Revel Score:
ENST00000370629 (MANE Select)
0.849
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.136656377C>A , CM000685.2:g.136656377C>A | GRCh38 |
| NC_000023.10:g.135738536C>A , CM000685.1:g.135738536C>A | GRCh37 |
| NC_000023.9:g.135566202C>A | NCBI36 |
| NG_007280.1:g.13201C>A , LRG_141:g.13201C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000695724.1:c.310C>A | ENSP00000512122.1:p.Arg104= | |
| ENST00000695725.1:c.157-2662C>A | ENSP00000512123.1:n.157-2662C>A | |
| ENST00000695726.1:n.2336C>A | ||
| ENST00000695729.1:n.3171C>A | ||
| ENST00000370629.7:c.368C>A MANE Select | ENSP00000359663.2:p.Ala123Glu | |
| ENST00000370628.2:c.346+1947C>A | ENSP00000359662.2:n.346+1947C>A | |
| ENST00000370629.6:c.368C>A | ENSP00000359663.2:p.Ala123Glu | |
| NM_000074.2:c.368C>A , LRG_141t1:c.368C>A | NP_000065.1:p.Ala123Glu | |
| NM_000074.3:c.368C>A MANE Select | NP_000065.1:p.Ala123Glu |