Canonical Allele Identifier: CA1310529447

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178566271T= , CM000664.2:g.178566271T= GRCh38
NC_000002.11:g.179430998T= , CM000664.1:g.179430998T= GRCh37
NC_000002.10:g.179139244T= NCBI36
NG_011618.3:g.269532A= , LRG_391:g.269532A=
NG_051363.1:g.48445T=

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.72157A= (TTN) ENSP00000343764.6:p.Thr24053=
ENST00000342175.11:c.53242A= (TTN) ENSP00000340554.6:p.Thr17748=
ENST00000359218.10:c.53041A= (TTN) ENSP00000352154.5:p.Thr17681=
ENST00000342175.10:c.53242A= (TTN) ENSP00000340554.6:p.Thr17748=
ENST00000342992.10:c.72157A= (TTN) ENSP00000343764.6:p.Thr24053=
ENST00000359218.9:c.53041A= (TTN) ENSP00000352154.5:p.Thr17681=
ENST00000460472.6:c.52666A= (TTN) ENSP00000434586.1:p.Thr17556=
ENST00000589042.5:c.79861A= (TTN) MANE Select ENSP00000467141.1:p.Thr26621=
ENST00000591111.5:c.74938A= (TTN) ENSP00000465570.1:p.Thr24980=
ENST00000615779.4:c.74938A= (TTN) ENSP00000483597.1:p.Thr24980=
NM_001256850.1:c.74938A= (TTN) NP_001243779.1:p.Thr24980=
NM_001267550.2:c.79861A= (TTN) MANE Select NP_001254479.2:p.Thr26621=
NM_003319.4:c.52666A= (TTN) NP_003310.4:p.Thr17556=
NM_133378.4:c.72157A= (TTN) NP_596869.4:p.Thr24053=
NM_133432.3:c.53041A= (TTN) NP_597676.3:p.Thr17681=
NM_133437.4:c.53242A= (TTN) NP_597681.4:p.Thr17748=
NR_038271.1:n.447-5029T= (TTN-AS1)
NR_038272.1:n.2044-16301T= (TTN-AS1)
XM_011511729.1:c.78958A= (TTN) XP_011510031.1:p.Thr26320=
XM_011511730.1:c.52852A= (TTN) XP_011510032.1:p.Thr17618=
XM_011511731.1:c.52711A= (TTN) XP_011510033.1:p.Thr17571=
XM_017004819.1:c.78754A= (TTN) XP_016860308.1:p.Thr26252=
XM_017004820.1:c.74152A= (TTN) XP_016860309.1:p.Thr24718=
XM_017004821.1:c.74149A= (TTN) XP_016860310.1:p.Thr24717=
XM_017004822.1:c.71191A= (TTN) XP_016860311.1:p.Thr23731=
XM_017004823.1:c.52807A= (TTN) XP_016860312.1:p.Thr17603=
XM_024453094.1:c.74302A= (TTN) XP_024308862.1:p.Thr24768=
XM_024453095.1:c.74299A= (TTN) XP_024308863.1:p.Thr24767=
XM_024453096.1:c.73732A= (TTN) XP_024308864.1:p.Thr24578=
XM_024453097.1:c.71074A= (TTN) XP_024308865.1:p.Thr23692=
XM_024453098.1:c.70993A= (TTN) XP_024308866.1:p.Thr23665=
XM_024453099.1:c.52756A= (TTN) XP_024308867.1:p.Thr17586=
XM_024453100.1:c.42610A= (TTN) XP_024308868.1:p.Thr14204=