Linked Data
ClinVar Variation Id:
497061
dbSNP Id:
rs796651993
gnomAD v2:
2-179468593-G-A
gnomAD v3:
2-178603866-G-A
gnomAD v4:
2-178603866-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.178603866G>A , CM000664.2:g.178603866G>A | GRCh38 |
| NC_000002.11:g.179468593G>A , CM000664.1:g.179468593G>A | GRCh37 |
| NC_000002.10:g.179176838G>A | NCBI36 |
| NG_011618.3:g.231937C>T , LRG_391:g.231937C>T | |
| NG_051363.1:g.86040G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000342992.11:c.47107+10C>T (TTN) | ENSP00000343764.6:n.47107+10C>T | |
| ENST00000342175.11:c.28192+10C>T (TTN) | ENSP00000340554.6:n.28192+10C>T | |
| ENST00000359218.10:c.27991+10C>T (TTN) | ENSP00000352154.5:n.27991+10C>T | |
| ENST00000342175.10:c.28192+10C>T (TTN) | ENSP00000340554.6:n.28192+10C>T | |
| ENST00000342992.10:c.47107+10C>T (TTN) | ENSP00000343764.6:n.47107+10C>T | |
| ENST00000359218.9:c.27991+10C>T (TTN) | ENSP00000352154.5:n.27991+10C>T | |
| ENST00000460472.6:c.27616+10C>T (TTN) | ENSP00000434586.1:n.27616+10C>T | |
| ENST00000589042.5:c.54811+10C>T (TTN) MANE Select | ENSP00000467141.1:n.54811+10C>T | |
| ENST00000591111.5:c.49888+10C>T (TTN) | ENSP00000465570.1:n.49888+10C>T | |
| ENST00000615779.4:c.49888+10C>T (TTN) | ENSP00000483597.1:n.49888+10C>T | |
| NM_001256850.1:c.49888+10C>T (TTN) | NP_001243779.1:n.49888+10C>T | |
| NM_001267550.2:c.54811+10C>T (TTN) MANE Select | NP_001254479.2:n.54811+10C>T | |
| NM_003319.4:c.27616+10C>T (TTN) | NP_003310.4:n.27616+10C>T | |
| NM_133378.4:c.47107+10C>T (TTN) | NP_596869.4:n.47107+10C>T | |
| NM_133432.3:c.27991+10C>T (TTN) | NP_597676.3:n.27991+10C>T | |
| NM_133437.4:c.28192+10C>T (TTN) | NP_597681.4:n.28192+10C>T | |
| NR_038271.1:n.683-4301G>A (TTN-AS1) | ||
| NR_038272.1:n.3918-865G>A (TTN-AS1) | ||
| XM_011511729.1:c.53908+10C>T (TTN) | XP_011510031.1:n.53908+10C>T | |
| XM_011511730.1:c.27802+10C>T (TTN) | XP_011510032.1:n.27802+10C>T | |
| XM_011511731.1:c.27661+10C>T (TTN) | XP_011510033.1:n.27661+10C>T | |
| XM_017004819.1:c.53704+10C>T (TTN) | XP_016860308.1:n.53704+10C>T | |
| XM_017004820.1:c.49102+10C>T (TTN) | XP_016860309.1:n.49102+10C>T | |
| XM_017004821.1:c.49099+10C>T (TTN) | XP_016860310.1:n.49099+10C>T | |
| XM_017004822.1:c.46141+10C>T (TTN) | XP_016860311.1:n.46141+10C>T | |
| XM_017004823.1:c.27757+10C>T (TTN) | XP_016860312.1:n.27757+10C>T | |
| XM_024453094.1:c.49252+10C>T (TTN) | XP_024308862.1:n.49252+10C>T | |
| XM_024453095.1:c.49249+10C>T (TTN) | XP_024308863.1:n.49249+10C>T | |
| XM_024453096.1:c.48682+10C>T (TTN) | XP_024308864.1:n.48682+10C>T | |
| XM_024453097.1:c.46024+10C>T (TTN) | XP_024308865.1:n.46024+10C>T | |
| XM_024453098.1:c.45943+10C>T (TTN) | XP_024308866.1:n.45943+10C>T | |
| XM_024453099.1:c.27706+10C>T (TTN) | XP_024308867.1:n.27706+10C>T | |
| XM_024453100.1:c.17560+10C>T (TTN) | XP_024308868.1:n.17560+10C>T |