Revel Score:
ENST00000215832 (MANE Select)
0.314
ENST00000415911
0.314
ENST00000398822
0.314
ENST00000544786
0.314
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.21772875C>G , CM000684.2:g.21772875C>G | GRCh38 |
| NC_000022.10:g.22127164C>G , CM000684.1:g.22127164C>G | GRCh37 |
| NC_000022.9:g.20457164C>G | NCBI36 |
| NG_023054.2:g.99806G>C , LRG_786:g.99806G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000215832.11:c.964G>C MANE Select | ENSP00000215832.7:p.Glu322Gln | |
| ENST00000215832.10:c.964G>C | ENSP00000215832.6:p.Glu322Gln | |
| ENST00000398822.7:c.964G>C | ENSP00000381803.3:p.Glu322Gln | |
| ENST00000544786.1:c.832G>C | ENSP00000440842.1:p.Glu278Gln | |
| NM_002745.4:c.964G>C , LRG_786t1:c.964G>C | NP_002736.3:p.Glu322Gln | |
| NM_138957.3:c.964G>C , LRG_786t2:c.964G>C | NP_620407.1:p.Glu322Gln | |
| NM_002745.5:c.964G>C MANE Select | NP_002736.3:p.Glu322Gln |