Canonical Allele Identifier: CA1310526766

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178559740_178559745delinsTAGTAC , CM000664.2:g.178559740_178559745delinsTAGTAC GRCh38
NC_000002.11:g.179424467_179424472delinsTAGTAC , CM000664.1:g.179424467_179424472delinsTAGTAC GRCh37
NC_000002.10:g.179132713_179132718delinsTAGTAC NCBI36
NG_011618.3:g.276058_276063delinsGTACTA , LRG_391:g.276058_276063delinsGTACTA
NG_051363.1:g.41914_41919delinsTAGTAC

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.78683_78688delinsGTACTA (TTN) ENSP00000343764.6:p.Arg26228=
ENST00000342175.11:c.59768_59773delinsGTACTA (TTN) ENSP00000340554.6:p.Arg19923=
ENST00000359218.10:c.59567_59572delinsGTACTA (TTN) ENSP00000352154.5:p.Arg19856=
ENST00000342175.10:c.59768_59773delinsGTACTA (TTN) ENSP00000340554.6:p.Arg19923=
ENST00000342992.10:c.78683_78688delinsGTACTA (TTN) ENSP00000343764.6:p.Arg26228=
ENST00000359218.9:c.59567_59572delinsGTACTA (TTN) ENSP00000352154.5:p.Arg19856=
ENST00000460472.6:c.59192_59197delinsGTACTA (TTN) ENSP00000434586.1:p.Arg19731=
ENST00000589042.5:c.86387_86392delinsGTACTA (TTN) MANE Select ENSP00000467141.1:p.Arg28796=
ENST00000591111.5:c.81464_81469delinsGTACTA (TTN) ENSP00000465570.1:p.Arg27155=
ENST00000615779.4:c.81464_81469delinsGTACTA (TTN) ENSP00000483597.1:p.Arg27155=
NM_001256850.1:c.81464_81469delinsGTACTA (TTN) NP_001243779.1:p.Arg27155=
NM_001267550.2:c.86387_86392delinsGTACTA (TTN) MANE Select NP_001254479.2:p.Arg28796=
NM_003319.4:c.59192_59197delinsGTACTA (TTN) NP_003310.4:p.Arg19731=
NM_133378.4:c.78683_78688delinsGTACTA (TTN) NP_596869.4:p.Arg26228=
NM_133432.3:c.59567_59572delinsGTACTA (TTN) NP_597676.3:p.Arg19856=
NM_133437.4:c.59768_59773delinsGTACTA (TTN) NP_597681.4:p.Arg19923=
NR_038271.1:n.447-11560_447-11555delinsTAGTAC (TTN-AS1)
NR_038272.1:n.2043+17379_2043+17384delinsTAGTAC (TTN-AS1)
XM_011511729.1:c.85484_85489delinsGTACTA (TTN) XP_011510031.1:p.Arg28495=
XM_011511730.1:c.59378_59383delinsGTACTA (TTN) XP_011510032.1:p.Arg19793=
XM_011511731.1:c.59237_59242delinsGTACTA (TTN) XP_011510033.1:p.Arg19746=
XM_017004819.1:c.85280_85285delinsGTACTA (TTN) XP_016860308.1:p.Arg28427=
XM_017004820.1:c.80678_80683delinsGTACTA (TTN) XP_016860309.1:p.Arg26893=
XM_017004821.1:c.80675_80680delinsGTACTA (TTN) XP_016860310.1:p.Arg26892=
XM_017004822.1:c.77717_77722delinsGTACTA (TTN) XP_016860311.1:p.Arg25906=
XM_017004823.1:c.59333_59338delinsGTACTA (TTN) XP_016860312.1:p.Arg19778=
XM_024453094.1:c.80828_80833delinsGTACTA (TTN) XP_024308862.1:p.Arg26943=
XM_024453095.1:c.80825_80830delinsGTACTA (TTN) XP_024308863.1:p.Arg26942=
XM_024453096.1:c.80258_80263delinsGTACTA (TTN) XP_024308864.1:p.Arg26753=
XM_024453097.1:c.77600_77605delinsGTACTA (TTN) XP_024308865.1:p.Arg25867=
XM_024453098.1:c.77519_77524delinsGTACTA (TTN) XP_024308866.1:p.Arg25840=
XM_024453099.1:c.59282_59287delinsGTACTA (TTN) XP_024308867.1:p.Arg19761=
XM_024453100.1:c.49136_49141delinsGTACTA (TTN) XP_024308868.1:p.Arg16379=