Revel Score:
ENST00000297268 (MANE Select)
0.263
ENST00000545487
0.263
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.94410478C>G , CM000669.2:g.94410478C>G | GRCh38 |
| NC_000007.13:g.94039790C>G , CM000669.1:g.94039790C>G | GRCh37 |
| NC_000007.12:g.93877726C>G | NCBI36 |
| NG_007405.1:g.20918C>G , LRG_2:g.20918C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000297268.11:c.1148C>G MANE Select | ENSP00000297268.6:p.Pro383Arg | |
| ENST00000297268.10:c.1148C>G | ENSP00000297268.6:p.Pro383Arg | |
| ENST00000620463.1:c.1142C>G | ENSP00000477719.1:p.Pro381Arg | |
| NM_000089.3:c.1148C>G , LRG_2t1:c.1148C>G | NP_000080.2:p.Pro383Arg | |
| NM_000089.4:c.1148C>G MANE Select | NP_000080.2:p.Pro383Arg |