Canonical Allele Identifier: CA2662125269

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178549816_178549818del , CM000664.2:g.178549816_178549818del GRCh38
NC_000002.11:g.179414543_179414545del , CM000664.1:g.179414543_179414545del GRCh37
NC_000002.10:g.179122789_179122791del NCBI36
NG_011618.3:g.285988_285990del , LRG_391:g.285988_285990del
NG_051363.1:g.31990_31992del

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.84203_84205del (TTN) ENSP00000343764.6:p.Lys28068del
ENST00000342175.11:c.65288_65290del (TTN) ENSP00000340554.6:p.Lys21763del
ENST00000359218.10:c.65087_65089del (TTN) ENSP00000352154.5:p.Lys21696del
ENST00000342175.10:c.65288_65290del (TTN) ENSP00000340554.6:p.Lys21763del
ENST00000342992.10:c.84203_84205del (TTN) ENSP00000343764.6:p.Lys28068del
ENST00000359218.9:c.65087_65089del (TTN) ENSP00000352154.5:p.Lys21696del
ENST00000460472.6:c.64712_64714del (TTN) ENSP00000434586.1:p.Lys21571del
ENST00000589042.5:c.91907_91909del (TTN) MANE Select ENSP00000467141.1:p.Lys30636del
ENST00000591111.5:c.86984_86986del (TTN) ENSP00000465570.1:p.Lys28995del
ENST00000615779.4:c.86984_86986del (TTN) ENSP00000483597.1:p.Lys28995del
NM_001256850.1:c.86984_86986del (TTN) NP_001243779.1:p.Lys28995del
NM_001267550.2:c.91907_91909del (TTN) MANE Select NP_001254479.2:p.Lys30636del
NM_003319.4:c.64712_64714del (TTN) NP_003310.4:p.Lys21571del
NM_133378.4:c.84203_84205del (TTN) NP_596869.4:p.Lys28068del
NM_133432.3:c.65087_65089del (TTN) NP_597676.3:p.Lys21696del
NM_133437.4:c.65288_65290del (TTN) NP_597681.4:p.Lys21763del
NR_038271.1:n.447-21484_447-21482del (TTN-AS1)
NR_038272.1:n.2043+7455_2043+7457del (TTN-AS1)
XM_011511729.1:c.91004_91006del (TTN) XP_011510031.1:p.Lys30335del
XM_011511730.1:c.64898_64900del (TTN) XP_011510032.1:p.Lys21633del
XM_011511731.1:c.64757_64759del (TTN) XP_011510033.1:p.Lys21586del
XM_017004819.1:c.90800_90802del (TTN) XP_016860308.1:p.Lys30267del
XM_017004820.1:c.86198_86200del (TTN) XP_016860309.1:p.Lys28733del
XM_017004821.1:c.86195_86197del (TTN) XP_016860310.1:p.Lys28732del
XM_017004822.1:c.83237_83239del (TTN) XP_016860311.1:p.Lys27746del
XM_017004823.1:c.64853_64855del (TTN) XP_016860312.1:p.Lys21618del
XM_024453094.1:c.86348_86350del (TTN) XP_024308862.1:p.Lys28783del
XM_024453095.1:c.86345_86347del (TTN) XP_024308863.1:p.Lys28782del
XM_024453096.1:c.85778_85780del (TTN) XP_024308864.1:p.Lys28593del
XM_024453097.1:c.83120_83122del (TTN) XP_024308865.1:p.Lys27707del
XM_024453098.1:c.83039_83041del (TTN) XP_024308866.1:p.Lys27680del
XM_024453099.1:c.64802_64804del (TTN) XP_024308867.1:p.Lys21601del
XM_024453100.1:c.54656_54658del (TTN) XP_024308868.1:p.Lys18219del