Revel Score:
ENST00000342992
0.518
ENST00000460472
0.518
ENST00000342175
0.518
ENST00000359218
0.518
ENST00000356127
0.518
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.178607487G>C , CM000664.2:g.178607487G>C | GRCh38 |
| NC_000002.11:g.179472214G>C , CM000664.1:g.179472214G>C | GRCh37 |
| NC_000002.10:g.179180459G>C | NCBI36 |
| NG_011618.3:g.228316C>G , LRG_391:g.228316C>G | |
| NG_051363.1:g.89661G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000342992.11:c.45497C>G (TTN) | ENSP00000343764.6:p.Ala15166Gly | |
| ENST00000342175.11:c.26582C>G (TTN) | ENSP00000340554.6:p.Ala8861Gly | |
| ENST00000359218.10:c.26381C>G (TTN) | ENSP00000352154.5:p.Ala8794Gly | |
| ENST00000342175.10:c.26582C>G (TTN) | ENSP00000340554.6:p.Ala8861Gly | |
| ENST00000342992.10:c.45497C>G (TTN) | ENSP00000343764.6:p.Ala15166Gly | |
| ENST00000359218.9:c.26381C>G (TTN) | ENSP00000352154.5:p.Ala8794Gly | |
| ENST00000460472.6:c.26006C>G (TTN) | ENSP00000434586.1:p.Ala8669Gly | |
| ENST00000589042.5:c.53201C>G (TTN) MANE Select | ENSP00000467141.1:p.Ala17734Gly | |
| ENST00000591111.5:c.48278C>G (TTN) | ENSP00000465570.1:p.Ala16093Gly | |
| ENST00000615779.4:c.48278C>G (TTN) | ENSP00000483597.1:p.Ala16093Gly | |
| NM_001256850.1:c.48278C>G (TTN) | NP_001243779.1:p.Ala16093Gly | |
| NM_001267550.2:c.53201C>G (TTN) MANE Select | NP_001254479.2:p.Ala17734Gly | |
| NM_003319.4:c.26006C>G (TTN) | NP_003310.4:p.Ala8669Gly | |
| NM_133378.4:c.45497C>G (TTN) | NP_596869.4:p.Ala15166Gly | |
| NM_133432.3:c.26381C>G (TTN) | NP_597676.3:p.Ala8794Gly | |
| NM_133437.4:c.26582C>G (TTN) | NP_597681.4:p.Ala8861Gly | |
| NR_038271.1:n.683-680G>C (TTN-AS1) | ||
| XM_011511729.1:c.52298C>G (TTN) | XP_011510031.1:p.Ala17433Gly | |
| XM_011511730.1:c.26192C>G (TTN) | XP_011510032.1:p.Ala8731Gly | |
| XM_011511731.1:c.26051C>G (TTN) | XP_011510033.1:p.Ala8684Gly | |
| XM_017004819.1:c.52094C>G (TTN) | XP_016860308.1:p.Ala17365Gly | |
| XM_017004820.1:c.47492C>G (TTN) | XP_016860309.1:p.Ala15831Gly | |
| XM_017004821.1:c.47489C>G (TTN) | XP_016860310.1:p.Ala15830Gly | |
| XM_017004822.1:c.44531C>G (TTN) | XP_016860311.1:p.Ala14844Gly | |
| XM_017004823.1:c.26147C>G (TTN) | XP_016860312.1:p.Ala8716Gly | |
| XM_024453094.1:c.47642C>G (TTN) | XP_024308862.1:p.Ala15881Gly | |
| XM_024453095.1:c.47639C>G (TTN) | XP_024308863.1:p.Ala15880Gly | |
| XM_024453096.1:c.47072C>G (TTN) | XP_024308864.1:p.Ala15691Gly | |
| XM_024453097.1:c.44414C>G (TTN) | XP_024308865.1:p.Ala14805Gly | |
| XM_024453098.1:c.44333C>G (TTN) | XP_024308866.1:p.Ala14778Gly | |
| XM_024453099.1:c.26096C>G (TTN) | XP_024308867.1:p.Ala8699Gly | |
| XM_024453100.1:c.15950C>G (TTN) | XP_024308868.1:p.Ala5317Gly |