MyVariant.info:
GRCh37
chr3:g.12626030T>G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.12584531T>G , CM000665.2:g.12584531T>G | GRCh38 |
| NC_000003.11:g.12626030T>G , CM000665.1:g.12626030T>G | GRCh37 |
| NC_000003.10:g.12601030T>G | NCBI36 |
| NG_007467.1:g.84649A>C , LRG_413:g.84649A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000423275.6:c.*1595A>C (RAF1) | ENSP00000401088.1:n.*1595A>C | |
| ENST00000432427.3:c.1247A>C (RAF1) | ||
| ENST00000460610.2:n.6242A>C (RAF1) | ||
| ENST00000471449.2:n.740A>C (RAF1) | ||
| ENST00000475353.2:n.4210A>C (RAF1) | ||
| ENST00000684903.1:c.*1607A>C (RAF1) | ENSP00000508612.1:n.*1607A>C | |
| ENST00000685348.1:c.*1641A>C (RAF1) | ENSP00000510285.1:n.*1641A>C | |
| ENST00000685437.1:c.1831A>C (RAF1) | ENSP00000508794.1:p.Arg611= | |
| ENST00000685653.1:c.1930A>C (RAF1) | ENSP00000509968.1:p.Arg644= | |
| ENST00000685697.1:n.2665A>C (RAF1) | ||
| ENST00000685738.1:c.*894A>C (RAF1) | ENSP00000510156.1:n.*894A>C | |
| ENST00000686409.1:n.5339A>C (RAF1) | ||
| ENST00000686455.1:n.4651A>C (RAF1) | ||
| ENST00000686762.1:c.*489A>C (RAF1) | ENSP00000509767.1:n.*489A>C | |
| ENST00000687257.1:n.4384A>C (RAF1) | ||
| ENST00000687326.1:c.*3222A>C (RAF1) | ENSP00000509665.1:n.*3222A>C | |
| ENST00000687505.1:n.2048A>C (RAF1) | ||
| ENST00000687923.1:c.1819A>C (RAF1) | ENSP00000510255.1:p.Arg607= | |
| ENST00000688269.1:n.2526A>C (RAF1) | ||
| ENST00000688444.1:n.4047A>C (RAF1) | ||
| ENST00000688543.1:c.1831A>C (RAF1) | ENSP00000509612.1:p.Arg611= | |
| ENST00000688625.1:c.*3299A>C (RAF1) | ENSP00000509522.1:n.*3299A>C | |
| ENST00000688803.1:n.3358A>C (RAF1) | ||
| ENST00000689097.1:c.*1607A>C (RAF1) | ENSP00000509756.1:n.*1607A>C | |
| ENST00000689389.1:c.1753A>C (RAF1) | ENSP00000510213.1:p.Arg585= | |
| ENST00000689418.1:c.*3825A>C (RAF1) | ENSP00000509467.1:n.*3825A>C | |
| ENST00000689540.1:n.4298A>C (RAF1) | ||
| ENST00000689876.1:c.*479A>C (RAF1) | ENSP00000508535.1:n.*479A>C | |
| ENST00000689914.1:c.*864A>C (RAF1) | ENSP00000509847.1:n.*864A>C | |
| ENST00000690397.1:c.1819A>C (RAF1) | ENSP00000508730.1:p.Arg607= | |
| ENST00000690460.1:c.1918A>C (RAF1) | ENSP00000509106.1:p.Arg640= | |
| ENST00000690585.1:c.656A>C (RAF1) | ||
| ENST00000690625.1:n.2966A>C (RAF1) | ||
| ENST00000691396.1:c.*1802A>C (RAF1) | ENSP00000510712.1:n.*1802A>C | |
| ENST00000691643.1:n.2983A>C (RAF1) | ||
| ENST00000691724.1:c.*887A>C (RAF1) | ENSP00000509255.1:n.*887A>C | |
| ENST00000691779.1:c.*1508A>C (RAF1) | ENSP00000508592.1:n.*1508A>C | |
| ENST00000691888.1:c.804A>C (RAF1) | ||
| ENST00000691899.1:c.1930A>C (RAF1) | ENSP00000508763.1:p.Arg644= | |
| ENST00000692069.1:n.4854A>C (RAF1) | ||
| ENST00000692093.1:c.1831A>C (RAF1) | ENSP00000509669.1:p.Arg611= | |
| ENST00000692311.1:n.2754A>C (RAF1) | ||
| ENST00000692558.1:n.4513A>C (RAF1) | ||
| ENST00000692773.1:c.*1667A>C (RAF1) | ENSP00000509055.1:n.*1667A>C | |
| ENST00000692830.1:c.*1675A>C (RAF1) | ENSP00000509461.1:n.*1675A>C | |
| ENST00000693312.1:c.1705A>C (RAF1) | ENSP00000508686.1:p.Arg569= | |
| ENST00000693664.1:c.*381A>C (RAF1) | ENSP00000509614.1:n.*381A>C | |
