Canonical Allele Identifier: CA1310511436

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178530073C= , CM000664.2:g.178530073C= GRCh38
NC_000002.11:g.179394800C= , CM000664.1:g.179394800C= GRCh37
NC_000002.10:g.179103046C= NCBI36
NG_011618.3:g.305730G= , LRG_391:g.305730G=
NG_051363.1:g.12247C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.98714G= (TTN) ENSP00000343764.6:p.Gly32905=
ENST00000342175.11:c.79799G= (TTN) ENSP00000340554.6:p.Gly26600=
ENST00000359218.10:c.79598G= (TTN) ENSP00000352154.5:p.Gly26533=
ENST00000342175.10:c.79799G= (TTN) ENSP00000340554.6:p.Gly26600=
ENST00000342992.10:c.98714G= (TTN) ENSP00000343764.6:p.Gly32905=
ENST00000359218.9:c.79598G= (TTN) ENSP00000352154.5:p.Gly26533=
ENST00000460472.6:c.79223G= (TTN) ENSP00000434586.1:p.Gly26408=
ENST00000589042.5:c.106418G= (TTN) MANE Select ENSP00000467141.1:p.Gly35473=
ENST00000591111.5:c.101495G= (TTN) ENSP00000465570.1:p.Gly33832=
ENST00000615779.4:c.101495G= (TTN) ENSP00000483597.1:p.Gly33832=
NM_001256850.1:c.101495G= (TTN) NP_001243779.1:p.Gly33832=
NM_001267550.2:c.106418G= (TTN) MANE Select NP_001254479.2:p.Gly35473=
NM_003319.4:c.79223G= (TTN) NP_003310.4:p.Gly26408=
NM_133378.4:c.98714G= (TTN) NP_596869.4:p.Gly32905=
NM_133432.3:c.79598G= (TTN) NP_597676.3:p.Gly26533=
NM_133437.4:c.79799G= (TTN) NP_597681.4:p.Gly26600=
NR_038271.1:n.446+6437C= (TTN-AS1)
NR_038272.1:n.220-5659C= (TTN-AS1)
XM_011511729.1:c.105515G= (TTN) XP_011510031.1:p.Gly35172=
XM_011511730.1:c.79409G= (TTN) XP_011510032.1:p.Gly26470=
XM_011511731.1:c.79268G= (TTN) XP_011510033.1:p.Gly26423=
XM_017004819.1:c.105311G= (TTN) XP_016860308.1:p.Gly35104=
XM_017004820.1:c.100709G= (TTN) XP_016860309.1:p.Gly33570=
XM_017004821.1:c.100706G= (TTN) XP_016860310.1:p.Gly33569=
XM_017004822.1:c.97748G= (TTN) XP_016860311.1:p.Gly32583=
XM_017004823.1:c.79364G= (TTN) XP_016860312.1:p.Gly26455=
XM_024453094.1:c.100859G= (TTN) XP_024308862.1:p.Gly33620=
XM_024453095.1:c.100856G= (TTN) XP_024308863.1:p.Gly33619=
XM_024453096.1:c.100289G= (TTN) XP_024308864.1:p.Gly33430=
XM_024453097.1:c.97631G= (TTN) XP_024308865.1:p.Gly32544=
XM_024453098.1:c.97550G= (TTN) XP_024308866.1:p.Gly32517=
XM_024453099.1:c.79313G= (TTN) XP_024308867.1:p.Gly26438=
XM_024453100.1:c.69167G= (TTN) XP_024308868.1:p.Gly23056=