Canonical Allele Identifier: CA351501620
Gene: RAF1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12590799C>G , CM000665.2:g.12590799C>G GRCh38
NC_000003.11:g.12632298C>G , CM000665.1:g.12632298C>G GRCh37
NC_000003.10:g.12607298C>G NCBI36
NG_007467.1:g.78381G>C , LRG_413:g.78381G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000423275.6:c.*1034G>C ENSP00000401088.1:n.*1034G>C
ENST00000432427.3:c.686G>C
ENST00000460610.2:n.163G>C
ENST00000465826.6:n.960G>C
ENST00000475353.2:n.1291G>C
ENST00000494557.2:n.1180G>C
ENST00000684903.1:c.*1046G>C ENSP00000508612.1:n.*1046G>C
ENST00000685348.1:c.*1046G>C ENSP00000510285.1:n.*1046G>C
ENST00000685437.1:c.1270G>C ENSP00000508794.1:p.Asp424His
ENST00000685653.1:c.1369G>C ENSP00000509968.1:p.Asp457His
ENST00000685738.1:c.*333G>C ENSP00000510156.1:n.*333G>C
ENST00000686409.1:n.2420G>C
ENST00000686455.1:n.1732G>C
ENST00000686762.1:c.1369G>C ENSP00000509767.1:p.Asp457His
ENST00000687257.1:n.1605G>C
ENST00000687326.1:c.*303G>C ENSP00000509665.1:n.*303G>C
ENST00000687505.1:n.1487G>C
ENST00000687923.1:c.1258G>C ENSP00000510255.1:p.Asp420His
ENST00000687940.1:n.1746G>C
ENST00000688269.1:n.1965G>C
ENST00000688326.1:c.802G>C
ENST00000688444.1:n.1695G>C
ENST00000688543.1:c.1270G>C ENSP00000509612.1:p.Asp424His
ENST00000688625.1:c.*947G>C ENSP00000509522.1:n.*947G>C
ENST00000688803.1:n.1600G>C
ENST00000688914.1:n.355G>C
ENST00000689097.1:c.*1046G>C ENSP00000509756.1:n.*1046G>C
ENST00000689389.1:c.1193+909G>C ENSP00000510213.1:n.1193+909G>C
ENST00000689418.1:c.*1046G>C ENSP00000509467.1:n.*1046G>C
ENST00000689481.1:c.*1046G>C ENSP00000510248.1:n.*1046G>C
ENST00000689540.1:n.1519G>C
ENST00000689876.1:c.1369G>C ENSP00000508535.1:p.Asp457His
ENST00000689914.1:c.*303G>C ENSP00000509847.1:n.*303G>C
ENST00000690397.1:c.1258G>C ENSP00000508730.1:p.Asp420His
ENST00000690460.1:c.1357G>C ENSP00000509106.1:p.Asp453His
ENST00000690585.1:c.261G>C
ENST00000690625.1:n.2405G>C
ENST00000691396.1:c.*1221G>C ENSP00000510712.1:n.*1221G>C
ENST00000691724.1:c.*326G>C ENSP00000509255.1:n.*326G>C
ENST00000691779.1:c.*947G>C ENSP00000508592.1:n.*947G>C
ENST00000691888.1:c.261G>C
ENST00000691899.1:c.1369G>C ENSP00000508763.1:p.Asp457His
ENST00000692069.1:n.1935G>C
ENST00000692093.1:c.1270G>C ENSP00000509669.1:p.Asp424His
ENST00000692311.1:n.2193G>C
ENST00000692558.1:n.1734G>C
ENST00000692773.1:c.*1106G>C ENSP00000509055.1:n.*1106G>C
ENST00000692830.1:c.*1114G>C ENSP00000509461.1:n.*1114G>C
ENST00000693069.1:c.*303G>C ENSP00000510072.1:n.*303G>C
