Revel Score:
ENST00000342992
0.692
ENST00000460472
0.692
ENST00000342175
0.692
ENST00000359218
0.692
ENST00000356127
0.692
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.178614652G>C , CM000664.2:g.178614652G>C | GRCh38 |
| NC_000002.11:g.179479379G>C , CM000664.1:g.179479379G>C | GRCh37 |
| NC_000002.10:g.179187624G>C | NCBI36 |
| NG_011618.3:g.221151C>G , LRG_391:g.221151C>G | |
| NG_051363.1:g.96826G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000342992.11:c.41158C>G (TTN) | ENSP00000343764.6:p.Pro13720Ala | |
| ENST00000342175.11:c.22243C>G (TTN) | ENSP00000340554.6:p.Pro7415Ala | |
| ENST00000359218.10:c.22042C>G (TTN) | ENSP00000352154.5:p.Pro7348Ala | |
| ENST00000342175.10:c.22243C>G (TTN) | ENSP00000340554.6:p.Pro7415Ala | |
| ENST00000342992.10:c.41158C>G (TTN) | ENSP00000343764.6:p.Pro13720Ala | |
| ENST00000359218.9:c.22042C>G (TTN) | ENSP00000352154.5:p.Pro7348Ala | |
| ENST00000460472.6:c.21667C>G (TTN) | ENSP00000434586.1:p.Pro7223Ala | |
| ENST00000589042.5:c.48862C>G (TTN) MANE Select | ENSP00000467141.1:p.Pro16288Ala | |
| ENST00000591111.5:c.43939C>G (TTN) | ENSP00000465570.1:p.Pro14647Ala | |
| ENST00000615779.4:c.43939C>G (TTN) | ENSP00000483597.1:p.Pro14647Ala | |
| NM_001256850.1:c.43939C>G (TTN) | NP_001243779.1:p.Pro14647Ala | |
| NM_001267550.2:c.48862C>G (TTN) MANE Select | NP_001254479.2:p.Pro16288Ala | |
| NM_003319.4:c.21667C>G (TTN) | NP_003310.4:p.Pro7223Ala | |
| NM_133378.4:c.41158C>G (TTN) | NP_596869.4:p.Pro13720Ala | |
| NM_133432.3:c.22042C>G (TTN) | NP_597676.3:p.Pro7348Ala | |
| NM_133437.4:c.22243C>G (TTN) | NP_597681.4:p.Pro7415Ala | |
| NR_038271.1:n.1400G>C (TTN-AS1) | ||
| XM_011511729.1:c.47959C>G (TTN) | XP_011510031.1:p.Pro15987Ala | |
| XM_011511730.1:c.21853C>G (TTN) | XP_011510032.1:p.Pro7285Ala | |
| XM_011511731.1:c.21712C>G (TTN) | XP_011510033.1:p.Pro7238Ala | |
| XM_017004819.1:c.47755C>G (TTN) | XP_016860308.1:p.Pro15919Ala | |
| XM_017004820.1:c.43153C>G (TTN) | XP_016860309.1:p.Pro14385Ala | |
| XM_017004821.1:c.43150C>G (TTN) | XP_016860310.1:p.Pro14384Ala | |
| XM_017004822.1:c.40192C>G (TTN) | XP_016860311.1:p.Pro13398Ala | |
| XM_017004823.1:c.21808C>G (TTN) | XP_016860312.1:p.Pro7270Ala | |
| XM_024453094.1:c.43303C>G (TTN) | XP_024308862.1:p.Pro14435Ala | |
| XM_024453095.1:c.43300C>G (TTN) | XP_024308863.1:p.Pro14434Ala | |
| XM_024453096.1:c.42733C>G (TTN) | XP_024308864.1:p.Pro14245Ala | |
| XM_024453097.1:c.40075C>G (TTN) | XP_024308865.1:p.Pro13359Ala | |
| XM_024453098.1:c.39994C>G (TTN) | XP_024308866.1:p.Pro13332Ala | |
| XM_024453099.1:c.21757C>G (TTN) | XP_024308867.1:p.Pro7253Ala | |
| XM_024453100.1:c.11611C>G (TTN) | XP_024308868.1:p.Pro3871Ala |