Linked Data
ClinVar Variation Id:
805233
dbSNP Id:
rs150702948
ExAC:
9:134393913 G / A
gnomAD v2:
9-134393913-G-A
gnomAD v3:
9-131518526-G-A
gnomAD v4:
9-131518526-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.131518526G>A , CM000671.2:g.131518526G>A | GRCh38 |
| NC_000009.11:g.134393913G>A , CM000671.1:g.134393913G>A | GRCh37 |
| NC_000009.10:g.133383734G>A | NCBI36 |
| NG_008896.1:g.20625G>A | |
| NG_008896.2:g.20625G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000341012.13:c.1192G>A | ENSP00000343034.7:p.Ala398Thr | |
| ENST00000404875.7:n.1894G>A | ||
| ENST00000423007.6:c.1411G>A | ENSP00000404119.2:p.Ala471Thr | |
| ENST00000677295.2:c.*1698G>A | ENSP00000504346.2:n.*1698G>A | |
| ENST00000678264.2:c.*1537G>A | ENSP00000503157.2:n.*1537G>A | |
| ENST00000682070.1:n.1819G>A | ||
| ENST00000682535.1:n.126G>A | ||
| ENST00000682539.1:c.292G>A | ||
| ENST00000682813.1:n.1619G>A | ||
| ENST00000683110.1:n.82G>A | ||
| ENST00000683392.1:n.4101G>A | ||
| ENST00000683712.1:n.1759G>A | ||
| ENST00000683900.1:n.3254G>A | ||
| ENST00000684062.1:n.2020G>A | ||
| ENST00000684579.1:n.3200G>A | ||
| ENST00000684679.1:n.581G>A | ||
| ENST00000341012.12:c.1192G>A | ENSP00000343034.7:p.Ala398Thr | |
| ENST00000372220.5:c.223G>A | ENSP00000361294.5:p.Ala75Thr | |
| ENST00000372228.9:c.1420G>A | ENSP00000361302.3:p.Ala474Thr | |
| ENST00000402686.8:c.1354G>A MANE Select | ENSP00000385797.4:p.Ala452Thr | |
| ENST00000676640.1:c.1354G>A | ENSP00000503281.1:p.Ala452Thr | |
| ENST00000676803.1:c.529G>A | ENSP00000503093.1:p.Ala177Thr | |
| ENST00000676835.1:c.*569G>A | ENSP00000502911.1:n.*569G>A | |
| ENST00000677029.1:c.898G>A | ENSP00000502936.1:p.Ala300Thr | |
| ENST00000677099.1:c.*1064G>A | ENSP00000504553.1:n.*1064G>A | |
| ENST00000677216.1:c.1003G>A | ENSP00000503772.1:p.Ala335Thr | |
| ENST00000677221.1:n.379G>A | ||
| ENST00000677295.1:c.*731G>A | ENSP00000504346.1:n.*731G>A | |
| ENST00000677444.1:c.1160G>A | ||
| ENST00000677586.1:n.835G>A | ||
| ENST00000677626.1:c.1003G>A | ENSP00000503552.1:p.Ala335Thr | |
| ENST00000677677.1:n.1314G>A | ||
| ENST00000677853.1:c.*362G>A | ENSP00000503488.1:n.*362G>A | |
| ENST00000677983.1:n.443G>A | ||
| ENST00000678202.1:n.374G>A | ||
| ENST00000678264.1:c.*731G>A | ENSP00000503157.1:n.*731G>A | |
| ENST00000678303.1:c.1264G>A | ENSP00000503696.1:p.Ala422Thr | |
| ENST00000678366.1:c.*1603G>A | ENSP00000504353.1:n.*1603G>A | |
| ENST00000678546.1:c.*1299G>A | ENSP00000503062.1:n.*1299G>A | |
| ENST00000678548.1:c.*1426G>A | ENSP00000503934.1:n.*1426G>A | |
