Revel Score:
ENST00000242839 (MANE Select)
0.959
ENST00000400366
0.959
ENST00000344297
0.959
ENST00000417240
0.959
ENST00000448424
0.959
ENST00000400370
0.959
ENST00000418097
0.959
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.51941111C>T , CM000675.2:g.51941111C>T | GRCh38 |
| NC_000013.10:g.52515247C>T , CM000675.1:g.52515247C>T | GRCh37 |
| NC_000013.9:g.51413248C>T | NCBI36 |
| NG_008806.1:g.75384G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000634296.2:c.*1176G>A | ENSP00000489512.2:n.*1176G>A | |
| ENST00000673864.2:c.*2270G>A | ENSP00000501045.2:n.*2270G>A | |
| ENST00000674147.2:c.2905G>A | ENSP00000500964.2:p.Gly969Arg | |
| ENST00000242839.10:c.3526G>A MANE Select | ENSP00000242839.5:p.Gly1176Arg | |
| ENST00000344297.9:c.2905G>A | ENSP00000342559.5:p.Gly969Arg | |
| ENST00000400366.6:c.3193G>A | ENSP00000383217.3:p.Gly1065Arg | |
| ENST00000448424.7:c.3274G>A | ENSP00000416738.3:p.Gly1092Arg | |
| ENST00000673772.1:c.3292G>A | ENSP00000501168.1:p.Gly1098Arg | |
| ENST00000673867.1:n.3665G>A | ||
| ENST00000674126.1:n.3889G>A | ||
| ENST00000674147.1:c.2461G>A | ENSP00000500964.1:p.Gly821Arg | |
| ENST00000242839.8:c.3526G>A | ENSP00000242839.4:p.Gly1176Arg | |
| ENST00000344297.8:c.2905G>A | ENSP00000342559.5:p.Gly969Arg | |
| ENST00000400366.5:c.3193G>A | ENSP00000383217.3:p.Gly1065Arg | |
| ENST00000400370.8:c.2236G>A | ENSP00000383221.3:p.Gly746Arg | |
| ENST00000418097.7:c.3331G>A | ENSP00000393343.2:p.Gly1111Arg | |
| ENST00000448424.6:c.3292G>A | ENSP00000416738.2:p.Gly1098Arg | |
| ENST00000634296.1:c.1304G>A | ||
| ENST00000634308.1:c.*627G>A | ENSP00000489234.1:n.*627G>A | |
| ENST00000634620.1:n.4270G>A | ||
| ENST00000634810.1:n.2871G>A | ||
| ENST00000634844.1:c.3382G>A | ENSP00000489398.1:p.Gly1128Arg | |
| NM_000053.3:c.3526G>A | NP_000044.2:p.Gly1176Arg | |
| NM_001005918.2:c.2905G>A | NP_001005918.1:p.Gly969Arg | |
| NM_001243182.1:c.3193G>A | NP_001230111.1:p.Gly1065Arg | |
| XM_005266423.2:c.3430G>A | XP_005266480.1:p.Gly1144Arg | |
| XM_005266424.3:c.3430G>A | XP_005266481.1:p.Gly1144Arg | |
| XM_005266427.2:c.3292G>A | XP_005266484.1:p.Gly1098Arg | |
| XM_005266428.1:c.3274G>A | XP_005266485.1:p.Gly1092Arg | |
| XM_005266430.3:c.3526G>A | XP_005266487.1:p.Gly1176Arg | |
| XM_005266431.2:c.3490G>A | XP_005266488.1:p.Gly1164Arg | |
| XM_005266432.2:c.3040G>A | XP_005266489.1:p.Gly1014Arg | |
| XM_006719837.2:c.3430G>A | XP_006719900.1:p.Gly1144Arg | |
| XM_006719838.1:c.1342G>A | XP_006719901.1:p.Gly448Arg | |
| XM_006719839.1:c.1159G>A | XP_006719902.1:p.Gly387Arg | |
| XM_011535117.1:c.3430G>A | XP_011533419.1:p.Gly1144Arg | |
| XM_011535118.1:c.3391G>A | XP_011533420.1:p.Gly1131Arg | |
| XM_011535119.1:c.3343G>A | XP_011533421.1:p.Gly1115Arg | |
| XM_011535120.1:c.3112G>A | XP_011533422.1:p.Gly1038Arg | |
| XM_011535121.1:c.3013G>A | XP_011533423.1:p.Gly1005Arg | |
| XM_011535122.1:c.2194G>A | XP_011533424.1:p.Gly732Arg | |
| XR_941601.1:n.3745G>A | ||
| XR_941602.1:n.3745G>A | ||
| XR_941603.1:n.3745G>A | ||
| XR_941604.1:n.3745G>A | ||
| NM_001330578.1:c.3292G>A | NP_001317507.1:p.Gly1098Arg | |
| NM_001330579.1:c.3274G>A | NP_001317508.1:p.Gly1092Arg | |
| XM_005266424.4:c.3430G>A | XP_005266481.1:p.Gly1144Arg | |
| XM_005266430.4:c.3526G>A | XP_005266487.1:p.Gly1176Arg | |
| XM_005266431.4:c.3490G>A | XP_005266488.1:p.Gly1164Arg | |
| XM_006719837.3:c.3430G>A | XP_006719900.1:p.Gly1144Arg | |
| XM_011535117.3:c.3430G>A | XP_011533419.1:p.Gly1144Arg | |
| XM_017020627.1:c.3430G>A | XP_016876116.1:p.Gly1144Arg | |
| NM_000053.4:c.3526G>A MANE Select | NP_000044.2:p.Gly1176Arg | |
| NM_001005918.3:c.2905G>A | NP_001005918.1:p.Gly969Arg | |
| NM_001330579.2:c.3274G>A | NP_001317508.1:p.Gly1092Arg | |
| NM_001243182.2:c.3193G>A | NP_001230111.1:p.Gly1065Arg | |
| NM_001330578.2:c.3292G>A | NP_001317507.1:p.Gly1098Arg |