Canonical Allele Identifier: CA2664502928
Gene: RAF1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12590965_12590969del , CM000665.2:g.12590965_12590969del GRCh38
NC_000003.11:g.12632464_12632468del , CM000665.1:g.12632464_12632468del GRCh37
NC_000003.10:g.12607464_12607468del NCBI36
NG_007467.1:g.78213_78217del , LRG_413:g.78213_78217del

Transcript Alleles

HGVS Amino-acid Change
ENST00000423275.6:c.*866_*870del ENSP00000401088.1:n.*866_*870del
ENST00000432427.3:c.518_522del
ENST00000465826.6:n.792_796del
ENST00000475353.2:n.1123_1127del
ENST00000494557.2:n.1012_1016del
ENST00000684903.1:c.*878_*882del ENSP00000508612.1:n.*878_*882del
ENST00000685348.1:c.*878_*882del ENSP00000510285.1:n.*878_*882del
ENST00000685437.1:c.1102_1106del ENSP00000508794.1:p.Arg368CysfsTer?
ENST00000685653.1:c.1201_1205del ENSP00000509968.1:p.Arg401CysfsTer?
ENST00000685738.1:c.*165_*169del ENSP00000510156.1:n.*165_*169del
ENST00000686409.1:n.2252_2256del
ENST00000686455.1:n.1564_1568del
ENST00000686762.1:c.1201_1205del ENSP00000509767.1:p.Arg401CysfsTer?
ENST00000687257.1:n.1437_1441del
ENST00000687326.1:c.*135_*139del ENSP00000509665.1:n.*135_*139del
ENST00000687505.1:n.1319_1323del
ENST00000687923.1:c.1090_1094del ENSP00000510255.1:p.Arg364CysfsTer?
ENST00000687940.1:n.1578_1582del
ENST00000688269.1:n.1797_1801del
ENST00000688326.1:c.634_638del
ENST00000688444.1:n.1527_1531del
ENST00000688543.1:c.1102_1106del ENSP00000509612.1:p.Arg368CysfsTer?
ENST00000688625.1:c.*779_*783del ENSP00000509522.1:n.*779_*783del
ENST00000688803.1:n.1432_1436del
ENST00000688914.1:n.187_191del
ENST00000689097.1:c.*878_*882del ENSP00000509756.1:n.*878_*882del
ENST00000689389.1:c.1193+741_1193+745del ENSP00000510213.1:n.1193+741_1193+745del
ENST00000689418.1:c.*878_*882del ENSP00000509467.1:n.*878_*882del
ENST00000689481.1:c.*878_*882del ENSP00000510248.1:n.*878_*882del
ENST00000689540.1:n.1351_1355del
ENST00000689876.1:c.1201_1205del ENSP00000508535.1:p.Arg401CysfsTer?
ENST00000689914.1:c.*135_*139del ENSP00000509847.1:n.*135_*139del
ENST00000690397.1:c.1090_1094del ENSP00000508730.1:p.Arg364CysfsTer?
ENST00000690460.1:c.1189_1193del ENSP00000509106.1:p.Arg397CysfsTer?
ENST00000690585.1:c.93_97del
ENST00000690625.1:n.2237_2241del
ENST00000691396.1:c.*1053_*1057del ENSP00000510712.1:n.*1053_*1057del
ENST00000691724.1:c.*158_*162del ENSP00000509255.1:n.*158_*162del
ENST00000691779.1:c.*779_*783del ENSP00000508592.1:n.*779_*783del
ENST00000691888.1:c.93_97del
ENST00000691899.1:c.1201_1205del ENSP00000508763.1:p.Arg401CysfsTer?
ENST00000692069.1:n.1767_1771del
ENST00000692093.1:c.1102_1106del ENSP00000509669.1:p.Arg368CysfsTer?
ENST00000692311.1:n.2025_2029del
ENST00000692558.1:n.1566_1570del
ENST00000692773.1:c.*938_*942del ENSP00000509055.1:n.*938_*942del
ENST00000692830.1:c.*946_*950del ENSP00000509461.1:n.*946_*950del
ENST00000693069.1:c.*135_*139del ENSP00000510072.1:n.*135_*139del
ENST00000693312.1:c.976_980del ENSP00000508686.1:p.Arg326CysfsTer?
ENST00000693664.1:c.1201_1205del ENSP00000509614.1:p.Arg401CysfsTer?
