Canonical Allele Identifier: CA1310524135

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178547638A= , CM000664.2:g.178547638A= GRCh38
NC_000002.11:g.179412365A= , CM000664.1:g.179412365A= GRCh37
NC_000002.10:g.179120611A= NCBI36
NG_011618.3:g.288165T= , LRG_391:g.288165T=
NG_051363.1:g.29812A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.86284T= (TTN) ENSP00000343764.6:p.Trp28762=
ENST00000342175.11:c.67369T= (TTN) ENSP00000340554.6:p.Trp22457=
ENST00000359218.10:c.67168T= (TTN) ENSP00000352154.5:p.Trp22390=
ENST00000342175.10:c.67369T= (TTN) ENSP00000340554.6:p.Trp22457=
ENST00000342992.10:c.86284T= (TTN) ENSP00000343764.6:p.Trp28762=
ENST00000359218.9:c.67168T= (TTN) ENSP00000352154.5:p.Trp22390=
ENST00000460472.6:c.66793T= (TTN) ENSP00000434586.1:p.Trp22265=
ENST00000589042.5:c.93988T= (TTN) MANE Select ENSP00000467141.1:p.Trp31330=
ENST00000591111.5:c.89065T= (TTN) ENSP00000465570.1:p.Trp29689=
ENST00000615779.4:c.89065T= (TTN) ENSP00000483597.1:p.Trp29689=
NM_001256850.1:c.89065T= (TTN) NP_001243779.1:p.Trp29689=
NM_001267550.2:c.93988T= (TTN) MANE Select NP_001254479.2:p.Trp31330=
NM_003319.4:c.66793T= (TTN) NP_003310.4:p.Trp22265=
NM_133378.4:c.86284T= (TTN) NP_596869.4:p.Trp28762=
NM_133432.3:c.67168T= (TTN) NP_597676.3:p.Trp22390=
NM_133437.4:c.67369T= (TTN) NP_597681.4:p.Trp22457=
NR_038271.1:n.447-23662A= (TTN-AS1)
NR_038272.1:n.2043+5277A= (TTN-AS1)
XM_011511729.1:c.93085T= (TTN) XP_011510031.1:p.Trp31029=
XM_011511730.1:c.66979T= (TTN) XP_011510032.1:p.Trp22327=
XM_011511731.1:c.66838T= (TTN) XP_011510033.1:p.Trp22280=
XM_017004819.1:c.92881T= (TTN) XP_016860308.1:p.Trp30961=
XM_017004820.1:c.88279T= (TTN) XP_016860309.1:p.Trp29427=
XM_017004821.1:c.88276T= (TTN) XP_016860310.1:p.Trp29426=
XM_017004822.1:c.85318T= (TTN) XP_016860311.1:p.Trp28440=
XM_017004823.1:c.66934T= (TTN) XP_016860312.1:p.Trp22312=
XM_024453094.1:c.88429T= (TTN) XP_024308862.1:p.Trp29477=
XM_024453095.1:c.88426T= (TTN) XP_024308863.1:p.Trp29476=
XM_024453096.1:c.87859T= (TTN) XP_024308864.1:p.Trp29287=
XM_024453097.1:c.85201T= (TTN) XP_024308865.1:p.Trp28401=
XM_024453098.1:c.85120T= (TTN) XP_024308866.1:p.Trp28374=
XM_024453099.1:c.66883T= (TTN) XP_024308867.1:p.Trp22295=
XM_024453100.1:c.56737T= (TTN) XP_024308868.1:p.Trp18913=