Canonical Allele Identifier: CA1310551141

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178618685A= , CM000664.2:g.178618685A= GRCh38
NC_000002.11:g.179483412A= , CM000664.1:g.179483412A= GRCh37
NC_000002.10:g.179191657A= NCBI36
NG_011618.3:g.217118T= , LRG_391:g.217118T=
NG_051363.1:g.100859A=

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.39161T= (TTN) ENSP00000343764.6:p.Phe13054=
ENST00000342175.11:c.20246T= (TTN) ENSP00000340554.6:p.Phe6749=
ENST00000359218.10:c.20045T= (TTN) ENSP00000352154.5:p.Phe6682=
ENST00000342175.10:c.20246T= (TTN) ENSP00000340554.6:p.Phe6749=
ENST00000342992.10:c.39161T= (TTN) ENSP00000343764.6:p.Phe13054=
ENST00000359218.9:c.20045T= (TTN) ENSP00000352154.5:p.Phe6682=
ENST00000460472.6:c.19670T= (TTN) ENSP00000434586.1:p.Phe6557=
ENST00000589042.5:c.46865T= (TTN) MANE Select ENSP00000467141.1:p.Phe15622=
ENST00000591111.5:c.41942T= (TTN) ENSP00000465570.1:p.Phe13981=
ENST00000615779.4:c.41942T= (TTN) ENSP00000483597.1:p.Phe13981=
NM_001256850.1:c.41942T= (TTN) NP_001243779.1:p.Phe13981=
NM_001267550.2:c.46865T= (TTN) MANE Select NP_001254479.2:p.Phe15622=
NM_003319.4:c.19670T= (TTN) NP_003310.4:p.Phe6557=
NM_133378.4:c.39161T= (TTN) NP_596869.4:p.Phe13054=
NM_133432.3:c.20045T= (TTN) NP_597676.3:p.Phe6682=
NM_133437.4:c.20246T= (TTN) NP_597681.4:p.Phe6749=
NR_038271.1:n.1605-1068A= (TTN-AS1)
XM_011511729.1:c.45962T= (TTN) XP_011510031.1:p.Phe15321=
XM_011511730.1:c.19856T= (TTN) XP_011510032.1:p.Phe6619=
XM_011511731.1:c.19715T= (TTN) XP_011510033.1:p.Phe6572=
XM_017004819.1:c.45758T= (TTN) XP_016860308.1:p.Phe15253=
XM_017004820.1:c.41156T= (TTN) XP_016860309.1:p.Phe13719=
XM_017004821.1:c.41153T= (TTN) XP_016860310.1:p.Phe13718=
XM_017004822.1:c.38195T= (TTN) XP_016860311.1:p.Phe12732=
XM_017004823.1:c.19811T= (TTN) XP_016860312.1:p.Phe6604=
XM_024453094.1:c.41306T= (TTN) XP_024308862.1:p.Phe13769=
XM_024453095.1:c.41303T= (TTN) XP_024308863.1:p.Phe13768=
XM_024453096.1:c.40736T= (TTN) XP_024308864.1:p.Phe13579=
XM_024453097.1:c.38078T= (TTN) XP_024308865.1:p.Phe12693=
XM_024453098.1:c.37997T= (TTN) XP_024308866.1:p.Phe12666=
XM_024453099.1:c.19760T= (TTN) XP_024308867.1:p.Phe6587=
XM_024453100.1:c.9614T= (TTN) XP_024308868.1:p.Phe3205=