Revel Score:
ENST00000342992
0.283
ENST00000460472
0.283
ENST00000342175
0.283
ENST00000359218
0.283
ENST00000356127
0.283
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.178614555T>A , CM000664.2:g.178614555T>A | GRCh38 |
| NC_000002.11:g.179479282T>A , CM000664.1:g.179479282T>A | GRCh37 |
| NC_000002.10:g.179187527T>A | NCBI36 |
| NG_011618.3:g.221248A>T , LRG_391:g.221248A>T | |
| NG_051363.1:g.96729T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000342992.11:c.41255A>T (TTN) | ENSP00000343764.6:p.Asp13752Val | |
| ENST00000342175.11:c.22340A>T (TTN) | ENSP00000340554.6:p.Asp7447Val | |
| ENST00000359218.10:c.22139A>T (TTN) | ENSP00000352154.5:p.Asp7380Val | |
| ENST00000342175.10:c.22340A>T (TTN) | ENSP00000340554.6:p.Asp7447Val | |
| ENST00000342992.10:c.41255A>T (TTN) | ENSP00000343764.6:p.Asp13752Val | |
| ENST00000359218.9:c.22139A>T (TTN) | ENSP00000352154.5:p.Asp7380Val | |
| ENST00000460472.6:c.21764A>T (TTN) | ENSP00000434586.1:p.Asp7255Val | |
| ENST00000589042.5:c.48959A>T (TTN) MANE Select | ENSP00000467141.1:p.Asp16320Val | |
| ENST00000591111.5:c.44036A>T (TTN) | ENSP00000465570.1:p.Asp14679Val | |
| ENST00000615779.4:c.44036A>T (TTN) | ENSP00000483597.1:p.Asp14679Val | |
| NM_001256850.1:c.44036A>T (TTN) | NP_001243779.1:p.Asp14679Val | |
| NM_001267550.2:c.48959A>T (TTN) MANE Select | NP_001254479.2:p.Asp16320Val | |
| NM_003319.4:c.21764A>T (TTN) | NP_003310.4:p.Asp7255Val | |
| NM_133378.4:c.41255A>T (TTN) | NP_596869.4:p.Asp13752Val | |
| NM_133432.3:c.22139A>T (TTN) | NP_597676.3:p.Asp7380Val | |
| NM_133437.4:c.22340A>T (TTN) | NP_597681.4:p.Asp7447Val | |
| NR_038271.1:n.1303T>A (TTN-AS1) | ||
| XM_011511729.1:c.48056A>T (TTN) | XP_011510031.1:p.Asp16019Val | |
| XM_011511730.1:c.21950A>T (TTN) | XP_011510032.1:p.Asp7317Val | |
| XM_011511731.1:c.21809A>T (TTN) | XP_011510033.1:p.Asp7270Val | |
| XM_017004819.1:c.47852A>T (TTN) | XP_016860308.1:p.Asp15951Val | |
| XM_017004820.1:c.43250A>T (TTN) | XP_016860309.1:p.Asp14417Val | |
| XM_017004821.1:c.43247A>T (TTN) | XP_016860310.1:p.Asp14416Val | |
| XM_017004822.1:c.40289A>T (TTN) | XP_016860311.1:p.Asp13430Val | |
| XM_017004823.1:c.21905A>T (TTN) | XP_016860312.1:p.Asp7302Val | |
| XM_024453094.1:c.43400A>T (TTN) | XP_024308862.1:p.Asp14467Val | |
| XM_024453095.1:c.43397A>T (TTN) | XP_024308863.1:p.Asp14466Val | |
| XM_024453096.1:c.42830A>T (TTN) | XP_024308864.1:p.Asp14277Val | |
| XM_024453097.1:c.40172A>T (TTN) | XP_024308865.1:p.Asp13391Val | |
| XM_024453098.1:c.40091A>T (TTN) | XP_024308866.1:p.Asp13364Val | |
| XM_024453099.1:c.21854A>T (TTN) | XP_024308867.1:p.Asp7285Val | |
| XM_024453100.1:c.11708A>T (TTN) | XP_024308868.1:p.Asp3903Val |