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.
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.17397099A= , CM000673.2:g.17397099A= | GRCh38 |
| NC_000011.9:g.17418646A= , CM000673.1:g.17418646A= | GRCh37 |
| NC_000011.8:g.17375222A= | NCBI36 |
| NG_008867.1:g.84804T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000524561.2:n.3537T= | ||
| ENST00000528374.2:c.568-41T= | ||
| ENST00000529967.6:n.2328-53T= | ||
| ENST00000532220.2:n.2184T= | ||
| ENST00000642611.2:n.4151T= | ||
| ENST00000644057.2:n.432-53T= | ||
| ENST00000645004.2:n.1488-53T= | ||
| ENST00000682051.1:n.4098T= | ||
| ENST00000682110.1:n.4151T= | ||
| ENST00000682140.1:c.3985+94T= | ENSP00000507829.1:n.3985+94T= | |
| ENST00000682185.1:n.5294-53T= | ||
| ENST00000682204.1:c.*2127-53T= | ENSP00000507094.1:n.*2127-53T= | |
| ENST00000682215.1:n.4518T= | ||
| ENST00000682288.1:c.*2420-53T= | ENSP00000507506.1:n.*2420-53T= | |
| ENST00000682442.1:n.4371T= | ||
| ENST00000682528.1:n.4228T= | ||
| ENST00000682673.1:n.4095T= | ||
| ENST00000682805.1:n.4518T= | ||
| ENST00000682965.1:c.*411-53T= | ENSP00000508229.1:n.*411-53T= | |
| ENST00000683093.1:n.4250T= | ||
| ENST00000683136.1:c.3872-53T= | ENSP00000507768.1:n.3872-53T= | |
| ENST00000683153.1:n.4193T= | ||
| ENST00000683365.1:n.4253T= | ||
| ENST00000683377.1:n.4151T= | ||
| ENST00000683456.1:c.*1126-53T= | ENSP00000508318.1:n.*1126-53T= | |
| ENST00000683522.1:n.4151T= | ||
| ENST00000683562.1:c.*2158-53T= | ENSP00000508265.1:n.*2158-53T= | |
| ENST00000683693.1:n.4598T= | ||
| ENST00000683725.1:c.3989-53T= | ENSP00000507496.1:n.3989-53T= | |
| ENST00000684010.1:n.4146T= | ||
| ENST00000684157.1:n.4151T= | ||
| ENST00000684253.1:n.4054T= | ||
| ENST00000684288.1:c.*2161-53T= | ENSP00000507143.1:n.*2161-53T= | |
| ENST00000684313.1:n.3583T= | ||
| ENST00000684332.1:n.4224T= | ||
| ENST00000684371.1:n.4257T= | ||
| ENST00000684404.1:n.4194T= | ||
| ENST00000684442.1:n.4428-53T= | ||
| ENST00000684555.1:c.*2201-53T= | ENSP00000507705.1:n.*2201-53T= | |
| ENST00000684571.1:c.3830-53T= | ENSP00000506935.1:n.3830-53T= | |
| ENST00000684593.1:c.*3694-53T= | ENSP00000507005.1:n.*3694-53T= | |
| ENST00000684711.1:c.*2385-53T= | ENSP00000506841.1:n.*2385-53T= | |
| ENST00000302539.9:c.3992-53T= | ENSP00000303960.4:n.3992-53T= | |
| ENST00000389817.8:c.3989-53T= MANE Select | ENSP00000374467.4:n.3989-53T= | |
| ENST00000642271.1:c.3986-53T= | ENSP00000493749.1:n.3986-53T= | |
| ENST00000642579.1:c.2073-83T= | ||
| ENST00000642611.1:n.4036T= | ||
| ENST00000642902.1:c.3771-53T= | ||
| ENST00000643260.1:c.3989-53T= | ENSP00000494450.1:n.3989-53T= | |
| ENST00000643562.1:c.*2058T= | ENSP00000496124.1:n.*2058T= | |
| ENST00000643925.1:c.2576T= | ||
| ENST00000644057.1:n.13T= | ||
| ENST00000644484.1:c.*2337T= | ENSP00000493558.1:n.*2337T= | |
