Linked Data
ClinVar Variation Id:
2740298
ClinVar RCV Id:
RCV003540195
MyVariant Identifiers:
chr3:g.12626385A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.12584886A>G , CM000665.2:g.12584886A>G | GRCh38 |
| NC_000003.11:g.12626385A>G , CM000665.1:g.12626385A>G | GRCh37 |
| NC_000003.10:g.12601385A>G | NCBI36 |
| NG_007467.1:g.84294T>C , LRG_413:g.84294T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000423275.6:c.*1429T>C (RAF1) | ENSP00000401088.1:n.*1429T>C | |
| ENST00000432427.3:c.1081T>C (RAF1) | ||
| ENST00000460610.2:n.6076T>C (RAF1) | ||
| ENST00000471449.2:n.574T>C (RAF1) | ||
| ENST00000475353.2:n.4044T>C (RAF1) | ||
| ENST00000684903.1:c.*1441T>C (RAF1) | ENSP00000508612.1:n.*1441T>C | |
| ENST00000685348.1:c.*1475T>C (RAF1) | ENSP00000510285.1:n.*1475T>C | |
| ENST00000685437.1:c.1665T>C (RAF1) | ENSP00000508794.1:p.Cys555= | |
| ENST00000685653.1:c.1764T>C (RAF1) | ENSP00000509968.1:p.Cys588= | |
| ENST00000685697.1:n.2499T>C (RAF1) | ||
| ENST00000685738.1:c.*728T>C (RAF1) | ENSP00000510156.1:n.*728T>C | |
| ENST00000686409.1:n.5173T>C (RAF1) | ||
| ENST00000686455.1:n.4485T>C (RAF1) | ||
| ENST00000686762.1:c.*323T>C (RAF1) | ENSP00000509767.1:n.*323T>C | |
| ENST00000687257.1:n.4218T>C (RAF1) | ||
| ENST00000687326.1:c.*3056T>C (RAF1) | ENSP00000509665.1:n.*3056T>C | |
| ENST00000687505.1:n.1882T>C (RAF1) | ||
| ENST00000687923.1:c.1653T>C (RAF1) | ENSP00000510255.1:p.Cys551= | |
| ENST00000688269.1:n.2360T>C (RAF1) | ||
| ENST00000688444.1:n.3881T>C (RAF1) | ||
| ENST00000688543.1:c.1665T>C (RAF1) | ENSP00000509612.1:p.Cys555= | |
| ENST00000688625.1:c.*3133T>C (RAF1) | ENSP00000509522.1:n.*3133T>C | |
| ENST00000688803.1:n.3192T>C (RAF1) | ||
| ENST00000689097.1:c.*1441T>C (RAF1) | ENSP00000509756.1:n.*1441T>C | |
| ENST00000689389.1:c.1587T>C (RAF1) | ENSP00000510213.1:p.Cys529= | |
| ENST00000689418.1:c.*3659T>C (RAF1) | ENSP00000509467.1:n.*3659T>C | |
| ENST00000689540.1:n.4132T>C (RAF1) | ||
| ENST00000689876.1:c.*313T>C (RAF1) | ENSP00000508535.1:n.*313T>C | |
| ENST00000689914.1:c.*698T>C (RAF1) | ENSP00000509847.1:n.*698T>C | |
| ENST00000690397.1:c.1653T>C (RAF1) | ENSP00000508730.1:p.Cys551= | |
| ENST00000690460.1:c.1752T>C (RAF1) | ENSP00000509106.1:p.Cys584= | |
| ENST00000690585.1:c.490T>C (RAF1) | ||
| ENST00000690625.1:n.2800T>C (RAF1) | ||
| ENST00000691396.1:c.*1636T>C (RAF1) | ENSP00000510712.1:n.*1636T>C | |
| ENST00000691643.1:n.2817T>C (RAF1) | ||
| ENST00000691724.1:c.*721T>C (RAF1) | ENSP00000509255.1:n.*721T>C | |
| ENST00000691779.1:c.*1342T>C (RAF1) | ENSP00000508592.1:n.*1342T>C | |
| ENST00000691888.1:c.638T>C (RAF1) | ||
| ENST00000691899.1:c.1764T>C (RAF1) | ENSP00000508763.1:p.Cys588= | |
| ENST00000692069.1:n.4688T>C (RAF1) | ||
| ENST00000692093.1:c.1665T>C (RAF1) | ENSP00000509669.1:p.Cys555= | |
| ENST00000692311.1:n.2588T>C (RAF1) | ||
| ENST00000692558.1:n.4347T>C (RAF1) | ||
| ENST00000692773.1:c.*1501T>C (RAF1) | ENSP00000509055.1:n.*1501T>C | |
| ENST00000692830.1:c.*1509T>C (RAF1) | ENSP00000509461.1:n.*1509T>C | |
| ENST00000693312.1:c.1539T>C (RAF1) | ENSP00000508686.1:p.Cys513= | |
