Revel Score:
ENST00000358127 (MANE Select)
0.917
ENST00000377849
0.917
ENST00000377853
0.917
ENST00000377852
0.917
ENST00000523241
0.917
ENST00000520154
0.917
ENST00000520281
0.917
ENST00000446742
0.917
ENST00000522003
0.917
ENST00000523145
0.917
ENST00000414447
0.917
ENST00000377847
0.917
ENST00000524340
0.917
gnomAD v4:
Joint Max Group AF
0.00000124 (NFE)
Exomes Max Group AF
0.00000132 (NFE)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.36966668G>A , CM000671.2:g.36966668G>A | GRCh38 |
| NC_000009.11:g.36966665G>A , CM000671.1:g.36966665G>A | GRCh37 |
| NC_000009.10:g.36956665G>A | NCBI36 |
| NG_033894.1:g.72812C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000358127.9:c.661C>T MANE Select | ENSP00000350844.4:p.Arg221Trp | |
| ENST00000377852.7:c.661C>T | ENSP00000367083.2:p.Arg221Trp | |
| ENST00000520154.6:c.661C>T | ENSP00000429291.1:p.Arg221Trp | |
| ENST00000523241.6:c.661C>T | ENSP00000429637.1:p.Arg221Trp | |
| ENST00000651550.1:c.337C>T | ENSP00000498443.1:p.Arg113Trp | |
| ENST00000358127.8:c.661C>T | ENSP00000350844.4:p.Arg221Trp | |
| ENST00000377840.6:c.661C>T | ENSP00000367071.2:p.Arg221Trp | |
| ENST00000377847.6:c.661C>T | ENSP00000367078.2:p.Arg221Trp | |
| ENST00000377852.6:c.661C>T | ENSP00000367083.2:p.Arg221Trp | |
| ENST00000377853.6:c.661C>T | ENSP00000367084.2:p.Arg221Trp | |
| ENST00000414447.5:c.532C>T | ENSP00000412188.1:p.Arg178Trp | |
| ENST00000446742.5:c.463C>T | ENSP00000404687.1:p.Arg155Trp | |
| ENST00000520154.5:c.661C>T | ENSP00000429291.1:p.Arg221Trp | |
| ENST00000520281.5:c.532C>T | ENSP00000430773.1:p.Arg178Trp | |
| ENST00000522003.5:c.337C>T | ENSP00000429359.1:p.Arg113Trp | |
| ENST00000522932.1:c.105+35980C>T | ||
| ENST00000523145.5:c.337C>T | ENSP00000429197.1:p.Arg113Trp | |
| ENST00000523241.5:c.661C>T | ENSP00000429637.1:p.Arg221Trp | |
| ENST00000523493.5:c.661C>T | ENSP00000431038.1:p.Arg221Trp | |
| ENST00000524340.5:c.85C>T | ENSP00000429404.1:p.Arg29Trp | |
| NM_001280547.1:c.661C>T | NP_001267476.1:p.Arg221Trp | |
| NM_001280548.1:c.661C>T | NP_001267477.1:p.Arg221Trp | |
| NM_001280549.1:c.661C>T | NP_001267478.1:p.Arg221Trp | |
| NM_001280550.1:c.661C>T | NP_001267479.1:p.Arg221Trp | |
| NM_001280551.1:c.337C>T | NP_001267480.1:p.Arg113Trp | |
| NM_001280552.1:c.661C>T | NP_001267481.1:p.Arg221Trp | |
| NM_001280553.1:c.532C>T | NP_001267482.1:p.Arg178Trp | |
| NM_001280554.1:c.532C>T | NP_001267483.1:p.Arg178Trp | |
| NM_001280555.1:c.463C>T | NP_001267484.1:p.Arg155Trp | |
| NM_001280556.1:c.337C>T | NP_001267485.1:p.Arg113Trp | |
| NM_016734.2:c.661C>T | NP_057953.1:p.Arg221Trp | |
| NR_103999.1:n.1109C>T | ||
| NR_104000.1:n.1109C>T | ||
| XM_005251481.3:c.658C>T | XP_005251538.1:p.Arg220Trp | |
| XM_011517896.1:c.661C>T | XP_011516198.1:p.Arg221Trp | |
| XM_011517897.1:c.658C>T | XP_011516199.1:p.Arg220Trp | |
| NM_016734.3:c.661C>T MANE Select | NP_057953.1:p.Arg221Trp | |
| NM_001280547.2:c.661C>T | NP_001267476.1:p.Arg221Trp | |
| NM_001280548.2:c.661C>T | NP_001267477.1:p.Arg221Trp | |
| NM_001280549.2:c.661C>T | NP_001267478.1:p.Arg221Trp | |
| NM_001280550.2:c.661C>T | NP_001267479.1:p.Arg221Trp | |
| NM_001280551.2:c.337C>T | NP_001267480.1:p.Arg113Trp | |
| NM_001280552.2:c.661C>T | NP_001267481.1:p.Arg221Trp | |
| NM_001280553.2:c.532C>T | NP_001267482.1:p.Arg178Trp | |
| NM_001280554.2:c.532C>T | NP_001267483.1:p.Arg178Trp | |
| NM_001280555.2:c.463C>T | NP_001267484.1:p.Arg155Trp | |
| NM_001280556.2:c.337C>T | NP_001267485.1:p.Arg113Trp | |
| NR_103999.2:n.898C>T | ||
| NR_104000.2:n.898C>T |