Revel Score:
ENST00000335295 (MANE Select)
0.972
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.5226614T>C , CM000673.2:g.5226614T>C | GRCh38 |
| NC_000011.9:g.5247844T>C , CM000673.1:g.5247844T>C | GRCh37 |
| NC_000011.8:g.5204420T>C | NCBI36 |
| NG_000007.3:g.71002A>G | |
| NG_059281.1:g.5458A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647020.1:c.278A>G | ENSP00000494175.1:p.His93Arg | |
| ENST00000335295.4:c.278A>G MANE Select | ENSP00000333994.3:p.His93Arg | |
| ENST00000475226.1:n.210A>G | ||
| ENST00000485743.1:n.329A>G | ||
| ENST00000633227.1:c.*94A>G | ENSP00000488004.1:n.*94A>G | |
| NM_000518.4:c.278A>G | NP_000509.1:p.His93Arg | |
| NM_000518.5:c.278A>G MANE Select | NP_000509.1:p.His93Arg |