Canonical Allele Identifier: CA2753331431

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178544466_178544467insTGTTTGGG , CM000664.2:g.178544466_178544467insTGTTTGGG GRCh38
NC_000002.11:g.179409193_179409194insTGTTTGGG , CM000664.1:g.179409193_179409194insTGTTTGGG GRCh37
NC_000002.10:g.179117439_179117440insTGTTTGGG NCBI36
NG_011618.3:g.291337_291338insCCAAACAC , LRG_391:g.291337_291338insCCAAACAC
NG_051363.1:g.26640_26641insTGTTTGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.88059_88060insCCAAACAC (TTN) ENSP00000343764.6:p.Thr29354ProfsTer24
ENST00000342175.11:c.69144_69145insCCAAACAC (TTN) ENSP00000340554.6:p.Thr23049ProfsTer24
ENST00000359218.10:c.68943_68944insCCAAACAC (TTN) ENSP00000352154.5:p.Thr22982ProfsTer24
ENST00000342175.10:c.69144_69145insCCAAACAC (TTN) ENSP00000340554.6:p.Thr23049ProfsTer24
ENST00000342992.10:c.88059_88060insCCAAACAC (TTN) ENSP00000343764.6:p.Thr29354ProfsTer24
ENST00000359218.9:c.68943_68944insCCAAACAC (TTN) ENSP00000352154.5:p.Thr22982ProfsTer24
ENST00000460472.6:c.68568_68569insCCAAACAC (TTN) ENSP00000434586.1:p.Thr22857ProfsTer24
ENST00000589042.5:c.95763_95764insCCAAACAC (TTN) MANE Select ENSP00000467141.1:p.Thr31922ProfsTer24
ENST00000591111.5:c.90840_90841insCCAAACAC (TTN) ENSP00000465570.1:p.Thr30281ProfsTer24
ENST00000615779.4:c.90840_90841insCCAAACAC (TTN) ENSP00000483597.1:p.Thr30281ProfsTer24
NM_001256850.1:c.90840_90841insCCAAACAC (TTN) NP_001243779.1:p.Thr30281ProfsTer24
NM_001267550.2:c.95763_95764insCCAAACAC (TTN) MANE Select NP_001254479.2:p.Thr31922ProfsTer24
NM_003319.4:c.68568_68569insCCAAACAC (TTN) NP_003310.4:p.Thr22857ProfsTer24
NM_133378.4:c.88059_88060insCCAAACAC (TTN) NP_596869.4:p.Thr29354ProfsTer24
NM_133432.3:c.68943_68944insCCAAACAC (TTN) NP_597676.3:p.Thr22982ProfsTer24
NM_133437.4:c.69144_69145insCCAAACAC (TTN) NP_597681.4:p.Thr23049ProfsTer24
NR_038271.1:n.446+20830_446+20831insTGTTTGGG (TTN-AS1)
NR_038272.1:n.2043+2105_2043+2106insTGTTTGGG (TTN-AS1)
XM_011511729.1:c.94860_94861insCCAAACAC (TTN) XP_011510031.1:p.Thr31621ProfsTer24
XM_011511730.1:c.68754_68755insCCAAACAC (TTN) XP_011510032.1:p.Thr22919ProfsTer24
XM_011511731.1:c.68613_68614insCCAAACAC (TTN) XP_011510033.1:p.Thr22872ProfsTer24
XM_017004819.1:c.94656_94657insCCAAACAC (TTN) XP_016860308.1:p.Thr31553ProfsTer24
XM_017004820.1:c.90054_90055insCCAAACAC (TTN) XP_016860309.1:p.Thr30019ProfsTer24
XM_017004821.1:c.90051_90052insCCAAACAC (TTN) XP_016860310.1:p.Thr30018ProfsTer24
XM_017004822.1:c.87093_87094insCCAAACAC (TTN) XP_016860311.1:p.Thr29032ProfsTer24
XM_017004823.1:c.68709_68710insCCAAACAC (TTN) XP_016860312.1:p.Thr22904ProfsTer24
XM_024453094.1:c.90204_90205insCCAAACAC (TTN) XP_024308862.1:p.Thr30069ProfsTer24
XM_024453095.1:c.90201_90202insCCAAACAC (TTN) XP_024308863.1:p.Thr30068ProfsTer24
XM_024453096.1:c.89634_89635insCCAAACAC (TTN) XP_024308864.1:p.Thr29879ProfsTer24
XM_024453097.1:c.86976_86977insCCAAACAC (TTN) XP_024308865.1:p.Thr28993ProfsTer24
XM_024453098.1:c.86895_86896insCCAAACAC (TTN) XP_024308866.1:p.Thr28966ProfsTer24
XM_024453099.1:c.68658_68659insCCAAACAC (TTN) XP_024308867.1:p.Thr22887ProfsTer24
XM_024453100.1:c.58512_58513insCCAAACAC (TTN) XP_024308868.1:p.Thr19505ProfsTer24