Revel Score:
ENST00000280362 (MANE Select)
0.539
gnomAD v2:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.112230210G>C , CM000673.2:g.112230210G>C | GRCh38 |
| NC_000011.9:g.112100933G>C , CM000673.1:g.112100933G>C | GRCh37 |
| NC_000011.8:g.111606143G>C | NCBI36 |
| NG_008743.1:g.8846G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000280362.8:c.166G>C MANE Select | ENSP00000280362.3:p.Val56Leu | |
| ENST00000280362.7:c.166G>C | ENSP00000280362.3:p.Val56Leu | |
| ENST00000524931.1:c.-39G>C | ENSP00000434688.1:n.-39G>C | |
| ENST00000525803.1:c.163+1537G>C | ENSP00000431750.1:n.163+1537G>C | |
| ENST00000528679.5:c.164-416G>C | ENSP00000435895.1:n.164-416G>C | |
| ENST00000531175.1:n.117G>C | ||
| ENST00000531673.5:c.164-416G>C | ENSP00000433469.1:n.164-416G>C | |
| NM_000317.2:c.166G>C | NP_000308.1:p.Val56Leu | |
| XM_011542943.1:c.127G>C | XP_011541245.1:p.Val43Leu | |
| NM_000317.3:c.166G>C MANE Select | NP_000308.1:p.Val56Leu |