| ENST00000678626.1:n.1051G>A | ||
| ENST00000678733.1:c.435G>A | ||
| ENST00000678739.1:c.*1680G>A | ENSP00000503806.1:n.*1680G>A | |
| ENST00000678795.1:n.441G>A | ||
| ENST00000678833.1:c.*801G>A | ENSP00000503893.1:n.*801G>A | |
| ENST00000678942.1:c.534G>A | ENSP00000504690.1:n.534G>A | |
| ENST00000679023.1:c.1192G>A | ENSP00000503718.1:p.Ala398Thr | |
| ENST00000679076.1:c.973G>A | ||
| ENST00000679111.1:c.1354G>A | ENSP00000504257.1:p.Ala452Thr | |
| ENST00000679189.1:c.1003G>A | ENSP00000503356.1:p.Ala335Thr | |
| ENST00000341012.11:c.1192G>A | ENSP00000343034.7:p.Ala398Thr | |
| ENST00000372220.4:c.217G>A | ENSP00000361294.4:p.Ala73Thr | |
| ENST00000372228.7:c.1420G>A | ENSP00000361302.3:p.Ala474Thr | |
| ENST00000402686.7:c.1354G>A | ENSP00000385797.3:p.Ala452Thr | |
| ENST00000404875.6:c.1003G>A | ENSP00000384531.2:p.Ala335Thr | |
| ENST00000423007.5:c.1354G>A | ENSP00000404119.1:p.Ala452Thr | |
| ENST00000485278.5:n.1909G>A | ||
| NM_001077365.1:c.1354G>A | NP_001070833.1:p.Ala452Thr | |
| NM_001077366.1:c.1192G>A | NP_001070834.1:p.Ala398Thr | |
| NM_001136113.1:c.1354G>A | NP_001129585.1:p.Ala452Thr | |
| NM_001136114.1:c.1003G>A | NP_001129586.1:p.Ala335Thr | |
| NM_007171.3:c.1420G>A | NP_009102.3:p.Ala474Thr | |
| XM_005272156.1:c.1420G>A | XP_005272213.1:p.Ala474Thr | |
| XM_005272158.1:c.1258G>A | XP_005272215.1:p.Ala420Thr | |
| XM_005272159.1:c.1069G>A | XP_005272216.1:p.Ala357Thr | |
| XM_005272162.1:c.223G>A | XP_005272219.1:p.Ala75Thr | |
| XM_006716932.1:c.1069G>A | XP_006716995.1:p.Ala357Thr | |
| XM_011518140.1:c.1273G>A | XP_011516442.1:p.Ala425Thr | |
| XM_011518141.1:c.1207G>A | XP_011516443.1:p.Ala403Thr | |
| XM_011518142.1:c.1111G>A | XP_011516444.1:p.Ala371Thr | |
| XM_011518143.1:c.1105G>A | XP_011516445.1:p.Ala369Thr | |
| XM_011518144.1:c.1420G>A | XP_011516446.1:p.Ala474Thr | |
| XM_011518145.1:c.964G>A | XP_011516447.1:p.Ala322Thr | |
| XM_011518146.1:c.1105G>A | XP_011516448.1:p.Ala369Thr | |
| XM_011518147.1:c.292G>A | XP_011516449.1:p.Ala98Thr | |
| XR_929703.1:n.1596G>A | ||
| NM_001353193.1:c.1420G>A | NP_001340122.1:p.Ala474Thr | |
| NM_001353194.1:c.1192G>A | NP_001340123.1:p.Ala398Thr | |
| NM_001353195.1:c.1003G>A | NP_001340124.1:p.Ala335Thr | |
| NM_001353196.1:c.1264G>A | NP_001340125.1:p.Ala422Thr | |
| NM_001353197.1:c.1258G>A | NP_001340126.1:p.Ala420Thr | |
| NM_001353198.1:c.1258G>A | NP_001340127.1:p.Ala420Thr | |
| NM_001353199.1:c.1069G>A | NP_001340128.1:p.Ala357Thr | |
