Canonical Allele Identifier: CA1310580126
Gene: TTN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178689202_178689203delinsGA , CM000664.2:g.178689202_178689203delinsGA GRCh38
NC_000002.11:g.179553929_179553930delinsGA , CM000664.1:g.179553929_179553930delinsGA GRCh37
NC_000002.10:g.179262174_179262175delinsGA NCBI36
NG_011618.3:g.146600_146601delinsTC , LRG_391:g.146600_146601delinsTC

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.28280-67_28280-66delinsTC ENSP00000343764.6:n.28280-67_28280-66deli...
ENST00000342175.11:c.13859-46886_13859-46885delinsTC ENSP00000340554.6:n.13859-46886_13859-468...
ENST00000359218.10:c.13658-46886_13658-46885delinsTC ENSP00000352154.5:n.13658-46886_13658-468...
ENST00000342175.10:c.13859-46886_13859-46885delinsTC ENSP00000340554.6:n.13859-46886_13859-468...
ENST00000342992.10:c.28280-67_28280-66delinsTC ENSP00000343764.6:n.28280-67_28280-66deli...
ENST00000359218.9:c.13658-46886_13658-46885delinsTC ENSP00000352154.5:n.13658-46886_13658-468...
ENST00000414766.5:c.1646-67_1646-66delinsTC ENSP00000401501.1:n.1646-67_1646-66delins...
ENST00000460472.6:c.13283-46886_13283-46885delinsTC ENSP00000434586.1:n.13283-46886_13283-468...
ENST00000589042.5:c.32012-67_32012-66delinsTC MANE Select ENSP00000467141.1:n.32012-67_32012-66deli...
ENST00000591111.5:c.31061-67_31061-66delinsTC ENSP00000465570.1:n.31061-67_31061-66deli...
ENST00000615779.4:c.31061-67_31061-66delinsTC ENSP00000483597.1:n.31061-67_31061-66deli...
NM_001256850.1:c.31061-67_31061-66delinsTC NP_001243779.1:n.31061-67_31061-66delinsT...
NM_001267550.2:c.32012-67_32012-66delinsTC MANE Select NP_001254479.2:n.32012-67_32012-66delinsT...
NM_003319.4:c.13283-46886_13283-46885delinsTC NP_003310.4:n.13283-46886_13283-46885deli...
NM_133378.4:c.28280-67_28280-66delinsTC NP_596869.4:n.28280-67_28280-66delinsTC
NM_133432.3:c.13658-46886_13658-46885delinsTC NP_597676.3:n.13658-46886_13658-46885deli...
NM_133437.4:c.13859-46886_13859-46885delinsTC NP_597681.4:n.13859-46886_13859-46885deli...
XM_011511729.1:c.31109-67_31109-66delinsTC XP_011510031.1:n.31109-67_31109-66delinsT...
XM_011511730.1:c.13469-46886_13469-46885delinsTC XP_011510032.1:n.13469-46886_13469-46885d...
XM_011511731.1:c.13328-46886_13328-46885delinsTC XP_011510033.1:n.13328-46886_13328-46885d...
XM_017004819.1:c.31064-67_31064-66delinsTC XP_016860308.1:n.31064-67_31064-66delinsT...
XM_017004820.1:c.28283-67_28283-66delinsTC XP_016860309.1:n.28283-67_28283-66delinsT...
XM_017004821.1:c.28280-67_28280-66delinsTC XP_016860310.1:n.28280-67_28280-66delinsT...
XM_017004822.1:c.31064-67_31064-66delinsTC XP_016860311.1:n.31064-67_31064-66delinsT...
XM_017004823.1:c.13424-46886_13424-46885delinsTC XP_016860312.1:n.13424-46886_13424-46885d...
XM_024453094.1:c.31064-67_31064-66delinsTC XP_024308862.1:n.31064-67_31064-66delinsT...
XM_024453095.1:c.31064-67_31064-66delinsTC XP_024308863.1:n.31064-67_31064-66delinsT...
XM_024453096.1:c.31064-67_31064-66delinsTC XP_024308864.1:n.31064-67_31064-66delinsT...
XM_024453097.1:c.30898+610_30898+611delinsTC XP_024308865.1:n.30898+610_30898+611delin...
XM_024453098.1:c.30898+610_30898+611delinsTC XP_024308866.1:n.30898+610_30898+611delin...
XM_024453099.1:c.13424-46886_13424-46885delinsTC XP_024308867.1:n.13424-46886_13424-46885d...