| ENST00000693664.1:c.*215T>C (RAF1) | ENSP00000509614.1:n.*215T>C | |
| ENST00000693705.1:c.*1143T>C (RAF1) | ENSP00000510697.1:n.*1143T>C | |
| ENST00000251849.9:c.1764T>C (RAF1) MANE Select | ENSP00000251849.4:p.Cys588= | |
| ENST00000442415.7:c.1824T>C (RAF1) | ENSP00000401888.2:p.Cys608= | |
| ENST00000676541.1:c.*2633A>G (MKRN2) | ENSP00000503730.1:n.*2633A>G | |
| ENST00000677142.1:c.*2633A>G (MKRN2) | ENSP00000504455.1:n.*2633A>G | |
| ENST00000677816.1:c.*1188A>G (MKRN2) | ENSP00000502893.1:n.*1188A>G | |
| ENST00000677941.1:n.2696A>G (MKRN2) | ||
| ENST00000251849.8:c.1764T>C (RAF1) | ENSP00000251849.4:p.Cys588= | |
| ENST00000423275.5:c.*1441T>C (RAF1) | ENSP00000401088.1:n.*1441T>C | |
| ENST00000432427.2:c.1401T>C (RAF1) | ENSP00000398591.2:p.Cys467= | |
| ENST00000442415.6:c.1824T>C (RAF1) | ENSP00000401888.2:p.Cys608= | |
| ENST00000471449.1:n.453T>C (RAF1) | ||
| NM_002880.3:c.1764T>C , LRG_413t1:c.1764T>C (RAF1) | NP_002871.1:p.Cys588= | |
| XM_005265355.1:c.1764T>C (RAF1) | XP_005265412.1:p.Cys588= | |
| XM_005265357.1:c.1665T>C (RAF1) | XP_005265414.1:p.Cys555= | |
| XM_005265358.3:c.1521T>C (RAF1) | XP_005265415.1:p.Cys507= | |
| XM_005265359.3:c.1422T>C (RAF1) | XP_005265416.1:p.Cys474= | |
| XM_011533974.1:c.1764T>C (RAF1) | XP_011532276.1:p.Cys588= | |
| XM_011533975.1:c.1521T>C (RAF1) | XP_011532277.1:p.Cys507= | |
| NM_001354689.1:c.1824T>C (RAF1) | NP_001341618.1:p.Cys608= | |
| NM_001354690.1:c.1764T>C (RAF1) | NP_001341619.1:p.Cys588= | |
| NM_001354691.1:c.1521T>C (RAF1) | NP_001341620.1:p.Cys507= | |
| NM_001354692.1:c.1521T>C (RAF1) | NP_001341621.1:p.Cys507= | |
| NM_001354693.1:c.1665T>C (RAF1) | NP_001341622.1:p.Cys555= | |
| NM_001354694.1:c.1581T>C (RAF1) | NP_001341623.1:p.Cys527= | |
| NM_001354695.1:c.1422T>C (RAF1) | NP_001341624.1:p.Cys474= | |
| NR_148940.1:n.2292T>C (RAF1) | ||
| NR_148941.1:n.2238T>C (RAF1) | ||
| NR_148942.1:n.2177T>C (RAF1) | ||
| XM_011533974.3:c.1764T>C (RAF1) | XP_011532276.1:p.Cys588= | |
| XM_017006966.1:c.1665T>C (RAF1) | XP_016862455.1:p.Cys555= | |
| NM_001354689.3:c.1824T>C (RAF1) | NP_001341618.1:p.Cys608= | |
| NM_001354690.2:c.1764T>C (RAF1) | NP_001341619.1:p.Cys588= | |
| NM_001354691.2:c.1521T>C (RAF1) | NP_001341620.1:p.Cys507= | |
| NM_001354692.2:c.1521T>C (RAF1) | NP_001341621.1:p.Cys507= | |
| NM_001354693.2:c.1665T>C (RAF1) | NP_001341622.1:p.Cys555= | |
| NM_001354694.2:c.1581T>C (RAF1) | NP_001341623.1:p.Cys527= | |
| NM_001354695.2:c.1422T>C (RAF1) | NP_001341624.1:p.Cys474= | |
| NR_148940.2:n.2208T>C (RAF1) | ||
| NR_148941.2:n.2154T>C (RAF1) | ||
| NR_148942.2:n.2093T>C (RAF1) | ||
| NM_001354690.3:c.1764T>C (RAF1) | NP_001341619.1:p.Cys588= | |
| NM_001354691.3:c.1521T>C (RAF1) | NP_001341620.1:p.Cys507= | |
| NM_001354692.3:c.1521T>C (RAF1) | NP_001341621.1:p.Cys507= | |
| NM_001354693.3:c.1665T>C (RAF1) | NP_001341622.1:p.Cys555= | |
| NM_001354694.3:c.1581T>C (RAF1) | NP_001341623.1:p.Cys527= | |
| NM_001354695.3:c.1422T>C (RAF1) | NP_001341624.1:p.Cys474= | |
| NM_002880.4:c.1764T>C (RAF1) MANE Select | NP_002871.1:p.Cys588= | |
| NR_148940.3:n.2208T>C (RAF1) | ||
| NR_148941.3:n.2154T>C (RAF1) | ||
| NR_148942.3:n.2093T>C (RAF1) |