Canonical Allele Identifier: CA1310520702

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178551062T= , CM000664.2:g.178551062T= GRCh38
NC_000002.11:g.179415789T= , CM000664.1:g.179415789T= GRCh37
NC_000002.10:g.179124035T= NCBI36
NG_011618.3:g.284741A= , LRG_391:g.284741A=
NG_051363.1:g.33236T=

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.83765A= (TTN) ENSP00000343764.6:p.Asp27922=
ENST00000342175.11:c.64850A= (TTN) ENSP00000340554.6:p.Asp21617=
ENST00000359218.10:c.64649A= (TTN) ENSP00000352154.5:p.Asp21550=
ENST00000342175.10:c.64850A= (TTN) ENSP00000340554.6:p.Asp21617=
ENST00000342992.10:c.83765A= (TTN) ENSP00000343764.6:p.Asp27922=
ENST00000359218.9:c.64649A= (TTN) ENSP00000352154.5:p.Asp21550=
ENST00000460472.6:c.64274A= (TTN) ENSP00000434586.1:p.Asp21425=
ENST00000589042.5:c.91469A= (TTN) MANE Select ENSP00000467141.1:p.Asp30490=
ENST00000591111.5:c.86546A= (TTN) ENSP00000465570.1:p.Asp28849=
ENST00000615779.4:c.86546A= (TTN) ENSP00000483597.1:p.Asp28849=
NM_001256850.1:c.86546A= (TTN) NP_001243779.1:p.Asp28849=
NM_001267550.2:c.91469A= (TTN) MANE Select NP_001254479.2:p.Asp30490=
NM_003319.4:c.64274A= (TTN) NP_003310.4:p.Asp21425=
NM_133378.4:c.83765A= (TTN) NP_596869.4:p.Asp27922=
NM_133432.3:c.64649A= (TTN) NP_597676.3:p.Asp21550=
NM_133437.4:c.64850A= (TTN) NP_597681.4:p.Asp21617=
NR_038271.1:n.447-20238T= (TTN-AS1)
NR_038272.1:n.2043+8701T= (TTN-AS1)
XM_011511729.1:c.90566A= (TTN) XP_011510031.1:p.Asp30189=
XM_011511730.1:c.64460A= (TTN) XP_011510032.1:p.Asp21487=
XM_011511731.1:c.64319A= (TTN) XP_011510033.1:p.Asp21440=
XM_017004819.1:c.90362A= (TTN) XP_016860308.1:p.Asp30121=
XM_017004820.1:c.85760A= (TTN) XP_016860309.1:p.Asp28587=
XM_017004821.1:c.85757A= (TTN) XP_016860310.1:p.Asp28586=
XM_017004822.1:c.82799A= (TTN) XP_016860311.1:p.Asp27600=
XM_017004823.1:c.64415A= (TTN) XP_016860312.1:p.Asp21472=
XM_024453094.1:c.85910A= (TTN) XP_024308862.1:p.Asp28637=
XM_024453095.1:c.85907A= (TTN) XP_024308863.1:p.Asp28636=
XM_024453096.1:c.85340A= (TTN) XP_024308864.1:p.Asp28447=
XM_024453097.1:c.82682A= (TTN) XP_024308865.1:p.Asp27561=
XM_024453098.1:c.82601A= (TTN) XP_024308866.1:p.Asp27534=
XM_024453099.1:c.64364A= (TTN) XP_024308867.1:p.Asp21455=
XM_024453100.1:c.54218A= (TTN) XP_024308868.1:p.Asp18073=