Revel Score:
ENST00000342992
0.782
ENST00000460472
0.782
ENST00000342175
0.782
ENST00000359218
0.782
ENST00000356127
0.782
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.178614657G>C , CM000664.2:g.178614657G>C | GRCh38 |
| NC_000002.11:g.179479384G>C , CM000664.1:g.179479384G>C | GRCh37 |
| NC_000002.10:g.179187629G>C | NCBI36 |
| NG_011618.3:g.221146C>G , LRG_391:g.221146C>G | |
| NG_051363.1:g.96831G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000342992.11:c.41153C>G (TTN) | ENSP00000343764.6:p.Pro13718Arg | |
| ENST00000342175.11:c.22238C>G (TTN) | ENSP00000340554.6:p.Pro7413Arg | |
| ENST00000359218.10:c.22037C>G (TTN) | ENSP00000352154.5:p.Pro7346Arg | |
| ENST00000342175.10:c.22238C>G (TTN) | ENSP00000340554.6:p.Pro7413Arg | |
| ENST00000342992.10:c.41153C>G (TTN) | ENSP00000343764.6:p.Pro13718Arg | |
| ENST00000359218.9:c.22037C>G (TTN) | ENSP00000352154.5:p.Pro7346Arg | |
| ENST00000460472.6:c.21662C>G (TTN) | ENSP00000434586.1:p.Pro7221Arg | |
| ENST00000589042.5:c.48857C>G (TTN) MANE Select | ENSP00000467141.1:p.Pro16286Arg | |
| ENST00000591111.5:c.43934C>G (TTN) | ENSP00000465570.1:p.Pro14645Arg | |
| ENST00000615779.4:c.43934C>G (TTN) | ENSP00000483597.1:p.Pro14645Arg | |
| NM_001256850.1:c.43934C>G (TTN) | NP_001243779.1:p.Pro14645Arg | |
| NM_001267550.2:c.48857C>G (TTN) MANE Select | NP_001254479.2:p.Pro16286Arg | |
| NM_003319.4:c.21662C>G (TTN) | NP_003310.4:p.Pro7221Arg | |
| NM_133378.4:c.41153C>G (TTN) | NP_596869.4:p.Pro13718Arg | |
| NM_133432.3:c.22037C>G (TTN) | NP_597676.3:p.Pro7346Arg | |
| NM_133437.4:c.22238C>G (TTN) | NP_597681.4:p.Pro7413Arg | |
| NR_038271.1:n.1405G>C (TTN-AS1) | ||
| XM_011511729.1:c.47954C>G (TTN) | XP_011510031.1:p.Pro15985Arg | |
| XM_011511730.1:c.21848C>G (TTN) | XP_011510032.1:p.Pro7283Arg | |
| XM_011511731.1:c.21707C>G (TTN) | XP_011510033.1:p.Pro7236Arg | |
| XM_017004819.1:c.47750C>G (TTN) | XP_016860308.1:p.Pro15917Arg | |
| XM_017004820.1:c.43148C>G (TTN) | XP_016860309.1:p.Pro14383Arg | |
| XM_017004821.1:c.43145C>G (TTN) | XP_016860310.1:p.Pro14382Arg | |
| XM_017004822.1:c.40187C>G (TTN) | XP_016860311.1:p.Pro13396Arg | |
| XM_017004823.1:c.21803C>G (TTN) | XP_016860312.1:p.Pro7268Arg | |
| XM_024453094.1:c.43298C>G (TTN) | XP_024308862.1:p.Pro14433Arg | |
| XM_024453095.1:c.43295C>G (TTN) | XP_024308863.1:p.Pro14432Arg | |
| XM_024453096.1:c.42728C>G (TTN) | XP_024308864.1:p.Pro14243Arg | |
| XM_024453097.1:c.40070C>G (TTN) | XP_024308865.1:p.Pro13357Arg | |
| XM_024453098.1:c.39989C>G (TTN) | XP_024308866.1:p.Pro13330Arg | |
| XM_024453099.1:c.21752C>G (TTN) | XP_024308867.1:p.Pro7251Arg | |
| XM_024453100.1:c.11606C>G (TTN) | XP_024308868.1:p.Pro3869Arg |