Canonical Allele Identifier: CA2586965323

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178546871del , CM000664.2:g.178546871del GRCh38
NC_000002.11:g.179411598del , CM000664.1:g.179411598del GRCh37
NC_000002.10:g.179119844del NCBI36
NG_011618.3:g.288933del , LRG_391:g.288933del
NG_051363.1:g.29045del

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.86854del (TTN) ENSP00000343764.6:p.Arg28952AspfsTer6
ENST00000342175.11:c.67939del (TTN) ENSP00000340554.6:p.Arg22647AspfsTer6
ENST00000359218.10:c.67738del (TTN) ENSP00000352154.5:p.Arg22580AspfsTer6
ENST00000342175.10:c.67939del (TTN) ENSP00000340554.6:p.Arg22647AspfsTer6
ENST00000342992.10:c.86854del (TTN) ENSP00000343764.6:p.Arg28952AspfsTer6
ENST00000359218.9:c.67738del (TTN) ENSP00000352154.5:p.Arg22580AspfsTer6
ENST00000460472.6:c.67363del (TTN) ENSP00000434586.1:p.Arg22455AspfsTer6
ENST00000589042.5:c.94558del (TTN) MANE Select ENSP00000467141.1:p.Arg31520AspfsTer6
ENST00000591111.5:c.89635del (TTN) ENSP00000465570.1:p.Arg29879AspfsTer6
ENST00000615779.4:c.89635del (TTN) ENSP00000483597.1:p.Arg29879AspfsTer6
NM_001256850.1:c.89635del (TTN) NP_001243779.1:p.Arg29879AspfsTer6
NM_001267550.2:c.94558del (TTN) MANE Select NP_001254479.2:p.Arg31520AspfsTer6
NM_003319.4:c.67363del (TTN) NP_003310.4:p.Arg22455AspfsTer6
NM_133378.4:c.86854del (TTN) NP_596869.4:p.Arg28952AspfsTer6
NM_133432.3:c.67738del (TTN) NP_597676.3:p.Arg22580AspfsTer6
NM_133437.4:c.67939del (TTN) NP_597681.4:p.Arg22647AspfsTer6
NR_038271.1:n.446+23235del (TTN-AS1)
NR_038272.1:n.2043+4510del (TTN-AS1)
XM_011511729.1:c.93655del (TTN) XP_011510031.1:p.Arg31219AspfsTer6
XM_011511730.1:c.67549del (TTN) XP_011510032.1:p.Arg22517AspfsTer6
XM_011511731.1:c.67408del (TTN) XP_011510033.1:p.Arg22470AspfsTer6
XM_017004819.1:c.93451del (TTN) XP_016860308.1:p.Arg31151AspfsTer6
XM_017004820.1:c.88849del (TTN) XP_016860309.1:p.Arg29617AspfsTer6
XM_017004821.1:c.88846del (TTN) XP_016860310.1:p.Arg29616AspfsTer6
XM_017004822.1:c.85888del (TTN) XP_016860311.1:p.Arg28630AspfsTer6
XM_017004823.1:c.67504del (TTN) XP_016860312.1:p.Arg22502AspfsTer6
XM_024453094.1:c.88999del (TTN) XP_024308862.1:p.Arg29667AspfsTer6
XM_024453095.1:c.88996del (TTN) XP_024308863.1:p.Arg29666AspfsTer6
XM_024453096.1:c.88429del (TTN) XP_024308864.1:p.Arg29477AspfsTer6
XM_024453097.1:c.85771del (TTN) XP_024308865.1:p.Arg28591AspfsTer6
XM_024453098.1:c.85690del (TTN) XP_024308866.1:p.Arg28564AspfsTer6
XM_024453099.1:c.67453del (TTN) XP_024308867.1:p.Arg22485AspfsTer6
XM_024453100.1:c.57307del (TTN) XP_024308868.1:p.Arg19103AspfsTer6