| ENST00000644675.1:c.*2161-53T= | ENSP00000494567.1:n.*2161-53T= | |
| ENST00000644757.1:c.*2367T= | ENSP00000495085.1:n.*2367T= | |
| ENST00000644772.1:c.4055-53T= | ENSP00000494321.1:n.4055-53T= | |
| ENST00000645004.1:n.1591T= | ||
| ENST00000645076.1:c.3188-53T= | ||
| ENST00000645417.1:c.1177-53T= | ||
| ENST00000645744.1:c.*2716T= | ENSP00000494564.1:n.*2716T= | |
| ENST00000645760.1:c.4357T= | ||
| ENST00000645884.1:c.*1219T= | ENSP00000495516.1:n.*1219T= | |
| ENST00000646003.1:c.*2038T= | ENSP00000495259.1:n.*2038T= | |
| ENST00000646207.1:c.*2826-53T= | ENSP00000495025.1:n.*2826-53T= | |
| ENST00000646276.1:c.*2355T= | ENSP00000496070.1:n.*2355T= | |
| ENST00000646592.1:c.3295-53T= | ||
| ENST00000646902.1:c.3986-83T= | ENSP00000494101.1:n.3986-83T= | |
| ENST00000646993.1:c.*2478T= | ENSP00000493720.1:n.*2478T= | |
| ENST00000647013.1:c.3995-53T= | ENSP00000496741.1:n.3995-53T= | |
| ENST00000647015.1:c.3740-53T= | ENSP00000495389.1:n.3740-53T= | |
| ENST00000647086.1:c.*3605-83T= | ENSP00000493677.1:n.*3605-83T= | |
| ENST00000647158.1:c.*2223T= | ENSP00000495744.1:n.*2223T= | |
| ENST00000302539.8:c.3992-53T= | ENSP00000303960.4:n.3992-53T= | |
| ENST00000389817.7:c.3989-53T= | ENSP00000374467.3:n.3989-53T= | |
| ENST00000527905.5:c.*958T= | ENSP00000431653.1:n.*958T= | |
| ENST00000528374.1:c.459-41T= | ||
| ENST00000531137.1:n.501T= | ||
| ENST00000531891.1:c.357-83T= | ||
| ENST00000532220.1:n.410T= | ||
| NM_000352.4:c.3989-53T= | NP_000343.2:n.3989-53T= | |
| NM_001287174.1:c.3992-53T= | NP_001274103.1:n.3992-53T= | |
| XM_011520331.1:c.3989-53T= | XP_011518633.1:n.3989-53T= | |
| XM_011520332.1:c.3992-53T= | XP_011518634.1:n.3992-53T= | |
| XM_011520333.1:c.2489-53T= | XP_011518635.1:n.2489-53T= | |
| XR_930890.1:n.4055-53T= | ||
| NM_001351295.1:c.4055-53T= | NP_001338224.1:n.4055-53T= | |
| NM_001351296.1:c.3989-53T= | NP_001338225.1:n.3989-53T= | |
| NM_001351297.1:c.3986-53T= | NP_001338226.1:n.3986-53T= | |
| NR_147094.1:n.4231T= | ||
| XM_017018197.2:c.4058-53T= | XP_016873686.1:n.4058-53T= | |
| XM_017018199.1:c.4055-53T= | XP_016873688.1:n.4055-53T= | |
| XM_017018201.2:c.4058-53T= | XP_016873690.1:n.4058-53T= | |
| XM_017018202.1:c.2555-53T= | XP_016873691.1:n.2555-53T= | |
| XM_017018204.1:c.1946-53T= | XP_016873693.1:n.1946-53T= | |
| XM_024448668.1:c.2357-53T= | XP_024304436.1:n.2357-53T= | |
| XR_001747945.2:n.4130-53T= | ||
| XR_001747946.2:n.4061-53T= | ||
| XR_002957189.1:n.4673T= | ||
| NM_000352.6:c.3989-53T= MANE Select | NP_000343.2:n.3989-53T= | |
| NM_001287174.2:c.3992-53T= | NP_001274103.1:n.3992-53T= | |
| NM_001351295.2:c.4055-53T= | NP_001338224.1:n.4055-53T= | |
| NM_001351296.2:c.3989-53T= | NP_001338225.1:n.3989-53T= | |
| NM_001351297.2:c.3986-53T= | NP_001338226.1:n.3986-53T= | |
| NR_147094.2:n.4231T= | ||
| NM_001287174.3:c.3992-53T= | NP_001274103.1:n.3992-53T= |