Canonical Allele Identifier: CA2702196643
Gene: RAF1 HGNC NCBI

Linked Data

dbSNP Id: rs2125377436

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12599711del , CM000665.2:g.12599711del GRCh38
NC_000003.11:g.12641210del , CM000665.1:g.12641210del GRCh37
NC_000003.10:g.12616210del NCBI36
NG_007467.1:g.69471del , LRG_413:g.69471del

Transcript Alleles

HGVS Amino-acid Change
ENST00000423275.6:c.*755del ENSP00000401088.1:n.*755del
ENST00000432427.3:c.410del
ENST00000465826.6:n.681del
ENST00000491290.2:n.1467del
ENST00000684903.1:c.*767del ENSP00000508612.1:n.*767del
ENST00000685348.1:c.*767del ENSP00000510285.1:n.*767del
ENST00000685437.1:c.991del ENSP00000508794.1:p.Tyr331IlefsTer11
ENST00000685653.1:c.1090del ENSP00000509968.1:p.Tyr364IlefsTer11
ENST00000685738.1:c.1090del ENSP00000510156.1:p.Tyr364IlefsTer8
ENST00000686409.1:n.2141del
ENST00000686455.1:n.1453del
ENST00000686479.1:n.1461del
ENST00000686762.1:c.1090del ENSP00000509767.1:p.Tyr364IlefsTer11
ENST00000687257.1:n.1326del
ENST00000687326.1:c.1090del ENSP00000509665.1:p.Tyr364IlefsTer9
ENST00000687486.1:c.282del
ENST00000687505.1:n.1208del
ENST00000687923.1:c.991del ENSP00000510255.1:p.Tyr331IlefsTer7
ENST00000687940.1:n.1467del
ENST00000688269.1:n.1686del
ENST00000688326.1:c.410del
ENST00000688444.1:n.1416del
ENST00000688543.1:c.991del ENSP00000509612.1:p.Tyr331IlefsTer11
ENST00000688625.1:c.*668del ENSP00000509522.1:n.*668del
ENST00000688803.1:n.1321del
ENST00000688914.1:n.76del
ENST00000689097.1:c.*767del ENSP00000509756.1:n.*767del
ENST00000689389.1:c.1090del ENSP00000510213.1:p.Tyr364IlefsTer11
ENST00000689418.1:c.*767del ENSP00000509467.1:n.*767del
ENST00000689481.1:c.*767del ENSP00000510248.1:n.*767del
ENST00000689540.1:n.1240del
ENST00000689876.1:c.1090del ENSP00000508535.1:p.Tyr364IlefsTer11
ENST00000689914.1:c.1090del ENSP00000509847.1:p.Tyr364IlefsTer9
ENST00000690397.1:c.979del ENSP00000508730.1:p.Tyr327IlefsTer11
ENST00000690460.1:c.1078del ENSP00000509106.1:p.Tyr360IlefsTer11
ENST00000690625.1:n.1393del
ENST00000691268.1:c.517del
ENST00000691396.1:c.*883del ENSP00000510712.1:n.*883del
ENST00000691724.1:c.*47del ENSP00000509255.1:n.*47del
ENST00000691779.1:c.*668del ENSP00000508592.1:n.*668del
ENST00000691899.1:c.1090del ENSP00000508763.1:p.Tyr364IlefsTer11
ENST00000692069.1:n.1656del
ENST00000692093.1:c.991del ENSP00000509669.1:p.Tyr331IlefsTer11
ENST00000692311.1:n.1914del
ENST00000692558.1:n.1455del
ENST00000692773.1:c.*827del ENSP00000509055.1:n.*827del
ENST00000692830.1:c.*835del ENSP00000509461.1:n.*835del
ENST00000693069.1:c.991del ENSP00000510072.1:p.Tyr331IlefsTer9
ENST00000693312.1:c.865del ENSP00000508686.1:p.Tyr289IlefsTer11
