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
dbSNP Id:
rs941961989
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.12584592T>A , CM000665.2:g.12584592T>A | GRCh38 |
| NC_000003.11:g.12626091T>A , CM000665.1:g.12626091T>A | GRCh37 |
| NC_000003.10:g.12601091T>A | NCBI36 |
| NG_007467.1:g.84588A>T , LRG_413:g.84588A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000423275.6:c.*1534A>T (RAF1) | ENSP00000401088.1:n.*1534A>T | |
| ENST00000432427.3:c.1186A>T (RAF1) | ||
| ENST00000460610.2:n.6181A>T (RAF1) | ||
| ENST00000471449.2:n.679A>T (RAF1) | ||
| ENST00000475353.2:n.4149A>T (RAF1) | ||
| ENST00000684903.1:c.*1546A>T (RAF1) | ENSP00000508612.1:n.*1546A>T | |
| ENST00000685348.1:c.*1580A>T (RAF1) | ENSP00000510285.1:n.*1580A>T | |
| ENST00000685437.1:c.1770A>T (RAF1) | ENSP00000508794.1:p.Pro590= | |
| ENST00000685653.1:c.1869A>T (RAF1) | ENSP00000509968.1:p.Pro623= | |
| ENST00000685697.1:n.2604A>T (RAF1) | ||
| ENST00000685738.1:c.*833A>T (RAF1) | ENSP00000510156.1:n.*833A>T | |
| ENST00000686409.1:n.5278A>T (RAF1) | ||
| ENST00000686455.1:n.4590A>T (RAF1) | ||
| ENST00000686762.1:c.*428A>T (RAF1) | ENSP00000509767.1:n.*428A>T | |
| ENST00000687257.1:n.4323A>T (RAF1) | ||
| ENST00000687326.1:c.*3161A>T (RAF1) | ENSP00000509665.1:n.*3161A>T | |
| ENST00000687505.1:n.1987A>T (RAF1) | ||
| ENST00000687923.1:c.1758A>T (RAF1) | ENSP00000510255.1:p.Pro586= | |
| ENST00000688269.1:n.2465A>T (RAF1) | ||
| ENST00000688444.1:n.3986A>T (RAF1) | ||
| ENST00000688543.1:c.1770A>T (RAF1) | ENSP00000509612.1:p.Pro590= | |
| ENST00000688625.1:c.*3238A>T (RAF1) | ENSP00000509522.1:n.*3238A>T | |
| ENST00000688803.1:n.3297A>T (RAF1) | ||
| ENST00000689097.1:c.*1546A>T (RAF1) | ENSP00000509756.1:n.*1546A>T | |
| ENST00000689389.1:c.1692A>T (RAF1) | ENSP00000510213.1:p.Pro564= | |
| ENST00000689418.1:c.*3764A>T (RAF1) | ENSP00000509467.1:n.*3764A>T | |
| ENST00000689540.1:n.4237A>T (RAF1) | ||
| ENST00000689876.1:c.*418A>T (RAF1) | ENSP00000508535.1:n.*418A>T | |
| ENST00000689914.1:c.*803A>T (RAF1) | ENSP00000509847.1:n.*803A>T | |
| ENST00000690397.1:c.1758A>T (RAF1) | ENSP00000508730.1:p.Pro586= | |
| ENST00000690460.1:c.1857A>T (RAF1) | ENSP00000509106.1:p.Pro619= | |
| ENST00000690585.1:c.595A>T (RAF1) | ||
| ENST00000690625.1:n.2905A>T (RAF1) | ||
| ENST00000691396.1:c.*1741A>T (RAF1) | ENSP00000510712.1:n.*1741A>T | |
| ENST00000691643.1:n.2922A>T (RAF1) | ||
| ENST00000691724.1:c.*826A>T (RAF1) | ENSP00000509255.1:n.*826A>T | |
| ENST00000691779.1:c.*1447A>T (RAF1) | ENSP00000508592.1:n.*1447A>T | |
| ENST00000691888.1:c.743A>T (RAF1) | ||
| ENST00000691899.1:c.1869A>T (RAF1) | ENSP00000508763.1:p.Pro623= | |
| ENST00000692069.1:n.4793A>T (RAF1) | ||
| ENST00000692093.1:c.1770A>T (RAF1) | ENSP00000509669.1:p.Pro590= | |
| ENST00000692311.1:n.2693A>T (RAF1) | ||
| ENST00000692558.1:n.4452A>T (RAF1) | ||
| ENST00000692773.1:c.*1606A>T (RAF1) | ENSP00000509055.1:n.*1606A>T | |
| ENST00000692830.1:c.*1614A>T (RAF1) | ENSP00000509461.1:n.*1614A>T | |
| ENST00000693312.1:c.1644A>T (RAF1) | ENSP00000508686.1:p.Pro548= | |
| ENST00000693664.1:c.*320A>T (RAF1) | ENSP00000509614.1:n.*320A>T | |
