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.17396376C= , CM000673.2:g.17396376C= | GRCh38 |
| NC_000011.9:g.17417923C= , CM000673.1:g.17417923C= | GRCh37 |
| NC_000011.8:g.17374499C= | NCBI36 |
| NG_008867.1:g.85527G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000524561.2:n.3721-446G= | ||
| ENST00000528374.2:c.711-446G= | ||
| ENST00000529967.6:n.2459-446G= | ||
| ENST00000532220.2:n.2907G= | ||
| ENST00000642611.2:n.4874G= | ||
| ENST00000644057.2:n.563-446G= | ||
| ENST00000645004.2:n.1619-446G= | ||
| ENST00000682051.1:n.4282-446G= | ||
| ENST00000682110.1:n.4335-446G= | ||
| ENST00000682140.1:c.3986-446G= | ENSP00000507829.1:n.3986-446G= | |
| ENST00000682185.1:n.5425-446G= | ||
| ENST00000682204.1:c.*2258-446G= | ENSP00000507094.1:n.*2258-446G= | |
| ENST00000682215.1:n.4702-446G= | ||
| ENST00000682288.1:c.*2551-446G= | ENSP00000507506.1:n.*2551-446G= | |
| ENST00000682442.1:n.4555-446G= | ||
| ENST00000682528.1:n.4412-446G= | ||
| ENST00000682673.1:n.4279-446G= | ||
| ENST00000682805.1:n.4740-446G= | ||
| ENST00000682965.1:c.*542-446G= | ENSP00000508229.1:n.*542-446G= | |
| ENST00000683093.1:n.4973G= | ||
| ENST00000683136.1:c.4003-446G= | ENSP00000507768.1:n.4003-446G= | |
| ENST00000683153.1:n.4377-446G= | ||
| ENST00000683365.1:n.4437-446G= | ||
| ENST00000683377.1:n.4335-446G= | ||
| ENST00000683456.1:c.*1257-446G= | ENSP00000508318.1:n.*1257-446G= | |
| ENST00000683522.1:n.4335-446G= | ||
| ENST00000683562.1:c.*2289-446G= | ENSP00000508265.1:n.*2289-446G= | |
| ENST00000683693.1:n.5321G= | ||
| ENST00000683725.1:c.4120-446G= | ENSP00000507496.1:n.4120-446G= | |
| ENST00000684010.1:n.4330-446G= | ||
| ENST00000684157.1:n.4874G= | ||
| ENST00000684253.1:n.4238-446G= | ||
| ENST00000684288.1:c.*2292-446G= | ENSP00000507143.1:n.*2292-446G= | |
| ENST00000684313.1:n.3767-446G= | ||
| ENST00000684332.1:n.4408-446G= | ||
| ENST00000684371.1:n.4441-446G= | ||
| ENST00000684404.1:n.4917G= | ||
| ENST00000684442.1:n.4559-446G= | ||
| ENST00000684555.1:c.*2332-446G= | ENSP00000507705.1:n.*2332-446G= | |
| ENST00000684571.1:c.3961-446G= | ENSP00000506935.1:n.3961-446G= | |
| ENST00000684593.1:c.*3825-446G= | ENSP00000507005.1:n.*3825-446G= | |
| ENST00000684711.1:c.*2516-446G= | ENSP00000506841.1:n.*2516-446G= | |
| ENST00000302539.9:c.4123-446G= | ENSP00000303960.4:n.4123-446G= | |
| ENST00000389817.8:c.4120-446G= MANE Select | ENSP00000374467.4:n.4120-446G= | |
| ENST00000642271.1:c.4117-446G= | ENSP00000493749.1:n.4117-446G= | |
| ENST00000642579.1:c.2174-446G= | ||
| ENST00000642611.1:n.4759G= | ||
| ENST00000642902.1:c.3902-446G= | ||
| ENST00000643260.1:c.4120-446G= | ENSP00000494450.1:n.4120-446G= | |
| ENST00000643562.1:c.*2242-446G= | ENSP00000496124.1:n.*2242-446G= | |
| ENST00000643925.1:c.2760-446G= | ||
| ENST00000644057.1:n.197-446G= | ||
| ENST00000644484.1:c.*3060G= | ENSP00000493558.1:n.*3060G= | |
