SUSPENSION NOTICE:2024-08-07T19:00:00-0500 — 2024-09-25T08:00:00-0500
New user registrations, changes to existing user profiles, and changes to user credentials will be suspended for several weeks.
This allows us to avoid multi-day, broad service outages as we continue to migrate off our current cloud hosting provider.
New user registrations, changes to existing user profiles, and changes to user credentials will be suspended for several weeks.
This allows us to avoid multi-day, broad service outages as we continue to migrate off our current cloud hosting provider.
Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.131518523T>A , CM000671.2:g.131518523T>A | GRCh38 |
| NC_000009.11:g.134393910T>A , CM000671.1:g.134393910T>A | GRCh37 |
| NC_000009.10:g.133383731T>A | NCBI36 |
| NG_008896.1:g.20622T>A | |
| NG_008896.2:g.20622T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000341012.13:c.1189T>A | ENSP00000343034.7:p.Ser397Thr | |
| ENST00000404875.7:n.1891T>A | ||
| ENST00000423007.6:c.1408T>A | ENSP00000404119.2:p.Ser470Thr | |
| ENST00000677295.2:c.*1695T>A | ENSP00000504346.2:n.*1695T>A | |
| ENST00000678264.2:c.*1534T>A | ENSP00000503157.2:n.*1534T>A | |
| ENST00000682070.1:n.1816T>A | ||
| ENST00000682535.1:n.123T>A | ||
| ENST00000682539.1:c.289T>A | ||
| ENST00000682813.1:n.1616T>A | ||
| ENST00000683110.1:n.79T>A | ||
| ENST00000683392.1:n.4098T>A | ||
| ENST00000683712.1:n.1756T>A | ||
| ENST00000683900.1:n.3251T>A | ||
| ENST00000684062.1:n.2017T>A | ||
| ENST00000684579.1:n.3197T>A | ||
| ENST00000684679.1:n.578T>A | ||
| ENST00000341012.12:c.1189T>A | ENSP00000343034.7:p.Ser397Thr | |
| ENST00000372220.5:c.220T>A | ENSP00000361294.5:p.Ser74Thr | |
| ENST00000372228.9:c.1417T>A | ENSP00000361302.3:p.Ser473Thr | |
| ENST00000402686.8:c.1351T>A MANE Select | ENSP00000385797.4:p.Ser451Thr | |
| ENST00000676640.1:c.1351T>A | ENSP00000503281.1:p.Ser451Thr | |
| ENST00000676803.1:c.526T>A | ENSP00000503093.1:p.Ser176Thr | |
| ENST00000676835.1:c.*566T>A | ENSP00000502911.1:n.*566T>A | |
| ENST00000677029.1:c.895T>A | ENSP00000502936.1:p.Ser299Thr | |
| ENST00000677099.1:c.*1061T>A | ENSP00000504553.1:n.*1061T>A | |
| ENST00000677216.1:c.1000T>A | ENSP00000503772.1:p.Ser334Thr | |
| ENST00000677221.1:n.376T>A | ||
| ENST00000677295.1:c.*728T>A | ENSP00000504346.1:n.*728T>A | |
| ENST00000677444.1:c.1157T>A | ||
| ENST00000677586.1:n.832T>A | ||
| ENST00000677626.1:c.1000T>A | ENSP00000503552.1:p.Ser334Thr | |
| ENST00000677677.1:n.1311T>A | ||
| ENST00000677853.1:c.*359T>A | ENSP00000503488.1:n.*359T>A | |
| ENST00000677983.1:n.440T>A | ||
| ENST00000678202.1:n.371T>A | ||
| ENST00000678264.1:c.*728T>A | ENSP00000503157.1:n.*728T>A | |