| NM_001353200.1:c.898G>A | NP_001340129.1:p.Ala300Thr | |
| NR_148391.1:n.1404G>A | ||
| NR_148392.1:n.1622G>A | ||
| NR_148393.1:n.1404G>A | ||
| NR_148394.1:n.1297G>A | ||
| NR_148395.1:n.1556G>A | ||
| NR_148396.1:n.1190G>A | ||
| NR_148397.1:n.1454G>A | ||
| NR_148398.1:n.1409G>A | ||
| NR_148399.1:n.1796G>A | ||
| NR_148400.1:n.1395G>A | ||
| XM_005272162.3:c.223G>A | XP_005272219.1:p.Ala75Thr | |
| XM_006716932.2:c.1069G>A | XP_006716995.1:p.Ala357Thr | |
| XM_011518140.2:c.1273G>A | XP_011516442.1:p.Ala425Thr | |
| XM_011518141.2:c.1207G>A | XP_011516443.1:p.Ala403Thr | |
| XM_011518142.2:c.1111G>A | XP_011516444.1:p.Ala371Thr | |
| XM_011518143.2:c.1105G>A | XP_011516445.1:p.Ala369Thr | |
| XM_011518145.2:c.964G>A | XP_011516447.1:p.Ala322Thr | |
| XM_017014205.2:c.223G>A | XP_016869694.1:p.Ala75Thr | |
| XM_024447380.1:c.223G>A | XP_024303148.1:p.Ala75Thr | |
| XM_024447381.1:c.529G>A | XP_024303149.1:p.Ala177Thr | |
| XM_024447382.1:c.223G>A | XP_024303150.1:p.Ala75Thr | |
| XR_001746160.2:n.1524G>A | ||
| XR_001746162.2:n.1590G>A | ||
| XR_001746164.1:n.1307G>A | ||
| XR_001746166.2:n.1741G>A | ||
| NM_001077365.2:c.1354G>A MANE Select | NP_001070833.1:p.Ala452Thr | |
| NM_001077366.2:c.1192G>A | NP_001070834.1:p.Ala398Thr | |
| NM_001136113.2:c.1354G>A | NP_001129585.1:p.Ala452Thr | |
| NM_001136114.2:c.1003G>A | NP_001129586.1:p.Ala335Thr | |
| NM_001353193.2:c.1420G>A | NP_001340122.2:p.Ala474Thr | |
| NM_001353194.2:c.1192G>A | NP_001340123.1:p.Ala398Thr | |
| NM_001353195.2:c.1003G>A | NP_001340124.1:p.Ala335Thr | |
| NM_001353196.2:c.1264G>A | NP_001340125.1:p.Ala422Thr | |
| NM_001353197.2:c.1258G>A | NP_001340126.2:p.Ala420Thr | |
| NM_001353198.2:c.1258G>A | NP_001340127.2:p.Ala420Thr | |
| NM_001353199.2:c.1069G>A | NP_001340128.2:p.Ala357Thr | |
| NM_001353200.2:c.898G>A | NP_001340129.1:p.Ala300Thr | |
| NM_001374689.1:c.1342G>A | NP_001361618.1:p.Ala448Thr | |
| NM_001374690.1:c.1354G>A | NP_001361619.1:p.Ala452Thr | |
| NM_001374691.1:c.1003G>A | NP_001361620.1:p.Ala335Thr | |
| NM_001374692.1:c.1003G>A | NP_001361621.1:p.Ala335Thr | |
| NM_001374693.1:c.1003G>A | NP_001361622.1:p.Ala335Thr | |
| NM_001374695.1:c.964G>A | NP_001361624.1:p.Ala322Thr | |
| NM_007171.4:c.1420G>A | NP_009102.4:p.Ala474Thr | |
| NR_148391.2:n.1388G>A | ||
| NR_148392.2:n.1606G>A | ||
| NR_148393.2:n.1388G>A | ||
| NR_148394.2:n.1281G>A | ||
| NR_148395.2:n.1540G>A | ||
| NR_148396.2:n.1174G>A | ||
| NR_148397.2:n.1438G>A | ||
| NR_148398.2:n.1393G>A | ||
| NR_148399.2:n.1780G>A | ||
| NR_148400.2:n.1379G>A |