Canonical Allele Identifier: CA1310521192

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178543925G= , CM000664.2:g.178543925G= GRCh38
NC_000002.11:g.179408652G= , CM000664.1:g.179408652G= GRCh37
NC_000002.10:g.179116898G= NCBI36
NG_011618.3:g.291878C= , LRG_391:g.291878C=
NG_051363.1:g.26099G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.88515C= (TTN) ENSP00000343764.6:p.Asp29505=
ENST00000342175.11:c.69600C= (TTN) ENSP00000340554.6:p.Asp23200=
ENST00000359218.10:c.69399C= (TTN) ENSP00000352154.5:p.Asp23133=
ENST00000342175.10:c.69600C= (TTN) ENSP00000340554.6:p.Asp23200=
ENST00000342992.10:c.88515C= (TTN) ENSP00000343764.6:p.Asp29505=
ENST00000359218.9:c.69399C= (TTN) ENSP00000352154.5:p.Asp23133=
ENST00000460472.6:c.69024C= (TTN) ENSP00000434586.1:p.Asp23008=
ENST00000589042.5:c.96219C= (TTN) MANE Select ENSP00000467141.1:p.Asp32073=
ENST00000591111.5:c.91296C= (TTN) ENSP00000465570.1:p.Asp30432=
ENST00000615779.4:c.91296C= (TTN) ENSP00000483597.1:p.Asp30432=
NM_001256850.1:c.91296C= (TTN) NP_001243779.1:p.Asp30432=
NM_001267550.2:c.96219C= (TTN) MANE Select NP_001254479.2:p.Asp32073=
NM_003319.4:c.69024C= (TTN) NP_003310.4:p.Asp23008=
NM_133378.4:c.88515C= (TTN) NP_596869.4:p.Asp29505=
NM_133432.3:c.69399C= (TTN) NP_597676.3:p.Asp23133=
NM_133437.4:c.69600C= (TTN) NP_597681.4:p.Asp23200=
NR_038271.1:n.446+20289G= (TTN-AS1)
NR_038272.1:n.2043+1564G= (TTN-AS1)
XM_011511729.1:c.95316C= (TTN) XP_011510031.1:p.Asp31772=
XM_011511730.1:c.69210C= (TTN) XP_011510032.1:p.Asp23070=
XM_011511731.1:c.69069C= (TTN) XP_011510033.1:p.Asp23023=
XM_017004819.1:c.95112C= (TTN) XP_016860308.1:p.Asp31704=
XM_017004820.1:c.90510C= (TTN) XP_016860309.1:p.Asp30170=
XM_017004821.1:c.90507C= (TTN) XP_016860310.1:p.Asp30169=
XM_017004822.1:c.87549C= (TTN) XP_016860311.1:p.Asp29183=
XM_017004823.1:c.69165C= (TTN) XP_016860312.1:p.Asp23055=
XM_024453094.1:c.90660C= (TTN) XP_024308862.1:p.Asp30220=
XM_024453095.1:c.90657C= (TTN) XP_024308863.1:p.Asp30219=
XM_024453096.1:c.90090C= (TTN) XP_024308864.1:p.Asp30030=
XM_024453097.1:c.87432C= (TTN) XP_024308865.1:p.Asp29144=
XM_024453098.1:c.87351C= (TTN) XP_024308866.1:p.Asp29117=
XM_024453099.1:c.69114C= (TTN) XP_024308867.1:p.Asp23038=
XM_024453100.1:c.58968C= (TTN) XP_024308868.1:p.Asp19656=