| ENST00000678303.1:c.1261T>A | ENSP00000503696.1:p.Ser421Thr | |
| ENST00000678366.1:c.*1600T>A | ENSP00000504353.1:n.*1600T>A | |
| ENST00000678546.1:c.*1296T>A | ENSP00000503062.1:n.*1296T>A | |
| ENST00000678548.1:c.*1423T>A | ENSP00000503934.1:n.*1423T>A | |
| ENST00000678626.1:n.1048T>A | ||
| ENST00000678733.1:c.432T>A | ||
| ENST00000678739.1:c.*1677T>A | ENSP00000503806.1:n.*1677T>A | |
| ENST00000678795.1:n.438T>A | ||
| ENST00000678833.1:c.*798T>A | ENSP00000503893.1:n.*798T>A | |
| ENST00000678942.1:c.531T>A | ENSP00000504690.1:n.531T>A | |
| ENST00000679023.1:c.1189T>A | ENSP00000503718.1:p.Ser397Thr | |
| ENST00000679076.1:c.970T>A | ||
| ENST00000679111.1:c.1351T>A | ENSP00000504257.1:p.Ser451Thr | |
| ENST00000679189.1:c.1000T>A | ENSP00000503356.1:p.Ser334Thr | |
| ENST00000341012.11:c.1189T>A | ENSP00000343034.7:p.Ser397Thr | |
| ENST00000372220.4:c.214T>A | ENSP00000361294.4:p.Ser72Thr | |
| ENST00000372228.7:c.1417T>A | ENSP00000361302.3:p.Ser473Thr | |
| ENST00000402686.7:c.1351T>A | ENSP00000385797.3:p.Ser451Thr | |
| ENST00000404875.6:c.1000T>A | ENSP00000384531.2:p.Ser334Thr | |
| ENST00000423007.5:c.1351T>A | ENSP00000404119.1:p.Ser451Thr | |
| ENST00000485278.5:n.1906T>A | ||
| NM_001077365.1:c.1351T>A | NP_001070833.1:p.Ser451Thr | |
| NM_001077366.1:c.1189T>A | NP_001070834.1:p.Ser397Thr | |
| NM_001136113.1:c.1351T>A | NP_001129585.1:p.Ser451Thr | |
| NM_001136114.1:c.1000T>A | NP_001129586.1:p.Ser334Thr | |
| NM_007171.3:c.1417T>A | NP_009102.3:p.Ser473Thr | |
| XM_005272156.1:c.1417T>A | XP_005272213.1:p.Ser473Thr | |
| XM_005272158.1:c.1255T>A | XP_005272215.1:p.Ser419Thr | |
| XM_005272159.1:c.1066T>A | XP_005272216.1:p.Ser356Thr | |
| XM_005272162.1:c.220T>A | XP_005272219.1:p.Ser74Thr | |
| XM_006716932.1:c.1066T>A | XP_006716995.1:p.Ser356Thr | |
| XM_011518140.1:c.1270T>A | XP_011516442.1:p.Ser424Thr | |
| XM_011518141.1:c.1204T>A | XP_011516443.1:p.Ser402Thr | |
| XM_011518142.1:c.1108T>A | XP_011516444.1:p.Ser370Thr | |
| XM_011518143.1:c.1102T>A | XP_011516445.1:p.Ser368Thr | |
| XM_011518144.1:c.1417T>A | XP_011516446.1:p.Ser473Thr | |
| XM_011518145.1:c.961T>A | XP_011516447.1:p.Ser321Thr | |
| XM_011518146.1:c.1102T>A | XP_011516448.1:p.Ser368Thr | |
| XM_011518147.1:c.289T>A | XP_011516449.1:p.Ser97Thr | |
| XR_929703.1:n.1593T>A | ||
| NM_001353193.1:c.1417T>A | NP_001340122.1:p.Ser473Thr | |
| NM_001353194.1:c.1189T>A | NP_001340123.1:p.Ser397Thr | |
| NM_001353195.1:c.1000T>A | NP_001340124.1:p.Ser334Thr | |
| NM_001353196.1:c.1261T>A | NP_001340125.1:p.Ser421Thr | |
| NM_001353197.1:c.1255T>A | NP_001340126.1:p.Ser419Thr | |
