Revel Score:
ENST00000262406 (MANE Select)
0.119
ENST00000449996
0.119
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.65225096G>T , CM000679.2:g.65225096G>T | GRCh38 |
| NC_000017.10:g.63221214G>T , CM000679.1:g.63221214G>T | GRCh37 |
| NC_000017.9:g.60651676G>T | NCBI36 |
| NG_013021.1:g.92759G>T | |
| NG_013021.2:g.92759G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262406.10:c.1502G>T MANE Select | ENSP00000262406.9:p.Arg501Leu | |
| ENST00000635833.1:c.1502G>T | ENSP00000490658.1:p.Arg501Leu | |
| ENST00000262406.9:c.1502G>T | ENSP00000262406.9:p.Arg501Leu | |
| ENST00000443584.7:c.1493G>T | ENSP00000405814.3:p.Arg498Leu | |
| ENST00000449996.7:c.1493G>T | ENSP00000396329.3:p.Arg498Leu | |
| ENST00000577595.1:n.1430G>T | ||
| ENST00000584234.5:c.*21G>T | ENSP00000463410.1:n.*21G>T | |
| NM_001081955.2:c.1493G>T | NP_001075424.1:p.Arg498Leu | |
| NM_003835.3:c.1502G>T | NP_003826.2:p.Arg501Leu | |
| XM_011525426.1:c.914G>T | XP_011523728.1:p.Arg305Leu | |
| XM_011525426.3:c.914G>T | XP_011523728.1:p.Arg305Leu | |
| NM_003835.4:c.1502G>T MANE Select | NP_003826.2:p.Arg501Leu | |
| NM_001081955.3:c.1493G>T | NP_001075424.1:p.Arg498Leu |