Canonical Allele Identifier: CA1310580449
Gene: TTN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178689918_178689922delinsTGTTA , CM000664.2:g.178689918_178689922delinsTGTTA GRCh38
NC_000002.11:g.179554645_179554649delinsTGTTA , CM000664.1:g.179554645_179554649delinsTGTTA GRCh37
NC_000002.10:g.179262890_179262894delinsTGTTA NCBI36
NG_011618.3:g.145881_145885delinsTAACA , LRG_391:g.145881_145885delinsTAACA

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.28031-26_28031-22delinsTAACA ENSP00000343764.6:n.28031-26_28031-22deli...
ENST00000342175.11:c.13859-47605_13859-47601delinsTAACA ENSP00000340554.6:n.13859-47605_13859-476...
ENST00000359218.10:c.13658-47605_13658-47601delinsTAACA ENSP00000352154.5:n.13658-47605_13658-476...
ENST00000342175.10:c.13859-47605_13859-47601delinsTAACA ENSP00000340554.6:n.13859-47605_13859-476...
ENST00000342992.10:c.28031-26_28031-22delinsTAACA ENSP00000343764.6:n.28031-26_28031-22deli...
ENST00000359218.9:c.13658-47605_13658-47601delinsTAACA ENSP00000352154.5:n.13658-47605_13658-476...
ENST00000414766.5:c.1397-26_1397-22delinsTAACA ENSP00000401501.1:n.1397-26_1397-22delins...
ENST00000460472.6:c.13283-47605_13283-47601delinsTAACA ENSP00000434586.1:n.13283-47605_13283-476...
ENST00000589042.5:c.31763-26_31763-22delinsTAACA MANE Select ENSP00000467141.1:n.31763-26_31763-22deli...
ENST00000591111.5:c.30812-26_30812-22delinsTAACA ENSP00000465570.1:n.30812-26_30812-22deli...
ENST00000615779.4:c.30812-26_30812-22delinsTAACA ENSP00000483597.1:n.30812-26_30812-22deli...
NM_001256850.1:c.30812-26_30812-22delinsTAACA NP_001243779.1:n.30812-26_30812-22delinsT...
NM_001267550.2:c.31763-26_31763-22delinsTAACA MANE Select NP_001254479.2:n.31763-26_31763-22delinsT...
NM_003319.4:c.13283-47605_13283-47601delinsTAACA NP_003310.4:n.13283-47605_13283-47601deli...
NM_133378.4:c.28031-26_28031-22delinsTAACA NP_596869.4:n.28031-26_28031-22delinsTAAC...
NM_133432.3:c.13658-47605_13658-47601delinsTAACA NP_597676.3:n.13658-47605_13658-47601deli...
NM_133437.4:c.13859-47605_13859-47601delinsTAACA NP_597681.4:n.13859-47605_13859-47601deli...
XM_011511729.1:c.30860-26_30860-22delinsTAACA XP_011510031.1:n.30860-26_30860-22delinsT...
XM_011511730.1:c.13469-47605_13469-47601delinsTAACA XP_011510032.1:n.13469-47605_13469-47601d...
XM_011511731.1:c.13328-47605_13328-47601delinsTAACA XP_011510033.1:n.13328-47605_13328-47601d...
XM_017004819.1:c.30815-26_30815-22delinsTAACA XP_016860308.1:n.30815-26_30815-22delinsT...
XM_017004820.1:c.28034-26_28034-22delinsTAACA XP_016860309.1:n.28034-26_28034-22delinsT...
XM_017004821.1:c.28031-26_28031-22delinsTAACA XP_016860310.1:n.28031-26_28031-22delinsT...
XM_017004822.1:c.30815-26_30815-22delinsTAACA XP_016860311.1:n.30815-26_30815-22delinsT...
XM_017004823.1:c.13424-47605_13424-47601delinsTAACA XP_016860312.1:n.13424-47605_13424-47601d...
XM_024453094.1:c.30815-26_30815-22delinsTAACA XP_024308862.1:n.30815-26_30815-22delinsT...
XM_024453095.1:c.30815-26_30815-22delinsTAACA XP_024308863.1:n.30815-26_30815-22delinsT...
XM_024453096.1:c.30815-26_30815-22delinsTAACA XP_024308864.1:n.30815-26_30815-22delinsT...
XM_024453097.1:c.30815-26_30815-22delinsTAACA XP_024308865.1:n.30815-26_30815-22delinsT...
XM_024453098.1:c.30815-26_30815-22delinsTAACA XP_024308866.1:n.30815-26_30815-22delinsT...
XM_024453099.1:c.13424-47605_13424-47601delinsTAACA XP_024308867.1:n.13424-47605_13424-47601d...