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_000003.12:g.12590934T= , CM000665.2:g.12590934T= | GRCh38 |
| NC_000003.11:g.12632433T= , CM000665.1:g.12632433T= | GRCh37 |
| NC_000003.10:g.12607433T= | NCBI36 |
| NG_007467.1:g.78246A= , LRG_413:g.78246A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000423275.6:c.*899A= | ENSP00000401088.1:n.*899A= | |
| ENST00000432427.3:c.551A= | ||
| ENST00000460610.2:n.28A= | ||
| ENST00000465826.6:n.825A= | ||
| ENST00000475353.2:n.1156A= | ||
| ENST00000494557.2:n.1045A= | ||
| ENST00000684903.1:c.*911A= | ENSP00000508612.1:n.*911A= | |
| ENST00000685348.1:c.*911A= | ENSP00000510285.1:n.*911A= | |
| ENST00000685437.1:c.1135A= | ENSP00000508794.1:p.Met379= | |
| ENST00000685653.1:c.1234A= | ENSP00000509968.1:p.Met412= | |
| ENST00000685738.1:c.*198A= | ENSP00000510156.1:n.*198A= | |
| ENST00000686409.1:n.2285A= | ||
| ENST00000686455.1:n.1597A= | ||
| ENST00000686762.1:c.1234A= | ENSP00000509767.1:p.Met412= | |
| ENST00000687257.1:n.1470A= | ||
| ENST00000687326.1:c.*168A= | ENSP00000509665.1:n.*168A= | |
| ENST00000687505.1:n.1352A= | ||
| ENST00000687923.1:c.1123A= | ENSP00000510255.1:p.Met375= | |
| ENST00000687940.1:n.1611A= | ||
| ENST00000688269.1:n.1830A= | ||
| ENST00000688326.1:c.667A= | ||
| ENST00000688444.1:n.1560A= | ||
| ENST00000688543.1:c.1135A= | ENSP00000509612.1:p.Met379= | |
| ENST00000688625.1:c.*812A= | ENSP00000509522.1:n.*812A= | |
| ENST00000688803.1:n.1465A= | ||
| ENST00000688914.1:n.220A= | ||
| ENST00000689097.1:c.*911A= | ENSP00000509756.1:n.*911A= | |
| ENST00000689389.1:c.1193+774A= | ENSP00000510213.1:n.1193+774A= | |
| ENST00000689418.1:c.*911A= | ENSP00000509467.1:n.*911A= | |
| ENST00000689481.1:c.*911A= | ENSP00000510248.1:n.*911A= | |
| ENST00000689540.1:n.1384A= | ||
| ENST00000689876.1:c.1234A= | ENSP00000508535.1:p.Met412= | |
| ENST00000689914.1:c.*168A= | ENSP00000509847.1:n.*168A= | |
| ENST00000690397.1:c.1123A= | ENSP00000508730.1:p.Met375= | |
| ENST00000690460.1:c.1222A= | ENSP00000509106.1:p.Met408= | |
| ENST00000690585.1:c.126A= | ||
| ENST00000690625.1:n.2270A= | ||
| ENST00000691396.1:c.*1086A= | ENSP00000510712.1:n.*1086A= | |
| ENST00000691724.1:c.*191A= | ENSP00000509255.1:n.*191A= | |
| ENST00000691779.1:c.*812A= | ENSP00000508592.1:n.*812A= | |
| ENST00000691888.1:c.126A= | ||
| ENST00000691899.1:c.1234A= | ENSP00000508763.1:p.Met412= | |
| ENST00000692069.1:n.1800A= | ||
| ENST00000692093.1:c.1135A= | ENSP00000509669.1:p.Met379= | |
| ENST00000692311.1:n.2058A= | ||
| ENST00000692558.1:n.1599A= | ||
| ENST00000692773.1:c.*971A= | ENSP00000509055.1:n.*971A= | |
| ENST00000692830.1:c.*979A= | ENSP00000509461.1:n.*979A= | |
| ENST00000693069.1:c.*168A= | ENSP00000510072.1:n.*168A= | |
