Revel Score:
ENST00000335295 (MANE Select)
0.969
ENST00000380315
0.969
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.5226783G>C , CM000673.2:g.5226783G>C | GRCh38 |
| NC_000011.9:g.5248013G>C , CM000673.1:g.5248013G>C | GRCh37 |
| NC_000011.8:g.5204589G>C | NCBI36 |
| NG_000007.3:g.70833C>G | |
| NG_059281.1:g.5289C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647020.1:c.109C>G | ENSP00000494175.1:p.Pro37Ala | |
| ENST00000335295.4:c.109C>G MANE Select | ENSP00000333994.3:p.Pro37Ala | |
| ENST00000380315.2:c.109C>G | ENSP00000369671.2:p.Pro37Ala | |
| ENST00000475226.1:n.41C>G | ||
| ENST00000485743.1:n.160C>G | ||
| ENST00000633227.1:c.93C>G | ENSP00000488004.1:p.Thr31= | |
| NM_000518.4:c.109C>G | NP_000509.1:p.Pro37Ala | |
| NM_000518.5:c.109C>G MANE Select | NP_000509.1:p.Pro37Ala |