Revel Score:
ENST00000342992
0.884
ENST00000460472
0.884
ENST00000342175
0.884
ENST00000359218
0.884
ENST00000356127
0.884
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.178614640A>G , CM000664.2:g.178614640A>G | GRCh38 |
| NC_000002.11:g.179479367A>G , CM000664.1:g.179479367A>G | GRCh37 |
| NC_000002.10:g.179187612A>G | NCBI36 |
| NG_011618.3:g.221163T>C , LRG_391:g.221163T>C | |
| NG_051363.1:g.96814A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000342992.11:c.41170T>C (TTN) | ENSP00000343764.6:p.Trp13724Arg | |
| ENST00000342175.11:c.22255T>C (TTN) | ENSP00000340554.6:p.Trp7419Arg | |
| ENST00000359218.10:c.22054T>C (TTN) | ENSP00000352154.5:p.Trp7352Arg | |
| ENST00000342175.10:c.22255T>C (TTN) | ENSP00000340554.6:p.Trp7419Arg | |
| ENST00000342992.10:c.41170T>C (TTN) | ENSP00000343764.6:p.Trp13724Arg | |
| ENST00000359218.9:c.22054T>C (TTN) | ENSP00000352154.5:p.Trp7352Arg | |
| ENST00000460472.6:c.21679T>C (TTN) | ENSP00000434586.1:p.Trp7227Arg | |
| ENST00000589042.5:c.48874T>C (TTN) MANE Select | ENSP00000467141.1:p.Trp16292Arg | |
| ENST00000591111.5:c.43951T>C (TTN) | ENSP00000465570.1:p.Trp14651Arg | |
| ENST00000615779.4:c.43951T>C (TTN) | ENSP00000483597.1:p.Trp14651Arg | |
| NM_001256850.1:c.43951T>C (TTN) | NP_001243779.1:p.Trp14651Arg | |
| NM_001267550.2:c.48874T>C (TTN) MANE Select | NP_001254479.2:p.Trp16292Arg | |
| NM_003319.4:c.21679T>C (TTN) | NP_003310.4:p.Trp7227Arg | |
| NM_133378.4:c.41170T>C (TTN) | NP_596869.4:p.Trp13724Arg | |
| NM_133432.3:c.22054T>C (TTN) | NP_597676.3:p.Trp7352Arg | |
| NM_133437.4:c.22255T>C (TTN) | NP_597681.4:p.Trp7419Arg | |
| NR_038271.1:n.1388A>G (TTN-AS1) | ||
| XM_011511729.1:c.47971T>C (TTN) | XP_011510031.1:p.Trp15991Arg | |
| XM_011511730.1:c.21865T>C (TTN) | XP_011510032.1:p.Trp7289Arg | |
| XM_011511731.1:c.21724T>C (TTN) | XP_011510033.1:p.Trp7242Arg | |
| XM_017004819.1:c.47767T>C (TTN) | XP_016860308.1:p.Trp15923Arg | |
| XM_017004820.1:c.43165T>C (TTN) | XP_016860309.1:p.Trp14389Arg | |
| XM_017004821.1:c.43162T>C (TTN) | XP_016860310.1:p.Trp14388Arg | |
| XM_017004822.1:c.40204T>C (TTN) | XP_016860311.1:p.Trp13402Arg | |
| XM_017004823.1:c.21820T>C (TTN) | XP_016860312.1:p.Trp7274Arg | |
| XM_024453094.1:c.43315T>C (TTN) | XP_024308862.1:p.Trp14439Arg | |
| XM_024453095.1:c.43312T>C (TTN) | XP_024308863.1:p.Trp14438Arg | |
| XM_024453096.1:c.42745T>C (TTN) | XP_024308864.1:p.Trp14249Arg | |
| XM_024453097.1:c.40087T>C (TTN) | XP_024308865.1:p.Trp13363Arg | |
| XM_024453098.1:c.40006T>C (TTN) | XP_024308866.1:p.Trp13336Arg | |
| XM_024453099.1:c.21769T>C (TTN) | XP_024308867.1:p.Trp7257Arg | |
| XM_024453100.1:c.11623T>C (TTN) | XP_024308868.1:p.Trp3875Arg |