Revel Score:
ENST00000342992
0.278
ENST00000460472
0.278
ENST00000342175
0.278
ENST00000359218
0.278
ENST00000356127
0.278
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.178614537G>A , CM000664.2:g.178614537G>A | GRCh38 |
| NC_000002.11:g.179479264G>A , CM000664.1:g.179479264G>A | GRCh37 |
| NC_000002.10:g.179187509G>A | NCBI36 |
| NG_011618.3:g.221266C>T , LRG_391:g.221266C>T | |
| NG_051363.1:g.96711G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000342992.11:c.41273C>T (TTN) | ENSP00000343764.6:p.Thr13758Ile | |
| ENST00000342175.11:c.22358C>T (TTN) | ENSP00000340554.6:p.Thr7453Ile | |
| ENST00000359218.10:c.22157C>T (TTN) | ENSP00000352154.5:p.Thr7386Ile | |
| ENST00000342175.10:c.22358C>T (TTN) | ENSP00000340554.6:p.Thr7453Ile | |
| ENST00000342992.10:c.41273C>T (TTN) | ENSP00000343764.6:p.Thr13758Ile | |
| ENST00000359218.9:c.22157C>T (TTN) | ENSP00000352154.5:p.Thr7386Ile | |
| ENST00000460472.6:c.21782C>T (TTN) | ENSP00000434586.1:p.Thr7261Ile | |
| ENST00000589042.5:c.48977C>T (TTN) MANE Select | ENSP00000467141.1:p.Thr16326Ile | |
| ENST00000591111.5:c.44054C>T (TTN) | ENSP00000465570.1:p.Thr14685Ile | |
| ENST00000615779.4:c.44054C>T (TTN) | ENSP00000483597.1:p.Thr14685Ile | |
| NM_001256850.1:c.44054C>T (TTN) | NP_001243779.1:p.Thr14685Ile | |
| NM_001267550.2:c.48977C>T (TTN) MANE Select | NP_001254479.2:p.Thr16326Ile | |
| NM_003319.4:c.21782C>T (TTN) | NP_003310.4:p.Thr7261Ile | |
| NM_133378.4:c.41273C>T (TTN) | NP_596869.4:p.Thr13758Ile | |
| NM_133432.3:c.22157C>T (TTN) | NP_597676.3:p.Thr7386Ile | |
| NM_133437.4:c.22358C>T (TTN) | NP_597681.4:p.Thr7453Ile | |
| NR_038271.1:n.1285G>A (TTN-AS1) | ||
| XM_011511729.1:c.48074C>T (TTN) | XP_011510031.1:p.Thr16025Ile | |
| XM_011511730.1:c.21968C>T (TTN) | XP_011510032.1:p.Thr7323Ile | |
| XM_011511731.1:c.21827C>T (TTN) | XP_011510033.1:p.Thr7276Ile | |
| XM_017004819.1:c.47870C>T (TTN) | XP_016860308.1:p.Thr15957Ile | |
| XM_017004820.1:c.43268C>T (TTN) | XP_016860309.1:p.Thr14423Ile | |
| XM_017004821.1:c.43265C>T (TTN) | XP_016860310.1:p.Thr14422Ile | |
| XM_017004822.1:c.40307C>T (TTN) | XP_016860311.1:p.Thr13436Ile | |
| XM_017004823.1:c.21923C>T (TTN) | XP_016860312.1:p.Thr7308Ile | |
| XM_024453094.1:c.43418C>T (TTN) | XP_024308862.1:p.Thr14473Ile | |
| XM_024453095.1:c.43415C>T (TTN) | XP_024308863.1:p.Thr14472Ile | |
| XM_024453096.1:c.42848C>T (TTN) | XP_024308864.1:p.Thr14283Ile | |
| XM_024453097.1:c.40190C>T (TTN) | XP_024308865.1:p.Thr13397Ile | |
| XM_024453098.1:c.40109C>T (TTN) | XP_024308866.1:p.Thr13370Ile | |
| XM_024453099.1:c.21872C>T (TTN) | XP_024308867.1:p.Thr7291Ile | |
| XM_024453100.1:c.11726C>T (TTN) | XP_024308868.1:p.Thr3909Ile |