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.131511425T>A , CM000671.2:g.131511425T>A | GRCh38 |
| NC_000009.11:g.134386812T>A , CM000671.1:g.134386812T>A | GRCh37 |
| NC_000009.10:g.133376633T>A | NCBI36 |
| NG_008896.1:g.13524T>A | |
| NG_008896.2:g.13524T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000341012.13:c.782T>A | ENSP00000343034.7:p.Val261Glu | |
| ENST00000404875.7:n.1316T>A | ||
| ENST00000423007.6:c.1001T>A | ENSP00000404119.2:p.Val334Glu | |
| ENST00000677295.2:c.*1283T>A | ENSP00000504346.2:n.*1283T>A | |
| ENST00000678264.2:c.*1127T>A | ENSP00000503157.2:n.*1127T>A | |
| ENST00000678942.2:c.*497T>A | ENSP00000504690.2:n.*497T>A | |
| ENST00000682070.1:n.1404T>A | ||
| ENST00000682813.1:n.1209T>A | ||
| ENST00000683134.1:c.311T>A | ||
| ENST00000683392.1:n.3691T>A | ||
| ENST00000683712.1:n.1344T>A | ||
| ENST00000683900.1:n.2271T>A | ||
| ENST00000684062.1:n.1610T>A | ||
| ENST00000684579.1:n.2785T>A | ||
| ENST00000341012.12:c.782T>A | ENSP00000343034.7:p.Val261Glu | |
| ENST00000372220.5:c.-145-616T>A | ENSP00000361294.5:n.-145-616T>A | |
| ENST00000372228.9:c.1010T>A | ENSP00000361302.3:p.Val337Glu | |
| ENST00000402686.8:c.944T>A MANE Select | ENSP00000385797.4:p.Val315Glu | |
| ENST00000415075.6:c.*397T>A | ENSP00000405149.2:n.*397T>A | |
| ENST00000676640.1:c.944T>A | ENSP00000503281.1:p.Val315Glu | |
| ENST00000676803.1:c.119T>A | ENSP00000503093.1:p.Val40Glu | |
| ENST00000676835.1:c.*154T>A | ENSP00000502911.1:n.*154T>A | |
| ENST00000677029.1:c.488T>A | ENSP00000502936.1:p.Val163Glu | |
| ENST00000677099.1:c.*654T>A | ENSP00000504553.1:n.*654T>A | |
| ENST00000677216.1:c.593T>A | ENSP00000503772.1:p.Val198Glu | |
| ENST00000677293.1:c.119T>A | ENSP00000504278.1:p.Val40Glu | |
| ENST00000677295.1:c.*316T>A | ENSP00000504346.1:n.*316T>A | |
| ENST00000677444.1:c.750T>A | ||
| ENST00000677586.1:n.425T>A | ||
| ENST00000677626.1:c.782T>A | ENSP00000503552.1:p.Val261Glu | |
| ENST00000677677.1:n.904T>A | ||
| ENST00000677853.1:c.525T>A | ENSP00000503488.1:p.Cys175Ter | |
| ENST00000677944.1:c.206T>A | ||
| ENST00000678264.1:c.*316T>A | ENSP00000503157.1:n.*316T>A | |
| ENST00000678303.1:c.854T>A | ENSP00000503696.1:p.Val285Glu | |
| ENST00000678366.1:c.*1193T>A | ENSP00000504353.1:n.*1193T>A | |
| ENST00000678546.1:c.*316T>A | ENSP00000503062.1:n.*316T>A | |
| ENST00000678548.1:c.*1011T>A | ENSP00000503934.1:n.*1011T>A | |
| ENST00000678626.1:n.636T>A | ||
| ENST00000678733.1:c.118T>A | ||
