Revel Score:
ENST00000369770
0.818
ENST00000485317
0.818
ENST00000440270
0.818
ENST00000316361 (MANE Select)
0.818
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.110603902C>A , CM000663.2:g.110603902C>A | GRCh38 |
| NC_000001.10:g.111146524C>A , CM000663.1:g.111146524C>A | GRCh37 |
| NC_000001.9:g.110948047C>A | NCBI36 |
| NG_027997.2:g.32573G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000316361.10:c.881G>T MANE Select | ENSP00000314520.4:p.Arg294Leu | |
| ENST00000485317.6:c.881G>T | ENSP00000433109.1:p.Arg294Leu | |
| ENST00000525120.2:n.361+1489G>T | ||
| ENST00000638477.2:c.119G>T | ENSP00000491354.1:p.Arg40Leu | |
| ENST00000638532.1:c.881G>T | ENSP00000491613.1:p.Arg294Leu | |
| ENST00000638616.2:c.881G>T | ENSP00000491977.1:p.Arg294Leu | |
| ENST00000639048.2:c.119G>T | ENSP00000491627.1:p.Arg40Leu | |
| ENST00000639227.1:n.649G>T | ||
| ENST00000639233.2:c.299G>T | ENSP00000492716.1:p.Arg100Leu | |
| ENST00000640450.1:n.989G>T | ||
| ENST00000640680.1:n.459+1489G>T | ||
| ENST00000640774.2:c.119G>T | ENSP00000492008.1:p.Arg40Leu | |
| ENST00000640956.1:c.515G>T | ENSP00000491647.1:p.Arg172Leu | |
| ENST00000675391.1:c.881G>T | ENSP00000502642.1:p.Arg294Leu | |
| ENST00000316361.8:c.881G>T | ENSP00000314520.4:p.Arg294Leu | |
| ENST00000369770.7:c.881G>T | ENSP00000358785.3:p.Arg294Leu | |
| ENST00000485317.5:c.881G>T | ENSP00000433109.1:p.Arg294Leu | |
| ENST00000633222.1:c.881G>T | ENSP00000487785.1:p.Arg294Leu | |
| NM_001204269.1:c.881G>T | NP_001191198.1:p.Arg294Leu | |
| NM_004974.3:c.881G>T | NP_004965.1:p.Arg294Leu | |
| XM_011541396.1:c.881G>T | XP_011539698.1:p.Arg294Leu | |
| XM_011541397.1:c.881G>T | XP_011539699.1:p.Arg294Leu | |
| XM_011541398.1:c.881G>T | XP_011539700.1:p.Arg294Leu | |
| XM_011541399.1:c.881G>T | XP_011539701.1:p.Arg294Leu | |
| XM_011541400.1:c.881G>T | XP_011539702.1:p.Arg294Leu | |
| XM_011541396.2:c.881G>T | XP_011539698.1:p.Arg294Leu | |
| XM_011541397.2:c.881G>T | XP_011539699.1:p.Arg294Leu | |
| XM_011541398.2:c.881G>T | XP_011539700.1:p.Arg294Leu | |
| XM_011541399.2:c.881G>T | XP_011539701.1:p.Arg294Leu | |
| XM_011541400.2:c.881G>T | XP_011539702.1:p.Arg294Leu | |
| XM_017001213.1:c.881G>T | XP_016856702.1:p.Arg294Leu | |
| NM_004974.4:c.881G>T MANE Select | NP_004965.1:p.Arg294Leu | |
| NM_001204269.2:c.881G>T | NP_001191198.1:p.Arg294Leu |