Linked Data
ClinVar Variation Id:
284672
dbSNP Id:
rs139289704
ExAC:
13:52544745 C / T
gnomAD v2:
13-52544745-C-T
gnomAD v3:
13-51970609-C-T
gnomAD v4:
13-51970609-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.51970609C>T , CM000675.2:g.51970609C>T | GRCh38 |
| NC_000013.10:g.52544745C>T , CM000675.1:g.52544745C>T | GRCh37 |
| NC_000013.9:g.51442746C>T | NCBI36 |
| NG_008806.1:g.45886G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000634296.2:c.1426G>A | ENSP00000489512.2:p.Ala476Thr | |
| ENST00000673864.2:c.*170G>A | ENSP00000501045.2:n.*170G>A | |
| ENST00000674147.2:c.1426G>A | ENSP00000500964.2:p.Ala476Thr | |
| ENST00000242839.10:c.1426G>A MANE Select | ENSP00000242839.5:p.Ala476Thr | |
| ENST00000344297.9:c.1426G>A | ENSP00000342559.5:p.Ala476Thr | |
| ENST00000400366.6:c.1093G>A | ENSP00000383217.3:p.Ala365Thr | |
| ENST00000448424.7:c.1426G>A | ENSP00000416738.3:p.Ala476Thr | |
| ENST00000483772.2:n.182G>A | ||
| ENST00000673772.1:c.1426G>A | ENSP00000501168.1:p.Ala476Thr | |
| ENST00000673789.1:n.382G>A | ||
| ENST00000673864.1:c.620G>A | ENSP00000501045.1:n.620G>A | |
| ENST00000674078.1:n.1527G>A | ||
| ENST00000674147.1:c.982G>A | ENSP00000500964.1:p.Ala328Thr | |
| ENST00000242839.8:c.1426G>A | ENSP00000242839.4:p.Ala476Thr | |
| ENST00000344297.8:c.1426G>A | ENSP00000342559.5:p.Ala476Thr | |
| ENST00000400366.5:c.1093G>A | ENSP00000383217.3:p.Ala365Thr | |
| ENST00000400370.8:c.1285+3326G>A | ENSP00000383221.3:n.1285+3326G>A | |
| ENST00000418097.7:c.1426G>A | ENSP00000393343.2:p.Ala476Thr | |
| ENST00000448424.6:c.1426G>A | ENSP00000416738.2:p.Ala476Thr | |
| ENST00000482841.6:n.1547G>A | ||
| ENST00000483772.1:n.182G>A | ||
| ENST00000634308.1:c.1426G>A | ENSP00000489234.1:p.Ala476Thr | |
| ENST00000634844.1:c.1426G>A | ENSP00000489398.1:p.Ala476Thr | |
| ENST00000635406.1:n.212-24131G>A | ||
| NM_000053.3:c.1426G>A | NP_000044.2:p.Ala476Thr | |
| NM_001005918.2:c.1426G>A | NP_001005918.1:p.Ala476Thr | |
| NM_001243182.1:c.1093G>A | NP_001230111.1:p.Ala365Thr | |
| XM_005266423.2:c.1330G>A | XP_005266480.1:p.Ala444Thr | |
| XM_005266424.3:c.1330G>A | XP_005266481.1:p.Ala444Thr | |
| XM_005266427.2:c.1426G>A | XP_005266484.1:p.Ala476Thr | |
| XM_005266428.1:c.1426G>A | XP_005266485.1:p.Ala476Thr | |
| XM_005266430.3:c.1426G>A | XP_005266487.1:p.Ala476Thr | |
| XM_005266431.2:c.1390G>A | XP_005266488.1:p.Ala464Thr | |
| XM_005266432.2:c.1426G>A | XP_005266489.1:p.Ala476Thr | |
| XM_006719837.2:c.1330G>A | XP_006719900.1:p.Ala444Thr | |
| XM_011535117.1:c.1330G>A | XP_011533419.1:p.Ala444Thr | |
| XM_011535118.1:c.1426G>A | XP_011533420.1:p.Ala476Thr | |
| XM_011535119.1:c.1426G>A | XP_011533421.1:p.Ala476Thr | |
| XM_011535120.1:c.1426G>A | XP_011533422.1:p.Ala476Thr | |
| XM_011535121.1:c.1426G>A | XP_011533423.1:p.Ala476Thr | |
| XM_011535122.1:c.94G>A | XP_011533424.1:p.Ala32Thr | |
| XR_941601.1:n.1645G>A | ||
| XR_941602.1:n.1645G>A | ||
| XR_941603.1:n.1645G>A | ||
| XR_941604.1:n.1645G>A | ||
| NM_001330578.1:c.1426G>A | NP_001317507.1:p.Ala476Thr | |
| NM_001330579.1:c.1426G>A | NP_001317508.1:p.Ala476Thr | |
| XM_005266424.4:c.1330G>A | XP_005266481.1:p.Ala444Thr | |
| XM_005266430.4:c.1426G>A | XP_005266487.1:p.Ala476Thr | |
| XM_005266431.4:c.1390G>A | XP_005266488.1:p.Ala464Thr | |
| XM_006719837.3:c.1330G>A | XP_006719900.1:p.Ala444Thr | |
| XM_011535117.3:c.1330G>A | XP_011533419.1:p.Ala444Thr | |
| XM_017020627.1:c.1330G>A | XP_016876116.1:p.Ala444Thr | |
| NM_000053.4:c.1426G>A MANE Select | NP_000044.2:p.Ala476Thr | |
| NM_001005918.3:c.1426G>A | NP_001005918.1:p.Ala476Thr | |
| NM_001330579.2:c.1426G>A | NP_001317508.1:p.Ala476Thr | |
| NM_001243182.2:c.1093G>A | NP_001230111.1:p.Ala365Thr | |
| NM_001330578.2:c.1426G>A | NP_001317507.1:p.Ala476Thr |