Canonical Allele Identifier: CA1310515522

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178537564G= , CM000664.2:g.178537564G= GRCh38
NC_000002.11:g.179402291G= , CM000664.1:g.179402291G= GRCh37
NC_000002.10:g.179110537G= NCBI36
NG_011618.3:g.298239C= , LRG_391:g.298239C=
NG_051363.1:g.19738G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.91939C= (TTN) ENSP00000343764.6:p.Arg30647=
ENST00000342175.11:c.73024C= (TTN) ENSP00000340554.6:p.Arg24342=
ENST00000359218.10:c.72823C= (TTN) ENSP00000352154.5:p.Arg24275=
ENST00000342175.10:c.73024C= (TTN) ENSP00000340554.6:p.Arg24342=
ENST00000342992.10:c.91939C= (TTN) ENSP00000343764.6:p.Arg30647=
ENST00000359218.9:c.72823C= (TTN) ENSP00000352154.5:p.Arg24275=
ENST00000460472.6:c.72448C= (TTN) ENSP00000434586.1:p.Arg24150=
ENST00000589042.5:c.99643C= (TTN) MANE Select ENSP00000467141.1:p.Arg33215=
ENST00000591111.5:c.94720C= (TTN) ENSP00000465570.1:p.Arg31574=
ENST00000615779.4:c.94720C= (TTN) ENSP00000483597.1:p.Arg31574=
NM_001256850.1:c.94720C= (TTN) NP_001243779.1:p.Arg31574=
NM_001267550.2:c.99643C= (TTN) MANE Select NP_001254479.2:p.Arg33215=
NM_003319.4:c.72448C= (TTN) NP_003310.4:p.Arg24150=
NM_133378.4:c.91939C= (TTN) NP_596869.4:p.Arg30647=
NM_133432.3:c.72823C= (TTN) NP_597676.3:p.Arg24275=
NM_133437.4:c.73024C= (TTN) NP_597681.4:p.Arg24342=
NR_038271.1:n.446+13928G= (TTN-AS1)
NR_038272.1:n.520G= (TTN-AS1)
XM_011511729.1:c.98740C= (TTN) XP_011510031.1:p.Arg32914=
XM_011511730.1:c.72634C= (TTN) XP_011510032.1:p.Arg24212=
XM_011511731.1:c.72493C= (TTN) XP_011510033.1:p.Arg24165=
XM_017004819.1:c.98536C= (TTN) XP_016860308.1:p.Arg32846=
XM_017004820.1:c.93934C= (TTN) XP_016860309.1:p.Arg31312=
XM_017004821.1:c.93931C= (TTN) XP_016860310.1:p.Arg31311=
XM_017004822.1:c.90973C= (TTN) XP_016860311.1:p.Arg30325=
XM_017004823.1:c.72589C= (TTN) XP_016860312.1:p.Arg24197=
XM_024453094.1:c.94084C= (TTN) XP_024308862.1:p.Arg31362=
XM_024453095.1:c.94081C= (TTN) XP_024308863.1:p.Arg31361=
XM_024453096.1:c.93514C= (TTN) XP_024308864.1:p.Arg31172=
XM_024453097.1:c.90856C= (TTN) XP_024308865.1:p.Arg30286=
XM_024453098.1:c.90775C= (TTN) XP_024308866.1:p.Arg30259=
XM_024453099.1:c.72538C= (TTN) XP_024308867.1:p.Arg24180=
XM_024453100.1:c.62392C= (TTN) XP_024308868.1:p.Arg20798=