Revel Score:
ENST00000342992
0.486
ENST00000460472
0.486
ENST00000342175
0.486
ENST00000359218
0.486
ENST00000356127
0.486
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.178614560A>C , CM000664.2:g.178614560A>C | GRCh38 |
| NC_000002.11:g.179479287A>C , CM000664.1:g.179479287A>C | GRCh37 |
| NC_000002.10:g.179187532A>C | NCBI36 |
| NG_011618.3:g.221243T>G , LRG_391:g.221243T>G | |
| NG_051363.1:g.96734A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000342992.11:c.41250T>G (TTN) | ENSP00000343764.6:p.Ile13750Met | |
| ENST00000342175.11:c.22335T>G (TTN) | ENSP00000340554.6:p.Ile7445Met | |
| ENST00000359218.10:c.22134T>G (TTN) | ENSP00000352154.5:p.Ile7378Met | |
| ENST00000342175.10:c.22335T>G (TTN) | ENSP00000340554.6:p.Ile7445Met | |
| ENST00000342992.10:c.41250T>G (TTN) | ENSP00000343764.6:p.Ile13750Met | |
| ENST00000359218.9:c.22134T>G (TTN) | ENSP00000352154.5:p.Ile7378Met | |
| ENST00000460472.6:c.21759T>G (TTN) | ENSP00000434586.1:p.Ile7253Met | |
| ENST00000589042.5:c.48954T>G (TTN) MANE Select | ENSP00000467141.1:p.Ile16318Met | |
| ENST00000591111.5:c.44031T>G (TTN) | ENSP00000465570.1:p.Ile14677Met | |
| ENST00000615779.4:c.44031T>G (TTN) | ENSP00000483597.1:p.Ile14677Met | |
| NM_001256850.1:c.44031T>G (TTN) | NP_001243779.1:p.Ile14677Met | |
| NM_001267550.2:c.48954T>G (TTN) MANE Select | NP_001254479.2:p.Ile16318Met | |
| NM_003319.4:c.21759T>G (TTN) | NP_003310.4:p.Ile7253Met | |
| NM_133378.4:c.41250T>G (TTN) | NP_596869.4:p.Ile13750Met | |
| NM_133432.3:c.22134T>G (TTN) | NP_597676.3:p.Ile7378Met | |
| NM_133437.4:c.22335T>G (TTN) | NP_597681.4:p.Ile7445Met | |
| NR_038271.1:n.1308A>C (TTN-AS1) | ||
| XM_011511729.1:c.48051T>G (TTN) | XP_011510031.1:p.Ile16017Met | |
| XM_011511730.1:c.21945T>G (TTN) | XP_011510032.1:p.Ile7315Met | |
| XM_011511731.1:c.21804T>G (TTN) | XP_011510033.1:p.Ile7268Met | |
| XM_017004819.1:c.47847T>G (TTN) | XP_016860308.1:p.Ile15949Met | |
| XM_017004820.1:c.43245T>G (TTN) | XP_016860309.1:p.Ile14415Met | |
| XM_017004821.1:c.43242T>G (TTN) | XP_016860310.1:p.Ile14414Met | |
| XM_017004822.1:c.40284T>G (TTN) | XP_016860311.1:p.Ile13428Met | |
| XM_017004823.1:c.21900T>G (TTN) | XP_016860312.1:p.Ile7300Met | |
| XM_024453094.1:c.43395T>G (TTN) | XP_024308862.1:p.Ile14465Met | |
| XM_024453095.1:c.43392T>G (TTN) | XP_024308863.1:p.Ile14464Met | |
| XM_024453096.1:c.42825T>G (TTN) | XP_024308864.1:p.Ile14275Met | |
| XM_024453097.1:c.40167T>G (TTN) | XP_024308865.1:p.Ile13389Met | |
| XM_024453098.1:c.40086T>G (TTN) | XP_024308866.1:p.Ile13362Met | |
| XM_024453099.1:c.21849T>G (TTN) | XP_024308867.1:p.Ile7283Met | |
| XM_024453100.1:c.11703T>G (TTN) | XP_024308868.1:p.Ile3901Met |