Linked Data
ClinVar Variation Id:
35725
dbSNP Id:
rs193922107
gnomAD v2:
13-52513227-G-A
gnomAD v4:
13-51939091-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.51939091G>A , CM000675.2:g.51939091G>A | GRCh38 |
| NC_000013.10:g.52513227G>A , CM000675.1:g.52513227G>A | GRCh37 |
| NC_000013.9:g.51411228G>A | NCBI36 |
| NG_008806.1:g.77404C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000634296.2:c.*1309C>T | ENSP00000489512.2:n.*1309C>T | |
| ENST00000673864.2:c.*2403C>T | ENSP00000501045.2:n.*2403C>T | |
| ENST00000674147.2:c.3038C>T | ENSP00000500964.2:p.Thr1013Met | |
| ENST00000242839.10:c.3659C>T MANE Select | ENSP00000242839.5:p.Thr1220Met | |
| ENST00000344297.9:c.3038C>T | ENSP00000342559.5:p.Thr1013Met | |
| ENST00000400366.6:c.3326C>T | ENSP00000383217.3:p.Thr1109Met | |
| ENST00000448424.7:c.3407C>T | ENSP00000416738.3:p.Thr1136Met | |
| ENST00000673696.1:n.900C>T | ||
| ENST00000673772.1:c.3425C>T | ENSP00000501168.1:p.Thr1142Met | |
| ENST00000673867.1:n.3798C>T | ||
| ENST00000673923.1:n.525C>T | ||
| ENST00000674147.1:c.2594C>T | ENSP00000500964.1:p.Thr865Met | |
| ENST00000242839.8:c.3659C>T | ENSP00000242839.4:p.Thr1220Met | |
| ENST00000344297.8:c.3038C>T | ENSP00000342559.5:p.Thr1013Met | |
| ENST00000400366.5:c.3326C>T | ENSP00000383217.3:p.Thr1109Met | |
| ENST00000400370.8:c.2369C>T | ENSP00000383221.3:p.Thr790Met | |
| ENST00000418097.7:c.3464C>T | ENSP00000393343.2:p.Thr1155Met | |
| ENST00000448424.6:c.3425C>T | ENSP00000416738.2:p.Thr1142Met | |
| ENST00000634296.1:c.1437C>T | ||
| ENST00000634308.1:c.*760C>T | ENSP00000489234.1:n.*760C>T | |
| ENST00000634620.1:n.4403C>T | ||
| ENST00000634810.1:n.3004C>T | ||
| ENST00000634844.1:c.3515C>T | ENSP00000489398.1:p.Thr1172Met | |
| NM_000053.3:c.3659C>T | NP_000044.2:p.Thr1220Met | |
| NM_001005918.2:c.3038C>T | NP_001005918.1:p.Thr1013Met | |
| NM_001243182.1:c.3326C>T | NP_001230111.1:p.Thr1109Met | |
| XM_005266423.2:c.3563C>T | XP_005266480.1:p.Thr1188Met | |
| XM_005266424.3:c.3563C>T | XP_005266481.1:p.Thr1188Met | |
| XM_005266427.2:c.3425C>T | XP_005266484.1:p.Thr1142Met | |
| XM_005266428.1:c.3407C>T | XP_005266485.1:p.Thr1136Met | |
| XM_005266430.3:c.3659C>T | XP_005266487.1:p.Thr1220Met | |
| XM_005266431.2:c.3623C>T | XP_005266488.1:p.Thr1208Met | |
| XM_005266432.2:c.3173C>T | XP_005266489.1:p.Thr1058Met | |
| XM_006719837.2:c.3563C>T | XP_006719900.1:p.Thr1188Met | |
| XM_006719838.1:c.1475C>T | XP_006719901.1:p.Thr492Met | |
| XM_006719839.1:c.1292C>T | XP_006719902.1:p.Thr431Met | |
| XM_011535117.1:c.3563C>T | XP_011533419.1:p.Thr1188Met | |
| XM_011535118.1:c.3524C>T | XP_011533420.1:p.Thr1175Met | |
| XM_011535119.1:c.3476C>T | XP_011533421.1:p.Thr1159Met | |
| XM_011535120.1:c.3245C>T | XP_011533422.1:p.Thr1082Met | |
| XM_011535121.1:c.3146C>T | XP_011533423.1:p.Thr1049Met | |
| XM_011535122.1:c.2327C>T | XP_011533424.1:p.Thr776Met | |
| XR_941601.1:n.3878C>T | ||
| XR_941602.1:n.3878C>T | ||
| XR_941603.1:n.3878C>T | ||
| XR_941604.1:n.3878C>T | ||
| NM_001330578.1:c.3425C>T | NP_001317507.1:p.Thr1142Met | |
| NM_001330579.1:c.3407C>T | NP_001317508.1:p.Thr1136Met | |
| XM_005266424.4:c.3563C>T | XP_005266481.1:p.Thr1188Met | |
| XM_005266430.4:c.3659C>T | XP_005266487.1:p.Thr1220Met | |
| XM_005266431.4:c.3623C>T | XP_005266488.1:p.Thr1208Met | |
| XM_006719837.3:c.3563C>T | XP_006719900.1:p.Thr1188Met | |
| XM_011535117.3:c.3563C>T | XP_011533419.1:p.Thr1188Met | |
| XM_017020627.1:c.3563C>T | XP_016876116.1:p.Thr1188Met | |
| NM_000053.4:c.3659C>T MANE Select | NP_000044.2:p.Thr1220Met | |
| NM_001005918.3:c.3038C>T | NP_001005918.1:p.Thr1013Met | |
| NM_001330579.2:c.3407C>T | NP_001317508.1:p.Thr1136Met | |
| NM_001243182.2:c.3326C>T | NP_001230111.1:p.Thr1109Met | |
| NM_001330578.2:c.3425C>T | NP_001317507.1:p.Thr1142Met |