM_011530274.1:c.363+35_364-45del XP_011528576.1:n.363+35_364-45del
XM_011530275.1:c.309+35_310-45del XP_011528577.1:n.309+35_310-45del
XM_011530271.2:c.600+35_601-45del XP_011528573.1:n.600+35_601-45del
XM_011530272.2:c.705+35_706-45del XP_011528574.1:n.705+35_706-45del
XM_011530273.2:c.705+35_706-45del XP_011528575.1:n.705+35_706-45del
XM_011530274.2:c.363+35_364-45del XP_011528576.1:n.363+35_364-45del
XM_024452260.1:c.600+35_601-45del XP_024308028.1:n.600+35_601-45del
XR_001755261.2:n.751+35_752-45del
XR_001755262.2:n.751+35_752-45del
NM_018006.5:c.705+35_706-45del MANE Select NP_060476.2:n.705+35_706-45del
NM_001282782.2:c.363+35_364-45del NP_001269711.1:n.363+35_364-45del
NM_001282783.2:c.285+35_286-45del NP_001269712.1:n.285+35_286-45del
NM_001282784.2:c.285+35_286-45del NP_001269713.1:n.285+35_286-45del
NM_001282785.2:c.705+35_706-45del NP_001269714.1:n.705+35_706-45del
NR_104240.2:n.701+35_702-45del
NR_104241.2:n.594+35_595-45del