Canonical Allele Identifier: CA261889

Linked Data

ClinVar Variation Id: 47131
dbSNP Id: rs397517633

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178594499del , CM000664.2:g.178594499del GRCh38
NC_000002.11:g.179459226del , CM000664.1:g.179459226del GRCh37
NC_000002.10:g.179167472del NCBI36
NG_011618.3:g.241304del , LRG_391:g.241304del
NG_051363.1:g.76673del

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.50291del (TTN) ENSP00000343764.6:p.His16764ProfsTer18
ENST00000342175.11:c.31376del (TTN) ENSP00000340554.6:p.His10459ProfsTer18
ENST00000359218.10:c.31175del (TTN) ENSP00000352154.5:p.His10392ProfsTer18
ENST00000342175.10:c.31376del (TTN) ENSP00000340554.6:p.His10459ProfsTer18
ENST00000342992.10:c.50291del (TTN) ENSP00000343764.6:p.His16764ProfsTer18
ENST00000359218.9:c.31175del (TTN) ENSP00000352154.5:p.His10392ProfsTer18
ENST00000460472.6:c.30800del (TTN) ENSP00000434586.1:p.His10267ProfsTer18
ENST00000589042.5:c.57995del (TTN) MANE Select ENSP00000467141.1:p.His19332ProfsTer18
ENST00000591111.5:c.53072del (TTN) ENSP00000465570.1:p.His17691ProfsTer18
ENST00000615779.4:c.53072del (TTN) ENSP00000483597.1:p.His17691ProfsTer18
NM_001256850.1:c.53072del (TTN) NP_001243779.1:p.His17691ProfsTer18
NM_001267550.2:c.57995del (TTN) MANE Select NP_001254479.2:p.His19332ProfsTer18
NM_003319.4:c.30800del (TTN) NP_003310.4:p.His10267ProfsTer18
NM_133378.4:c.50291del (TTN) NP_596869.4:p.His16764ProfsTer18
NM_133432.3:c.31175del (TTN) NP_597676.3:p.His10392ProfsTer18
NM_133437.4:c.31376del (TTN) NP_597681.4:p.His10459ProfsTer18
NR_038271.1:n.597-3097del (TTN-AS1)
NR_038272.1:n.3365-3097del (TTN-AS1)
XM_011511729.1:c.57092del (TTN) XP_011510031.1:p.His19031ProfsTer18
XM_011511730.1:c.30986del (TTN) XP_011510032.1:p.His10329ProfsTer18
XM_011511731.1:c.30845del (TTN) XP_011510033.1:p.His10282ProfsTer18
XM_017004819.1:c.56888del (TTN) XP_016860308.1:p.His18963ProfsTer18
XM_017004820.1:c.52286del (TTN) XP_016860309.1:p.His17429ProfsTer18
XM_017004821.1:c.52283del (TTN) XP_016860310.1:p.His17428ProfsTer18
XM_017004822.1:c.49325del (TTN) XP_016860311.1:p.His16442ProfsTer18
XM_017004823.1:c.30941del (TTN) XP_016860312.1:p.His10314ProfsTer18
XM_024453094.1:c.52436del (TTN) XP_024308862.1:p.His17479ProfsTer18
XM_024453095.1:c.52433del (TTN) XP_024308863.1:p.His17478ProfsTer18
XM_024453096.1:c.51866del (TTN) XP_024308864.1:p.His17289ProfsTer18
XM_024453097.1:c.49208del (TTN) XP_024308865.1:p.His16403ProfsTer18
XM_024453098.1:c.49127del (TTN) XP_024308866.1:p.His16376ProfsTer18
XM_024453099.1:c.30890del (TTN) XP_024308867.1:p.His10297ProfsTer18
XM_024453100.1:c.20744del (TTN) XP_024308868.1:p.His6915ProfsTer18