| ENST00000693705.1:c.*1309A>C (RAF1) | ENSP00000510697.1:n.*1309A>C | |
| ENST00000251849.9:c.1930A>C (RAF1) MANE Select | ENSP00000251849.4:p.Arg644= | |
| ENST00000442415.7:c.1990A>C (RAF1) | ENSP00000401888.2:p.Arg664= | |
| ENST00000676541.1:c.*2278T>G (MKRN2) | ENSP00000503730.1:n.*2278T>G | |
| ENST00000677142.1:c.*2278T>G (MKRN2) | ENSP00000504455.1:n.*2278T>G | |
| ENST00000677816.1:c.*833T>G (MKRN2) | ENSP00000502893.1:n.*833T>G | |
| ENST00000677941.1:n.2341T>G (MKRN2) | ||
| ENST00000251849.8:c.1930A>C (RAF1) | ENSP00000251849.4:p.Arg644= | |
| ENST00000423275.5:c.*1607A>C (RAF1) | ENSP00000401088.1:n.*1607A>C | |
| ENST00000432427.2:c.1567A>C (RAF1) | ENSP00000398591.2:p.Arg523= | |
| ENST00000442415.6:c.1990A>C (RAF1) | ENSP00000401888.2:p.Arg664= | |
| ENST00000471449.1:n.619A>C (RAF1) | ||
| NM_002880.3:c.1930A>C , LRG_413t1:c.1930A>C (RAF1) | NP_002871.1:p.Arg644= | |
| XM_005265355.1:c.1930A>C (RAF1) | XP_005265412.1:p.Arg644= | |
| XM_005265357.1:c.1831A>C (RAF1) | XP_005265414.1:p.Arg611= | |
| XM_005265358.3:c.1687A>C (RAF1) | XP_005265415.1:p.Arg563= | |
| XM_005265359.3:c.1588A>C (RAF1) | XP_005265416.1:p.Arg530= | |
| XM_011533974.1:c.1930A>C (RAF1) | XP_011532276.1:p.Arg644= | |
| XM_011533975.1:c.1687A>C (RAF1) | XP_011532277.1:p.Arg563= | |
| NM_001354689.1:c.1990A>C (RAF1) | NP_001341618.1:p.Arg664= | |
| NM_001354690.1:c.1930A>C (RAF1) | NP_001341619.1:p.Arg644= | |
| NM_001354691.1:c.1687A>C (RAF1) | NP_001341620.1:p.Arg563= | |
| NM_001354692.1:c.1687A>C (RAF1) | NP_001341621.1:p.Arg563= | |
| NM_001354693.1:c.1831A>C (RAF1) | NP_001341622.1:p.Arg611= | |
| NM_001354694.1:c.1747A>C (RAF1) | NP_001341623.1:p.Arg583= | |
| NM_001354695.1:c.1588A>C (RAF1) | NP_001341624.1:p.Arg530= | |
| NR_148940.1:n.2458A>C (RAF1) | ||
| NR_148941.1:n.2404A>C (RAF1) | ||
| NR_148942.1:n.2343A>C (RAF1) | ||
| XM_011533974.3:c.1930A>C (RAF1) | XP_011532276.1:p.Arg644= | |
| XM_017006966.1:c.1831A>C (RAF1) | XP_016862455.1:p.Arg611= | |
| NM_001354689.3:c.1990A>C (RAF1) | NP_001341618.1:p.Arg664= | |
| NM_001354690.2:c.1930A>C (RAF1) | NP_001341619.1:p.Arg644= | |
| NM_001354691.2:c.1687A>C (RAF1) | NP_001341620.1:p.Arg563= | |
| NM_001354692.2:c.1687A>C (RAF1) | NP_001341621.1:p.Arg563= | |
| NM_001354693.2:c.1831A>C (RAF1) | NP_001341622.1:p.Arg611= | |
| NM_001354694.2:c.1747A>C (RAF1) | NP_001341623.1:p.Arg583= | |
| NM_001354695.2:c.1588A>C (RAF1) | NP_001341624.1:p.Arg530= | |
| NR_148940.2:n.2374A>C (RAF1) | ||
| NR_148941.2:n.2320A>C (RAF1) | ||
| NR_148942.2:n.2259A>C (RAF1) | ||
| NM_001354690.3:c.1930A>C (RAF1) | NP_001341619.1:p.Arg644= | |
| NM_001354691.3:c.1687A>C (RAF1) | NP_001341620.1:p.Arg563= | |
| NM_001354692.3:c.1687A>C (RAF1) | NP_001341621.1:p.Arg563= | |
| NM_001354693.3:c.1831A>C (RAF1) | NP_001341622.1:p.Arg611= | |
| NM_001354694.3:c.1747A>C (RAF1) | NP_001341623.1:p.Arg583= | |
| NM_001354695.3:c.1588A>C (RAF1) | NP_001341624.1:p.Arg530= | |
| NM_002880.4:c.1930A>C (RAF1) MANE Select | NP_002871.1:p.Arg644= | |
| NR_148940.3:n.2374A>C (RAF1) | ||
| NR_148941.3:n.2320A>C (RAF1) | ||
| NR_148942.3:n.2259A>C (RAF1) |