Canonical Allele Identifier: CA1310521199

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178551753C= , CM000664.2:g.178551753C= GRCh38
NC_000002.11:g.179416480C= , CM000664.1:g.179416480C= GRCh37
NC_000002.10:g.179124726C= NCBI36
NG_011618.3:g.284050G= , LRG_391:g.284050G=
NG_051363.1:g.33927C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.83443G= (TTN) ENSP00000343764.6:p.Glu27815=
ENST00000342175.11:c.64528G= (TTN) ENSP00000340554.6:p.Glu21510=
ENST00000359218.10:c.64327G= (TTN) ENSP00000352154.5:p.Glu21443=
ENST00000342175.10:c.64528G= (TTN) ENSP00000340554.6:p.Glu21510=
ENST00000342992.10:c.83443G= (TTN) ENSP00000343764.6:p.Glu27815=
ENST00000359218.9:c.64327G= (TTN) ENSP00000352154.5:p.Glu21443=
ENST00000460472.6:c.63952G= (TTN) ENSP00000434586.1:p.Glu21318=
ENST00000589042.5:c.91147G= (TTN) MANE Select ENSP00000467141.1:p.Glu30383=
ENST00000591111.5:c.86224G= (TTN) ENSP00000465570.1:p.Glu28742=
ENST00000615779.4:c.86224G= (TTN) ENSP00000483597.1:p.Glu28742=
NM_001256850.1:c.86224G= (TTN) NP_001243779.1:p.Glu28742=
NM_001267550.2:c.91147G= (TTN) MANE Select NP_001254479.2:p.Glu30383=
NM_003319.4:c.63952G= (TTN) NP_003310.4:p.Glu21318=
NM_133378.4:c.83443G= (TTN) NP_596869.4:p.Glu27815=
NM_133432.3:c.64327G= (TTN) NP_597676.3:p.Glu21443=
NM_133437.4:c.64528G= (TTN) NP_597681.4:p.Glu21510=
NR_038271.1:n.447-19547C= (TTN-AS1)
NR_038272.1:n.2043+9392C= (TTN-AS1)
XM_011511729.1:c.90244G= (TTN) XP_011510031.1:p.Glu30082=
XM_011511730.1:c.64138G= (TTN) XP_011510032.1:p.Glu21380=
XM_011511731.1:c.63997G= (TTN) XP_011510033.1:p.Glu21333=
XM_017004819.1:c.90040G= (TTN) XP_016860308.1:p.Glu30014=
XM_017004820.1:c.85438G= (TTN) XP_016860309.1:p.Glu28480=
XM_017004821.1:c.85435G= (TTN) XP_016860310.1:p.Glu28479=
XM_017004822.1:c.82477G= (TTN) XP_016860311.1:p.Glu27493=
XM_017004823.1:c.64093G= (TTN) XP_016860312.1:p.Glu21365=
XM_024453094.1:c.85588G= (TTN) XP_024308862.1:p.Glu28530=
XM_024453095.1:c.85585G= (TTN) XP_024308863.1:p.Glu28529=
XM_024453096.1:c.85018G= (TTN) XP_024308864.1:p.Glu28340=
XM_024453097.1:c.82360G= (TTN) XP_024308865.1:p.Glu27454=
XM_024453098.1:c.82279G= (TTN) XP_024308866.1:p.Glu27427=
XM_024453099.1:c.64042G= (TTN) XP_024308867.1:p.Glu21348=
XM_024453100.1:c.53896G= (TTN) XP_024308868.1:p.Glu17966=