| ENST00000678739.1:c.*1265T>A | ENSP00000503806.1:n.*1265T>A | |
| ENST00000678833.1:c.*391T>A | ENSP00000503893.1:n.*391T>A | |
| ENST00000678942.1:c.119T>A | ENSP00000504690.1:p.Val40Glu | |
| ENST00000679023.1:c.782T>A | ENSP00000503718.1:p.Val261Glu | |
| ENST00000679073.1:c.322T>A | ENSP00000504356.1:n.322T>A | |
| ENST00000679076.1:c.558T>A | ||
| ENST00000679111.1:c.944T>A | ENSP00000504257.1:p.Val315Glu | |
| ENST00000679189.1:c.593T>A | ENSP00000503356.1:p.Val198Glu | |
| ENST00000341012.11:c.782T>A | ENSP00000343034.7:p.Val261Glu | |
| ENST00000372228.7:c.1010T>A | ENSP00000361302.3:p.Val337Glu | |
| ENST00000402686.7:c.944T>A | ENSP00000385797.3:p.Val315Glu | |
| ENST00000404875.6:c.593T>A | ENSP00000384531.2:p.Val198Glu | |
| ENST00000415075.5:c.336T>A | ENSP00000405149.1:p.Cys112Ter | |
| ENST00000423007.5:c.944T>A | ENSP00000404119.1:p.Val315Glu | |
| ENST00000441334.5:c.659T>A | ENSP00000395060.1:p.Val220Glu | |
| ENST00000462375.5:n.765T>A | ||
| ENST00000485278.5:n.926T>A | ||
| NM_001077365.1:c.944T>A | NP_001070833.1:p.Val315Glu | |
| NM_001077366.1:c.782T>A | NP_001070834.1:p.Val261Glu | |
| NM_001136113.1:c.944T>A | NP_001129585.1:p.Val315Glu | |
| NM_001136114.1:c.593T>A | NP_001129586.1:p.Val198Glu | |
| NM_007171.3:c.1010T>A | NP_009102.3:p.Val337Glu | |
| XM_005272156.1:c.1010T>A | XP_005272213.1:p.Val337Glu | |
| XM_005272158.1:c.848T>A | XP_005272215.1:p.Val283Glu | |
| XM_005272159.1:c.659T>A | XP_005272216.1:p.Val220Glu | |
| XM_005272162.1:c.-193T>A | XP_005272219.1:n.-193T>A | |
| XM_006716932.1:c.659T>A | XP_006716995.1:p.Val220Glu | |
| XM_011518140.1:c.863T>A | XP_011516442.1:p.Val288Glu | |
| XM_011518141.1:c.797T>A | XP_011516443.1:p.Val266Glu | |
| XM_011518142.1:c.701T>A | XP_011516444.1:p.Val234Glu | |
| XM_011518143.1:c.690T>A | XP_011516445.1:p.Cys230Ter | |
| XM_011518144.1:c.1010T>A | XP_011516446.1:p.Val337Glu | |
| XM_011518145.1:c.554T>A | XP_011516447.1:p.Val185Glu | |
| XM_011518146.1:c.690T>A | XP_011516448.1:p.Cys230Ter | |
| XR_929703.1:n.1186T>A | ||
| NM_001353193.1:c.1010T>A | NP_001340122.1:p.Val337Glu | |
| NM_001353194.1:c.782T>A | NP_001340123.1:p.Val261Glu | |
| NM_001353195.1:c.593T>A | NP_001340124.1:p.Val198Glu | |
| NM_001353196.1:c.854T>A | NP_001340125.1:p.Val285Glu | |
| NM_001353197.1:c.848T>A | NP_001340126.1:p.Val283Glu | |
| NM_001353198.1:c.848T>A | NP_001340127.1:p.Val283Glu | |
| NM_001353199.1:c.659T>A | NP_001340128.1:p.Val220Glu | |
| NM_001353200.1:c.488T>A | NP_001340129.1:p.Val163Glu | |
