Revel Score:
ENST00000237014 (MANE Select)
0.948
ENST00000432547
0.948
ENST00000541025
0.948
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.31595125C>G , CM000680.2:g.31595125C>G | GRCh38 |
| NC_000018.9:g.29175088C>G , CM000680.1:g.29175088C>G | GRCh37 |
| NC_000018.8:g.27429086C>G | NCBI36 |
| NG_009490.1:g.8359C>G , LRG_416:g.8359C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000237014.8:c.206C>G MANE Select | ENSP00000237014.4:p.Thr69Ser | |
| ENST00000610404.5:c.110C>G | ENSP00000477599.2:p.Thr37Ser | |
| ENST00000649620.1:c.206C>G | ENSP00000497927.1:p.Thr69Ser | |
| ENST00000237014.7:c.206C>G | ENSP00000237014.3:p.Thr69Ser | |
| ENST00000541025.2:n.232C>G | ||
| ENST00000610404.4:c.206C>G | ENSP00000477599.1:p.Thr69Ser | |
| ENST00000613781.1:c.206C>G | ENSP00000479174.1:p.Thr69Ser | |
| NM_000371.3:c.206C>G , LRG_416t1:c.206C>G | NP_000362.1:p.Thr69Ser | |
| NM_000371.4:c.206C>G MANE Select | NP_000362.1:p.Thr69Ser |