Revel Score:
ENST00000378823 (MANE Select)
0.651
ENST00000265335
0.651
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.132642210T>C , CM000667.2:g.132642210T>C | GRCh38 |
| NC_000005.9:g.131977902T>C , CM000667.1:g.131977902T>C | GRCh37 |
| NC_000005.8:g.132005801T>C | NCBI36 |
| NG_021151.1:g.90287T>C | |
| NG_021151.2:g.90234T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378823.8:c.3785T>C (RAD50) MANE Select | ENSP00000368100.4:p.Phe1262Ser | |
| ENST00000638452.2:c.3488T>C | ENSP00000492349.2:p.Phe1163Ser | |
| ENST00000638504.1:n.3393T>C | ||
| ENST00000638568.2:c.3488T>C | ENSP00000491158.2:p.Phe1163Ser | |
| ENST00000639899.1:n.4304T>C | ||
| ENST00000640655.2:c.3488T>C | ENSP00000491596.2:p.Phe1163Ser | |
| ENST00000651249.1:c.621T>C (RAD50) | ||
| ENST00000378823.7:c.3785T>C (RAD50) | ENSP00000368100.4:p.Phe1262Ser | |
| ENST00000455677.1:c.388-795T>C (RAD50) | ||
| ENST00000533482.5:c.*3411T>C (RAD50) | ENSP00000431225.1:n.*3411T>C | |
| NM_005732.3:c.3785T>C (RAD50) | NP_005723.2:p.Phe1262Ser | |
| NR_132125.1:n.177A>G (TH2LCRR) | ||
| NR_132126.1:n.175-3945A>G (TH2LCRR) | ||
| NM_005732.4:c.3785T>C (RAD50) MANE Select | NP_005723.2:p.Phe1262Ser |