Canonical Allele Identifier: CA1310537028

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178584471A= , CM000664.2:g.178584471A= GRCh38
NC_000002.11:g.179449198A= , CM000664.1:g.179449198A= GRCh37
NC_000002.10:g.179157444A= NCBI36
NG_011618.3:g.251332T= , LRG_391:g.251332T=
NG_051363.1:g.66645A=

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.57376T= (TTN) ENSP00000343764.6:p.Tyr19126=
ENST00000342175.11:c.38461T= (TTN) ENSP00000340554.6:p.Tyr12821=
ENST00000359218.10:c.38260T= (TTN) ENSP00000352154.5:p.Tyr12754=
ENST00000342175.10:c.38461T= (TTN) ENSP00000340554.6:p.Tyr12821=
ENST00000342992.10:c.57376T= (TTN) ENSP00000343764.6:p.Tyr19126=
ENST00000359218.9:c.38260T= (TTN) ENSP00000352154.5:p.Tyr12754=
ENST00000460472.6:c.37885T= (TTN) ENSP00000434586.1:p.Tyr12629=
ENST00000589042.5:c.65080T= (TTN) MANE Select ENSP00000467141.1:p.Tyr21694=
ENST00000591111.5:c.60157T= (TTN) ENSP00000465570.1:p.Tyr20053=
ENST00000615779.4:c.60157T= (TTN) ENSP00000483597.1:p.Tyr20053=
NM_001256850.1:c.60157T= (TTN) NP_001243779.1:p.Tyr20053=
NM_001267550.2:c.65080T= (TTN) MANE Select NP_001254479.2:p.Tyr21694=
NM_003319.4:c.37885T= (TTN) NP_003310.4:p.Tyr12629=
NM_133378.4:c.57376T= (TTN) NP_596869.4:p.Tyr19126=
NM_133432.3:c.38260T= (TTN) NP_597676.3:p.Tyr12754=
NM_133437.4:c.38461T= (TTN) NP_597681.4:p.Tyr12821=
NR_038271.1:n.596+13022A= (TTN-AS1)
NR_038272.1:n.2768-102A= (TTN-AS1)
XM_011511729.1:c.64177T= (TTN) XP_011510031.1:p.Tyr21393=
XM_011511730.1:c.38071T= (TTN) XP_011510032.1:p.Tyr12691=
XM_011511731.1:c.37930T= (TTN) XP_011510033.1:p.Tyr12644=
XM_017004819.1:c.63973T= (TTN) XP_016860308.1:p.Tyr21325=
XM_017004820.1:c.59371T= (TTN) XP_016860309.1:p.Tyr19791=
XM_017004821.1:c.59368T= (TTN) XP_016860310.1:p.Tyr19790=
XM_017004822.1:c.56410T= (TTN) XP_016860311.1:p.Tyr18804=
XM_017004823.1:c.38026T= (TTN) XP_016860312.1:p.Tyr12676=
XM_024453094.1:c.59521T= (TTN) XP_024308862.1:p.Tyr19841=
XM_024453095.1:c.59518T= (TTN) XP_024308863.1:p.Tyr19840=
XM_024453096.1:c.58951T= (TTN) XP_024308864.1:p.Tyr19651=
XM_024453097.1:c.56293T= (TTN) XP_024308865.1:p.Tyr18765=
XM_024453098.1:c.56212T= (TTN) XP_024308866.1:p.Tyr18738=
XM_024453099.1:c.37975T= (TTN) XP_024308867.1:p.Tyr12659=
XM_024453100.1:c.27829T= (TTN) XP_024308868.1:p.Tyr9277=