Canonical Allele Identifier: CA541675304
Gene: RAF1 HGNC NCBI

Linked Data

dbSNP Id: rs1559407634

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12590853del , CM000665.2:g.12590853del GRCh38
NC_000003.11:g.12632352del , CM000665.1:g.12632352del GRCh37
NC_000003.10:g.12607352del NCBI36
NG_007467.1:g.78328del , LRG_413:g.78328del

Transcript Alleles

HGVS Amino-acid Change
ENST00000423275.6:c.*981del ENSP00000401088.1:n.*981del
ENST00000432427.3:c.633del
ENST00000460610.2:n.110del
ENST00000465826.6:n.907del
ENST00000475353.2:n.1238del
ENST00000494557.2:n.1127del
ENST00000684903.1:c.*993del ENSP00000508612.1:n.*993del
ENST00000685348.1:c.*993del ENSP00000510285.1:n.*993del
ENST00000685437.1:c.1217del ENSP00000508794.1:p.Lys406SerfsTer7
ENST00000685653.1:c.1316del ENSP00000509968.1:p.Lys439SerfsTer7
ENST00000685738.1:c.*280del ENSP00000510156.1:n.*280del
ENST00000686409.1:n.2367del
ENST00000686455.1:n.1679del
ENST00000686762.1:c.1316del ENSP00000509767.1:p.Lys439SerfsTer7
ENST00000687257.1:n.1552del
ENST00000687326.1:c.*250del ENSP00000509665.1:n.*250del
ENST00000687505.1:n.1434del
ENST00000687923.1:c.1205del ENSP00000510255.1:p.Lys402SerfsTer7
ENST00000687940.1:n.1693del
ENST00000688269.1:n.1912del
ENST00000688326.1:c.749del
ENST00000688444.1:n.1642del
ENST00000688543.1:c.1217del ENSP00000509612.1:p.Lys406SerfsTer7
ENST00000688625.1:c.*894del ENSP00000509522.1:n.*894del
ENST00000688803.1:n.1547del
ENST00000688914.1:n.302del
ENST00000689097.1:c.*993del ENSP00000509756.1:n.*993del
ENST00000689389.1:c.1193+856del ENSP00000510213.1:n.1193+856del
ENST00000689418.1:c.*993del ENSP00000509467.1:n.*993del
ENST00000689481.1:c.*993del ENSP00000510248.1:n.*993del
ENST00000689540.1:n.1466del
ENST00000689876.1:c.1316del ENSP00000508535.1:p.Lys439SerfsTer7
ENST00000689914.1:c.*250del ENSP00000509847.1:n.*250del
ENST00000690397.1:c.1205del ENSP00000508730.1:p.Lys402SerfsTer7
ENST00000690460.1:c.1304del ENSP00000509106.1:p.Lys435SerfsTer7
ENST00000690585.1:c.208del
ENST00000690625.1:n.2352del
ENST00000691396.1:c.*1168del ENSP00000510712.1:n.*1168del
ENST00000691724.1:c.*273del ENSP00000509255.1:n.*273del
ENST00000691779.1:c.*894del ENSP00000508592.1:n.*894del
ENST00000691888.1:c.208del
ENST00000691899.1:c.1316del ENSP00000508763.1:p.Lys439SerfsTer7
ENST00000692069.1:n.1882del
ENST00000692093.1:c.1217del ENSP00000509669.1:p.Lys406SerfsTer7
ENST00000692311.1:n.2140del
ENST00000692558.1:n.1681del
ENST00000692773.1:c.*1053del ENSP00000509055.1:n.*1053del
ENST00000692830.1:c.*1061del ENSP00000509461.1:n.*1061del
ENST00000693069.1:c.*250del ENSP00000510072.1:n.*250del
ENST00000693312.1:c.1091del ENSP00000508686.1:p.Lys364SerfsTer7