| NR_148391.1:n.994T>A | ||
| NR_148392.1:n.1212T>A | ||
| NR_148393.1:n.994T>A | ||
| NR_148394.1:n.882T>A | ||
| NR_148395.1:n.1146T>A | ||
| NR_148396.1:n.775T>A | ||
| NR_148397.1:n.1039T>A | ||
| NR_148398.1:n.994T>A | ||
| NR_148399.1:n.1386T>A | ||
| NR_148400.1:n.980T>A | ||
| XM_005272162.3:c.-193T>A | XP_005272219.1:n.-193T>A | |
| XM_006716932.2:c.659T>A | XP_006716995.1:p.Val220Glu | |
| XM_011518140.2:c.863T>A | XP_011516442.1:p.Val288Glu | |
| XM_011518141.2:c.797T>A | XP_011516443.1:p.Val266Glu | |
| XM_011518142.2:c.701T>A | XP_011516444.1:p.Val234Glu | |
| XM_011518143.2:c.690T>A | XP_011516445.1:p.Cys230Ter | |
| XM_011518145.2:c.554T>A | XP_011516447.1:p.Val185Glu | |
| XM_017014205.2:c.-193T>A | XP_016869694.1:n.-193T>A | |
| XM_024447380.1:c.-193T>A | XP_024303148.1:n.-193T>A | |
| XM_024447381.1:c.119T>A | XP_024303149.1:p.Val40Glu | |
| XM_024447382.1:c.-193T>A | XP_024303150.1:n.-193T>A | |
| XR_001746160.2:n.1114T>A | ||
| XR_001746162.2:n.1180T>A | ||
| XR_001746164.1:n.892T>A | ||
| XR_001746166.2:n.1331T>A | ||
| NM_001077365.2:c.944T>A MANE Select | NP_001070833.1:p.Val315Glu | |
| NM_001077366.2:c.782T>A | NP_001070834.1:p.Val261Glu | |
| NM_001136113.2:c.944T>A | NP_001129585.1:p.Val315Glu | |
| NM_001136114.2:c.593T>A | NP_001129586.1:p.Val198Glu | |
| NM_001353193.2:c.1010T>A | NP_001340122.2:p.Val337Glu | |
| NM_001353194.2:c.782T>A | NP_001340123.1:p.Val261Glu | |
| NM_001353195.2:c.593T>A | NP_001340124.1:p.Val198Glu | |
| NM_001353196.2:c.854T>A | NP_001340125.1:p.Val285Glu | |
| NM_001353197.2:c.848T>A | NP_001340126.2:p.Val283Glu | |
| NM_001353198.2:c.848T>A | NP_001340127.2:p.Val283Glu | |
| NM_001353199.2:c.659T>A | NP_001340128.2:p.Val220Glu | |
| NM_001353200.2:c.488T>A | NP_001340129.1:p.Val163Glu | |
| NM_001374689.1:c.927T>A | NP_001361618.1:p.Cys309Ter | |
| NM_001374690.1:c.944T>A | NP_001361619.1:p.Val315Glu | |
| NM_001374691.1:c.593T>A | NP_001361620.1:p.Val198Glu | |
| NM_001374692.1:c.593T>A | NP_001361621.1:p.Val198Glu | |
| NM_001374693.1:c.782T>A | NP_001361622.1:p.Val261Glu | |
| NM_001374695.1:c.554T>A | NP_001361624.1:p.Val185Glu | |
| NM_007171.4:c.1010T>A | NP_009102.4:p.Val337Glu | |
| NR_148391.2:n.978T>A | ||
| NR_148392.2:n.1196T>A | ||
| NR_148393.2:n.978T>A | ||
| NR_148394.2:n.866T>A | ||
| NR_148395.2:n.1130T>A | ||
| NR_148396.2:n.759T>A | ||
| NR_148397.2:n.1023T>A | ||
| NR_148398.2:n.978T>A | ||
| NR_148399.2:n.1370T>A | ||
| NR_148400.2:n.964T>A |