Canonical Allele Identifier: CA645514477
Gene: TTN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178740592_178740593delinsTT , CM000664.2:g.178740592_178740593delinsTT GRCh38
NC_000002.11:g.179605319_179605320delinsTT , CM000664.1:g.179605319_179605320delinsTT GRCh37
NC_000002.10:g.179313564_179313565delinsTT NCBI36
NG_011618.3:g.95210_95211delinsAA , LRG_391:g.95210_95211delinsAA

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.10361-2233_10361-2232delinsAA ENSP00000343764.6:n.10361-2233_10361-2232...
ENST00000342175.11:c.12127_12128delinsAA ENSP00000340554.6:p.Pro4043Lys
ENST00000359218.10:c.11926_11927delinsAA ENSP00000352154.5:p.Pro3976Lys
ENST00000342175.10:c.12127_12128delinsAA ENSP00000340554.6:p.Pro4043Lys
ENST00000342992.10:c.10361-2233_10361-2232delinsAA ENSP00000343764.6:n.10361-2233_10361-2232...
ENST00000359218.9:c.11926_11927delinsAA ENSP00000352154.5:p.Pro3976Lys
ENST00000460472.6:c.11551_11552delinsAA ENSP00000434586.1:p.Pro3851Lys
ENST00000589042.5:c.12640_12641delinsAA MANE Select ENSP00000467141.1:p.Pro4214Lys
ENST00000591111.5:c.11689_11690delinsAA ENSP00000465570.1:p.Pro3897Lys
ENST00000615779.4:c.11689_11690delinsAA ENSP00000483597.1:p.Pro3897Lys
NM_001256850.1:c.11689_11690delinsAA NP_001243779.1:p.Pro3897Lys
NM_001267550.2:c.12640_12641delinsAA MANE Select NP_001254479.2:p.Pro4214Lys
NM_003319.4:c.11551_11552delinsAA NP_003310.4:p.Pro3851Lys
NM_133378.4:c.10361-2233_10361-2232delinsAA NP_596869.4:n.10361-2233_10361-2232delins...
NM_133432.3:c.11926_11927delinsAA NP_597676.3:p.Pro3976Lys
NM_133437.4:c.12127_12128delinsAA NP_597681.4:p.Pro4043Lys
XM_011511729.1:c.11737_11738delinsAA XP_011510031.1:p.Pro3913Lys
XM_011511730.1:c.11737_11738delinsAA XP_011510032.1:p.Pro3913Lys
XM_011511731.1:c.11596_11597delinsAA XP_011510033.1:p.Pro3866Lys
XM_017004819.1:c.11692_11693delinsAA XP_016860308.1:p.Pro3898Lys
XM_017004820.1:c.10364-2233_10364-2232delinsAA XP_016860309.1:n.10364-2233_10364-2232del...
XM_017004821.1:c.10361-2233_10361-2232delinsAA XP_016860310.1:n.10361-2233_10361-2232del...
XM_017004822.1:c.11692_11693delinsAA XP_016860311.1:p.Pro3898Lys
XM_017004823.1:c.11692_11693delinsAA XP_016860312.1:p.Pro3898Lys
XM_024453094.1:c.11692_11693delinsAA XP_024308862.1:p.Pro3898Lys
XM_024453095.1:c.11692_11693delinsAA XP_024308863.1:p.Pro3898Lys
XM_024453096.1:c.11692_11693delinsAA XP_024308864.1:p.Pro3898Lys
XM_024453097.1:c.11692_11693delinsAA XP_024308865.1:p.Pro3898Lys
XM_024453098.1:c.11692_11693delinsAA XP_024308866.1:p.Pro3898Lys
XM_024453099.1:c.11692_11693delinsAA XP_024308867.1:p.Pro3898Lys