Canonical Allele Identifier: CA1310551138

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178618680T= , CM000664.2:g.178618680T= GRCh38
NC_000002.11:g.179483407T= , CM000664.1:g.179483407T= GRCh37
NC_000002.10:g.179191652T= NCBI36
NG_011618.3:g.217123A= , LRG_391:g.217123A=
NG_051363.1:g.100854T=

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.39166A= (TTN) ENSP00000343764.6:p.Ile13056=
ENST00000342175.11:c.20251A= (TTN) ENSP00000340554.6:p.Ile6751=
ENST00000359218.10:c.20050A= (TTN) ENSP00000352154.5:p.Ile6684=
ENST00000342175.10:c.20251A= (TTN) ENSP00000340554.6:p.Ile6751=
ENST00000342992.10:c.39166A= (TTN) ENSP00000343764.6:p.Ile13056=
ENST00000359218.9:c.20050A= (TTN) ENSP00000352154.5:p.Ile6684=
ENST00000460472.6:c.19675A= (TTN) ENSP00000434586.1:p.Ile6559=
ENST00000589042.5:c.46870A= (TTN) MANE Select ENSP00000467141.1:p.Ile15624=
ENST00000591111.5:c.41947A= (TTN) ENSP00000465570.1:p.Ile13983=
ENST00000615779.4:c.41947A= (TTN) ENSP00000483597.1:p.Ile13983=
NM_001256850.1:c.41947A= (TTN) NP_001243779.1:p.Ile13983=
NM_001267550.2:c.46870A= (TTN) MANE Select NP_001254479.2:p.Ile15624=
NM_003319.4:c.19675A= (TTN) NP_003310.4:p.Ile6559=
NM_133378.4:c.39166A= (TTN) NP_596869.4:p.Ile13056=
NM_133432.3:c.20050A= (TTN) NP_597676.3:p.Ile6684=
NM_133437.4:c.20251A= (TTN) NP_597681.4:p.Ile6751=
NR_038271.1:n.1605-1073T= (TTN-AS1)
XM_011511729.1:c.45967A= (TTN) XP_011510031.1:p.Ile15323=
XM_011511730.1:c.19861A= (TTN) XP_011510032.1:p.Ile6621=
XM_011511731.1:c.19720A= (TTN) XP_011510033.1:p.Ile6574=
XM_017004819.1:c.45763A= (TTN) XP_016860308.1:p.Ile15255=
XM_017004820.1:c.41161A= (TTN) XP_016860309.1:p.Ile13721=
XM_017004821.1:c.41158A= (TTN) XP_016860310.1:p.Ile13720=
XM_017004822.1:c.38200A= (TTN) XP_016860311.1:p.Ile12734=
XM_017004823.1:c.19816A= (TTN) XP_016860312.1:p.Ile6606=
XM_024453094.1:c.41311A= (TTN) XP_024308862.1:p.Ile13771=
XM_024453095.1:c.41308A= (TTN) XP_024308863.1:p.Ile13770=
XM_024453096.1:c.40741A= (TTN) XP_024308864.1:p.Ile13581=
XM_024453097.1:c.38083A= (TTN) XP_024308865.1:p.Ile12695=
XM_024453098.1:c.38002A= (TTN) XP_024308866.1:p.Ile12668=
XM_024453099.1:c.19765A= (TTN) XP_024308867.1:p.Ile6589=
XM_024453100.1:c.9619A= (TTN) XP_024308868.1:p.Ile3207=