Canonical Allele Identifier: CA261882

Linked Data

ClinVar Variation Id: 47119
ClinVar RCV Id: RCV000040389
dbSNP Id: rs397517628

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178597956del , CM000664.2:g.178597956del GRCh38
NC_000002.11:g.179462683del , CM000664.1:g.179462683del GRCh37
NC_000002.10:g.179170928del NCBI36
NG_011618.3:g.237848del , LRG_391:g.237848del
NG_051363.1:g.80130del

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.49511del (TTN) ENSP00000343764.6:p.Gly16504GlufsTer12
ENST00000342175.11:c.30596del (TTN) ENSP00000340554.6:p.Gly10199GlufsTer12
ENST00000359218.10:c.30395del (TTN) ENSP00000352154.5:p.Gly10132GlufsTer12
ENST00000342175.10:c.30596del (TTN) ENSP00000340554.6:p.Gly10199GlufsTer12
ENST00000342992.10:c.49511del (TTN) ENSP00000343764.6:p.Gly16504GlufsTer12
ENST00000359218.9:c.30395del (TTN) ENSP00000352154.5:p.Gly10132GlufsTer12
ENST00000460472.6:c.30020del (TTN) ENSP00000434586.1:p.Gly10007GlufsTer12
ENST00000589042.5:c.57215del (TTN) MANE Select ENSP00000467141.1:p.Gly19072GlufsTer12
ENST00000591111.5:c.52292del (TTN) ENSP00000465570.1:p.Gly17431GlufsTer12
ENST00000615779.4:c.52292del (TTN) ENSP00000483597.1:p.Gly17431GlufsTer12
NM_001256850.1:c.52292del (TTN) NP_001243779.1:p.Gly17431GlufsTer12
NM_001267550.2:c.57215del (TTN) MANE Select NP_001254479.2:p.Gly19072GlufsTer12
NM_003319.4:c.30020del (TTN) NP_003310.4:p.Gly10007GlufsTer12
NM_133378.4:c.49511del (TTN) NP_596869.4:p.Gly16504GlufsTer12
NM_133432.3:c.30395del (TTN) NP_597676.3:p.Gly10132GlufsTer12
NM_133437.4:c.30596del (TTN) NP_597681.4:p.Gly10199GlufsTer12
NR_038271.1:n.682+275del (TTN-AS1)
NR_038272.1:n.3450+275del (TTN-AS1)
XM_011511729.1:c.56312del (TTN) XP_011510031.1:p.Gly18771GlufsTer12
XM_011511730.1:c.30206del (TTN) XP_011510032.1:p.Gly10069GlufsTer12
XM_011511731.1:c.30065del (TTN) XP_011510033.1:p.Gly10022GlufsTer12
XM_017004819.1:c.56108del (TTN) XP_016860308.1:p.Gly18703GlufsTer12
XM_017004820.1:c.51506del (TTN) XP_016860309.1:p.Gly17169GlufsTer12
XM_017004821.1:c.51503del (TTN) XP_016860310.1:p.Gly17168GlufsTer12
XM_017004822.1:c.48545del (TTN) XP_016860311.1:p.Gly16182GlufsTer12
XM_017004823.1:c.30161del (TTN) XP_016860312.1:p.Gly10054GlufsTer12
XM_024453094.1:c.51656del (TTN) XP_024308862.1:p.Gly17219GlufsTer12
XM_024453095.1:c.51653del (TTN) XP_024308863.1:p.Gly17218GlufsTer12
XM_024453096.1:c.51086del (TTN) XP_024308864.1:p.Gly17029GlufsTer12
XM_024453097.1:c.48428del (TTN) XP_024308865.1:p.Gly16143GlufsTer12
XM_024453098.1:c.48347del (TTN) XP_024308866.1:p.Gly16116GlufsTer12
XM_024453099.1:c.30110del (TTN) XP_024308867.1:p.Gly10037GlufsTer12
XM_024453100.1:c.19964del (TTN) XP_024308868.1:p.Gly6655GlufsTer12