Canonical Allele Identifier: CA1310520627

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178543291A= , CM000664.2:g.178543291A= GRCh38
NC_000002.11:g.179408018A= , CM000664.1:g.179408018A= GRCh37
NC_000002.10:g.179116264A= NCBI36
NG_011618.3:g.292512T= , LRG_391:g.292512T=
NG_051363.1:g.25465A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.88978T= (TTN) ENSP00000343764.6:p.Tyr29660=
ENST00000342175.11:c.70063T= (TTN) ENSP00000340554.6:p.Tyr23355=
ENST00000359218.10:c.69862T= (TTN) ENSP00000352154.5:p.Tyr23288=
ENST00000342175.10:c.70063T= (TTN) ENSP00000340554.6:p.Tyr23355=
ENST00000342992.10:c.88978T= (TTN) ENSP00000343764.6:p.Tyr29660=
ENST00000359218.9:c.69862T= (TTN) ENSP00000352154.5:p.Tyr23288=
ENST00000460472.6:c.69487T= (TTN) ENSP00000434586.1:p.Tyr23163=
ENST00000589042.5:c.96682T= (TTN) MANE Select ENSP00000467141.1:p.Tyr32228=
ENST00000591111.5:c.91759T= (TTN) ENSP00000465570.1:p.Tyr30587=
ENST00000615779.4:c.91759T= (TTN) ENSP00000483597.1:p.Tyr30587=
NM_001256850.1:c.91759T= (TTN) NP_001243779.1:p.Tyr30587=
NM_001267550.2:c.96682T= (TTN) MANE Select NP_001254479.2:p.Tyr32228=
NM_003319.4:c.69487T= (TTN) NP_003310.4:p.Tyr23163=
NM_133378.4:c.88978T= (TTN) NP_596869.4:p.Tyr29660=
NM_133432.3:c.69862T= (TTN) NP_597676.3:p.Tyr23288=
NM_133437.4:c.70063T= (TTN) NP_597681.4:p.Tyr23355=
NR_038271.1:n.446+19655A= (TTN-AS1)
NR_038272.1:n.2043+930A= (TTN-AS1)
XM_011511729.1:c.95779T= (TTN) XP_011510031.1:p.Tyr31927=
XM_011511730.1:c.69673T= (TTN) XP_011510032.1:p.Tyr23225=
XM_011511731.1:c.69532T= (TTN) XP_011510033.1:p.Tyr23178=
XM_017004819.1:c.95575T= (TTN) XP_016860308.1:p.Tyr31859=
XM_017004820.1:c.90973T= (TTN) XP_016860309.1:p.Tyr30325=
XM_017004821.1:c.90970T= (TTN) XP_016860310.1:p.Tyr30324=
XM_017004822.1:c.88012T= (TTN) XP_016860311.1:p.Tyr29338=
XM_017004823.1:c.69628T= (TTN) XP_016860312.1:p.Tyr23210=
XM_024453094.1:c.91123T= (TTN) XP_024308862.1:p.Tyr30375=
XM_024453095.1:c.91120T= (TTN) XP_024308863.1:p.Tyr30374=
XM_024453096.1:c.90553T= (TTN) XP_024308864.1:p.Tyr30185=
XM_024453097.1:c.87895T= (TTN) XP_024308865.1:p.Tyr29299=
XM_024453098.1:c.87814T= (TTN) XP_024308866.1:p.Tyr29272=
XM_024453099.1:c.69577T= (TTN) XP_024308867.1:p.Tyr23193=
XM_024453100.1:c.59431T= (TTN) XP_024308868.1:p.Tyr19811=