Canonical Allele Identifier: CA2662125713

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178530397del , CM000664.2:g.178530397del GRCh38
NC_000002.11:g.179395124del , CM000664.1:g.179395124del GRCh37
NC_000002.10:g.179103370del NCBI36
NG_011618.3:g.305410del , LRG_391:g.305410del
NG_051363.1:g.12571del

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.98518del (TTN) ENSP00000343764.6:p.Thr32840LeufsTer14
ENST00000342175.11:c.79603del (TTN) ENSP00000340554.6:p.Thr26535LeufsTer14
ENST00000359218.10:c.79402del (TTN) ENSP00000352154.5:p.Thr26468LeufsTer14
ENST00000342175.10:c.79603del (TTN) ENSP00000340554.6:p.Thr26535LeufsTer14
ENST00000342992.10:c.98518del (TTN) ENSP00000343764.6:p.Thr32840LeufsTer14
ENST00000359218.9:c.79402del (TTN) ENSP00000352154.5:p.Thr26468LeufsTer14
ENST00000460472.6:c.79027del (TTN) ENSP00000434586.1:p.Thr26343LeufsTer14
ENST00000589042.5:c.106222del (TTN) MANE Select ENSP00000467141.1:p.Thr35408LeufsTer14
ENST00000591111.5:c.101299del (TTN) ENSP00000465570.1:p.Thr33767LeufsTer14
ENST00000615779.4:c.101299del (TTN) ENSP00000483597.1:p.Thr33767LeufsTer14
NM_001256850.1:c.101299del (TTN) NP_001243779.1:p.Thr33767LeufsTer14
NM_001267550.2:c.106222del (TTN) MANE Select NP_001254479.2:p.Thr35408LeufsTer14
NM_003319.4:c.79027del (TTN) NP_003310.4:p.Thr26343LeufsTer14
NM_133378.4:c.98518del (TTN) NP_596869.4:p.Thr32840LeufsTer14
NM_133432.3:c.79402del (TTN) NP_597676.3:p.Thr26468LeufsTer14
NM_133437.4:c.79603del (TTN) NP_597681.4:p.Thr26535LeufsTer14
NR_038271.1:n.446+6761del (TTN-AS1)
NR_038272.1:n.220-5335del (TTN-AS1)
XM_011511729.1:c.105319del (TTN) XP_011510031.1:p.Thr35107LeufsTer14
XM_011511730.1:c.79213del (TTN) XP_011510032.1:p.Thr26405LeufsTer14
XM_011511731.1:c.79072del (TTN) XP_011510033.1:p.Thr26358LeufsTer14
XM_017004819.1:c.105115del (TTN) XP_016860308.1:p.Thr35039LeufsTer14
XM_017004820.1:c.100513del (TTN) XP_016860309.1:p.Thr33505LeufsTer14
XM_017004821.1:c.100510del (TTN) XP_016860310.1:p.Thr33504LeufsTer14
XM_017004822.1:c.97552del (TTN) XP_016860311.1:p.Thr32518LeufsTer14
XM_017004823.1:c.79168del (TTN) XP_016860312.1:p.Thr26390LeufsTer14
XM_024453094.1:c.100663del (TTN) XP_024308862.1:p.Thr33555LeufsTer14
XM_024453095.1:c.100660del (TTN) XP_024308863.1:p.Thr33554LeufsTer14
XM_024453096.1:c.100093del (TTN) XP_024308864.1:p.Thr33365LeufsTer14
XM_024453097.1:c.97435del (TTN) XP_024308865.1:p.Thr32479LeufsTer14
XM_024453098.1:c.97354del (TTN) XP_024308866.1:p.Thr32452LeufsTer14
XM_024453099.1:c.79117del (TTN) XP_024308867.1:p.Thr26373LeufsTer14
XM_024453100.1:c.68971del (TTN) XP_024308868.1:p.Thr22991LeufsTer14