Canonical Allele Identifier: CA2753331448

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178613978dup , CM000664.2:g.178613978dup GRCh38
NC_000002.11:g.179478705dup , CM000664.1:g.179478705dup GRCh37
NC_000002.10:g.179186950dup NCBI36
NG_011618.3:g.221825dup , LRG_391:g.221825dup
NG_051363.1:g.96152dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.41642-41dup (TTN) ENSP00000343764.6:n.41642-41dup
ENST00000342175.11:c.22727-41dup (TTN) ENSP00000340554.6:n.22727-41dup
ENST00000359218.10:c.22526-41dup (TTN) ENSP00000352154.5:n.22526-41dup
ENST00000342175.10:c.22727-41dup (TTN) ENSP00000340554.6:n.22727-41dup
ENST00000342992.10:c.41642-41dup (TTN) ENSP00000343764.6:n.41642-41dup
ENST00000359218.9:c.22526-41dup (TTN) ENSP00000352154.5:n.22526-41dup
ENST00000460472.6:c.22151-41dup (TTN) ENSP00000434586.1:n.22151-41dup
ENST00000589042.5:c.49346-41dup (TTN) MANE Select ENSP00000467141.1:n.49346-41dup
ENST00000591111.5:c.44423-41dup (TTN) ENSP00000465570.1:n.44423-41dup
ENST00000615779.4:c.44423-41dup (TTN) ENSP00000483597.1:n.44423-41dup
NM_001256850.1:c.44423-41dup (TTN) NP_001243779.1:n.44423-41dup
NM_001267550.2:c.49346-41dup (TTN) MANE Select NP_001254479.2:n.49346-41dup
NM_003319.4:c.22151-41dup (TTN) NP_003310.4:n.22151-41dup
NM_133378.4:c.41642-41dup (TTN) NP_596869.4:n.41642-41dup
NM_133432.3:c.22526-41dup (TTN) NP_597676.3:n.22526-41dup
NM_133437.4:c.22727-41dup (TTN) NP_597681.4:n.22727-41dup
NR_038271.1:n.783-57dup (TTN-AS1)
XM_011511729.1:c.48443-41dup (TTN) XP_011510031.1:n.48443-41dup
XM_011511730.1:c.22337-41dup (TTN) XP_011510032.1:n.22337-41dup
XM_011511731.1:c.22196-41dup (TTN) XP_011510033.1:n.22196-41dup
XM_017004819.1:c.48239-41dup (TTN) XP_016860308.1:n.48239-41dup
XM_017004820.1:c.43637-41dup (TTN) XP_016860309.1:n.43637-41dup
XM_017004821.1:c.43634-41dup (TTN) XP_016860310.1:n.43634-41dup
XM_017004822.1:c.40676-41dup (TTN) XP_016860311.1:n.40676-41dup
XM_017004823.1:c.22292-41dup (TTN) XP_016860312.1:n.22292-41dup
XM_024453094.1:c.43787-41dup (TTN) XP_024308862.1:n.43787-41dup
XM_024453095.1:c.43784-41dup (TTN) XP_024308863.1:n.43784-41dup
XM_024453096.1:c.43217-41dup (TTN) XP_024308864.1:n.43217-41dup
XM_024453097.1:c.40559-41dup (TTN) XP_024308865.1:n.40559-41dup
XM_024453098.1:c.40478-41dup (TTN) XP_024308866.1:n.40478-41dup
XM_024453099.1:c.22241-41dup (TTN) XP_024308867.1:n.22241-41dup
XM_024453100.1:c.12095-41dup (TTN) XP_024308868.1:n.12095-41dup