Canonical Allele Identifier: CA1310540314

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178593050A= , CM000664.2:g.178593050A= GRCh38
NC_000002.11:g.179457777A= , CM000664.1:g.179457777A= GRCh37
NC_000002.10:g.179166023A= NCBI36
NG_011618.3:g.242753T= , LRG_391:g.242753T=
NG_051363.1:g.75224A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.51365T= (TTN) ENSP00000343764.6:p.Ile17122=
ENST00000342175.11:c.32450T= (TTN) ENSP00000340554.6:p.Ile10817=
ENST00000359218.10:c.32249T= (TTN) ENSP00000352154.5:p.Ile10750=
ENST00000342175.10:c.32450T= (TTN) ENSP00000340554.6:p.Ile10817=
ENST00000342992.10:c.51365T= (TTN) ENSP00000343764.6:p.Ile17122=
ENST00000359218.9:c.32249T= (TTN) ENSP00000352154.5:p.Ile10750=
ENST00000460472.6:c.31874T= (TTN) ENSP00000434586.1:p.Ile10625=
ENST00000589042.5:c.59069T= (TTN) MANE Select ENSP00000467141.1:p.Ile19690=
ENST00000591111.5:c.54146T= (TTN) ENSP00000465570.1:p.Ile18049=
ENST00000615779.4:c.54146T= (TTN) ENSP00000483597.1:p.Ile18049=
NM_001256850.1:c.54146T= (TTN) NP_001243779.1:p.Ile18049=
NM_001267550.2:c.59069T= (TTN) MANE Select NP_001254479.2:p.Ile19690=
NM_003319.4:c.31874T= (TTN) NP_003310.4:p.Ile10625=
NM_133378.4:c.51365T= (TTN) NP_596869.4:p.Ile17122=
NM_133432.3:c.32249T= (TTN) NP_597676.3:p.Ile10750=
NM_133437.4:c.32450T= (TTN) NP_597681.4:p.Ile10817=
NR_038271.1:n.597-4546A= (TTN-AS1)
NR_038272.1:n.3364+1736A= (TTN-AS1)
XM_011511729.1:c.58166T= (TTN) XP_011510031.1:p.Ile19389=
XM_011511730.1:c.32060T= (TTN) XP_011510032.1:p.Ile10687=
XM_011511731.1:c.31919T= (TTN) XP_011510033.1:p.Ile10640=
XM_017004819.1:c.57962T= (TTN) XP_016860308.1:p.Ile19321=
XM_017004820.1:c.53360T= (TTN) XP_016860309.1:p.Ile17787=
XM_017004821.1:c.53357T= (TTN) XP_016860310.1:p.Ile17786=
XM_017004822.1:c.50399T= (TTN) XP_016860311.1:p.Ile16800=
XM_017004823.1:c.32015T= (TTN) XP_016860312.1:p.Ile10672=
XM_024453094.1:c.53510T= (TTN) XP_024308862.1:p.Ile17837=
XM_024453095.1:c.53507T= (TTN) XP_024308863.1:p.Ile17836=
XM_024453096.1:c.52940T= (TTN) XP_024308864.1:p.Ile17647=
XM_024453097.1:c.50282T= (TTN) XP_024308865.1:p.Ile16761=
XM_024453098.1:c.50201T= (TTN) XP_024308866.1:p.Ile16734=
XM_024453099.1:c.31964T= (TTN) XP_024308867.1:p.Ile10655=
XM_024453100.1:c.21818T= (TTN) XP_024308868.1:p.Ile7273=