ENST00000693664.1:c.1316del ENSP00000509614.1:p.Lys439SerfsTer7
ENST00000693705.1:c.*993del ENSP00000510697.1:n.*993del
ENST00000251849.9:c.1316del MANE Select ENSP00000251849.4:p.Lys439SerfsTer7
ENST00000442415.7:c.1376del ENSP00000401888.2:p.Lys459SerfsTer7
ENST00000251849.8:c.1316del ENSP00000251849.4:p.Lys439SerfsTer7
ENST00000423275.5:c.*993del ENSP00000401088.1:n.*993del
ENST00000432427.2:c.953del ENSP00000398591.2:p.Lys318SerfsTer7
ENST00000442415.6:c.1376del ENSP00000401888.2:p.Lys459SerfsTer7
ENST00000460610.1:n.273del
ENST00000465826.5:n.673del
ENST00000475353.1:n.484del
ENST00000494557.1:n.332del
NM_002880.3:c.1316del , LRG_413t1:c.1316del NP_002871.1:p.Lys439SerfsTer7
XM_005265355.1:c.1316del XP_005265412.1:p.Lys439SerfsTer7
XM_005265357.1:c.1217del XP_005265414.1:p.Lys406SerfsTer7
XM_005265358.3:c.1073del XP_005265415.1:p.Lys358SerfsTer7
XM_005265359.3:c.974del XP_005265416.1:p.Lys325SerfsTer7
XM_005265360.1:c.1316del XP_005265417.1:p.Lys439SerfsTer7
XM_011533974.1:c.1316del XP_011532276.1:p.Lys439SerfsTer7
XM_011533975.1:c.1073del XP_011532277.1:p.Lys358SerfsTer7
NM_001354689.1:c.1376del NP_001341618.1:p.Lys459SerfsTer7
NM_001354690.1:c.1316del NP_001341619.1:p.Lys439SerfsTer7
NM_001354691.1:c.1073del NP_001341620.1:p.Lys358SerfsTer7
NM_001354692.1:c.1073del NP_001341621.1:p.Lys358SerfsTer7
NM_001354693.1:c.1217del NP_001341622.1:p.Lys406SerfsTer7
NM_001354694.1:c.1133del NP_001341623.1:p.Lys378SerfsTer7
NM_001354695.1:c.974del NP_001341624.1:p.Lys325SerfsTer7
NR_148940.1:n.1844del
NR_148941.1:n.1790del
NR_148942.1:n.1729del
XM_011533974.3:c.1316del XP_011532276.1:p.Lys439SerfsTer7
XM_017006966.1:c.1217del XP_016862455.1:p.Lys406SerfsTer7
NM_001354689.3:c.1376del NP_001341618.1:p.Lys459SerfsTer7
NM_001354690.2:c.1316del NP_001341619.1:p.Lys439SerfsTer7
NM_001354691.2:c.1073del NP_001341620.1:p.Lys358SerfsTer7
NM_001354692.2:c.1073del NP_001341621.1:p.Lys358SerfsTer7
NM_001354693.2:c.1217del NP_001341622.1:p.Lys406SerfsTer7
NM_001354694.2:c.1133del NP_001341623.1:p.Lys378SerfsTer7
NM_001354695.2:c.974del NP_001341624.1:p.Lys325SerfsTer7
NR_148940.2:n.1760del
NR_148941.2:n.1706del
NR_148942.2:n.1645del
NM_001354690.3:c.1316del NP_001341619.1:p.Lys439SerfsTer7
NM_001354691.3:c.1073del NP_001341620.1:p.Lys358SerfsTer7
NM_001354692.3:c.1073del NP_001341621.1:p.Lys358SerfsTer7
NM_001354693.3:c.1217del NP_001341622.1:p.Lys406SerfsTer7
NM_001354694.3:c.1133del NP_001341623.1:p.Lys378SerfsTer7
NM_001354695.3:c.974del NP_001341624.1:p.Lys325SerfsTer7
NM_002880.4:c.1316del MANE Select NP_002871.1:p.Lys439SerfsTer7
NR_148940.3:n.1760del
NR_148941.3:n.1706del
NR_148942.3:n.1645del