Revel Score:
ENST00000370629 (MANE Select)
0.706
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.136656393T>G , CM000685.2:g.136656393T>G | GRCh38 |
| NC_000023.10:g.135738552T>G , CM000685.1:g.135738552T>G | GRCh37 |
| NC_000023.9:g.135566218T>G | NCBI36 |
| NG_007280.1:g.13217T>G , LRG_141:g.13217T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000695724.1:c.*2T>G | ENSP00000512122.1:n.*2T>G | |
| ENST00000695725.1:c.157-2646T>G | ENSP00000512123.1:n.157-2646T>G | |
| ENST00000695726.1:n.2352T>G | ||
| ENST00000695729.1:n.3187T>G | ||
| ENST00000370629.7:c.384T>G MANE Select | ENSP00000359663.2:p.Ser128Arg | |
| ENST00000370628.2:c.346+1963T>G | ENSP00000359662.2:n.346+1963T>G | |
| ENST00000370629.6:c.384T>G | ENSP00000359663.2:p.Ser128Arg | |
| NM_000074.2:c.384T>G , LRG_141t1:c.384T>G | NP_000065.1:p.Ser128Arg | |
| NM_000074.3:c.384T>G MANE Select | NP_000065.1:p.Ser128Arg |