Revel Score:
ENST00000311895 (MANE Select)
0.677
ENST00000389138
0.677
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.13947845G>T , CM000678.2:g.13947845G>T | GRCh38 |
| NC_000016.9:g.14041702G>T , CM000678.1:g.14041702G>T | GRCh37 |
| NC_000016.8:g.13949203G>T | NCBI36 |
| NG_011442.1:g.32689G>T , LRG_463:g.32689G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682617.1:c.2387G>T | ENSP00000507912.1:p.Arg796Leu | |
| ENST00000683962.1:c.*1943G>T | ENSP00000506854.1:n.*1943G>T | |
| ENST00000311895.8:c.2249G>T MANE Select | ENSP00000310520.7:p.Arg750Leu | |
| ENST00000311895.7:c.2249G>T | ENSP00000310520.7:p.Arg750Leu | |
| ENST00000389138.7:n.1526G>T | ||
| ENST00000462862.1:c.562G>T | ENSP00000461322.1:n.562G>T | |
| NM_005236.2:c.2249G>T , LRG_463t1:c.2249G>T | NP_005227.1:p.Arg750Leu | |
| XM_011522424.1:c.2387G>T | XP_011520726.1:p.Arg796Leu | |
| XM_011522425.1:c.1706G>T | XP_011520727.1:p.Arg569Leu | |
| XM_011522426.1:c.1460G>T | XP_011520728.1:p.Arg487Leu | |
| XM_011522427.1:c.899G>T | XP_011520729.1:p.Arg300Leu | |
| XR_932805.1:n.2408G>T | ||
| XM_011522424.3:c.2387G>T | XP_011520726.1:p.Arg796Leu | |
| XM_017023043.2:c.1460G>T | XP_016878532.1:p.Arg487Leu | |
| NM_005236.3:c.2249G>T MANE Select | NP_005227.1:p.Arg750Leu |