ENST00000693664.1:c.1090del ENSP00000509614.1:p.Tyr364IlefsTer11
ENST00000693705.1:c.*767del ENSP00000510697.1:n.*767del
ENST00000251849.9:c.1090del MANE Select ENSP00000251849.4:p.Tyr364IlefsTer11
ENST00000442415.7:c.1150del ENSP00000401888.2:p.Tyr384IlefsTer11
ENST00000251849.8:c.1090del ENSP00000251849.4:p.Tyr364IlefsTer11
ENST00000423275.5:c.*767del ENSP00000401088.1:n.*767del
ENST00000432427.2:c.727del ENSP00000398591.2:p.Tyr243IlefsTer11
ENST00000442415.6:c.1150del ENSP00000401888.2:p.Tyr384IlefsTer11
ENST00000460610.1:n.47del
ENST00000465826.5:n.334del
NM_002880.3:c.1090del , LRG_413t1:c.1090del NP_002871.1:p.Tyr364IlefsTer11
XM_005265355.1:c.1090del XP_005265412.1:p.Tyr364IlefsTer11
XM_005265357.1:c.991del XP_005265414.1:p.Tyr331IlefsTer11
XM_005265358.3:c.847del XP_005265415.1:p.Tyr283IlefsTer11
XM_005265359.3:c.748del XP_005265416.1:p.Tyr250IlefsTer11
XM_005265360.1:c.1090del XP_005265417.1:p.Tyr364IlefsTer11
XM_011533974.1:c.1090del XP_011532276.1:p.Tyr364IlefsTer11
XM_011533975.1:c.847del XP_011532277.1:p.Tyr283IlefsTer11
NM_001354689.1:c.1150del NP_001341618.1:p.Tyr384IlefsTer11
NM_001354690.1:c.1090del NP_001341619.1:p.Tyr364IlefsTer11
NM_001354691.1:c.847del NP_001341620.1:p.Tyr283IlefsTer11
NM_001354692.1:c.847del NP_001341621.1:p.Tyr283IlefsTer11
NM_001354693.1:c.991del NP_001341622.1:p.Tyr331IlefsTer11
NM_001354694.1:c.907del NP_001341623.1:p.Tyr303IlefsTer11
NM_001354695.1:c.748del NP_001341624.1:p.Tyr250IlefsTer11
NR_148940.1:n.1505del
NR_148941.1:n.1505del
NR_148942.1:n.1503del
XM_011533974.3:c.1090del XP_011532276.1:p.Tyr364IlefsTer11
XM_017006966.1:c.991del XP_016862455.1:p.Tyr331IlefsTer11
XR_001740227.1:n.1322del
NM_001354689.3:c.1150del NP_001341618.1:p.Tyr384IlefsTer11
NM_001354690.2:c.1090del NP_001341619.1:p.Tyr364IlefsTer11
NM_001354691.2:c.847del NP_001341620.1:p.Tyr283IlefsTer11
NM_001354692.2:c.847del NP_001341621.1:p.Tyr283IlefsTer11
NM_001354693.2:c.991del NP_001341622.1:p.Tyr331IlefsTer11
NM_001354694.2:c.907del NP_001341623.1:p.Tyr303IlefsTer11
NM_001354695.2:c.748del NP_001341624.1:p.Tyr250IlefsTer11
NR_148940.2:n.1421del
NR_148941.2:n.1421del
NR_148942.2:n.1419del
NM_001354690.3:c.1090del NP_001341619.1:p.Tyr364IlefsTer11
NM_001354691.3:c.847del NP_001341620.1:p.Tyr283IlefsTer11
NM_001354692.3:c.847del NP_001341621.1:p.Tyr283IlefsTer11
NM_001354693.3:c.991del NP_001341622.1:p.Tyr331IlefsTer11
NM_001354694.3:c.907del NP_001341623.1:p.Tyr303IlefsTer11
NM_001354695.3:c.748del NP_001341624.1:p.Tyr250IlefsTer11
NM_002880.4:c.1090del MANE Select NP_002871.1:p.Tyr364IlefsTer11
NR_148940.3:n.1421del
NR_148941.3:n.1421del
NR_148942.3:n.1419del