Canonical Allele Identifier: CA2662152343
Gene: TTN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178733473_178733475del , CM000664.2:g.178733473_178733475del GRCh38
NC_000002.11:g.179598200_179598202del , CM000664.1:g.179598200_179598202del GRCh37
NC_000002.10:g.179306445_179306447del NCBI36
NG_011618.3:g.102331_102333del , LRG_391:g.102331_102333del

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.12089_12091del ENSP00000343764.6:p.Ala4030del
ENST00000342175.11:c.13858+4610_13858+4612del ENSP00000340554.6:n.13858+4610_13858+4612...
ENST00000359218.10:c.13657+4610_13657+4612del ENSP00000352154.5:n.13657+4610_13657+4612...
ENST00000342175.10:c.13858+4610_13858+4612del ENSP00000340554.6:n.13858+4610_13858+4612...
ENST00000342992.10:c.12089_12091del ENSP00000343764.6:p.Ala4030del
ENST00000359218.9:c.13657+4610_13657+4612del ENSP00000352154.5:n.13657+4610_13657+4612...
ENST00000460472.6:c.13282+4610_13282+4612del ENSP00000434586.1:n.13282+4610_13282+4612...
ENST00000589042.5:c.15821_15823del MANE Select ENSP00000467141.1:p.Ala5274del
ENST00000591111.5:c.14870_14872del ENSP00000465570.1:p.Ala4957del
ENST00000615779.4:c.14870_14872del ENSP00000483597.1:p.Ala4957del
NM_001256850.1:c.14870_14872del NP_001243779.1:p.Ala4957del
NM_001267550.2:c.15821_15823del MANE Select NP_001254479.2:p.Ala5274del
NM_003319.4:c.13282+4610_13282+4612del NP_003310.4:n.13282+4610_13282+4612del
NM_133378.4:c.12089_12091del NP_596869.4:p.Ala4030del
NM_133432.3:c.13657+4610_13657+4612del NP_597676.3:n.13657+4610_13657+4612del
NM_133437.4:c.13858+4610_13858+4612del NP_597681.4:n.13858+4610_13858+4612del
XM_011511729.1:c.14918_14920del XP_011510031.1:p.Ala4973del
XM_011511730.1:c.13468+4610_13468+4612del XP_011510032.1:n.13468+4610_13468+4612del...
XM_011511731.1:c.13327+4610_13327+4612del XP_011510033.1:n.13327+4610_13327+4612del...
XM_017004819.1:c.14873_14875del XP_016860308.1:p.Ala4958del
XM_017004820.1:c.12092_12094del XP_016860309.1:p.Ala4031del
XM_017004821.1:c.12089_12091del XP_016860310.1:p.Ala4030del
XM_017004822.1:c.14873_14875del XP_016860311.1:p.Ala4958del
XM_017004823.1:c.13423+4610_13423+4612del XP_016860312.1:n.13423+4610_13423+4612del...
XM_024453094.1:c.14873_14875del XP_024308862.1:p.Ala4958del
XM_024453095.1:c.14873_14875del XP_024308863.1:p.Ala4958del
XM_024453096.1:c.14873_14875del XP_024308864.1:p.Ala4958del
XM_024453097.1:c.14873_14875del XP_024308865.1:p.Ala4958del
XM_024453098.1:c.14873_14875del XP_024308866.1:p.Ala4958del
XM_024453099.1:c.13423+4610_13423+4612del XP_024308867.1:n.13423+4610_13423+4612del...