Canonical Allele Identifier: CA1310521278

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178551847A= , CM000664.2:g.178551847A= GRCh38
NC_000002.11:g.179416574A= , CM000664.1:g.179416574A= GRCh37
NC_000002.10:g.179124820A= NCBI36
NG_011618.3:g.283956T= , LRG_391:g.283956T=
NG_051363.1:g.34021A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.83349T= (TTN) ENSP00000343764.6:p.Asp27783=
ENST00000342175.11:c.64434T= (TTN) ENSP00000340554.6:p.Asp21478=
ENST00000359218.10:c.64233T= (TTN) ENSP00000352154.5:p.Asp21411=
ENST00000342175.10:c.64434T= (TTN) ENSP00000340554.6:p.Asp21478=
ENST00000342992.10:c.83349T= (TTN) ENSP00000343764.6:p.Asp27783=
ENST00000359218.9:c.64233T= (TTN) ENSP00000352154.5:p.Asp21411=
ENST00000460472.6:c.63858T= (TTN) ENSP00000434586.1:p.Asp21286=
ENST00000589042.5:c.91053T= (TTN) MANE Select ENSP00000467141.1:p.Asp30351=
ENST00000591111.5:c.86130T= (TTN) ENSP00000465570.1:p.Asp28710=
ENST00000615779.4:c.86130T= (TTN) ENSP00000483597.1:p.Asp28710=
NM_001256850.1:c.86130T= (TTN) NP_001243779.1:p.Asp28710=
NM_001267550.2:c.91053T= (TTN) MANE Select NP_001254479.2:p.Asp30351=
NM_003319.4:c.63858T= (TTN) NP_003310.4:p.Asp21286=
NM_133378.4:c.83349T= (TTN) NP_596869.4:p.Asp27783=
NM_133432.3:c.64233T= (TTN) NP_597676.3:p.Asp21411=
NM_133437.4:c.64434T= (TTN) NP_597681.4:p.Asp21478=
NR_038271.1:n.447-19453A= (TTN-AS1)
NR_038272.1:n.2043+9486A= (TTN-AS1)
XM_011511729.1:c.90150T= (TTN) XP_011510031.1:p.Asp30050=
XM_011511730.1:c.64044T= (TTN) XP_011510032.1:p.Asp21348=
XM_011511731.1:c.63903T= (TTN) XP_011510033.1:p.Asp21301=
XM_017004819.1:c.89946T= (TTN) XP_016860308.1:p.Asp29982=
XM_017004820.1:c.85344T= (TTN) XP_016860309.1:p.Asp28448=
XM_017004821.1:c.85341T= (TTN) XP_016860310.1:p.Asp28447=
XM_017004822.1:c.82383T= (TTN) XP_016860311.1:p.Asp27461=
XM_017004823.1:c.63999T= (TTN) XP_016860312.1:p.Asp21333=
XM_024453094.1:c.85494T= (TTN) XP_024308862.1:p.Asp28498=
XM_024453095.1:c.85491T= (TTN) XP_024308863.1:p.Asp28497=
XM_024453096.1:c.84924T= (TTN) XP_024308864.1:p.Asp28308=
XM_024453097.1:c.82266T= (TTN) XP_024308865.1:p.Asp27422=
XM_024453098.1:c.82185T= (TTN) XP_024308866.1:p.Asp27395=
XM_024453099.1:c.63948T= (TTN) XP_024308867.1:p.Asp21316=
XM_024453100.1:c.53802T= (TTN) XP_024308868.1:p.Asp17934=