Canonical Allele Identifier: CA2586970743

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178530565del , CM000664.2:g.178530565del GRCh38
NC_000002.11:g.179395292del , CM000664.1:g.179395292del GRCh37
NC_000002.10:g.179103538del NCBI36
NG_011618.3:g.305238del , LRG_391:g.305238del
NG_051363.1:g.12739del

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.98346del (TTN) ENSP00000343764.6:p.Glu32783AsnfsTer?
ENST00000342175.11:c.79431del (TTN) ENSP00000340554.6:p.Glu26478AsnfsTer?
ENST00000359218.10:c.79230del (TTN) ENSP00000352154.5:p.Glu26411AsnfsTer?
ENST00000342175.10:c.79431del (TTN) ENSP00000340554.6:p.Glu26478AsnfsTer?
ENST00000342992.10:c.98346del (TTN) ENSP00000343764.6:p.Glu32783AsnfsTer?
ENST00000359218.9:c.79230del (TTN) ENSP00000352154.5:p.Glu26411AsnfsTer?
ENST00000460472.6:c.78855del (TTN) ENSP00000434586.1:p.Glu26286AsnfsTer?
ENST00000589042.5:c.106050del (TTN) MANE Select ENSP00000467141.1:p.Glu35351AsnfsTer?
ENST00000591111.5:c.101127del (TTN) ENSP00000465570.1:p.Glu33710AsnfsTer?
ENST00000615779.4:c.101127del (TTN) ENSP00000483597.1:p.Glu33710AsnfsTer?
NM_001256850.1:c.101127del (TTN) NP_001243779.1:p.Glu33710AsnfsTer?
NM_001267550.2:c.106050del (TTN) MANE Select NP_001254479.2:p.Glu35351AsnfsTer?
NM_003319.4:c.78855del (TTN) NP_003310.4:p.Glu26286AsnfsTer?
NM_133378.4:c.98346del (TTN) NP_596869.4:p.Glu32783AsnfsTer?
NM_133432.3:c.79230del (TTN) NP_597676.3:p.Glu26411AsnfsTer?
NM_133437.4:c.79431del (TTN) NP_597681.4:p.Glu26478AsnfsTer?
NR_038271.1:n.446+6929del (TTN-AS1)
NR_038272.1:n.220-5167del (TTN-AS1)
XM_011511729.1:c.105147del (TTN) XP_011510031.1:p.Glu35050AsnfsTer?
XM_011511730.1:c.79041del (TTN) XP_011510032.1:p.Glu26348AsnfsTer?
XM_011511731.1:c.78900del (TTN) XP_011510033.1:p.Glu26301AsnfsTer?
XM_017004819.1:c.104943del (TTN) XP_016860308.1:p.Glu34982AsnfsTer?
XM_017004820.1:c.100341del (TTN) XP_016860309.1:p.Glu33448AsnfsTer?
XM_017004821.1:c.100338del (TTN) XP_016860310.1:p.Glu33447AsnfsTer?
XM_017004822.1:c.97380del (TTN) XP_016860311.1:p.Glu32461AsnfsTer?
XM_017004823.1:c.78996del (TTN) XP_016860312.1:p.Glu26333AsnfsTer?
XM_024453094.1:c.100491del (TTN) XP_024308862.1:p.Glu33498AsnfsTer?
XM_024453095.1:c.100488del (TTN) XP_024308863.1:p.Glu33497AsnfsTer?
XM_024453096.1:c.99921del (TTN) XP_024308864.1:p.Glu33308AsnfsTer?
XM_024453097.1:c.97263del (TTN) XP_024308865.1:p.Glu32422AsnfsTer?
XM_024453098.1:c.97182del (TTN) XP_024308866.1:p.Glu32395AsnfsTer?
XM_024453099.1:c.78945del (TTN) XP_024308867.1:p.Glu26316AsnfsTer?
XM_024453100.1:c.68799del (TTN) XP_024308868.1:p.Glu22934AsnfsTer?