Canonical Allele Identifier: CA1310530744

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178568838T= , CM000664.2:g.178568838T= GRCh38
NC_000002.11:g.179433565T= , CM000664.1:g.179433565T= GRCh37
NC_000002.10:g.179141811T= NCBI36
NG_011618.3:g.266965A= , LRG_391:g.266965A=
NG_051363.1:g.51012T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.69590A= (TTN) ENSP00000343764.6:p.Glu23197=
ENST00000342175.11:c.50675A= (TTN) ENSP00000340554.6:p.Glu16892=
ENST00000359218.10:c.50474A= (TTN) ENSP00000352154.5:p.Glu16825=
ENST00000342175.10:c.50675A= (TTN) ENSP00000340554.6:p.Glu16892=
ENST00000342992.10:c.69590A= (TTN) ENSP00000343764.6:p.Glu23197=
ENST00000359218.9:c.50474A= (TTN) ENSP00000352154.5:p.Glu16825=
ENST00000460472.6:c.50099A= (TTN) ENSP00000434586.1:p.Glu16700=
ENST00000589042.5:c.77294A= (TTN) MANE Select ENSP00000467141.1:p.Glu25765=
ENST00000591111.5:c.72371A= (TTN) ENSP00000465570.1:p.Glu24124=
ENST00000615779.4:c.72371A= (TTN) ENSP00000483597.1:p.Glu24124=
NM_001256850.1:c.72371A= (TTN) NP_001243779.1:p.Glu24124=
NM_001267550.2:c.77294A= (TTN) MANE Select NP_001254479.2:p.Glu25765=
NM_003319.4:c.50099A= (TTN) NP_003310.4:p.Glu16700=
NM_133378.4:c.69590A= (TTN) NP_596869.4:p.Glu23197=
NM_133432.3:c.50474A= (TTN) NP_597676.3:p.Glu16825=
NM_133437.4:c.50675A= (TTN) NP_597681.4:p.Glu16892=
NR_038271.1:n.447-2462T= (TTN-AS1)
NR_038272.1:n.2044-13734T= (TTN-AS1)
XM_011511729.1:c.76391A= (TTN) XP_011510031.1:p.Glu25464=
XM_011511730.1:c.50285A= (TTN) XP_011510032.1:p.Glu16762=
XM_011511731.1:c.50144A= (TTN) XP_011510033.1:p.Glu16715=
XM_017004819.1:c.76187A= (TTN) XP_016860308.1:p.Glu25396=
XM_017004820.1:c.71585A= (TTN) XP_016860309.1:p.Glu23862=
XM_017004821.1:c.71582A= (TTN) XP_016860310.1:p.Glu23861=
XM_017004822.1:c.68624A= (TTN) XP_016860311.1:p.Glu22875=
XM_017004823.1:c.50240A= (TTN) XP_016860312.1:p.Glu16747=
XM_024453094.1:c.71735A= (TTN) XP_024308862.1:p.Glu23912=
XM_024453095.1:c.71732A= (TTN) XP_024308863.1:p.Glu23911=
XM_024453096.1:c.71165A= (TTN) XP_024308864.1:p.Glu23722=
XM_024453097.1:c.68507A= (TTN) XP_024308865.1:p.Glu22836=
XM_024453098.1:c.68426A= (TTN) XP_024308866.1:p.Glu22809=
XM_024453099.1:c.50189A= (TTN) XP_024308867.1:p.Glu16730=
XM_024453100.1:c.40043A= (TTN) XP_024308868.1:p.Glu13348=