Canonical Allele Identifier: CA1310547591

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178610041A= , CM000664.2:g.178610041A= GRCh38
NC_000002.11:g.179474768A= , CM000664.1:g.179474768A= GRCh37
NC_000002.10:g.179183013A= NCBI36
NG_011618.3:g.225762T= , LRG_391:g.225762T=
NG_051363.1:g.92215A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.43732+49T= (TTN) ENSP00000343764.6:n.43732+49T=
ENST00000342175.11:c.24817+49T= (TTN) ENSP00000340554.6:n.24817+49T=
ENST00000359218.10:c.24616+49T= (TTN) ENSP00000352154.5:n.24616+49T=
ENST00000342175.10:c.24817+49T= (TTN) ENSP00000340554.6:n.24817+49T=
ENST00000342992.10:c.43732+49T= (TTN) ENSP00000343764.6:n.43732+49T=
ENST00000359218.9:c.24616+49T= (TTN) ENSP00000352154.5:n.24616+49T=
ENST00000460472.6:c.24241+49T= (TTN) ENSP00000434586.1:n.24241+49T=
ENST00000589042.5:c.51436+49T= (TTN) MANE Select ENSP00000467141.1:n.51436+49T=
ENST00000591111.5:c.46513+49T= (TTN) ENSP00000465570.1:n.46513+49T=
ENST00000615779.4:c.46513+49T= (TTN) ENSP00000483597.1:n.46513+49T=
NM_001256850.1:c.46513+49T= (TTN) NP_001243779.1:n.46513+49T=
NM_001267550.2:c.51436+49T= (TTN) MANE Select NP_001254479.2:n.51436+49T=
NM_003319.4:c.24241+49T= (TTN) NP_003310.4:n.24241+49T=
NM_133378.4:c.43732+49T= (TTN) NP_596869.4:n.43732+49T=
NM_133432.3:c.24616+49T= (TTN) NP_597676.3:n.24616+49T=
NM_133437.4:c.24817+49T= (TTN) NP_597681.4:n.24817+49T=
NR_038271.1:n.782+1775A= (TTN-AS1)
XM_011511729.1:c.50533+49T= (TTN) XP_011510031.1:n.50533+49T=
XM_011511730.1:c.24427+49T= (TTN) XP_011510032.1:n.24427+49T=
XM_011511731.1:c.24286+49T= (TTN) XP_011510033.1:n.24286+49T=
XM_017004819.1:c.50329+49T= (TTN) XP_016860308.1:n.50329+49T=
XM_017004820.1:c.45727+49T= (TTN) XP_016860309.1:n.45727+49T=
XM_017004821.1:c.45724+49T= (TTN) XP_016860310.1:n.45724+49T=
XM_017004822.1:c.42766+49T= (TTN) XP_016860311.1:n.42766+49T=
XM_017004823.1:c.24382+49T= (TTN) XP_016860312.1:n.24382+49T=
XM_024453094.1:c.45877+49T= (TTN) XP_024308862.1:n.45877+49T=
XM_024453095.1:c.45874+49T= (TTN) XP_024308863.1:n.45874+49T=
XM_024453096.1:c.45307+49T= (TTN) XP_024308864.1:n.45307+49T=
XM_024453097.1:c.42649+49T= (TTN) XP_024308865.1:n.42649+49T=
XM_024453098.1:c.42568+49T= (TTN) XP_024308866.1:n.42568+49T=
XM_024453099.1:c.24331+49T= (TTN) XP_024308867.1:n.24331+49T=
XM_024453100.1:c.14185+49T= (TTN) XP_024308868.1:n.14185+49T=