| ENST00000644675.1:c.*2292-446G= | ENSP00000494567.1:n.*2292-446G= | |
| ENST00000644757.1:c.*3090G= | ENSP00000495085.1:n.*3090G= | |
| ENST00000644772.1:c.4186-446G= | ENSP00000494321.1:n.4186-446G= | |
| ENST00000645004.1:n.1813-446G= | ||
| ENST00000645076.1:c.3319-446G= | ||
| ENST00000645417.1:c.1308-446G= | ||
| ENST00000645744.1:c.*3439G= | ENSP00000494564.1:n.*3439G= | |
| ENST00000645760.1:c.4541-446G= | ||
| ENST00000645884.1:c.*1403-446G= | ENSP00000495516.1:n.*1403-446G= | |
| ENST00000646003.1:c.*2222-446G= | ENSP00000495259.1:n.*2222-446G= | |
| ENST00000646207.1:c.*2957-446G= | ENSP00000495025.1:n.*2957-446G= | |
| ENST00000646276.1:c.*3078G= | ENSP00000496070.1:n.*3078G= | |
| ENST00000646592.1:c.3426-446G= | ||
| ENST00000646902.1:c.4087-446G= | ENSP00000494101.1:n.4087-446G= | |
| ENST00000646993.1:c.*2662-446G= | ENSP00000493720.1:n.*2662-446G= | |
| ENST00000647013.1:c.4126-446G= | ENSP00000496741.1:n.4126-446G= | |
| ENST00000647015.1:c.3871-446G= | ENSP00000495389.1:n.3871-446G= | |
| ENST00000647086.1:c.*3706-446G= | ENSP00000493677.1:n.*3706-446G= | |
| ENST00000647158.1:c.*2407-446G= | ENSP00000495744.1:n.*2407-446G= | |
| ENST00000302539.8:c.4123-446G= | ENSP00000303960.4:n.4123-446G= | |
| ENST00000389817.7:c.4120-446G= | ENSP00000374467.3:n.4120-446G= | |
| ENST00000528374.1:c.602-446G= | ||
| ENST00000532220.1:n.594-446G= | ||
| NM_000352.4:c.4120-446G= | NP_000343.2:n.4120-446G= | |
| NM_001287174.1:c.4123-446G= | NP_001274103.1:n.4123-446G= | |
| XM_011520331.1:c.4120-446G= | XP_011518633.1:n.4120-446G= | |
| XM_011520332.1:c.4123-446G= | XP_011518634.1:n.4123-446G= | |
| XM_011520333.1:c.2620-446G= | XP_011518635.1:n.2620-446G= | |
| XR_930890.1:n.4186-446G= | ||
| NM_001351295.1:c.4186-446G= | NP_001338224.1:n.4186-446G= | |
| NM_001351296.1:c.4120-446G= | NP_001338225.1:n.4120-446G= | |
| NM_001351297.1:c.4117-446G= | NP_001338226.1:n.4117-446G= | |
| NR_147094.1:n.4415-446G= | ||
| XM_017018197.2:c.4189-446G= | XP_016873686.1:n.4189-446G= | |
| XM_017018199.1:c.4186-446G= | XP_016873688.1:n.4186-446G= | |
| XM_017018201.2:c.4189-446G= | XP_016873690.1:n.4189-446G= | |
| XM_017018202.1:c.2686-446G= | XP_016873691.1:n.2686-446G= | |
| XM_017018204.1:c.2077-446G= | XP_016873693.1:n.2077-446G= | |
| XM_024448668.1:c.2488-446G= | XP_024304436.1:n.2488-446G= | |
| XR_001747945.2:n.4261-446G= | ||
| XR_001747946.2:n.4192-446G= | ||
| XR_002957189.1:n.5396G= | ||
| NM_000352.6:c.4120-446G= MANE Select | NP_000343.2:n.4120-446G= | |
| NM_001287174.2:c.4123-446G= | NP_001274103.1:n.4123-446G= | |
| NM_001351295.2:c.4186-446G= | NP_001338224.1:n.4186-446G= | |
| NM_001351296.2:c.4120-446G= | NP_001338225.1:n.4120-446G= | |
| NM_001351297.2:c.4117-446G= | NP_001338226.1:n.4117-446G= | |
| NR_147094.2:n.4415-446G= | ||
| NM_001287174.3:c.4123-446G= | NP_001274103.1:n.4123-446G= |