Canonical Allele Identifier: CA1310526711

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178559639_178559640delinsCA , CM000664.2:g.178559639_178559640delinsCA GRCh38
NC_000002.11:g.179424366_179424367delinsCA , CM000664.1:g.179424366_179424367delinsCA GRCh37
NC_000002.10:g.179132612_179132613delinsCA NCBI36
NG_011618.3:g.276163_276164delinsTG , LRG_391:g.276163_276164delinsTG
NG_051363.1:g.41813_41814delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.78788_78789delinsTG (TTN) ENSP00000343764.6:p.Leu26263=
ENST00000342175.11:c.59873_59874delinsTG (TTN) ENSP00000340554.6:p.Leu19958=
ENST00000359218.10:c.59672_59673delinsTG (TTN) ENSP00000352154.5:p.Leu19891=
ENST00000342175.10:c.59873_59874delinsTG (TTN) ENSP00000340554.6:p.Leu19958=
ENST00000342992.10:c.78788_78789delinsTG (TTN) ENSP00000343764.6:p.Leu26263=
ENST00000359218.9:c.59672_59673delinsTG (TTN) ENSP00000352154.5:p.Leu19891=
ENST00000460472.6:c.59297_59298delinsTG (TTN) ENSP00000434586.1:p.Leu19766=
ENST00000589042.5:c.86492_86493delinsTG (TTN) MANE Select ENSP00000467141.1:p.Leu28831=
ENST00000591111.5:c.81569_81570delinsTG (TTN) ENSP00000465570.1:p.Leu27190=
ENST00000615779.4:c.81569_81570delinsTG (TTN) ENSP00000483597.1:p.Leu27190=
NM_001256850.1:c.81569_81570delinsTG (TTN) NP_001243779.1:p.Leu27190=
NM_001267550.2:c.86492_86493delinsTG (TTN) MANE Select NP_001254479.2:p.Leu28831=
NM_003319.4:c.59297_59298delinsTG (TTN) NP_003310.4:p.Leu19766=
NM_133378.4:c.78788_78789delinsTG (TTN) NP_596869.4:p.Leu26263=
NM_133432.3:c.59672_59673delinsTG (TTN) NP_597676.3:p.Leu19891=
NM_133437.4:c.59873_59874delinsTG (TTN) NP_597681.4:p.Leu19958=
NR_038271.1:n.447-11661_447-11660delinsCA (TTN-AS1)
NR_038272.1:n.2043+17278_2043+17279delinsCA (TTN-AS1)
XM_011511729.1:c.85589_85590delinsTG (TTN) XP_011510031.1:p.Leu28530=
XM_011511730.1:c.59483_59484delinsTG (TTN) XP_011510032.1:p.Leu19828=
XM_011511731.1:c.59342_59343delinsTG (TTN) XP_011510033.1:p.Leu19781=
XM_017004819.1:c.85385_85386delinsTG (TTN) XP_016860308.1:p.Leu28462=
XM_017004820.1:c.80783_80784delinsTG (TTN) XP_016860309.1:p.Leu26928=
XM_017004821.1:c.80780_80781delinsTG (TTN) XP_016860310.1:p.Leu26927=
XM_017004822.1:c.77822_77823delinsTG (TTN) XP_016860311.1:p.Leu25941=
XM_017004823.1:c.59438_59439delinsTG (TTN) XP_016860312.1:p.Leu19813=
XM_024453094.1:c.80933_80934delinsTG (TTN) XP_024308862.1:p.Leu26978=
XM_024453095.1:c.80930_80931delinsTG (TTN) XP_024308863.1:p.Leu26977=
XM_024453096.1:c.80363_80364delinsTG (TTN) XP_024308864.1:p.Leu26788=
XM_024453097.1:c.77705_77706delinsTG (TTN) XP_024308865.1:p.Leu25902=
XM_024453098.1:c.77624_77625delinsTG (TTN) XP_024308866.1:p.Leu25875=
XM_024453099.1:c.59387_59388delinsTG (TTN) XP_024308867.1:p.Leu19796=
XM_024453100.1:c.49241_49242delinsTG (TTN) XP_024308868.1:p.Leu16414=