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
MyVariant Identifiers:
chr3:g.12626445T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.12584946T>A , CM000665.2:g.12584946T>A | GRCh38 |
| NC_000003.11:g.12626445T>A , CM000665.1:g.12626445T>A | GRCh37 |
| NC_000003.10:g.12601445T>A | NCBI36 |
| NG_007467.1:g.84234A>T , LRG_413:g.84234A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000423275.6:c.*1369A>T (RAF1) | ENSP00000401088.1:n.*1369A>T | |
| ENST00000432427.3:c.1021A>T (RAF1) | ||
| ENST00000460610.2:n.6016A>T (RAF1) | ||
| ENST00000471449.2:n.514A>T (RAF1) | ||
| ENST00000475353.2:n.3984A>T (RAF1) | ||
| ENST00000684903.1:c.*1381A>T (RAF1) | ENSP00000508612.1:n.*1381A>T | |
| ENST00000685348.1:c.*1415A>T (RAF1) | ENSP00000510285.1:n.*1415A>T | |
| ENST00000685437.1:c.1605A>T (RAF1) | ENSP00000508794.1:p.Pro535= | |
| ENST00000685653.1:c.1704A>T (RAF1) | ENSP00000509968.1:p.Pro568= | |
| ENST00000685697.1:n.2439A>T (RAF1) | ||
| ENST00000685738.1:c.*668A>T (RAF1) | ENSP00000510156.1:n.*668A>T | |
| ENST00000686409.1:n.5113A>T (RAF1) | ||
| ENST00000686455.1:n.4425A>T (RAF1) | ||
| ENST00000686762.1:c.*263A>T (RAF1) | ENSP00000509767.1:n.*263A>T | |
| ENST00000687257.1:n.4158A>T (RAF1) | ||
| ENST00000687326.1:c.*2996A>T (RAF1) | ENSP00000509665.1:n.*2996A>T | |
| ENST00000687505.1:n.1822A>T (RAF1) | ||
| ENST00000687923.1:c.1593A>T (RAF1) | ENSP00000510255.1:p.Pro531= | |
| ENST00000688269.1:n.2300A>T (RAF1) | ||
| ENST00000688444.1:n.3821A>T (RAF1) | ||
| ENST00000688543.1:c.1605A>T (RAF1) | ENSP00000509612.1:p.Pro535= | |
| ENST00000688625.1:c.*3073A>T (RAF1) | ENSP00000509522.1:n.*3073A>T | |
| ENST00000688803.1:n.3132A>T (RAF1) | ||
| ENST00000688914.1:n.1117A>T (RAF1) | ||
| ENST00000689097.1:c.*1381A>T (RAF1) | ENSP00000509756.1:n.*1381A>T | |
| ENST00000689389.1:c.1527A>T (RAF1) | ENSP00000510213.1:p.Pro509= | |
| ENST00000689418.1:c.*3599A>T (RAF1) | ENSP00000509467.1:n.*3599A>T | |
| ENST00000689540.1:n.4072A>T (RAF1) | ||
| ENST00000689876.1:c.*253A>T (RAF1) | ENSP00000508535.1:n.*253A>T | |
| ENST00000689914.1:c.*638A>T (RAF1) | ENSP00000509847.1:n.*638A>T | |
| ENST00000690397.1:c.1593A>T (RAF1) | ENSP00000508730.1:p.Pro531= | |
| ENST00000690460.1:c.1692A>T (RAF1) | ENSP00000509106.1:p.Pro564= | |
| ENST00000690585.1:c.430A>T (RAF1) | ||
| ENST00000690625.1:n.2740A>T (RAF1) | ||
| ENST00000691396.1:c.*1576A>T (RAF1) | ENSP00000510712.1:n.*1576A>T | |
| ENST00000691643.1:n.2757A>T (RAF1) | ||
| ENST00000691724.1:c.*661A>T (RAF1) | ENSP00000509255.1:n.*661A>T | |
| ENST00000691779.1:c.*1282A>T (RAF1) | ENSP00000508592.1:n.*1282A>T | |
| ENST00000691888.1:c.578A>T (RAF1) | ||
| ENST00000691899.1:c.1704A>T (RAF1) | ENSP00000508763.1:p.Pro568= | |
| ENST00000692069.1:n.4628A>T (RAF1) | ||
| ENST00000692093.1:c.1605A>T (RAF1) | ENSP00000509669.1:p.Pro535= | |
| ENST00000692311.1:n.2528A>T (RAF1) | ||
| ENST00000692558.1:n.4287A>T (RAF1) | ||
| ENST00000692773.1:c.*1441A>T (RAF1) | ENSP00000509055.1:n.*1441A>T | |
| ENST00000692830.1:c.*1449A>T (RAF1) | ENSP00000509461.1:n.*1449A>T | |
| ENST00000693312.1:c.1479A>T (RAF1) | ENSP00000508686.1:p.Pro493= | |