ENST00000693312.1:c.1144G>C ENSP00000508686.1:p.Asp382His
ENST00000693664.1:c.1369G>C ENSP00000509614.1:p.Asp457His
ENST00000693705.1:c.*1046G>C ENSP00000510697.1:n.*1046G>C
ENST00000251849.9:c.1369G>C MANE Select ENSP00000251849.4:p.Asp457His
ENST00000442415.7:c.1429G>C ENSP00000401888.2:p.Asp477His
ENST00000251849.8:c.1369G>C ENSP00000251849.4:p.Asp457His
ENST00000423275.5:c.*1046G>C ENSP00000401088.1:n.*1046G>C
ENST00000432427.2:c.1006G>C ENSP00000398591.2:p.Asp336His
ENST00000442415.6:c.1429G>C ENSP00000401888.2:p.Asp477His
ENST00000460610.1:n.326G>C
ENST00000465826.5:n.726G>C
ENST00000475353.1:n.537G>C
ENST00000494557.1:n.385G>C
NM_002880.3:c.1369G>C , LRG_413t1:c.1369G>C NP_002871.1:p.Asp457His
XM_005265355.1:c.1369G>C XP_005265412.1:p.Asp457His
XM_005265357.1:c.1270G>C XP_005265414.1:p.Asp424His
XM_005265358.3:c.1126G>C XP_005265415.1:p.Asp376His
XM_005265359.3:c.1027G>C XP_005265416.1:p.Asp343His
XM_005265360.1:c.1369G>C XP_005265417.1:p.Asp457His
XM_011533974.1:c.1369G>C XP_011532276.1:p.Asp457His
XM_011533975.1:c.1126G>C XP_011532277.1:p.Asp376His
NM_001354689.1:c.1429G>C NP_001341618.1:p.Asp477His
NM_001354690.1:c.1369G>C NP_001341619.1:p.Asp457His
NM_001354691.1:c.1126G>C NP_001341620.1:p.Asp376His
NM_001354692.1:c.1126G>C NP_001341621.1:p.Asp376His
NM_001354693.1:c.1270G>C NP_001341622.1:p.Asp424His
NM_001354694.1:c.1186G>C NP_001341623.1:p.Asp396His
NM_001354695.1:c.1027G>C NP_001341624.1:p.Asp343His
NR_148940.1:n.1897G>C
NR_148941.1:n.1843G>C
NR_148942.1:n.1782G>C
XM_011533974.3:c.1369G>C XP_011532276.1:p.Asp457His
XM_017006966.1:c.1270G>C XP_016862455.1:p.Asp424His
NM_001354689.3:c.1429G>C NP_001341618.1:p.Asp477His
NM_001354690.2:c.1369G>C NP_001341619.1:p.Asp457His
NM_001354691.2:c.1126G>C NP_001341620.1:p.Asp376His
NM_001354692.2:c.1126G>C NP_001341621.1:p.Asp376His
NM_001354693.2:c.1270G>C NP_001341622.1:p.Asp424His
NM_001354694.2:c.1186G>C NP_001341623.1:p.Asp396His
NM_001354695.2:c.1027G>C NP_001341624.1:p.Asp343His
NR_148940.2:n.1813G>C
NR_148941.2:n.1759G>C
NR_148942.2:n.1698G>C
NM_001354690.3:c.1369G>C NP_001341619.1:p.Asp457His
NM_001354691.3:c.1126G>C NP_001341620.1:p.Asp376His
NM_001354692.3:c.1126G>C NP_001341621.1:p.Asp376His
NM_001354693.3:c.1270G>C NP_001341622.1:p.Asp424His
NM_001354694.3:c.1186G>C NP_001341623.1:p.Asp396His
NM_001354695.3:c.1027G>C NP_001341624.1:p.Asp343His
NM_002880.4:c.1369G>C MANE Select NP_002871.1:p.Asp457His
NR_148940.3:n.1813G>C
NR_148941.3:n.1759G>C
NR_148942.3:n.1698G>C