Revel Score:
ENST00000342992
0.115
ENST00000460472
0.115
ENST00000342175
0.115
ENST00000359218
0.115
ENST00000356127
0.115
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.178614544T>C , CM000664.2:g.178614544T>C | GRCh38 |
| NC_000002.11:g.179479271T>C , CM000664.1:g.179479271T>C | GRCh37 |
| NC_000002.10:g.179187516T>C | NCBI36 |
| NG_011618.3:g.221259A>G , LRG_391:g.221259A>G | |
| NG_051363.1:g.96718T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000342992.11:c.41266A>G (TTN) | ENSP00000343764.6:p.Ser13756Gly | |
| ENST00000342175.11:c.22351A>G (TTN) | ENSP00000340554.6:p.Ser7451Gly | |
| ENST00000359218.10:c.22150A>G (TTN) | ENSP00000352154.5:p.Ser7384Gly | |
| ENST00000342175.10:c.22351A>G (TTN) | ENSP00000340554.6:p.Ser7451Gly | |
| ENST00000342992.10:c.41266A>G (TTN) | ENSP00000343764.6:p.Ser13756Gly | |
| ENST00000359218.9:c.22150A>G (TTN) | ENSP00000352154.5:p.Ser7384Gly | |
| ENST00000460472.6:c.21775A>G (TTN) | ENSP00000434586.1:p.Ser7259Gly | |
| ENST00000589042.5:c.48970A>G (TTN) MANE Select | ENSP00000467141.1:p.Ser16324Gly | |
| ENST00000591111.5:c.44047A>G (TTN) | ENSP00000465570.1:p.Ser14683Gly | |
| ENST00000615779.4:c.44047A>G (TTN) | ENSP00000483597.1:p.Ser14683Gly | |
| NM_001256850.1:c.44047A>G (TTN) | NP_001243779.1:p.Ser14683Gly | |
| NM_001267550.2:c.48970A>G (TTN) MANE Select | NP_001254479.2:p.Ser16324Gly | |
| NM_003319.4:c.21775A>G (TTN) | NP_003310.4:p.Ser7259Gly | |
| NM_133378.4:c.41266A>G (TTN) | NP_596869.4:p.Ser13756Gly | |
| NM_133432.3:c.22150A>G (TTN) | NP_597676.3:p.Ser7384Gly | |
| NM_133437.4:c.22351A>G (TTN) | NP_597681.4:p.Ser7451Gly | |
| NR_038271.1:n.1292T>C (TTN-AS1) | ||
| XM_011511729.1:c.48067A>G (TTN) | XP_011510031.1:p.Ser16023Gly | |
| XM_011511730.1:c.21961A>G (TTN) | XP_011510032.1:p.Ser7321Gly | |
| XM_011511731.1:c.21820A>G (TTN) | XP_011510033.1:p.Ser7274Gly | |
| XM_017004819.1:c.47863A>G (TTN) | XP_016860308.1:p.Ser15955Gly | |
| XM_017004820.1:c.43261A>G (TTN) | XP_016860309.1:p.Ser14421Gly | |
| XM_017004821.1:c.43258A>G (TTN) | XP_016860310.1:p.Ser14420Gly | |
| XM_017004822.1:c.40300A>G (TTN) | XP_016860311.1:p.Ser13434Gly | |
| XM_017004823.1:c.21916A>G (TTN) | XP_016860312.1:p.Ser7306Gly | |
| XM_024453094.1:c.43411A>G (TTN) | XP_024308862.1:p.Ser14471Gly | |
| XM_024453095.1:c.43408A>G (TTN) | XP_024308863.1:p.Ser14470Gly | |
| XM_024453096.1:c.42841A>G (TTN) | XP_024308864.1:p.Ser14281Gly | |
| XM_024453097.1:c.40183A>G (TTN) | XP_024308865.1:p.Ser13395Gly | |
| XM_024453098.1:c.40102A>G (TTN) | XP_024308866.1:p.Ser13368Gly | |
| XM_024453099.1:c.21865A>G (TTN) | XP_024308867.1:p.Ser7289Gly | |
| XM_024453100.1:c.11719A>G (TTN) | XP_024308868.1:p.Ser3907Gly |