Canonical Allele Identifier: CA1310520598

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178543262A= , CM000664.2:g.178543262A= GRCh38
NC_000002.11:g.179407989A= , CM000664.1:g.179407989A= GRCh37
NC_000002.10:g.179116235A= NCBI36
NG_011618.3:g.292541T= , LRG_391:g.292541T=
NG_051363.1:g.25436A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.89007T= (TTN) ENSP00000343764.6:p.Tyr29669=
ENST00000342175.11:c.70092T= (TTN) ENSP00000340554.6:p.Tyr23364=
ENST00000359218.10:c.69891T= (TTN) ENSP00000352154.5:p.Tyr23297=
ENST00000342175.10:c.70092T= (TTN) ENSP00000340554.6:p.Tyr23364=
ENST00000342992.10:c.89007T= (TTN) ENSP00000343764.6:p.Tyr29669=
ENST00000359218.9:c.69891T= (TTN) ENSP00000352154.5:p.Tyr23297=
ENST00000460472.6:c.69516T= (TTN) ENSP00000434586.1:p.Tyr23172=
ENST00000589042.5:c.96711T= (TTN) MANE Select ENSP00000467141.1:p.Tyr32237=
ENST00000591111.5:c.91788T= (TTN) ENSP00000465570.1:p.Tyr30596=
ENST00000615779.4:c.91788T= (TTN) ENSP00000483597.1:p.Tyr30596=
NM_001256850.1:c.91788T= (TTN) NP_001243779.1:p.Tyr30596=
NM_001267550.2:c.96711T= (TTN) MANE Select NP_001254479.2:p.Tyr32237=
NM_003319.4:c.69516T= (TTN) NP_003310.4:p.Tyr23172=
NM_133378.4:c.89007T= (TTN) NP_596869.4:p.Tyr29669=
NM_133432.3:c.69891T= (TTN) NP_597676.3:p.Tyr23297=
NM_133437.4:c.70092T= (TTN) NP_597681.4:p.Tyr23364=
NR_038271.1:n.446+19626A= (TTN-AS1)
NR_038272.1:n.2043+901A= (TTN-AS1)
XM_011511729.1:c.95808T= (TTN) XP_011510031.1:p.Tyr31936=
XM_011511730.1:c.69702T= (TTN) XP_011510032.1:p.Tyr23234=
XM_011511731.1:c.69561T= (TTN) XP_011510033.1:p.Tyr23187=
XM_017004819.1:c.95604T= (TTN) XP_016860308.1:p.Tyr31868=
XM_017004820.1:c.91002T= (TTN) XP_016860309.1:p.Tyr30334=
XM_017004821.1:c.90999T= (TTN) XP_016860310.1:p.Tyr30333=
XM_017004822.1:c.88041T= (TTN) XP_016860311.1:p.Tyr29347=
XM_017004823.1:c.69657T= (TTN) XP_016860312.1:p.Tyr23219=
XM_024453094.1:c.91152T= (TTN) XP_024308862.1:p.Tyr30384=
XM_024453095.1:c.91149T= (TTN) XP_024308863.1:p.Tyr30383=
XM_024453096.1:c.90582T= (TTN) XP_024308864.1:p.Tyr30194=
XM_024453097.1:c.87924T= (TTN) XP_024308865.1:p.Tyr29308=
XM_024453098.1:c.87843T= (TTN) XP_024308866.1:p.Tyr29281=
XM_024453099.1:c.69606T= (TTN) XP_024308867.1:p.Tyr23202=
XM_024453100.1:c.59460T= (TTN) XP_024308868.1:p.Tyr19820=