ENST00000693705.1:c.*878_*882del ENSP00000510697.1:n.*878_*882del
ENST00000251849.9:c.1201_1205del MANE Select ENSP00000251849.4:p.Arg401CysfsTer?
ENST00000442415.7:c.1261_1265del ENSP00000401888.2:p.Arg421CysfsTer?
ENST00000251849.8:c.1201_1205del ENSP00000251849.4:p.Arg401CysfsTer?
ENST00000423275.5:c.*878_*882del ENSP00000401088.1:n.*878_*882del
ENST00000432427.2:c.838_842del ENSP00000398591.2:p.Arg280CysfsTer?
ENST00000442415.6:c.1261_1265del ENSP00000401888.2:p.Arg421CysfsTer?
ENST00000460610.1:n.158_162del
ENST00000465826.5:n.558_562del
ENST00000475353.1:n.369_373del
ENST00000494557.1:n.217_221del
NM_002880.3:c.1201_1205del , LRG_413t1:c.1201_1205del NP_002871.1:p.Arg401CysfsTer?
XM_005265355.1:c.1201_1205del XP_005265412.1:p.Arg401CysfsTer?
XM_005265357.1:c.1102_1106del XP_005265414.1:p.Arg368CysfsTer?
XM_005265358.3:c.958_962del XP_005265415.1:p.Arg320CysfsTer?
XM_005265359.3:c.859_863del XP_005265416.1:p.Arg287CysfsTer?
XM_005265360.1:c.1201_1205del XP_005265417.1:p.Arg401CysfsTer?
XM_011533974.1:c.1201_1205del XP_011532276.1:p.Arg401CysfsTer?
XM_011533975.1:c.958_962del XP_011532277.1:p.Arg320CysfsTer?
NM_001354689.1:c.1261_1265del NP_001341618.1:p.Arg421CysfsTer?
NM_001354690.1:c.1201_1205del NP_001341619.1:p.Arg401CysfsTer?
NM_001354691.1:c.958_962del NP_001341620.1:p.Arg320CysfsTer?
NM_001354692.1:c.958_962del NP_001341621.1:p.Arg320CysfsTer?
NM_001354693.1:c.1102_1106del NP_001341622.1:p.Arg368CysfsTer?
NM_001354694.1:c.1018_1022del NP_001341623.1:p.Arg340CysfsTer?
NM_001354695.1:c.859_863del NP_001341624.1:p.Arg287CysfsTer?
NR_148940.1:n.1729_1733del
NR_148941.1:n.1675_1679del
NR_148942.1:n.1614_1618del
XM_011533974.3:c.1201_1205del XP_011532276.1:p.Arg401CysfsTer?
XM_017006966.1:c.1102_1106del XP_016862455.1:p.Arg368CysfsTer?
XR_001740227.1:n.1492_1496del
NM_001354689.3:c.1261_1265del NP_001341618.1:p.Arg421CysfsTer?
NM_001354690.2:c.1201_1205del NP_001341619.1:p.Arg401CysfsTer?
NM_001354691.2:c.958_962del NP_001341620.1:p.Arg320CysfsTer?
NM_001354692.2:c.958_962del NP_001341621.1:p.Arg320CysfsTer?
NM_001354693.2:c.1102_1106del NP_001341622.1:p.Arg368CysfsTer?
NM_001354694.2:c.1018_1022del NP_001341623.1:p.Arg340CysfsTer?
NM_001354695.2:c.859_863del NP_001341624.1:p.Arg287CysfsTer?
NR_148940.2:n.1645_1649del
NR_148941.2:n.1591_1595del
NR_148942.2:n.1530_1534del
NM_001354690.3:c.1201_1205del NP_001341619.1:p.Arg401CysfsTer?
NM_001354691.3:c.958_962del NP_001341620.1:p.Arg320CysfsTer?
NM_001354692.3:c.958_962del NP_001341621.1:p.Arg320CysfsTer?
NM_001354693.3:c.1102_1106del NP_001341622.1:p.Arg368CysfsTer?
NM_001354694.3:c.1018_1022del NP_001341623.1:p.Arg340CysfsTer?
NM_001354695.3:c.859_863del NP_001341624.1:p.Arg287CysfsTer?
NM_002880.4:c.1201_1205del MANE Select NP_002871.1:p.Arg401CysfsTer?
NR_148940.3:n.1645_1649del
NR_148941.3:n.1591_1595del
NR_148942.3:n.1530_1534del