Linked Data
dbSNP Id:
rs1187873982
gnomAD v2:
3-12625838-C-CA
gnomAD v3:
3-12584339-C-CA
gnomAD v4:
3-12584339-C-CA
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.12584342dup , CM000665.2:g.12584342dup | GRCh38 |
| NC_000003.11:g.12625841dup , CM000665.1:g.12625841dup | GRCh37 |
| NC_000003.10:g.12600841dup | NCBI36 |
| NG_007467.1:g.84840dup , LRG_413:g.84840dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000423275.6:c.*1786dup (RAF1) | ENSP00000401088.1:n.*1786dup | |
| ENST00000432427.3:c.1438dup (RAF1) | ||
| ENST00000460610.2:n.6433dup (RAF1) | ||
| ENST00000471449.2:n.931dup (RAF1) | ||
| ENST00000475353.2:n.4401dup (RAF1) | ||
| ENST00000684903.1:c.*1798dup (RAF1) | ENSP00000508612.1:n.*1798dup | |
| ENST00000685348.1:c.*1832dup (RAF1) | ENSP00000510285.1:n.*1832dup | |
| ENST00000685437.1:c.*174dup (RAF1) | ENSP00000508794.1:n.*174dup | |
| ENST00000685653.1:c.*174dup (RAF1) | ENSP00000509968.1:n.*174dup | |
| ENST00000685697.1:n.2856dup (RAF1) | ||
| ENST00000685738.1:c.*1085dup (RAF1) | ENSP00000510156.1:n.*1085dup | |
| ENST00000686409.1:n.5530dup (RAF1) | ||
| ENST00000686455.1:n.4842dup (RAF1) | ||
| ENST00000686762.1:c.*680dup (RAF1) | ENSP00000509767.1:n.*680dup | |
| ENST00000687257.1:n.4575dup (RAF1) | ||
| ENST00000687326.1:c.*3413dup (RAF1) | ENSP00000509665.1:n.*3413dup | |
| ENST00000687505.1:n.2239dup (RAF1) | ||
| ENST00000687923.1:c.*174dup (RAF1) | ENSP00000510255.1:n.*174dup | |
| ENST00000688269.1:n.2717dup (RAF1) | ||
| ENST00000688444.1:n.4238dup (RAF1) | ||
| ENST00000688543.1:c.*174dup (RAF1) | ENSP00000509612.1:n.*174dup | |
| ENST00000688625.1:c.*3490dup (RAF1) | ENSP00000509522.1:n.*3490dup | |
| ENST00000688803.1:n.3549dup (RAF1) | ||
| ENST00000689097.1:c.*1798dup (RAF1) | ENSP00000509756.1:n.*1798dup | |
| ENST00000689389.1:c.*174dup (RAF1) | ENSP00000510213.1:n.*174dup | |
| ENST00000689418.1:c.*4016dup (RAF1) | ENSP00000509467.1:n.*4016dup | |
| ENST00000689540.1:n.4489dup (RAF1) | ||
| ENST00000689876.1:c.*670dup (RAF1) | ENSP00000508535.1:n.*670dup | |
| ENST00000689914.1:c.*1055dup (RAF1) | ENSP00000509847.1:n.*1055dup | |
| ENST00000690397.1:c.*174dup (RAF1) | ENSP00000508730.1:n.*174dup | |
| ENST00000690460.1:c.*174dup (RAF1) | ENSP00000509106.1:n.*174dup | |
| ENST00000690585.1:c.847dup (RAF1) | ||
| ENST00000690625.1:n.3157dup (RAF1) | ||
| ENST00000691396.1:c.*1993dup (RAF1) | ENSP00000510712.1:n.*1993dup | |
| ENST00000691643.1:n.3174dup (RAF1) | ||
| ENST00000691724.1:c.*1078dup (RAF1) | ENSP00000509255.1:n.*1078dup | |
| ENST00000691779.1:c.*1699dup (RAF1) | ENSP00000508592.1:n.*1699dup | |
| ENST00000691888.1:c.995dup (RAF1) | ||
| ENST00000691899.1:c.*174dup (RAF1) | ENSP00000508763.1:n.*174dup | |
| ENST00000692069.1:n.5045dup (RAF1) | ||
| ENST00000692093.1:c.*174dup (RAF1) | ENSP00000509669.1:n.*174dup | |
| ENST00000692311.1:n.2945dup (RAF1) | ||
| ENST00000692558.1:n.4704dup (RAF1) | ||
| ENST00000692773.1:c.*1858dup (RAF1) | ENSP00000509055.1:n.*1858dup | |
| ENST00000692830.1:c.*1866dup (RAF1) | ENSP00000509461.1:n.*1866dup | |
| ENST00000693312.1:c.*174dup (RAF1) | ENSP00000508686.1:n.*174dup | |
