Canonical Allele Identifier: CA1310550942

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178618176_178618177delinsTA , CM000664.2:g.178618176_178618177delinsTA GRCh38
NC_000002.11:g.179482903_179482904delinsTA , CM000664.1:g.179482903_179482904delinsTA GRCh37
NC_000002.10:g.179191148_179191149delinsTA NCBI36
NG_011618.3:g.217626_217627delinsTA , LRG_391:g.217626_217627delinsTA
NG_051363.1:g.100350_100351delinsTA

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.39565+12_39565+13delinsTA (TTN) ENSP00000343764.6:n.39565+12_39565+13deli...
ENST00000342175.11:c.20650+12_20650+13delinsTA (TTN) ENSP00000340554.6:n.20650+12_20650+13deli...
ENST00000359218.10:c.20449+12_20449+13delinsTA (TTN) ENSP00000352154.5:n.20449+12_20449+13deli...
ENST00000342175.10:c.20650+12_20650+13delinsTA (TTN) ENSP00000340554.6:n.20650+12_20650+13deli...
ENST00000342992.10:c.39565+12_39565+13delinsTA (TTN) ENSP00000343764.6:n.39565+12_39565+13deli...
ENST00000359218.9:c.20449+12_20449+13delinsTA (TTN) ENSP00000352154.5:n.20449+12_20449+13deli...
ENST00000460472.6:c.20074+12_20074+13delinsTA (TTN) ENSP00000434586.1:n.20074+12_20074+13deli...
ENST00000589042.5:c.47269+12_47269+13delinsTA (TTN) MANE Select ENSP00000467141.1:n.47269+12_47269+13deli...
ENST00000591111.5:c.42346+12_42346+13delinsTA (TTN) ENSP00000465570.1:n.42346+12_42346+13deli...
ENST00000615779.4:c.42346+12_42346+13delinsTA (TTN) ENSP00000483597.1:n.42346+12_42346+13deli...
NM_001256850.1:c.42346+12_42346+13delinsTA (TTN) NP_001243779.1:n.42346+12_42346+13delinsT...
NM_001267550.2:c.47269+12_47269+13delinsTA (TTN) MANE Select NP_001254479.2:n.47269+12_47269+13delinsT...
NM_003319.4:c.20074+12_20074+13delinsTA (TTN) NP_003310.4:n.20074+12_20074+13delinsTA
NM_133378.4:c.39565+12_39565+13delinsTA (TTN) NP_596869.4:n.39565+12_39565+13delinsTA
NM_133432.3:c.20449+12_20449+13delinsTA (TTN) NP_597676.3:n.20449+12_20449+13delinsTA
NM_133437.4:c.20650+12_20650+13delinsTA (TTN) NP_597681.4:n.20650+12_20650+13delinsTA
NR_038271.1:n.1605-1577_1605-1576delinsTA (TTN-AS1)
XM_011511729.1:c.46366+12_46366+13delinsTA (TTN) XP_011510031.1:n.46366+12_46366+13delinsT...
XM_011511730.1:c.20260+12_20260+13delinsTA (TTN) XP_011510032.1:n.20260+12_20260+13delinsT...
XM_011511731.1:c.20119+12_20119+13delinsTA (TTN) XP_011510033.1:n.20119+12_20119+13delinsT...
XM_017004819.1:c.46162+12_46162+13delinsTA (TTN) XP_016860308.1:n.46162+12_46162+13delinsT...
XM_017004820.1:c.41560+12_41560+13delinsTA (TTN) XP_016860309.1:n.41560+12_41560+13delinsT...
XM_017004821.1:c.41557+12_41557+13delinsTA (TTN) XP_016860310.1:n.41557+12_41557+13delinsT...
XM_017004822.1:c.38599+12_38599+13delinsTA (TTN) XP_016860311.1:n.38599+12_38599+13delinsT...
XM_017004823.1:c.20215+12_20215+13delinsTA (TTN) XP_016860312.1:n.20215+12_20215+13delinsT...
XM_024453094.1:c.41710+12_41710+13delinsTA (TTN) XP_024308862.1:n.41710+12_41710+13delinsT...
XM_024453095.1:c.41707+12_41707+13delinsTA (TTN) XP_024308863.1:n.41707+12_41707+13delinsT...
XM_024453096.1:c.41140+12_41140+13delinsTA (TTN) XP_024308864.1:n.41140+12_41140+13delinsT...
XM_024453097.1:c.38482+12_38482+13delinsTA (TTN) XP_024308865.1:n.38482+12_38482+13delinsT...
XM_024453098.1:c.38401+12_38401+13delinsTA (TTN) XP_024308866.1:n.38401+12_38401+13delinsT...
XM_024453099.1:c.20164+12_20164+13delinsTA (TTN) XP_024308867.1:n.20164+12_20164+13delinsT...
XM_024453100.1:c.10018+12_10018+13delinsTA (TTN) XP_024308868.1:n.10018+12_10018+13delinsT...