Canonical Allele Identifier: CA1310551174

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178618779A= , CM000664.2:g.178618779A= GRCh38
NC_000002.11:g.179483506A= , CM000664.1:g.179483506A= GRCh37
NC_000002.10:g.179191751A= NCBI36
NG_011618.3:g.217024T= , LRG_391:g.217024T=
NG_051363.1:g.100953A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.39067T= (TTN) ENSP00000343764.6:p.Tyr13023=
ENST00000342175.11:c.20152T= (TTN) ENSP00000340554.6:p.Tyr6718=
ENST00000359218.10:c.19951T= (TTN) ENSP00000352154.5:p.Tyr6651=
ENST00000342175.10:c.20152T= (TTN) ENSP00000340554.6:p.Tyr6718=
ENST00000342992.10:c.39067T= (TTN) ENSP00000343764.6:p.Tyr13023=
ENST00000359218.9:c.19951T= (TTN) ENSP00000352154.5:p.Tyr6651=
ENST00000460472.6:c.19576T= (TTN) ENSP00000434586.1:p.Tyr6526=
ENST00000589042.5:c.46771T= (TTN) MANE Select ENSP00000467141.1:p.Tyr15591=
ENST00000591111.5:c.41848T= (TTN) ENSP00000465570.1:p.Tyr13950=
ENST00000615779.4:c.41848T= (TTN) ENSP00000483597.1:p.Tyr13950=
NM_001256850.1:c.41848T= (TTN) NP_001243779.1:p.Tyr13950=
NM_001267550.2:c.46771T= (TTN) MANE Select NP_001254479.2:p.Tyr15591=
NM_003319.4:c.19576T= (TTN) NP_003310.4:p.Tyr6526=
NM_133378.4:c.39067T= (TTN) NP_596869.4:p.Tyr13023=
NM_133432.3:c.19951T= (TTN) NP_597676.3:p.Tyr6651=
NM_133437.4:c.20152T= (TTN) NP_597681.4:p.Tyr6718=
NR_038271.1:n.1605-974A= (TTN-AS1)
XM_011511729.1:c.45868T= (TTN) XP_011510031.1:p.Tyr15290=
XM_011511730.1:c.19762T= (TTN) XP_011510032.1:p.Tyr6588=
XM_011511731.1:c.19621T= (TTN) XP_011510033.1:p.Tyr6541=
XM_017004819.1:c.45664T= (TTN) XP_016860308.1:p.Tyr15222=
XM_017004820.1:c.41062T= (TTN) XP_016860309.1:p.Tyr13688=
XM_017004821.1:c.41059T= (TTN) XP_016860310.1:p.Tyr13687=
XM_017004822.1:c.38101T= (TTN) XP_016860311.1:p.Tyr12701=
XM_017004823.1:c.19717T= (TTN) XP_016860312.1:p.Tyr6573=
XM_024453094.1:c.41212T= (TTN) XP_024308862.1:p.Tyr13738=
XM_024453095.1:c.41209T= (TTN) XP_024308863.1:p.Tyr13737=
XM_024453096.1:c.40642T= (TTN) XP_024308864.1:p.Tyr13548=
XM_024453097.1:c.37984T= (TTN) XP_024308865.1:p.Tyr12662=
XM_024453098.1:c.37903T= (TTN) XP_024308866.1:p.Tyr12635=
XM_024453099.1:c.19666T= (TTN) XP_024308867.1:p.Tyr6556=
XM_024453100.1:c.9520T= (TTN) XP_024308868.1:p.Tyr3174=