Canonical Allele Identifier: CA1989806

Linked Data

dbSNP Id: rs748727364

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178568924_178568926dup , CM000664.2:g.178568924_178568926dup GRCh38
NC_000002.11:g.179433651_179433653dup , CM000664.1:g.179433651_179433653dup GRCh37
NC_000002.10:g.179141897_179141899dup NCBI36
NG_011618.3:g.266877_266879dup , LRG_391:g.266877_266879dup
NG_051363.1:g.51098_51100dup

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.69502_69504dup (TTN) ENSP00000343764.6:p.Glu23168_Met23169insG...
ENST00000342175.11:c.50587_50589dup (TTN) ENSP00000340554.6:p.Glu16863_Met16864insG...
ENST00000359218.10:c.50386_50388dup (TTN) ENSP00000352154.5:p.Glu16796_Met16797insG...
ENST00000342175.10:c.50587_50589dup (TTN) ENSP00000340554.6:p.Glu16863_Met16864insG...
ENST00000342992.10:c.69502_69504dup (TTN) ENSP00000343764.6:p.Glu23168_Met23169insG...
ENST00000359218.9:c.50386_50388dup (TTN) ENSP00000352154.5:p.Glu16796_Met16797insG...
ENST00000460472.6:c.50011_50013dup (TTN) ENSP00000434586.1:p.Glu16671_Met16672insG...
ENST00000589042.5:c.77206_77208dup (TTN) MANE Select ENSP00000467141.1:p.Glu25736_Met25737insG...
ENST00000591111.5:c.72283_72285dup (TTN) ENSP00000465570.1:p.Glu24095_Met24096insG...
ENST00000615779.4:c.72283_72285dup (TTN) ENSP00000483597.1:p.Glu24095_Met24096insG...
NM_001256850.1:c.72283_72285dup (TTN) NP_001243779.1:p.Glu24095_Met24096insGlu
NM_001267550.2:c.77206_77208dup (TTN) MANE Select NP_001254479.2:p.Glu25736_Met25737insGlu
NM_003319.4:c.50011_50013dup (TTN) NP_003310.4:p.Glu16671_Met16672insGlu
NM_133378.4:c.69502_69504dup (TTN) NP_596869.4:p.Glu23168_Met23169insGlu
NM_133432.3:c.50386_50388dup (TTN) NP_597676.3:p.Glu16796_Met16797insGlu
NM_133437.4:c.50587_50589dup (TTN) NP_597681.4:p.Glu16863_Met16864insGlu
NR_038271.1:n.447-2376_447-2374dup (TTN-AS1)
NR_038272.1:n.2044-13648_2044-13646dup (TTN-AS1)
XM_011511729.1:c.76303_76305dup (TTN) XP_011510031.1:p.Glu25435_Met25436insGlu
XM_011511730.1:c.50197_50199dup (TTN) XP_011510032.1:p.Glu16733_Met16734insGlu
XM_011511731.1:c.50056_50058dup (TTN) XP_011510033.1:p.Glu16686_Met16687insGlu
XM_017004819.1:c.76099_76101dup (TTN) XP_016860308.1:p.Glu25367_Met25368insGlu
XM_017004820.1:c.71497_71499dup (TTN) XP_016860309.1:p.Glu23833_Met23834insGlu
XM_017004821.1:c.71494_71496dup (TTN) XP_016860310.1:p.Glu23832_Met23833insGlu
XM_017004822.1:c.68536_68538dup (TTN) XP_016860311.1:p.Glu22846_Met22847insGlu
XM_017004823.1:c.50152_50154dup (TTN) XP_016860312.1:p.Glu16718_Met16719insGlu
XM_024453094.1:c.71647_71649dup (TTN) XP_024308862.1:p.Glu23883_Met23884insGlu
XM_024453095.1:c.71644_71646dup (TTN) XP_024308863.1:p.Glu23882_Met23883insGlu
XM_024453096.1:c.71077_71079dup (TTN) XP_024308864.1:p.Glu23693_Met23694insGlu
XM_024453097.1:c.68419_68421dup (TTN) XP_024308865.1:p.Glu22807_Met22808insGlu
XM_024453098.1:c.68338_68340dup (TTN) XP_024308866.1:p.Glu22780_Met22781insGlu
XM_024453099.1:c.50101_50103dup (TTN) XP_024308867.1:p.Glu16701_Met16702insGlu
XM_024453100.1:c.39955_39957dup (TTN) XP_024308868.1:p.Glu13319_Met13320insGlu