Canonical Allele Identifier: CA2753331437

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178544466_178544467insT , CM000664.2:g.178544466_178544467insT GRCh38
NC_000002.11:g.179409193_179409194insT , CM000664.1:g.179409193_179409194insT GRCh37
NC_000002.10:g.179117439_179117440insT NCBI36
NG_011618.3:g.291336_291337insA , LRG_391:g.291336_291337insA
NG_051363.1:g.26640_26641insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.88058_88059insA (TTN) ENSP00000343764.6:p.Thr29354HisfsTer6
ENST00000342175.11:c.69143_69144insA (TTN) ENSP00000340554.6:p.Thr23049HisfsTer6
ENST00000359218.10:c.68942_68943insA (TTN) ENSP00000352154.5:p.Thr22982HisfsTer6
ENST00000342175.10:c.69143_69144insA (TTN) ENSP00000340554.6:p.Thr23049HisfsTer6
ENST00000342992.10:c.88058_88059insA (TTN) ENSP00000343764.6:p.Thr29354HisfsTer6
ENST00000359218.9:c.68942_68943insA (TTN) ENSP00000352154.5:p.Thr22982HisfsTer6
ENST00000460472.6:c.68567_68568insA (TTN) ENSP00000434586.1:p.Thr22857HisfsTer6
ENST00000589042.5:c.95762_95763insA (TTN) MANE Select ENSP00000467141.1:p.Thr31922HisfsTer6
ENST00000591111.5:c.90839_90840insA (TTN) ENSP00000465570.1:p.Thr30281HisfsTer6
ENST00000615779.4:c.90839_90840insA (TTN) ENSP00000483597.1:p.Thr30281HisfsTer6
NM_001256850.1:c.90839_90840insA (TTN) NP_001243779.1:p.Thr30281HisfsTer6
NM_001267550.2:c.95762_95763insA (TTN) MANE Select NP_001254479.2:p.Thr31922HisfsTer6
NM_003319.4:c.68567_68568insA (TTN) NP_003310.4:p.Thr22857HisfsTer6
NM_133378.4:c.88058_88059insA (TTN) NP_596869.4:p.Thr29354HisfsTer6
NM_133432.3:c.68942_68943insA (TTN) NP_597676.3:p.Thr22982HisfsTer6
NM_133437.4:c.69143_69144insA (TTN) NP_597681.4:p.Thr23049HisfsTer6
NR_038271.1:n.446+20830_446+20831insT (TTN-AS1)
NR_038272.1:n.2043+2105_2043+2106insT (TTN-AS1)
XM_011511729.1:c.94859_94860insA (TTN) XP_011510031.1:p.Thr31621HisfsTer6
XM_011511730.1:c.68753_68754insA (TTN) XP_011510032.1:p.Thr22919HisfsTer6
XM_011511731.1:c.68612_68613insA (TTN) XP_011510033.1:p.Thr22872HisfsTer6
XM_017004819.1:c.94655_94656insA (TTN) XP_016860308.1:p.Thr31553HisfsTer6
XM_017004820.1:c.90053_90054insA (TTN) XP_016860309.1:p.Thr30019HisfsTer6
XM_017004821.1:c.90050_90051insA (TTN) XP_016860310.1:p.Thr30018HisfsTer6
XM_017004822.1:c.87092_87093insA (TTN) XP_016860311.1:p.Thr29032HisfsTer6
XM_017004823.1:c.68708_68709insA (TTN) XP_016860312.1:p.Thr22904HisfsTer6
XM_024453094.1:c.90203_90204insA (TTN) XP_024308862.1:p.Thr30069HisfsTer6
XM_024453095.1:c.90200_90201insA (TTN) XP_024308863.1:p.Thr30068HisfsTer6
XM_024453096.1:c.89633_89634insA (TTN) XP_024308864.1:p.Thr29879HisfsTer6
XM_024453097.1:c.86975_86976insA (TTN) XP_024308865.1:p.Thr28993HisfsTer6
XM_024453098.1:c.86894_86895insA (TTN) XP_024308866.1:p.Thr28966HisfsTer6
XM_024453099.1:c.68657_68658insA (TTN) XP_024308867.1:p.Thr22887HisfsTer6
XM_024453100.1:c.58511_58512insA (TTN) XP_024308868.1:p.Thr19505HisfsTer6