Canonical Allele Identifier: CA1346233259
Gene: RAF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12590894T= , CM000665.2:g.12590894T= GRCh38
NC_000003.11:g.12632393T= , CM000665.1:g.12632393T= GRCh37
NC_000003.10:g.12607393T= NCBI36
NG_007467.1:g.78286A= , LRG_413:g.78286A=

Transcript Alleles

HGVS Amino-acid change
ENST00000423275.6:c.*939A= ENSP00000401088.1:n.*939A=
ENST00000432427.3:c.591A=
ENST00000460610.2:n.68A=
ENST00000465826.6:n.865A=
ENST00000475353.2:n.1196A=
ENST00000494557.2:n.1085A=
ENST00000684903.1:c.*951A= ENSP00000508612.1:n.*951A=
ENST00000685348.1:c.*951A= ENSP00000510285.1:n.*951A=
ENST00000685437.1:c.1175A= ENSP00000508794.1:p.Glu392=
ENST00000685653.1:c.1274A= ENSP00000509968.1:p.Glu425=
ENST00000685738.1:c.*238A= ENSP00000510156.1:n.*238A=
ENST00000686409.1:n.2325A=
ENST00000686455.1:n.1637A=
ENST00000686762.1:c.1274A= ENSP00000509767.1:p.Glu425=
ENST00000687257.1:n.1510A=
ENST00000687326.1:c.*208A= ENSP00000509665.1:n.*208A=
ENST00000687505.1:n.1392A=
ENST00000687923.1:c.1163A= ENSP00000510255.1:p.Glu388=
ENST00000687940.1:n.1651A=
ENST00000688269.1:n.1870A=
ENST00000688326.1:c.707A=
ENST00000688444.1:n.1600A=
ENST00000688543.1:c.1175A= ENSP00000509612.1:p.Glu392=
ENST00000688625.1:c.*852A= ENSP00000509522.1:n.*852A=
ENST00000688803.1:n.1505A=
ENST00000688914.1:n.260A=
ENST00000689097.1:c.*951A= ENSP00000509756.1:n.*951A=
ENST00000689389.1:c.1193+814A= ENSP00000510213.1:n.1193+814A=
ENST00000689418.1:c.*951A= ENSP00000509467.1:n.*951A=
ENST00000689481.1:c.*951A= ENSP00000510248.1:n.*951A=
ENST00000689540.1:n.1424A=
ENST00000689876.1:c.1274A= ENSP00000508535.1:p.Glu425=
ENST00000689914.1:c.*208A= ENSP00000509847.1:n.*208A=
ENST00000690397.1:c.1163A= ENSP00000508730.1:p.Glu388=
ENST00000690460.1:c.1262A= ENSP00000509106.1:p.Glu421=
ENST00000690585.1:c.166A=
ENST00000690625.1:n.2310A=
ENST00000691396.1:c.*1126A= ENSP00000510712.1:n.*1126A=
ENST00000691724.1:c.*231A= ENSP00000509255.1:n.*231A=
ENST00000691779.1:c.*852A= ENSP00000508592.1:n.*852A=
ENST00000691888.1:c.166A=
ENST00000691899.1:c.1274A= ENSP00000508763.1:p.Glu425=
ENST00000692069.1:n.1840A=
ENST00000692093.1:c.1175A= ENSP00000509669.1:p.Glu392=
ENST00000692311.1:n.2098A=
ENST00000692558.1:n.1639A=
ENST00000692773.1:c.*1011A= ENSP00000509055.1:n.*1011A=
ENST00000692830.1:c.*1019A= ENSP00000509461.1:n.*1019A=
ENST00000693069.1:c.*208A= ENSP00000510072.1:n.*208A=
ENST00000693312.1:c.1049A= ENSP00000508686.1:p.Glu350=
ENST00000693664.1:c.1274A= ENSP00000509614.1:p.Glu425=
ENST00000693705.1:c.*951A= ENSP00000510697.1:n.*951A=
ENST00000251849.9:c.1274A= MANE Select ENSP00000251849.4:p.Glu425=
ENST00000442415.7:c.1334A= ENSP00000401888.2:p.Glu445=
ENST00000251849.8:c.1274A= ENSP00000251849.4:p.Glu425=
ENST00000423275.5:c.*951A= ENSP00000401088.1:n.*951A=
ENST00000432427.2:c.911A= ENSP00000398591.2:p.Glu304=
ENST00000442415.6:c.1334A= ENSP00000401888.2:p.Glu445=
ENST00000460610.1:n.231A=
ENST00000465826.5:n.631A=
ENST00000475353.1:n.442A=
ENST00000494557.1:n.290A=
NM_002880.3:c.1274A= , LRG_413t1:c.1274A= NP_002871.1:p.Glu425=
XM_005265355.1:c.1274A= XP_005265412.1:p.Glu425=
XM_005265357.1:c.1175A= XP_005265414.1:p.Glu392=
XM_005265358.3:c.1031A= XP_005265415.1:p.Glu344=
XM_005265359.3:c.932A= XP_005265416.1:p.Glu311=
XM_005265360.1:c.1274A= XP_005265417.1:p.Glu425=
XM_011533974.1:c.1274A= XP_011532276.1:p.Glu425=
XM_011533975.1:c.1031A= XP_011532277.1:p.Glu344=
NM_001354689.1:c.1334A= NP_001341618.1:p.Glu445=
NM_001354690.1:c.1274A= NP_001341619.1:p.Glu425=
NM_001354691.1:c.1031A= NP_001341620.1:p.Glu344=
NM_001354692.1:c.1031A= NP_001341621.1:p.Glu344=
NM_001354693.1:c.1175A= NP_001341622.1:p.Glu392=
NM_001354694.1:c.1091A= NP_001341623.1:p.Glu364=
NM_001354695.1:c.932A= NP_001341624.1:p.Glu311=
NR_148940.1:n.1802A=
NR_148941.1:n.1748A=
NR_148942.1:n.1687A=
XM_011533974.3:c.1274A= XP_011532276.1:p.Glu425=
XM_017006966.1:c.1175A= XP_016862455.1:p.Glu392=
NM_001354689.3:c.1334A= NP_001341618.1:p.Glu445=
NM_001354690.2:c.1274A= NP_001341619.1:p.Glu425=
NM_001354691.2:c.1031A= NP_001341620.1:p.Glu344=
NM_001354692.2:c.1031A= NP_001341621.1:p.Glu344=
NM_001354693.2:c.1175A= NP_001341622.1:p.Glu392=
NM_001354694.2:c.1091A= NP_001341623.1:p.Glu364=
NM_001354695.2:c.932A= NP_001341624.1:p.Glu311=
NR_148940.2:n.1718A=
NR_148941.2:n.1664A=
NR_148942.2:n.1603A=
NM_001354690.3:c.1274A= NP_001341619.1:p.Glu425=
NM_001354691.3:c.1031A= NP_001341620.1:p.Glu344=
NM_001354692.3:c.1031A= NP_001341621.1:p.Glu344=
NM_001354693.3:c.1175A= NP_001341622.1:p.Glu392=
NM_001354694.3:c.1091A= NP_001341623.1:p.Glu364=
NM_001354695.3:c.932A= NP_001341624.1:p.Glu311=
NM_002880.4:c.1274A= MANE Select NP_002871.1:p.Glu425=
NR_148940.3:n.1718A=
NR_148941.3:n.1664A=
NR_148942.3:n.1603A=