Canonical Allele Identifier: CA2662146136
Gene: TTN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178689203_178689216del , CM000664.2:g.178689203_178689216del GRCh38
NC_000002.11:g.179553930_179553943del , CM000664.1:g.179553930_179553943del GRCh37
NC_000002.10:g.179262175_179262188del NCBI36
NG_011618.3:g.146589_146602del , LRG_391:g.146589_146602del

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.28279+76_28280-65del ENSP00000343764.6:n.28279+76_28280-65del
ENST00000342175.11:c.13859-46897_13859-46884del ENSP00000340554.6:n.13859-46897_13859-468...
ENST00000359218.10:c.13658-46897_13658-46884del ENSP00000352154.5:n.13658-46897_13658-468...
ENST00000342175.10:c.13859-46897_13859-46884del ENSP00000340554.6:n.13859-46897_13859-468...
ENST00000342992.10:c.28279+76_28280-65del ENSP00000343764.6:n.28279+76_28280-65del
ENST00000359218.9:c.13658-46897_13658-46884del ENSP00000352154.5:n.13658-46897_13658-468...
ENST00000414766.5:c.1645+76_1646-65del ENSP00000401501.1:n.1645+76_1646-65del
ENST00000460472.6:c.13283-46897_13283-46884del ENSP00000434586.1:n.13283-46897_13283-468...
ENST00000589042.5:c.32011+76_32012-65del MANE Select ENSP00000467141.1:n.32011+76_32012-65del
ENST00000591111.5:c.31060+76_31061-65del ENSP00000465570.1:n.31060+76_31061-65del
ENST00000615779.4:c.31060+76_31061-65del ENSP00000483597.1:n.31060+76_31061-65del
NM_001256850.1:c.31060+76_31061-65del NP_001243779.1:n.31060+76_31061-65del
NM_001267550.2:c.32011+76_32012-65del MANE Select NP_001254479.2:n.32011+76_32012-65del
NM_003319.4:c.13283-46897_13283-46884del NP_003310.4:n.13283-46897_13283-46884del
NM_133378.4:c.28279+76_28280-65del NP_596869.4:n.28279+76_28280-65del
NM_133432.3:c.13658-46897_13658-46884del NP_597676.3:n.13658-46897_13658-46884del
NM_133437.4:c.13859-46897_13859-46884del NP_597681.4:n.13859-46897_13859-46884del
XM_011511729.1:c.31108+76_31109-65del XP_011510031.1:n.31108+76_31109-65del
XM_011511730.1:c.13469-46897_13469-46884del XP_011510032.1:n.13469-46897_13469-46884d...
XM_011511731.1:c.13328-46897_13328-46884del XP_011510033.1:n.13328-46897_13328-46884d...
XM_017004819.1:c.31063+76_31064-65del XP_016860308.1:n.31063+76_31064-65del
XM_017004820.1:c.28282+76_28283-65del XP_016860309.1:n.28282+76_28283-65del
XM_017004821.1:c.28279+76_28280-65del XP_016860310.1:n.28279+76_28280-65del
XM_017004822.1:c.31063+76_31064-65del XP_016860311.1:n.31063+76_31064-65del
XM_017004823.1:c.13424-46897_13424-46884del XP_016860312.1:n.13424-46897_13424-46884d...
XM_024453094.1:c.31063+76_31064-65del XP_024308862.1:n.31063+76_31064-65del
XM_024453095.1:c.31063+76_31064-65del XP_024308863.1:n.31063+76_31064-65del
XM_024453096.1:c.31063+76_31064-65del XP_024308864.1:n.31063+76_31064-65del
XM_024453097.1:c.30898+599_30898+612del XP_024308865.1:n.30898+599_30898+612del
XM_024453098.1:c.30898+599_30898+612del XP_024308866.1:n.30898+599_30898+612del
XM_024453099.1:c.13424-46897_13424-46884del XP_024308867.1:n.13424-46897_13424-46884d...