Revel Score:
ENST00000348295
0.065
ENST00000382578
0.065
ENST00000382565
0.065
ENST00000382563
0.065
ENST00000544772
0.065
ENST00000328354
0.065
ENST00000404276 (MANE Select)
0.065
ENST00000405598
0.065
ENST00000382580
0.065
ENST00000403642
0.065
ENST00000402731
0.065
gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.00105476 (MID)
Genomes Max Group AF
0.00007908 (NFE)
Exomes Max Group AF
0.00113568 (MID)
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.28687973C>A , CM000684.2:g.28687973C>A | GRCh38 |
| NC_000022.10:g.29083961C>A , CM000684.1:g.29083961C>A | GRCh37 |
| NC_000022.9:g.27413961C>A | NCBI36 |
| NG_008150.1:g.58862G>T | |
| NG_008150.2:g.58894G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000711048.1:c.*291G>T | ENSP00000518557.1:n.*291G>T | |
| ENST00000402731.6:c.1355G>T | ENSP00000384835.2:p.Arg452Leu | |
| ENST00000404276.6:c.1556G>T MANE Select | ENSP00000385747.1:p.Arg519Leu | |
| ENST00000425190.7:c.893G>T | ENSP00000390244.2:p.Arg298Leu | |
| ENST00000464581.6:c.896G>T | ENSP00000483777.2:p.Arg299Leu | |
| ENST00000648295.1:n.1108G>T | ||
| ENST00000649563.1:c.893G>T | ENSP00000496928.1:p.Arg298Leu | |
| ENST00000650281.1:c.1556G>T | ENSP00000497000.1:p.Arg519Leu | |
| ENST00000328354.10:c.1556G>T | ENSP00000329178.6:p.Arg519Leu | |
| ENST00000348295.7:c.1469G>T | ENSP00000329012.5:p.Arg490Leu | |
| ENST00000382580.6:c.1685G>T | ENSP00000372023.2:p.Arg562Leu | |
| ENST00000402731.5:c.1469G>T | ENSP00000384835.1:p.Arg490Leu | |
| ENST00000403642.5:c.1283G>T | ENSP00000384919.1:p.Arg428Leu | |
| ENST00000404276.5:c.1556G>T | ENSP00000385747.1:p.Arg519Leu | |
| ENST00000405598.5:c.1556G>T | ENSP00000386087.1:p.Arg519Leu | |
| ENST00000416671.5:c.*1046G>T | ENSP00000402225.1:n.*1046G>T | |
| ENST00000417588.5:c.1465G>T | ENSP00000412901.1:n.1465G>T | |
| ENST00000433728.5:c.1494G>T | ENSP00000404400.1:n.1494G>T | |
| ENST00000434810.5:c.754G>T | ||
| ENST00000448511.5:c.1446G>T | ENSP00000404567.1:n.1446G>T | |
| ENST00000456369.5:c.358G>T | ||
| ENST00000472807.1:n.290G>T | ||
| NM_001005735.1:c.1685G>T | NP_001005735.1:p.Arg562Leu | |
| NM_001257387.1:c.893G>T | NP_001244316.1:p.Arg298Leu | |
| NM_007194.3:c.1556G>T | NP_009125.1:p.Arg519Leu | |
| NM_145862.2:c.1469G>T | NP_665861.1:p.Arg490Leu | |
| XM_006724114.2:c.1076G>T | XP_006724177.1:p.Arg359Leu | |
| XM_006724116.2:c.1013G>T | XP_006724179.2:p.Arg338Leu | |
| XM_011529839.1:c.1715G>T | XP_011528141.1:p.Arg572Leu | |
| XM_011529840.1:c.1628G>T | XP_011528142.1:p.Arg543Leu | |
| XM_011529841.1:c.1484G>T | XP_011528143.1:p.Arg495Leu | |
| XM_011529842.1:c.1385G>T | XP_011528144.1:p.Arg462Leu | |
| XM_011529843.1:c.1355G>T | XP_011528145.1:p.Arg452Leu | |
| XM_011529845.1:c.893G>T | XP_011528147.1:p.Arg298Leu | |
| XR_937805.1:n.1715G>T | ||
| NM_001349956.1:c.1355G>T | NP_001336885.1:p.Arg452Leu | |
| NM_007194.4:c.1556G>T MANE Select | NP_009125.1:p.Arg519Leu | |
| XM_006724114.3:c.1109G>T | XP_006724177.2:p.Arg370Leu | |
| XM_011529839.2:c.1715G>T | XP_011528141.1:p.Arg572Leu | |
| XM_011529840.3:c.1628G>T | XP_011528142.1:p.Arg543Leu | |
| XM_011529842.2:c.1385G>T | XP_011528144.1:p.Arg462Leu | |
| XM_011529845.2:c.893G>T | XP_011528147.1:p.Arg298Leu | |
| XM_017028560.1:c.1679G>T | XP_016884049.1:p.Arg560Leu | |
| XM_017028561.2:c.893G>T | XP_016884050.1:p.Arg298Leu | |
| XM_024452148.1:c.1586G>T | XP_024307916.1:p.Arg529Leu | |
| XM_024452149.1:c.1499G>T | XP_024307917.1:p.Arg500Leu | |
| XR_937805.2:n.1726G>T | ||
| NM_001005735.2:c.1685G>T | NP_001005735.1:p.Arg562Leu | |
| NM_001257387.2:c.893G>T | NP_001244316.1:p.Arg298Leu | |
| NM_001349956.2:c.1355G>T | NP_001336885.1:p.Arg452Leu |