Revel Score:
ENST00000342992
0.432
ENST00000460472
0.432
ENST00000342175
0.432
ENST00000359218
0.432
ENST00000356127
0.432
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.178614551A>C , CM000664.2:g.178614551A>C | GRCh38 |
| NC_000002.11:g.179479278A>C , CM000664.1:g.179479278A>C | GRCh37 |
| NC_000002.10:g.179187523A>C | NCBI36 |
| NG_011618.3:g.221252T>G , LRG_391:g.221252T>G | |
| NG_051363.1:g.96725A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000342992.11:c.41259T>G (TTN) | ENSP00000343764.6:p.Ser13753Arg | |
| ENST00000342175.11:c.22344T>G (TTN) | ENSP00000340554.6:p.Ser7448Arg | |
| ENST00000359218.10:c.22143T>G (TTN) | ENSP00000352154.5:p.Ser7381Arg | |
| ENST00000342175.10:c.22344T>G (TTN) | ENSP00000340554.6:p.Ser7448Arg | |
| ENST00000342992.10:c.41259T>G (TTN) | ENSP00000343764.6:p.Ser13753Arg | |
| ENST00000359218.9:c.22143T>G (TTN) | ENSP00000352154.5:p.Ser7381Arg | |
| ENST00000460472.6:c.21768T>G (TTN) | ENSP00000434586.1:p.Ser7256Arg | |
| ENST00000589042.5:c.48963T>G (TTN) MANE Select | ENSP00000467141.1:p.Ser16321Arg | |
| ENST00000591111.5:c.44040T>G (TTN) | ENSP00000465570.1:p.Ser14680Arg | |
| ENST00000615779.4:c.44040T>G (TTN) | ENSP00000483597.1:p.Ser14680Arg | |
| NM_001256850.1:c.44040T>G (TTN) | NP_001243779.1:p.Ser14680Arg | |
| NM_001267550.2:c.48963T>G (TTN) MANE Select | NP_001254479.2:p.Ser16321Arg | |
| NM_003319.4:c.21768T>G (TTN) | NP_003310.4:p.Ser7256Arg | |
| NM_133378.4:c.41259T>G (TTN) | NP_596869.4:p.Ser13753Arg | |
| NM_133432.3:c.22143T>G (TTN) | NP_597676.3:p.Ser7381Arg | |
| NM_133437.4:c.22344T>G (TTN) | NP_597681.4:p.Ser7448Arg | |
| NR_038271.1:n.1299A>C (TTN-AS1) | ||
| XM_011511729.1:c.48060T>G (TTN) | XP_011510031.1:p.Ser16020Arg | |
| XM_011511730.1:c.21954T>G (TTN) | XP_011510032.1:p.Ser7318Arg | |
| XM_011511731.1:c.21813T>G (TTN) | XP_011510033.1:p.Ser7271Arg | |
| XM_017004819.1:c.47856T>G (TTN) | XP_016860308.1:p.Ser15952Arg | |
| XM_017004820.1:c.43254T>G (TTN) | XP_016860309.1:p.Ser14418Arg | |
| XM_017004821.1:c.43251T>G (TTN) | XP_016860310.1:p.Ser14417Arg | |
| XM_017004822.1:c.40293T>G (TTN) | XP_016860311.1:p.Ser13431Arg | |
| XM_017004823.1:c.21909T>G (TTN) | XP_016860312.1:p.Ser7303Arg | |
| XM_024453094.1:c.43404T>G (TTN) | XP_024308862.1:p.Ser14468Arg | |
| XM_024453095.1:c.43401T>G (TTN) | XP_024308863.1:p.Ser14467Arg | |
| XM_024453096.1:c.42834T>G (TTN) | XP_024308864.1:p.Ser14278Arg | |
| XM_024453097.1:c.40176T>G (TTN) | XP_024308865.1:p.Ser13392Arg | |
| XM_024453098.1:c.40095T>G (TTN) | XP_024308866.1:p.Ser13365Arg | |
| XM_024453099.1:c.21858T>G (TTN) | XP_024308867.1:p.Ser7286Arg | |
| XM_024453100.1:c.11712T>G (TTN) | XP_024308868.1:p.Ser3904Arg |