| ENST00000693312.1:c.1009A= | ENSP00000508686.1:p.Met337= | |
| ENST00000693664.1:c.1234A= | ENSP00000509614.1:p.Met412= | |
| ENST00000693705.1:c.*911A= | ENSP00000510697.1:n.*911A= | |
| ENST00000251849.9:c.1234A= MANE Select | ENSP00000251849.4:p.Met412= | |
| ENST00000442415.7:c.1294A= | ENSP00000401888.2:p.Met432= | |
| ENST00000251849.8:c.1234A= | ENSP00000251849.4:p.Met412= | |
| ENST00000423275.5:c.*911A= | ENSP00000401088.1:n.*911A= | |
| ENST00000432427.2:c.871A= | ENSP00000398591.2:p.Met291= | |
| ENST00000442415.6:c.1294A= | ENSP00000401888.2:p.Met432= | |
| ENST00000460610.1:n.191A= | ||
| ENST00000465826.5:n.591A= | ||
| ENST00000475353.1:n.402A= | ||
| ENST00000494557.1:n.250A= | ||
| NM_002880.3:c.1234A= , LRG_413t1:c.1234A= | NP_002871.1:p.Met412= | |
| XM_005265355.1:c.1234A= | XP_005265412.1:p.Met412= | |
| XM_005265357.1:c.1135A= | XP_005265414.1:p.Met379= | |
| XM_005265358.3:c.991A= | XP_005265415.1:p.Met331= | |
| XM_005265359.3:c.892A= | XP_005265416.1:p.Met298= | |
| XM_005265360.1:c.1234A= | XP_005265417.1:p.Met412= | |
| XM_011533974.1:c.1234A= | XP_011532276.1:p.Met412= | |
| XM_011533975.1:c.991A= | XP_011532277.1:p.Met331= | |
| NM_001354689.1:c.1294A= | NP_001341618.1:p.Met432= | |
| NM_001354690.1:c.1234A= | NP_001341619.1:p.Met412= | |
| NM_001354691.1:c.991A= | NP_001341620.1:p.Met331= | |
| NM_001354692.1:c.991A= | NP_001341621.1:p.Met331= | |
| NM_001354693.1:c.1135A= | NP_001341622.1:p.Met379= | |
| NM_001354694.1:c.1051A= | NP_001341623.1:p.Met351= | |
| NM_001354695.1:c.892A= | NP_001341624.1:p.Met298= | |
| NR_148940.1:n.1762A= | ||
| NR_148941.1:n.1708A= | ||
| NR_148942.1:n.1647A= | ||
| XM_011533974.3:c.1234A= | XP_011532276.1:p.Met412= | |
| XM_017006966.1:c.1135A= | XP_016862455.1:p.Met379= | |
| NM_001354689.3:c.1294A= | NP_001341618.1:p.Met432= | |
| NM_001354690.2:c.1234A= | NP_001341619.1:p.Met412= | |
| NM_001354691.2:c.991A= | NP_001341620.1:p.Met331= | |
| NM_001354692.2:c.991A= | NP_001341621.1:p.Met331= | |
| NM_001354693.2:c.1135A= | NP_001341622.1:p.Met379= | |
| NM_001354694.2:c.1051A= | NP_001341623.1:p.Met351= | |
| NM_001354695.2:c.892A= | NP_001341624.1:p.Met298= | |
| NR_148940.2:n.1678A= | ||
| NR_148941.2:n.1624A= | ||
| NR_148942.2:n.1563A= | ||
| NM_001354690.3:c.1234A= | NP_001341619.1:p.Met412= | |
| NM_001354691.3:c.991A= | NP_001341620.1:p.Met331= | |
| NM_001354692.3:c.991A= | NP_001341621.1:p.Met331= | |
| NM_001354693.3:c.1135A= | NP_001341622.1:p.Met379= | |
| NM_001354694.3:c.1051A= | NP_001341623.1:p.Met351= | |
| NM_001354695.3:c.892A= | NP_001341624.1:p.Met298= | |
| NM_002880.4:c.1234A= MANE Select | NP_002871.1:p.Met412= | |
| NR_148940.3:n.1678A= | ||
| NR_148941.3:n.1624A= | ||
| NR_148942.3:n.1563A= |