| NM_001353198.1:c.1255T>A | NP_001340127.1:p.Ser419Thr | |
| NM_001353199.1:c.1066T>A | NP_001340128.1:p.Ser356Thr | |
| NM_001353200.1:c.895T>A | NP_001340129.1:p.Ser299Thr | |
| NR_148391.1:n.1401T>A | ||
| NR_148392.1:n.1619T>A | ||
| NR_148393.1:n.1401T>A | ||
| NR_148394.1:n.1294T>A | ||
| NR_148395.1:n.1553T>A | ||
| NR_148396.1:n.1187T>A | ||
| NR_148397.1:n.1451T>A | ||
| NR_148398.1:n.1406T>A | ||
| NR_148399.1:n.1793T>A | ||
| NR_148400.1:n.1392T>A | ||
| XM_005272162.3:c.220T>A | XP_005272219.1:p.Ser74Thr | |
| XM_006716932.2:c.1066T>A | XP_006716995.1:p.Ser356Thr | |
| XM_011518140.2:c.1270T>A | XP_011516442.1:p.Ser424Thr | |
| XM_011518141.2:c.1204T>A | XP_011516443.1:p.Ser402Thr | |
| XM_011518142.2:c.1108T>A | XP_011516444.1:p.Ser370Thr | |
| XM_011518143.2:c.1102T>A | XP_011516445.1:p.Ser368Thr | |
| XM_011518145.2:c.961T>A | XP_011516447.1:p.Ser321Thr | |
| XM_017014205.2:c.220T>A | XP_016869694.1:p.Ser74Thr | |
| XM_024447380.1:c.220T>A | XP_024303148.1:p.Ser74Thr | |
| XM_024447381.1:c.526T>A | XP_024303149.1:p.Ser176Thr | |
| XM_024447382.1:c.220T>A | XP_024303150.1:p.Ser74Thr | |
| XR_001746160.2:n.1521T>A | ||
| XR_001746162.2:n.1587T>A | ||
| XR_001746164.1:n.1304T>A | ||
| XR_001746166.2:n.1738T>A | ||
| NM_001077365.2:c.1351T>A MANE Select | NP_001070833.1:p.Ser451Thr | |
| NM_001077366.2:c.1189T>A | NP_001070834.1:p.Ser397Thr | |
| NM_001136113.2:c.1351T>A | NP_001129585.1:p.Ser451Thr | |
| NM_001136114.2:c.1000T>A | NP_001129586.1:p.Ser334Thr | |
| NM_001353193.2:c.1417T>A | NP_001340122.2:p.Ser473Thr | |
| NM_001353194.2:c.1189T>A | NP_001340123.1:p.Ser397Thr | |
| NM_001353195.2:c.1000T>A | NP_001340124.1:p.Ser334Thr | |
| NM_001353196.2:c.1261T>A | NP_001340125.1:p.Ser421Thr | |
| NM_001353197.2:c.1255T>A | NP_001340126.2:p.Ser419Thr | |
| NM_001353198.2:c.1255T>A | NP_001340127.2:p.Ser419Thr | |
| NM_001353199.2:c.1066T>A | NP_001340128.2:p.Ser356Thr | |
| NM_001353200.2:c.895T>A | NP_001340129.1:p.Ser299Thr | |
| NM_001374689.1:c.1339T>A | NP_001361618.1:p.Ser447Thr | |
| NM_001374690.1:c.1351T>A | NP_001361619.1:p.Ser451Thr | |
| NM_001374691.1:c.1000T>A | NP_001361620.1:p.Ser334Thr | |
| NM_001374692.1:c.1000T>A | NP_001361621.1:p.Ser334Thr | |
| NM_001374693.1:c.1000T>A | NP_001361622.1:p.Ser334Thr | |
| NM_001374695.1:c.961T>A | NP_001361624.1:p.Ser321Thr | |
| NM_007171.4:c.1417T>A | NP_009102.4:p.Ser473Thr | |
| NR_148391.2:n.1385T>A | ||
| NR_148392.2:n.1603T>A | ||
| NR_148393.2:n.1385T>A | ||
| NR_148394.2:n.1278T>A | ||
| NR_148395.2:n.1537T>A | ||
| NR_148396.2:n.1171T>A | ||
| NR_148397.2:n.1435T>A | ||
| NR_148398.2:n.1390T>A | ||
| NR_148399.2:n.1777T>A | ||
| NR_148400.2:n.1376T>A |