Canonical Allele Identifier: CA1310514276

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178527031A= , CM000664.2:g.178527031A= GRCh38
NC_000002.11:g.179391758A= , CM000664.1:g.179391758A= GRCh37
NC_000002.10:g.179100004A= NCBI36
NG_011618.3:g.308772T= , LRG_391:g.308772T=
NG_051363.1:g.9205A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.100253T= (TTN) ENSP00000343764.6:p.Ile33418=
ENST00000342175.11:c.81338T= (TTN) ENSP00000340554.6:p.Ile27113=
ENST00000359218.10:c.81137T= (TTN) ENSP00000352154.5:p.Ile27046=
ENST00000342175.10:c.81338T= (TTN) ENSP00000340554.6:p.Ile27113=
ENST00000342992.10:c.100253T= (TTN) ENSP00000343764.6:p.Ile33418=
ENST00000359218.9:c.81137T= (TTN) ENSP00000352154.5:p.Ile27046=
ENST00000460472.6:c.80762T= (TTN) ENSP00000434586.1:p.Ile26921=
ENST00000589042.5:c.107957T= (TTN) MANE Select ENSP00000467141.1:p.Ile35986=
ENST00000591111.5:c.103034T= (TTN) ENSP00000465570.1:p.Ile34345=
ENST00000615779.4:c.103034T= (TTN) ENSP00000483597.1:p.Ile34345=
NM_001256850.1:c.103034T= (TTN) NP_001243779.1:p.Ile34345=
NM_001267550.2:c.107957T= (TTN) MANE Select NP_001254479.2:p.Ile35986=
NM_003319.4:c.80762T= (TTN) NP_003310.4:p.Ile26921=
NM_133378.4:c.100253T= (TTN) NP_596869.4:p.Ile33418=
NM_133432.3:c.81137T= (TTN) NP_597676.3:p.Ile27046=
NM_133437.4:c.81338T= (TTN) NP_597681.4:p.Ile27113=
NR_038271.1:n.446+3395A= (TTN-AS1)
NR_038272.1:n.219+3395A= (TTN-AS1)
XM_011511729.1:c.107054T= (TTN) XP_011510031.1:p.Ile35685=
XM_011511730.1:c.80948T= (TTN) XP_011510032.1:p.Ile26983=
XM_011511731.1:c.80807T= (TTN) XP_011510033.1:p.Ile26936=
XM_017004819.1:c.106850T= (TTN) XP_016860308.1:p.Ile35617=
XM_017004820.1:c.102248T= (TTN) XP_016860309.1:p.Ile34083=
XM_017004821.1:c.102245T= (TTN) XP_016860310.1:p.Ile34082=
XM_017004822.1:c.99287T= (TTN) XP_016860311.1:p.Ile33096=
XM_017004823.1:c.80903T= (TTN) XP_016860312.1:p.Ile26968=
XM_024453094.1:c.102398T= (TTN) XP_024308862.1:p.Ile34133=
XM_024453095.1:c.102395T= (TTN) XP_024308863.1:p.Ile34132=
XM_024453096.1:c.101828T= (TTN) XP_024308864.1:p.Ile33943=
XM_024453097.1:c.99170T= (TTN) XP_024308865.1:p.Ile33057=
XM_024453098.1:c.99089T= (TTN) XP_024308866.1:p.Ile33030=
XM_024453099.1:c.80852T= (TTN) XP_024308867.1:p.Ile26951=
XM_024453100.1:c.70706T= (TTN) XP_024308868.1:p.Ile23569=