Canonical Allele Identifier: CA10581845

Linked Data

ClinVar Variation Id: 238840
dbSNP Id: rs878854332

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178571525del , CM000664.2:g.178571525del GRCh38
NC_000002.11:g.179436252del , CM000664.1:g.179436252del GRCh37
NC_000002.10:g.179144498del NCBI36
NG_011618.3:g.264279del , LRG_391:g.264279del
NG_051363.1:g.53699del

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.66904del (TTN) ENSP00000343764.6:p.Ala22302LeufsTer4
ENST00000342175.11:c.47989del (TTN) ENSP00000340554.6:p.Ala15997LeufsTer4
ENST00000359218.10:c.47788del (TTN) ENSP00000352154.5:p.Ala15930LeufsTer4
ENST00000342175.10:c.47989del (TTN) ENSP00000340554.6:p.Ala15997LeufsTer4
ENST00000342992.10:c.66904del (TTN) ENSP00000343764.6:p.Ala22302LeufsTer4
ENST00000359218.9:c.47788del (TTN) ENSP00000352154.5:p.Ala15930LeufsTer4
ENST00000460472.6:c.47413del (TTN) ENSP00000434586.1:p.Ala15805LeufsTer4
ENST00000589042.5:c.74608del (TTN) MANE Select ENSP00000467141.1:p.Ala24870LeufsTer4
ENST00000591111.5:c.69685del (TTN) ENSP00000465570.1:p.Ala23229LeufsTer4
ENST00000615779.4:c.69685del (TTN) ENSP00000483597.1:p.Ala23229LeufsTer4
NM_001256850.1:c.69685del (TTN) NP_001243779.1:p.Ala23229LeufsTer4
NM_001267550.2:c.74608del (TTN) MANE Select NP_001254479.2:p.Ala24870LeufsTer4
NM_003319.4:c.47413del (TTN) NP_003310.4:p.Ala15805LeufsTer4
NM_133378.4:c.66904del (TTN) NP_596869.4:p.Ala22302LeufsTer4
NM_133432.3:c.47788del (TTN) NP_597676.3:p.Ala15930LeufsTer4
NM_133437.4:c.47989del (TTN) NP_597681.4:p.Ala15997LeufsTer4
NR_038271.1:n.596+76del (TTN-AS1)
NR_038272.1:n.2044-11047del (TTN-AS1)
XM_011511729.1:c.73705del (TTN) XP_011510031.1:p.Ala24569LeufsTer4
XM_011511730.1:c.47599del (TTN) XP_011510032.1:p.Ala15867LeufsTer4
XM_011511731.1:c.47458del (TTN) XP_011510033.1:p.Ala15820LeufsTer4
XM_017004819.1:c.73501del (TTN) XP_016860308.1:p.Ala24501LeufsTer4
XM_017004820.1:c.68899del (TTN) XP_016860309.1:p.Ala22967LeufsTer4
XM_017004821.1:c.68896del (TTN) XP_016860310.1:p.Ala22966LeufsTer4
XM_017004822.1:c.65938del (TTN) XP_016860311.1:p.Ala21980LeufsTer4
XM_017004823.1:c.47554del (TTN) XP_016860312.1:p.Ala15852LeufsTer4
XM_024453094.1:c.69049del (TTN) XP_024308862.1:p.Ala23017LeufsTer4
XM_024453095.1:c.69046del (TTN) XP_024308863.1:p.Ala23016LeufsTer4
XM_024453096.1:c.68479del (TTN) XP_024308864.1:p.Ala22827LeufsTer4
XM_024453097.1:c.65821del (TTN) XP_024308865.1:p.Ala21941LeufsTer4
XM_024453098.1:c.65740del (TTN) XP_024308866.1:p.Ala21914LeufsTer4
XM_024453099.1:c.47503del (TTN) XP_024308867.1:p.Ala15835LeufsTer4
XM_024453100.1:c.37357del (TTN) XP_024308868.1:p.Ala12453LeufsTer4