Canonical Allele Identifier: CA1310521268

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178551835T= , CM000664.2:g.178551835T= GRCh38
NC_000002.11:g.179416562T= , CM000664.1:g.179416562T= GRCh37
NC_000002.10:g.179124808T= NCBI36
NG_011618.3:g.283968A= , LRG_391:g.283968A=
NG_051363.1:g.34009T=

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.83361A= (TTN) ENSP00000343764.6:p.Glu27787=
ENST00000342175.11:c.64446A= (TTN) ENSP00000340554.6:p.Glu21482=
ENST00000359218.10:c.64245A= (TTN) ENSP00000352154.5:p.Glu21415=
ENST00000342175.10:c.64446A= (TTN) ENSP00000340554.6:p.Glu21482=
ENST00000342992.10:c.83361A= (TTN) ENSP00000343764.6:p.Glu27787=
ENST00000359218.9:c.64245A= (TTN) ENSP00000352154.5:p.Glu21415=
ENST00000460472.6:c.63870A= (TTN) ENSP00000434586.1:p.Glu21290=
ENST00000589042.5:c.91065A= (TTN) MANE Select ENSP00000467141.1:p.Glu30355=
ENST00000591111.5:c.86142A= (TTN) ENSP00000465570.1:p.Glu28714=
ENST00000615779.4:c.86142A= (TTN) ENSP00000483597.1:p.Glu28714=
NM_001256850.1:c.86142A= (TTN) NP_001243779.1:p.Glu28714=
NM_001267550.2:c.91065A= (TTN) MANE Select NP_001254479.2:p.Glu30355=
NM_003319.4:c.63870A= (TTN) NP_003310.4:p.Glu21290=
NM_133378.4:c.83361A= (TTN) NP_596869.4:p.Glu27787=
NM_133432.3:c.64245A= (TTN) NP_597676.3:p.Glu21415=
NM_133437.4:c.64446A= (TTN) NP_597681.4:p.Glu21482=
NR_038271.1:n.447-19465T= (TTN-AS1)
NR_038272.1:n.2043+9474T= (TTN-AS1)
XM_011511729.1:c.90162A= (TTN) XP_011510031.1:p.Glu30054=
XM_011511730.1:c.64056A= (TTN) XP_011510032.1:p.Glu21352=
XM_011511731.1:c.63915A= (TTN) XP_011510033.1:p.Glu21305=
XM_017004819.1:c.89958A= (TTN) XP_016860308.1:p.Glu29986=
XM_017004820.1:c.85356A= (TTN) XP_016860309.1:p.Glu28452=
XM_017004821.1:c.85353A= (TTN) XP_016860310.1:p.Glu28451=
XM_017004822.1:c.82395A= (TTN) XP_016860311.1:p.Glu27465=
XM_017004823.1:c.64011A= (TTN) XP_016860312.1:p.Glu21337=
XM_024453094.1:c.85506A= (TTN) XP_024308862.1:p.Glu28502=
XM_024453095.1:c.85503A= (TTN) XP_024308863.1:p.Glu28501=
XM_024453096.1:c.84936A= (TTN) XP_024308864.1:p.Glu28312=
XM_024453097.1:c.82278A= (TTN) XP_024308865.1:p.Glu27426=
XM_024453098.1:c.82197A= (TTN) XP_024308866.1:p.Glu27399=
XM_024453099.1:c.63960A= (TTN) XP_024308867.1:p.Glu21320=
XM_024453100.1:c.53814A= (TTN) XP_024308868.1:p.Glu17938=