Revel Score:
ENST00000342992
0.835
ENST00000460472
0.835
ENST00000342175
0.835
ENST00000359218
0.835
ENST00000356127
0.835
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.178614663C>A , CM000664.2:g.178614663C>A | GRCh38 |
| NC_000002.11:g.179479390C>A , CM000664.1:g.179479390C>A | GRCh37 |
| NC_000002.10:g.179187635C>A | NCBI36 |
| NG_011618.3:g.221140G>T , LRG_391:g.221140G>T | |
| NG_051363.1:g.96837C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000342992.11:c.41147G>T (TTN) | ENSP00000343764.6:p.Gly13716Val | |
| ENST00000342175.11:c.22232G>T (TTN) | ENSP00000340554.6:p.Gly7411Val | |
| ENST00000359218.10:c.22031G>T (TTN) | ENSP00000352154.5:p.Gly7344Val | |
| ENST00000342175.10:c.22232G>T (TTN) | ENSP00000340554.6:p.Gly7411Val | |
| ENST00000342992.10:c.41147G>T (TTN) | ENSP00000343764.6:p.Gly13716Val | |
| ENST00000359218.9:c.22031G>T (TTN) | ENSP00000352154.5:p.Gly7344Val | |
| ENST00000460472.6:c.21656G>T (TTN) | ENSP00000434586.1:p.Gly7219Val | |
| ENST00000589042.5:c.48851G>T (TTN) MANE Select | ENSP00000467141.1:p.Gly16284Val | |
| ENST00000591111.5:c.43928G>T (TTN) | ENSP00000465570.1:p.Gly14643Val | |
| ENST00000615779.4:c.43928G>T (TTN) | ENSP00000483597.1:p.Gly14643Val | |
| NM_001256850.1:c.43928G>T (TTN) | NP_001243779.1:p.Gly14643Val | |
| NM_001267550.2:c.48851G>T (TTN) MANE Select | NP_001254479.2:p.Gly16284Val | |
| NM_003319.4:c.21656G>T (TTN) | NP_003310.4:p.Gly7219Val | |
| NM_133378.4:c.41147G>T (TTN) | NP_596869.4:p.Gly13716Val | |
| NM_133432.3:c.22031G>T (TTN) | NP_597676.3:p.Gly7344Val | |
| NM_133437.4:c.22232G>T (TTN) | NP_597681.4:p.Gly7411Val | |
| NR_038271.1:n.1411C>A (TTN-AS1) | ||
| XM_011511729.1:c.47948G>T (TTN) | XP_011510031.1:p.Gly15983Val | |
| XM_011511730.1:c.21842G>T (TTN) | XP_011510032.1:p.Gly7281Val | |
| XM_011511731.1:c.21701G>T (TTN) | XP_011510033.1:p.Gly7234Val | |
| XM_017004819.1:c.47744G>T (TTN) | XP_016860308.1:p.Gly15915Val | |
| XM_017004820.1:c.43142G>T (TTN) | XP_016860309.1:p.Gly14381Val | |
| XM_017004821.1:c.43139G>T (TTN) | XP_016860310.1:p.Gly14380Val | |
| XM_017004822.1:c.40181G>T (TTN) | XP_016860311.1:p.Gly13394Val | |
| XM_017004823.1:c.21797G>T (TTN) | XP_016860312.1:p.Gly7266Val | |
| XM_024453094.1:c.43292G>T (TTN) | XP_024308862.1:p.Gly14431Val | |
| XM_024453095.1:c.43289G>T (TTN) | XP_024308863.1:p.Gly14430Val | |
| XM_024453096.1:c.42722G>T (TTN) | XP_024308864.1:p.Gly14241Val | |
| XM_024453097.1:c.40064G>T (TTN) | XP_024308865.1:p.Gly13355Val | |
| XM_024453098.1:c.39983G>T (TTN) | XP_024308866.1:p.Gly13328Val | |
| XM_024453099.1:c.21746G>T (TTN) | XP_024308867.1:p.Gly7249Val | |
| XM_024453100.1:c.11600G>T (TTN) | XP_024308868.1:p.Gly3867Val |