Canonical Allele Identifier: CA2577511196
Gene: RAF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12599696_12599700dup , CM000665.2:g.12599696_12599700dup GRCh38
NC_000003.11:g.12641195_12641199dup , CM000665.1:g.12641195_12641199dup GRCh37
NC_000003.10:g.12616195_12616199dup NCBI36
NG_007467.1:g.69480_69484dup , LRG_413:g.69480_69484dup

Transcript Alleles

HGVS Amino-acid change
ENST00000423275.6:c.*764_*768dup ENSP00000401088.1:n.*764_*768dup
ENST00000432427.3:c.419_423dup
ENST00000465826.6:n.690_694dup
ENST00000491290.2:n.1476_1480dup
ENST00000684903.1:c.*776_*780dup ENSP00000508612.1:n.*776_*780dup
ENST00000685348.1:c.*776_*780dup ENSP00000510285.1:n.*776_*780dup
ENST00000685437.1:c.1000_1004dup ENSP00000508794.1:p.Trp335Ter
ENST00000685653.1:c.1099_1103dup ENSP00000509968.1:p.Trp368Ter
ENST00000685738.1:c.1099_1103dup ENSP00000510156.1:p.Trp368Ter
ENST00000686409.1:n.2150_2154dup
ENST00000686455.1:n.1462_1466dup
ENST00000686479.1:n.1470_1474dup
ENST00000686762.1:c.1099_1103dup ENSP00000509767.1:p.Trp368Ter
ENST00000687257.1:n.1335_1339dup
ENST00000687326.1:c.1099_1103dup ENSP00000509665.1:p.Trp368Ter
ENST00000687486.1:c.291_295dup
ENST00000687505.1:n.1217_1221dup
ENST00000687923.1:c.997+3_997+7dup ENSP00000510255.1:n.997+3_997+7dup
ENST00000687940.1:n.1476_1480dup
ENST00000688269.1:n.1695_1699dup
ENST00000688326.1:c.419_423dup
ENST00000688444.1:n.1425_1429dup
ENST00000688543.1:c.1000_1004dup ENSP00000509612.1:p.Trp335Ter
ENST00000688625.1:c.*677_*681dup ENSP00000509522.1:n.*677_*681dup
ENST00000688803.1:n.1330_1334dup
ENST00000688914.1:n.85_89dup
ENST00000689097.1:c.*776_*780dup ENSP00000509756.1:n.*776_*780dup
ENST00000689389.1:c.1099_1103dup ENSP00000510213.1:p.Trp368Ter
ENST00000689418.1:c.*776_*780dup ENSP00000509467.1:n.*776_*780dup
ENST00000689481.1:c.*776_*780dup ENSP00000510248.1:n.*776_*780dup
ENST00000689540.1:n.1249_1253dup
ENST00000689876.1:c.1099_1103dup ENSP00000508535.1:p.Trp368Ter
ENST00000689914.1:c.1099_1103dup ENSP00000509847.1:p.Trp368Ter
ENST00000690397.1:c.988_992dup ENSP00000508730.1:p.Trp331Ter
ENST00000690460.1:c.1087_1091dup ENSP00000509106.1:p.Trp364Ter
ENST00000690625.1:n.1402_1406dup
ENST00000691268.1:c.526_530dup
ENST00000691396.1:c.*892_*896dup ENSP00000510712.1:n.*892_*896dup
ENST00000691724.1:c.*56_*60dup ENSP00000509255.1:n.*56_*60dup
ENST00000691779.1:c.*677_*681dup ENSP00000508592.1:n.*677_*681dup
ENST00000691899.1:c.1099_1103dup ENSP00000508763.1:p.Trp368Ter
ENST00000692069.1:n.1665_1669dup
ENST00000692093.1:c.1000_1004dup ENSP00000509669.1:p.Trp335Ter
ENST00000692311.1:n.1923_1927dup
ENST00000692558.1:n.1464_1468dup
ENST00000692773.1:c.*836_*840dup ENSP00000509055.1:n.*836_*840dup
ENST00000692830.1:c.*844_*848dup ENSP00000509461.1:n.*844_*848dup