| ENST00000693664.1:c.*572dup (RAF1) | ENSP00000509614.1:n.*572dup | |
| ENST00000693705.1:c.*1500dup (RAF1) | ENSP00000510697.1:n.*1500dup | |
| ENST00000251849.9:c.*174dup (RAF1) MANE Select | ENSP00000251849.4:n.*174dup | |
| ENST00000442415.7:c.*174dup (RAF1) | ENSP00000401888.2:n.*174dup | |
| ENST00000676541.1:c.*2089dup (MKRN2) | ENSP00000503730.1:n.*2089dup | |
| ENST00000677142.1:c.*2089dup (MKRN2) | ENSP00000504455.1:n.*2089dup | |
| ENST00000677816.1:c.*644dup (MKRN2) | ENSP00000502893.1:n.*644dup | |
| ENST00000677941.1:n.2152dup (MKRN2) | ||
| ENST00000251849.8:c.*174dup (RAF1) | ENSP00000251849.4:n.*174dup | |
| ENST00000423275.5:c.*1798dup (RAF1) | ENSP00000401088.1:n.*1798dup | |
| ENST00000432427.2:c.1758dup (RAF1) | ENSP00000398591.2:n.1758dup | |
| ENST00000442415.6:c.*174dup (RAF1) | ENSP00000401888.2:n.*174dup | |
| NM_002880.3:c.*174dup , LRG_413t1:c.*174dup (RAF1) | NP_002871.1:n.*174dup | |
| XM_005265355.1:c.*174dup (RAF1) | XP_005265412.1:n.*174dup | |
| XM_005265357.1:c.*174dup (RAF1) | XP_005265414.1:n.*174dup | |
| XM_005265358.3:c.*174dup (RAF1) | XP_005265415.1:n.*174dup | |
| XM_005265359.3:c.*174dup (RAF1) | XP_005265416.1:n.*174dup | |
| XM_011533974.1:c.*174dup (RAF1) | XP_011532276.1:n.*174dup | |
| XM_011533975.1:c.*174dup (RAF1) | XP_011532277.1:n.*174dup | |
| NM_001354689.1:c.*174dup (RAF1) | NP_001341618.1:n.*174dup | |
| NM_001354690.1:c.*174dup (RAF1) | NP_001341619.1:n.*174dup | |
| NM_001354691.1:c.*174dup (RAF1) | NP_001341620.1:n.*174dup | |
| NM_001354692.1:c.*174dup (RAF1) | NP_001341621.1:n.*174dup | |
| NM_001354693.1:c.*174dup (RAF1) | NP_001341622.1:n.*174dup | |
| NM_001354694.1:c.*174dup (RAF1) | NP_001341623.1:n.*174dup | |
| NM_001354695.1:c.*174dup (RAF1) | NP_001341624.1:n.*174dup | |
| NR_148940.1:n.2649dup (RAF1) | ||
| NR_148941.1:n.2595dup (RAF1) | ||
| NR_148942.1:n.2534dup (RAF1) | ||
| XM_011533974.3:c.*174dup (RAF1) | XP_011532276.1:n.*174dup | |
| XM_017006966.1:c.*174dup (RAF1) | XP_016862455.1:n.*174dup | |
| NM_001354689.3:c.*174dup (RAF1) | NP_001341618.1:n.*174dup | |
| NM_001354690.2:c.*174dup (RAF1) | NP_001341619.1:n.*174dup | |
| NM_001354691.2:c.*174dup (RAF1) | NP_001341620.1:n.*174dup | |
| NM_001354692.2:c.*174dup (RAF1) | NP_001341621.1:n.*174dup | |
| NM_001354693.2:c.*174dup (RAF1) | NP_001341622.1:n.*174dup | |
| NM_001354694.2:c.*174dup (RAF1) | NP_001341623.1:n.*174dup | |
| NM_001354695.2:c.*174dup (RAF1) | NP_001341624.1:n.*174dup | |
| NR_148940.2:n.2565dup (RAF1) | ||
| NR_148941.2:n.2511dup (RAF1) | ||
| NR_148942.2:n.2450dup (RAF1) | ||
| NM_001354690.3:c.*174dup (RAF1) | NP_001341619.1:n.*174dup | |
| NM_001354691.3:c.*174dup (RAF1) | NP_001341620.1:n.*174dup | |
| NM_001354692.3:c.*174dup (RAF1) | NP_001341621.1:n.*174dup | |
| NM_001354693.3:c.*174dup (RAF1) | NP_001341622.1:n.*174dup | |
| NM_001354694.3:c.*174dup (RAF1) | NP_001341623.1:n.*174dup | |
| NM_001354695.3:c.*174dup (RAF1) | NP_001341624.1:n.*174dup | |
| NM_002880.4:c.*174dup (RAF1) MANE Select | NP_002871.1:n.*174dup | |
| NR_148940.3:n.2565dup (RAF1) | ||
| NR_148941.3:n.2511dup (RAF1) | ||
| NR_148942.3:n.2450dup (RAF1) |