| ENST00000693664.1:c.*155A>T (RAF1) | ENSP00000509614.1:n.*155A>T | |
| ENST00000693705.1:c.*1083A>T (RAF1) | ENSP00000510697.1:n.*1083A>T | |
| ENST00000251849.9:c.1704A>T (RAF1) MANE Select | ENSP00000251849.4:p.Pro568= | |
| ENST00000442415.7:c.1764A>T (RAF1) | ENSP00000401888.2:p.Pro588= | |
| ENST00000676541.1:c.*2693T>A (MKRN2) | ENSP00000503730.1:n.*2693T>A | |
| ENST00000677142.1:c.*2693T>A (MKRN2) | ENSP00000504455.1:n.*2693T>A | |
| ENST00000677816.1:c.*1248T>A (MKRN2) | ENSP00000502893.1:n.*1248T>A | |
| ENST00000677941.1:n.2756T>A (MKRN2) | ||
| ENST00000251849.8:c.1704A>T (RAF1) | ENSP00000251849.4:p.Pro568= | |
| ENST00000423275.5:c.*1381A>T (RAF1) | ENSP00000401088.1:n.*1381A>T | |
| ENST00000432427.2:c.1341A>T (RAF1) | ENSP00000398591.2:p.Pro447= | |
| ENST00000442415.6:c.1764A>T (RAF1) | ENSP00000401888.2:p.Pro588= | |
| ENST00000471449.1:n.393A>T (RAF1) | ||
| NM_002880.3:c.1704A>T , LRG_413t1:c.1704A>T (RAF1) | NP_002871.1:p.Pro568= | |
| XM_005265355.1:c.1704A>T (RAF1) | XP_005265412.1:p.Pro568= | |
| XM_005265357.1:c.1605A>T (RAF1) | XP_005265414.1:p.Pro535= | |
| XM_005265358.3:c.1461A>T (RAF1) | XP_005265415.1:p.Pro487= | |
| XM_005265359.3:c.1362A>T (RAF1) | XP_005265416.1:p.Pro454= | |
| XM_011533974.1:c.1704A>T (RAF1) | XP_011532276.1:p.Pro568= | |
| XM_011533975.1:c.1461A>T (RAF1) | XP_011532277.1:p.Pro487= | |
| NM_001354689.1:c.1764A>T (RAF1) | NP_001341618.1:p.Pro588= | |
| NM_001354690.1:c.1704A>T (RAF1) | NP_001341619.1:p.Pro568= | |
| NM_001354691.1:c.1461A>T (RAF1) | NP_001341620.1:p.Pro487= | |
| NM_001354692.1:c.1461A>T (RAF1) | NP_001341621.1:p.Pro487= | |
| NM_001354693.1:c.1605A>T (RAF1) | NP_001341622.1:p.Pro535= | |
| NM_001354694.1:c.1521A>T (RAF1) | NP_001341623.1:p.Pro507= | |
| NM_001354695.1:c.1362A>T (RAF1) | NP_001341624.1:p.Pro454= | |
| NR_148940.1:n.2232A>T (RAF1) | ||
| NR_148941.1:n.2178A>T (RAF1) | ||
| NR_148942.1:n.2117A>T (RAF1) | ||
| XM_011533974.3:c.1704A>T (RAF1) | XP_011532276.1:p.Pro568= | |
| XM_017006966.1:c.1605A>T (RAF1) | XP_016862455.1:p.Pro535= | |
| NM_001354689.3:c.1764A>T (RAF1) | NP_001341618.1:p.Pro588= | |
| NM_001354690.2:c.1704A>T (RAF1) | NP_001341619.1:p.Pro568= | |
| NM_001354691.2:c.1461A>T (RAF1) | NP_001341620.1:p.Pro487= | |
| NM_001354692.2:c.1461A>T (RAF1) | NP_001341621.1:p.Pro487= | |
| NM_001354693.2:c.1605A>T (RAF1) | NP_001341622.1:p.Pro535= | |
| NM_001354694.2:c.1521A>T (RAF1) | NP_001341623.1:p.Pro507= | |
| NM_001354695.2:c.1362A>T (RAF1) | NP_001341624.1:p.Pro454= | |
| NR_148940.2:n.2148A>T (RAF1) | ||
| NR_148941.2:n.2094A>T (RAF1) | ||
| NR_148942.2:n.2033A>T (RAF1) | ||
| NM_001354690.3:c.1704A>T (RAF1) | NP_001341619.1:p.Pro568= | |
| NM_001354691.3:c.1461A>T (RAF1) | NP_001341620.1:p.Pro487= | |
| NM_001354692.3:c.1461A>T (RAF1) | NP_001341621.1:p.Pro487= | |
| NM_001354693.3:c.1605A>T (RAF1) | NP_001341622.1:p.Pro535= | |
| NM_001354694.3:c.1521A>T (RAF1) | NP_001341623.1:p.Pro507= | |
| NM_001354695.3:c.1362A>T (RAF1) | NP_001341624.1:p.Pro454= | |
| NM_002880.4:c.1704A>T (RAF1) MANE Select | NP_002871.1:p.Pro568= | |
| NR_148940.3:n.2148A>T (RAF1) | ||
| NR_148941.3:n.2094A>T (RAF1) | ||
| NR_148942.3:n.2033A>T (RAF1) |