ENST00000693069.1:c.1000_1004dup ENSP00000510072.1:p.Trp335Ter
ENST00000693312.1:c.874_878dup ENSP00000508686.1:p.Trp293Ter
ENST00000693664.1:c.1099_1103dup ENSP00000509614.1:p.Trp368Ter
ENST00000693705.1:c.*776_*780dup ENSP00000510697.1:n.*776_*780dup
ENST00000251849.9:c.1099_1103dup MANE Select ENSP00000251849.4:p.Trp368Ter
ENST00000442415.7:c.1159_1163dup ENSP00000401888.2:p.Trp388Ter
ENST00000251849.8:c.1099_1103dup ENSP00000251849.4:p.Trp368Ter
ENST00000423275.5:c.*776_*780dup ENSP00000401088.1:n.*776_*780dup
ENST00000432427.2:c.736_740dup ENSP00000398591.2:p.Trp247Ter
ENST00000442415.6:c.1159_1163dup ENSP00000401888.2:p.Trp388Ter
ENST00000460610.1:n.56_60dup
ENST00000465826.5:n.343_347dup
NM_002880.3:c.1099_1103dup , LRG_413t1:c.1099_1103dup NP_002871.1:p.Trp368Ter
XM_005265355.1:c.1099_1103dup XP_005265412.1:p.Trp368Ter
XM_005265357.1:c.1000_1004dup XP_005265414.1:p.Trp335Ter
XM_005265358.3:c.856_860dup XP_005265415.1:p.Trp287Ter
XM_005265359.3:c.757_761dup XP_005265416.1:p.Trp254Ter
XM_005265360.1:c.1099_1103dup XP_005265417.1:p.Trp368Ter
XM_011533974.1:c.1099_1103dup XP_011532276.1:p.Trp368Ter
XM_011533975.1:c.856_860dup XP_011532277.1:p.Trp287Ter
NM_001354689.1:c.1159_1163dup NP_001341618.1:p.Trp388Ter
NM_001354690.1:c.1099_1103dup NP_001341619.1:p.Trp368Ter
NM_001354691.1:c.856_860dup NP_001341620.1:p.Trp287Ter
NM_001354692.1:c.856_860dup NP_001341621.1:p.Trp287Ter
NM_001354693.1:c.1000_1004dup NP_001341622.1:p.Trp335Ter
NM_001354694.1:c.916_920dup NP_001341623.1:p.Trp307Ter
NM_001354695.1:c.757_761dup NP_001341624.1:p.Trp254Ter
NR_148940.1:n.1514_1518dup
NR_148941.1:n.1514_1518dup
NR_148942.1:n.1512_1516dup
XM_011533974.3:c.1099_1103dup XP_011532276.1:p.Trp368Ter
XM_017006966.1:c.1000_1004dup XP_016862455.1:p.Trp335Ter
XR_001740227.1:n.1331_1335dup
NM_001354689.3:c.1159_1163dup NP_001341618.1:p.Trp388Ter
NM_001354690.2:c.1099_1103dup NP_001341619.1:p.Trp368Ter
NM_001354691.2:c.856_860dup NP_001341620.1:p.Trp287Ter
NM_001354692.2:c.856_860dup NP_001341621.1:p.Trp287Ter
NM_001354693.2:c.1000_1004dup NP_001341622.1:p.Trp335Ter
NM_001354694.2:c.916_920dup NP_001341623.1:p.Trp307Ter
NM_001354695.2:c.757_761dup NP_001341624.1:p.Trp254Ter
NR_148940.2:n.1430_1434dup
NR_148941.2:n.1430_1434dup
NR_148942.2:n.1428_1432dup
NM_001354690.3:c.1099_1103dup NP_001341619.1:p.Trp368Ter
NM_001354691.3:c.856_860dup NP_001341620.1:p.Trp287Ter
NM_001354692.3:c.856_860dup NP_001341621.1:p.Trp287Ter
NM_001354693.3:c.1000_1004dup NP_001341622.1:p.Trp335Ter
NM_001354694.3:c.916_920dup NP_001341623.1:p.Trp307Ter
NM_001354695.3:c.757_761dup NP_001341624.1:p.Trp254Ter
NM_002880.4:c.1099_1103dup MANE Select NP_002871.1:p.Trp368Ter
NR_148940.3:n.1430_1434dup
NR_148941.3:n.1430_1434dup
NR_148942.3:n.1428_1432dup