Canonical Allele Identifier: CA1310511433

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178530072T= , CM000664.2:g.178530072T= GRCh38
NC_000002.11:g.179394799T= , CM000664.1:g.179394799T= GRCh37
NC_000002.10:g.179103045T= NCBI36
NG_011618.3:g.305731A= , LRG_391:g.305731A=
NG_051363.1:g.12246T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.98715A= (TTN) ENSP00000343764.6:p.Gly32905=
ENST00000342175.11:c.79800A= (TTN) ENSP00000340554.6:p.Gly26600=
ENST00000359218.10:c.79599A= (TTN) ENSP00000352154.5:p.Gly26533=
ENST00000342175.10:c.79800A= (TTN) ENSP00000340554.6:p.Gly26600=
ENST00000342992.10:c.98715A= (TTN) ENSP00000343764.6:p.Gly32905=
ENST00000359218.9:c.79599A= (TTN) ENSP00000352154.5:p.Gly26533=
ENST00000460472.6:c.79224A= (TTN) ENSP00000434586.1:p.Gly26408=
ENST00000589042.5:c.106419A= (TTN) MANE Select ENSP00000467141.1:p.Gly35473=
ENST00000591111.5:c.101496A= (TTN) ENSP00000465570.1:p.Gly33832=
ENST00000615779.4:c.101496A= (TTN) ENSP00000483597.1:p.Gly33832=
NM_001256850.1:c.101496A= (TTN) NP_001243779.1:p.Gly33832=
NM_001267550.2:c.106419A= (TTN) MANE Select NP_001254479.2:p.Gly35473=
NM_003319.4:c.79224A= (TTN) NP_003310.4:p.Gly26408=
NM_133378.4:c.98715A= (TTN) NP_596869.4:p.Gly32905=
NM_133432.3:c.79599A= (TTN) NP_597676.3:p.Gly26533=
NM_133437.4:c.79800A= (TTN) NP_597681.4:p.Gly26600=
NR_038271.1:n.446+6436T= (TTN-AS1)
NR_038272.1:n.220-5660T= (TTN-AS1)
XM_011511729.1:c.105516A= (TTN) XP_011510031.1:p.Gly35172=
XM_011511730.1:c.79410A= (TTN) XP_011510032.1:p.Gly26470=
XM_011511731.1:c.79269A= (TTN) XP_011510033.1:p.Gly26423=
XM_017004819.1:c.105312A= (TTN) XP_016860308.1:p.Gly35104=
XM_017004820.1:c.100710A= (TTN) XP_016860309.1:p.Gly33570=
XM_017004821.1:c.100707A= (TTN) XP_016860310.1:p.Gly33569=
XM_017004822.1:c.97749A= (TTN) XP_016860311.1:p.Gly32583=
XM_017004823.1:c.79365A= (TTN) XP_016860312.1:p.Gly26455=
XM_024453094.1:c.100860A= (TTN) XP_024308862.1:p.Gly33620=
XM_024453095.1:c.100857A= (TTN) XP_024308863.1:p.Gly33619=
XM_024453096.1:c.100290A= (TTN) XP_024308864.1:p.Gly33430=
XM_024453097.1:c.97632A= (TTN) XP_024308865.1:p.Gly32544=
XM_024453098.1:c.97551A= (TTN) XP_024308866.1:p.Gly32517=
XM_024453099.1:c.79314A= (TTN) XP_024308867.1:p.Gly26438=
XM_024453100.1:c.69168A= (TTN) XP_024308868.1:p.Gly23056=