Revel Score:
ENST00000342992
0.444
ENST00000460472
0.444
ENST00000342175
0.444
ENST00000359218
0.444
ENST00000356127
0.444
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.178586613C>T , CM000664.2:g.178586613C>T | GRCh38 |
| NC_000002.11:g.179451340C>T , CM000664.1:g.179451340C>T | GRCh37 |
| NC_000002.10:g.179159586C>T | NCBI36 |
| NG_011618.3:g.249190G>A , LRG_391:g.249190G>A | |
| NG_051363.1:g.68787C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000342992.11:c.56584G>A (TTN) | ENSP00000343764.6:p.Gly18862Ser | |
| ENST00000342175.11:c.37669G>A (TTN) | ENSP00000340554.6:p.Gly12557Ser | |
| ENST00000359218.10:c.37468G>A (TTN) | ENSP00000352154.5:p.Gly12490Ser | |
| ENST00000342175.10:c.37669G>A (TTN) | ENSP00000340554.6:p.Gly12557Ser | |
| ENST00000342992.10:c.56584G>A (TTN) | ENSP00000343764.6:p.Gly18862Ser | |
| ENST00000359218.9:c.37468G>A (TTN) | ENSP00000352154.5:p.Gly12490Ser | |
| ENST00000460472.6:c.37093G>A (TTN) | ENSP00000434586.1:p.Gly12365Ser | |
| ENST00000589042.5:c.64288G>A (TTN) MANE Select | ENSP00000467141.1:p.Gly21430Ser | |
| ENST00000591111.5:c.59365G>A (TTN) | ENSP00000465570.1:p.Gly19789Ser | |
| ENST00000615779.4:c.59365G>A (TTN) | ENSP00000483597.1:p.Gly19789Ser | |
| NM_001256850.1:c.59365G>A (TTN) | NP_001243779.1:p.Gly19789Ser | |
| NM_001267550.2:c.64288G>A (TTN) MANE Select | NP_001254479.2:p.Gly21430Ser | |
| NM_003319.4:c.37093G>A (TTN) | NP_003310.4:p.Gly12365Ser | |
| NM_133378.4:c.56584G>A (TTN) | NP_596869.4:p.Gly18862Ser | |
| NM_133432.3:c.37468G>A (TTN) | NP_597676.3:p.Gly12490Ser | |
| NM_133437.4:c.37669G>A (TTN) | NP_597681.4:p.Gly12557Ser | |
| NR_038271.1:n.597-10983C>T (TTN-AS1) | ||
| NR_038272.1:n.3188+1620C>T (TTN-AS1) | ||
| XM_011511729.1:c.63385G>A (TTN) | XP_011510031.1:p.Gly21129Ser | |
| XM_011511730.1:c.37279G>A (TTN) | XP_011510032.1:p.Gly12427Ser | |
| XM_011511731.1:c.37138G>A (TTN) | XP_011510033.1:p.Gly12380Ser | |
| XM_017004819.1:c.63181G>A (TTN) | XP_016860308.1:p.Gly21061Ser | |
| XM_017004820.1:c.58579G>A (TTN) | XP_016860309.1:p.Gly19527Ser | |
| XM_017004821.1:c.58576G>A (TTN) | XP_016860310.1:p.Gly19526Ser | |
| XM_017004822.1:c.55618G>A (TTN) | XP_016860311.1:p.Gly18540Ser | |
| XM_017004823.1:c.37234G>A (TTN) | XP_016860312.1:p.Gly12412Ser | |
| XM_024453094.1:c.58729G>A (TTN) | XP_024308862.1:p.Gly19577Ser | |
| XM_024453095.1:c.58726G>A (TTN) | XP_024308863.1:p.Gly19576Ser | |
| XM_024453096.1:c.58159G>A (TTN) | XP_024308864.1:p.Gly19387Ser | |
| XM_024453097.1:c.55501G>A (TTN) | XP_024308865.1:p.Gly18501Ser | |
| XM_024453098.1:c.55420G>A (TTN) | XP_024308866.1:p.Gly18474Ser | |
| XM_024453099.1:c.37183G>A (TTN) | XP_024308867.1:p.Gly12395Ser | |
| XM_024453100.1:c.27037G>A (TTN) | XP_024308868.1:p.Gly9013Ser |