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_000023.11:g.154032417_154032418del , CM000685.2:g.154032417_154032418del | GRCh38 |
| NC_000023.10:g.153297868_153297869del , CM000685.1:g.153297868_153297869del | GRCh37 |
| NC_000023.9:g.152951062_152951063del | NCBI36 |
| NG_007107.2:g.109711_109712del | |
| NG_007107.3:g.109687_109688del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000303391.11:c.167_168del MANE Plus Clinical | ENSP00000301948.6:p.Pro56ArgfsTer? | |
| ENST00000453960.7:c.203_204del MANE Select | ENSP00000395535.2:p.Pro68ArgfsTer? | |
| ENST00000303391.10:c.167_168del | ENSP00000301948.6:p.Pro56ArgfsTer? | |
| ENST00000369957.5:c.*221_*222del | ENSP00000358973.4:n.*221_*222del | |
| ENST00000407218.5:c.203_204del | ENSP00000384865.2:p.Pro68ArgfsTer? | |
| ENST00000453960.6:c.203_204del | ENSP00000395535.2:p.Pro68ArgfsTer? | |
| ENST00000486506.5:n.2515_2516del | ||
| ENST00000496908.5:n.298_299del | ||
| ENST00000611468.1:c.155_156del | ENSP00000479736.1:p.Pro52ArgfsTer? | |
| ENST00000619732.4:c.167_168del | ENSP00000480973.1:p.Pro56ArgfsTer? | |
| ENST00000622433.4:c.155_156del | ENSP00000484470.1:p.Pro52ArgfsTer? | |
| ENST00000628176.2:c.167_168del | ENSP00000486978.1:p.Pro56ArgfsTer? | |
| ENST00000631210.1:n.446_447del | ||
| NM_001110792.1:c.203_204del | NP_001104262.1:p.Pro68ArgfsTer? | |
| NM_001316337.1:c.-113_-112del | NP_001303266.1:n.-113_-112del | |
| NM_004992.3:c.167_168del | NP_004983.1:p.Pro56ArgfsTer? | |
| XM_005274681.3:c.167_168del | XP_005274738.1:p.Pro56ArgfsTer? | |
| XM_005274682.3:c.-113_-112del | XP_005274739.1:n.-113_-112del | |
| XM_005274683.3:c.-113_-112del | XP_005274740.1:n.-113_-112del | |
| XM_011531166.1:c.-113_-112del | XP_011529468.1:n.-113_-112del | |
| XM_006724819.3:c.-394_-393del | XP_006724882.1:n.-394_-393del | |
| XM_011531166.2:c.-113_-112del | XP_011529468.1:n.-113_-112del | |
| XM_024452383.1:c.-113_-112del | XP_024308151.1:n.-113_-112del | |
| XM_024452384.1:c.-113_-112del | XP_024308152.1:n.-113_-112del | |
| NM_001110792.2:c.203_204del MANE Select | NP_001104262.1:p.Pro68ArgfsTer? | |
| NM_001316337.2:c.-113_-112del | NP_001303266.1:n.-113_-112del | |
| NM_001369391.2:c.-113_-112del | NP_001356320.1:n.-113_-112del | |
| NM_001369392.2:c.-113_-112del | NP_001356321.1:n.-113_-112del | |
| NM_001369393.2:c.-113_-112del | NP_001356322.1:n.-113_-112del | |
| NM_001369394.1:c.-113_-112del | NP_001356323.1:n.-113_-112del | |
| NM_001369394.2:c.-113_-112del | NP_001356323.1:n.-113_-112del | |
| NM_001386137.1:c.-394_-393del | NP_001373066.1:n.-394_-393del | |
| NM_001386138.1:c.-394_-393del | NP_001373067.1:n.-394_-393del | |
| NM_001386139.1:c.-394_-393del | NP_001373068.1:n.-394_-393del | |
| NM_004992.4:c.167_168del MANE Plus Clinical | NP_004983.1:p.Pro56ArgfsTer? |