| ENST00000693705.1:c.*1248A>T (RAF1) | ENSP00000510697.1:n.*1248A>T | |
| ENST00000251849.9:c.1869A>T (RAF1) MANE Select | ENSP00000251849.4:p.Pro623= | |
| ENST00000442415.7:c.1929A>T (RAF1) | ENSP00000401888.2:p.Pro643= | |
| ENST00000676541.1:c.*2339T>A (MKRN2) | ENSP00000503730.1:n.*2339T>A | |
| ENST00000677142.1:c.*2339T>A (MKRN2) | ENSP00000504455.1:n.*2339T>A | |
| ENST00000677816.1:c.*894T>A (MKRN2) | ENSP00000502893.1:n.*894T>A | |
| ENST00000677941.1:n.2402T>A (MKRN2) | ||
| ENST00000251849.8:c.1869A>T (RAF1) | ENSP00000251849.4:p.Pro623= | |
| ENST00000423275.5:c.*1546A>T (RAF1) | ENSP00000401088.1:n.*1546A>T | |
| ENST00000432427.2:c.1506A>T (RAF1) | ENSP00000398591.2:p.Pro502= | |
| ENST00000442415.6:c.1929A>T (RAF1) | ENSP00000401888.2:p.Pro643= | |
| ENST00000471449.1:n.558A>T (RAF1) | ||
| NM_002880.3:c.1869A>T , LRG_413t1:c.1869A>T (RAF1) | NP_002871.1:p.Pro623= | |
| XM_005265355.1:c.1869A>T (RAF1) | XP_005265412.1:p.Pro623= | |
| XM_005265357.1:c.1770A>T (RAF1) | XP_005265414.1:p.Pro590= | |
| XM_005265358.3:c.1626A>T (RAF1) | XP_005265415.1:p.Pro542= | |
| XM_005265359.3:c.1527A>T (RAF1) | XP_005265416.1:p.Pro509= | |
| XM_011533974.1:c.1869A>T (RAF1) | XP_011532276.1:p.Pro623= | |
| XM_011533975.1:c.1626A>T (RAF1) | XP_011532277.1:p.Pro542= | |
| NM_001354689.1:c.1929A>T (RAF1) | NP_001341618.1:p.Pro643= | |
| NM_001354690.1:c.1869A>T (RAF1) | NP_001341619.1:p.Pro623= | |
| NM_001354691.1:c.1626A>T (RAF1) | NP_001341620.1:p.Pro542= | |
| NM_001354692.1:c.1626A>T (RAF1) | NP_001341621.1:p.Pro542= | |
| NM_001354693.1:c.1770A>T (RAF1) | NP_001341622.1:p.Pro590= | |
| NM_001354694.1:c.1686A>T (RAF1) | NP_001341623.1:p.Pro562= | |
| NM_001354695.1:c.1527A>T (RAF1) | NP_001341624.1:p.Pro509= | |
| NR_148940.1:n.2397A>T (RAF1) | ||
| NR_148941.1:n.2343A>T (RAF1) | ||
| NR_148942.1:n.2282A>T (RAF1) | ||
| XM_011533974.3:c.1869A>T (RAF1) | XP_011532276.1:p.Pro623= | |
| XM_017006966.1:c.1770A>T (RAF1) | XP_016862455.1:p.Pro590= | |
| NM_001354689.3:c.1929A>T (RAF1) | NP_001341618.1:p.Pro643= | |
| NM_001354690.2:c.1869A>T (RAF1) | NP_001341619.1:p.Pro623= | |
| NM_001354691.2:c.1626A>T (RAF1) | NP_001341620.1:p.Pro542= | |
| NM_001354692.2:c.1626A>T (RAF1) | NP_001341621.1:p.Pro542= | |
| NM_001354693.2:c.1770A>T (RAF1) | NP_001341622.1:p.Pro590= | |
| NM_001354694.2:c.1686A>T (RAF1) | NP_001341623.1:p.Pro562= | |
| NM_001354695.2:c.1527A>T (RAF1) | NP_001341624.1:p.Pro509= | |
| NR_148940.2:n.2313A>T (RAF1) | ||
| NR_148941.2:n.2259A>T (RAF1) | ||
| NR_148942.2:n.2198A>T (RAF1) | ||
| NM_001354690.3:c.1869A>T (RAF1) | NP_001341619.1:p.Pro623= | |
| NM_001354691.3:c.1626A>T (RAF1) | NP_001341620.1:p.Pro542= | |
| NM_001354692.3:c.1626A>T (RAF1) | NP_001341621.1:p.Pro542= | |
| NM_001354693.3:c.1770A>T (RAF1) | NP_001341622.1:p.Pro590= | |
| NM_001354694.3:c.1686A>T (RAF1) | NP_001341623.1:p.Pro562= | |
| NM_001354695.3:c.1527A>T (RAF1) | NP_001341624.1:p.Pro509= | |
| NM_002880.4:c.1869A>T (RAF1) MANE Select | NP_002871.1:p.Pro623= | |
| NR_148940.3:n.2313A>T (RAF1) | ||
| NR_148941.3:n.2259A>T (RAF1) | ||
| NR_148942.3:n.2198A>T (RAF1) |