Canonical Allele Identifier: CA1310522961

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178546306_178546308delinsGAT , CM000664.2:g.178546306_178546308delinsGAT GRCh38
NC_000002.11:g.179411033_179411035delinsGAT , CM000664.1:g.179411033_179411035delinsGAT GRCh37
NC_000002.10:g.179119279_179119281delinsGAT NCBI36
NG_011618.3:g.289495_289497delinsATC , LRG_391:g.289495_289497delinsATC
NG_051363.1:g.28480_28482delinsGAT

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.87319_87321delinsATC (TTN) ENSP00000343764.6:p.Ile29107=
ENST00000342175.11:c.68404_68406delinsATC (TTN) ENSP00000340554.6:p.Ile22802=
ENST00000359218.10:c.68203_68205delinsATC (TTN) ENSP00000352154.5:p.Ile22735=
ENST00000342175.10:c.68404_68406delinsATC (TTN) ENSP00000340554.6:p.Ile22802=
ENST00000342992.10:c.87319_87321delinsATC (TTN) ENSP00000343764.6:p.Ile29107=
ENST00000359218.9:c.68203_68205delinsATC (TTN) ENSP00000352154.5:p.Ile22735=
ENST00000460472.6:c.67828_67830delinsATC (TTN) ENSP00000434586.1:p.Ile22610=
ENST00000589042.5:c.95023_95025delinsATC (TTN) MANE Select ENSP00000467141.1:p.Ile31675=
ENST00000591111.5:c.90100_90102delinsATC (TTN) ENSP00000465570.1:p.Ile30034=
ENST00000615779.4:c.90100_90102delinsATC (TTN) ENSP00000483597.1:p.Ile30034=
NM_001256850.1:c.90100_90102delinsATC (TTN) NP_001243779.1:p.Ile30034=
NM_001267550.2:c.95023_95025delinsATC (TTN) MANE Select NP_001254479.2:p.Ile31675=
NM_003319.4:c.67828_67830delinsATC (TTN) NP_003310.4:p.Ile22610=
NM_133378.4:c.87319_87321delinsATC (TTN) NP_596869.4:p.Ile29107=
NM_133432.3:c.68203_68205delinsATC (TTN) NP_597676.3:p.Ile22735=
NM_133437.4:c.68404_68406delinsATC (TTN) NP_597681.4:p.Ile22802=
NR_038271.1:n.446+22670_446+22672delinsGAT (TTN-AS1)
NR_038272.1:n.2043+3945_2043+3947delinsGAT (TTN-AS1)
XM_011511729.1:c.94120_94122delinsATC (TTN) XP_011510031.1:p.Ile31374=
XM_011511730.1:c.68014_68016delinsATC (TTN) XP_011510032.1:p.Ile22672=
XM_011511731.1:c.67873_67875delinsATC (TTN) XP_011510033.1:p.Ile22625=
XM_017004819.1:c.93916_93918delinsATC (TTN) XP_016860308.1:p.Ile31306=
XM_017004820.1:c.89314_89316delinsATC (TTN) XP_016860309.1:p.Ile29772=
XM_017004821.1:c.89311_89313delinsATC (TTN) XP_016860310.1:p.Ile29771=
XM_017004822.1:c.86353_86355delinsATC (TTN) XP_016860311.1:p.Ile28785=
XM_017004823.1:c.67969_67971delinsATC (TTN) XP_016860312.1:p.Ile22657=
XM_024453094.1:c.89464_89466delinsATC (TTN) XP_024308862.1:p.Ile29822=
XM_024453095.1:c.89461_89463delinsATC (TTN) XP_024308863.1:p.Ile29821=
XM_024453096.1:c.88894_88896delinsATC (TTN) XP_024308864.1:p.Ile29632=
XM_024453097.1:c.86236_86238delinsATC (TTN) XP_024308865.1:p.Ile28746=
XM_024453098.1:c.86155_86157delinsATC (TTN) XP_024308866.1:p.Ile28719=
XM_024453099.1:c.67918_67920delinsATC (TTN) XP_024308867.1:p.Ile22640=
XM_024453100.1:c.57772_57774delinsATC (TTN) XP_024308868.1:p.Ile19258=