Canonical Allele Identifier: CA1039717945
Gene: TTN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178689013_178689027dup , CM000664.2:g.178689013_178689027dup GRCh38
NC_000002.11:g.179553740_179553754dup , CM000664.1:g.179553740_179553754dup GRCh37
NC_000002.10:g.179261985_179261999dup NCBI36
NG_011618.3:g.146785_146799dup , LRG_391:g.146785_146799dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.28363+35_28363+49dup ENSP00000343764.6:n.28363+35_28363+49dup
ENST00000342175.11:c.13859-46701_13859-46687dup ENSP00000340554.6:n.13859-46701_13859-46687dup
ENST00000359218.10:c.13658-46701_13658-46687dup ENSP00000352154.5:n.13658-46701_13658-46687dup
ENST00000342175.10:c.13859-46701_13859-46687dup ENSP00000340554.6:n.13859-46701_13859-46687dup
ENST00000342992.10:c.28363+35_28363+49dup ENSP00000343764.6:n.28363+35_28363+49dup
ENST00000359218.9:c.13658-46701_13658-46687dup ENSP00000352154.5:n.13658-46701_13658-46687dup
ENST00000414766.5:c.1729+35_1729+49dup ENSP00000401501.1:n.1729+35_1729+49dup
ENST00000460472.6:c.13283-46701_13283-46687dup ENSP00000434586.1:n.13283-46701_13283-46687dup
ENST00000589042.5:c.32095+35_32095+49dup MANE Select ENSP00000467141.1:n.32095+35_32095+49dup
ENST00000591111.5:c.31144+35_31144+49dup ENSP00000465570.1:n.31144+35_31144+49dup
ENST00000615779.4:c.31144+35_31144+49dup ENSP00000483597.1:n.31144+35_31144+49dup
NM_001256850.1:c.31144+35_31144+49dup NP_001243779.1:n.31144+35_31144+49dup
NM_001267550.2:c.32095+35_32095+49dup MANE Select NP_001254479.2:n.32095+35_32095+49dup
NM_003319.4:c.13283-46701_13283-46687dup NP_003310.4:n.13283-46701_13283-46687dup
NM_133378.4:c.28363+35_28363+49dup NP_596869.4:n.28363+35_28363+49dup
NM_133432.3:c.13658-46701_13658-46687dup NP_597676.3:n.13658-46701_13658-46687dup
NM_133437.4:c.13859-46701_13859-46687dup NP_597681.4:n.13859-46701_13859-46687dup
XM_011511729.1:c.31192+35_31192+49dup XP_011510031.1:n.31192+35_31192+49dup
XM_011511730.1:c.13469-46701_13469-46687dup XP_011510032.1:n.13469-46701_13469-46687dup
XM_011511731.1:c.13328-46701_13328-46687dup XP_011510033.1:n.13328-46701_13328-46687dup
XM_017004819.1:c.31147+35_31147+49dup XP_016860308.1:n.31147+35_31147+49dup
XM_017004820.1:c.28366+35_28366+49dup XP_016860309.1:n.28366+35_28366+49dup
XM_017004821.1:c.28363+35_28363+49dup XP_016860310.1:n.28363+35_28363+49dup
XM_017004822.1:c.31147+35_31147+49dup XP_016860311.1:n.31147+35_31147+49dup
XM_017004823.1:c.13424-46701_13424-46687dup XP_016860312.1:n.13424-46701_13424-46687dup
XM_024453094.1:c.31147+35_31147+49dup XP_024308862.1:n.31147+35_31147+49dup
XM_024453095.1:c.31147+35_31147+49dup XP_024308863.1:n.31147+35_31147+49dup
XM_024453096.1:c.31147+35_31147+49dup XP_024308864.1:n.31147+35_31147+49dup
XM_024453097.1:c.30898+795_30898+809dup XP_024308865.1:n.30898+795_30898+809dup
XM_024453098.1:c.30898+795_30898+809dup XP_024308866.1:n.30898+795_30898+809dup
XM_024453099.1:c.13424-46701_13424-46687dup XP_024308867.1:n.13424-46701_13424-46687dup