Canonical Allele Identifier: CA1346233248
Gene: RAF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12590889T= , CM000665.2:g.12590889T= GRCh38
NC_000003.11:g.12632388T= , CM000665.1:g.12632388T= GRCh37
NC_000003.10:g.12607388T= NCBI36
NG_007467.1:g.78291A= , LRG_413:g.78291A=

Transcript Alleles

HGVS Amino-acid change
ENST00000423275.6:c.*944A= ENSP00000401088.1:n.*944A=
ENST00000432427.3:c.596A=
ENST00000460610.2:n.73A=
ENST00000465826.6:n.870A=
ENST00000475353.2:n.1201A=
ENST00000494557.2:n.1090A=
ENST00000684903.1:c.*956A= ENSP00000508612.1:n.*956A=
ENST00000685348.1:c.*956A= ENSP00000510285.1:n.*956A=
ENST00000685437.1:c.1180A= ENSP00000508794.1:p.Ser394=
ENST00000685653.1:c.1279A= ENSP00000509968.1:p.Ser427=
ENST00000685738.1:c.*243A= ENSP00000510156.1:n.*243A=
ENST00000686409.1:n.2330A=
ENST00000686455.1:n.1642A=
ENST00000686762.1:c.1279A= ENSP00000509767.1:p.Ser427=
ENST00000687257.1:n.1515A=
ENST00000687326.1:c.*213A= ENSP00000509665.1:n.*213A=
ENST00000687505.1:n.1397A=
ENST00000687923.1:c.1168A= ENSP00000510255.1:p.Ser390=
ENST00000687940.1:n.1656A=
ENST00000688269.1:n.1875A=
ENST00000688326.1:c.712A=
ENST00000688444.1:n.1605A=
ENST00000688543.1:c.1180A= ENSP00000509612.1:p.Ser394=
ENST00000688625.1:c.*857A= ENSP00000509522.1:n.*857A=
ENST00000688803.1:n.1510A=
ENST00000688914.1:n.265A=
ENST00000689097.1:c.*956A= ENSP00000509756.1:n.*956A=
ENST00000689389.1:c.1193+819A= ENSP00000510213.1:n.1193+819A=
ENST00000689418.1:c.*956A= ENSP00000509467.1:n.*956A=
ENST00000689481.1:c.*956A= ENSP00000510248.1:n.*956A=
ENST00000689540.1:n.1429A=
ENST00000689876.1:c.1279A= ENSP00000508535.1:p.Ser427=
ENST00000689914.1:c.*213A= ENSP00000509847.1:n.*213A=
ENST00000690397.1:c.1168A= ENSP00000508730.1:p.Ser390=
ENST00000690460.1:c.1267A= ENSP00000509106.1:p.Ser423=
ENST00000690585.1:c.171A=
ENST00000690625.1:n.2315A=
ENST00000691396.1:c.*1131A= ENSP00000510712.1:n.*1131A=
ENST00000691724.1:c.*236A= ENSP00000509255.1:n.*236A=
ENST00000691779.1:c.*857A= ENSP00000508592.1:n.*857A=
ENST00000691888.1:c.171A=
ENST00000691899.1:c.1279A= ENSP00000508763.1:p.Ser427=
ENST00000692069.1:n.1845A=
ENST00000692093.1:c.1180A= ENSP00000509669.1:p.Ser394=
ENST00000692311.1:n.2103A=
ENST00000692558.1:n.1644A=
ENST00000692773.1:c.*1016A= ENSP00000509055.1:n.*1016A=
ENST00000692830.1:c.*1024A= ENSP00000509461.1:n.*1024A=
ENST00000693069.1:c.*213A= ENSP00000510072.1:n.*213A=
ENST00000693312.1:c.1054A= ENSP00000508686.1:p.Ser352=
ENST00000693664.1:c.1279A= ENSP00000509614.1:p.Ser427=
ENST00000693705.1:c.*956A= ENSP00000510697.1:n.*956A=
ENST00000251849.9:c.1279A= MANE Select ENSP00000251849.4:p.Ser427=
ENST00000442415.7:c.1339A= ENSP00000401888.2:p.Ser447=
ENST00000251849.8:c.1279A= ENSP00000251849.4:p.Ser427=
ENST00000423275.5:c.*956A= ENSP00000401088.1:n.*956A=
ENST00000432427.2:c.916A= ENSP00000398591.2:p.Ser306=
ENST00000442415.6:c.1339A= ENSP00000401888.2:p.Ser447=
ENST00000460610.1:n.236A=
ENST00000465826.5:n.636A=
ENST00000475353.1:n.447A=
ENST00000494557.1:n.295A=
NM_002880.3:c.1279A= , LRG_413t1:c.1279A= NP_002871.1:p.Ser427=
XM_005265355.1:c.1279A= XP_005265412.1:p.Ser427=
XM_005265357.1:c.1180A= XP_005265414.1:p.Ser394=
XM_005265358.3:c.1036A= XP_005265415.1:p.Ser346=
XM_005265359.3:c.937A= XP_005265416.1:p.Ser313=
XM_005265360.1:c.1279A= XP_005265417.1:p.Ser427=
XM_011533974.1:c.1279A= XP_011532276.1:p.Ser427=
XM_011533975.1:c.1036A= XP_011532277.1:p.Ser346=
NM_001354689.1:c.1339A= NP_001341618.1:p.Ser447=
NM_001354690.1:c.1279A= NP_001341619.1:p.Ser427=
NM_001354691.1:c.1036A= NP_001341620.1:p.Ser346=
NM_001354692.1:c.1036A= NP_001341621.1:p.Ser346=
NM_001354693.1:c.1180A= NP_001341622.1:p.Ser394=
NM_001354694.1:c.1096A= NP_001341623.1:p.Ser366=
NM_001354695.1:c.937A= NP_001341624.1:p.Ser313=
NR_148940.1:n.1807A=
NR_148941.1:n.1753A=
NR_148942.1:n.1692A=
XM_011533974.3:c.1279A= XP_011532276.1:p.Ser427=
XM_017006966.1:c.1180A= XP_016862455.1:p.Ser394=
NM_001354689.3:c.1339A= NP_001341618.1:p.Ser447=
NM_001354690.2:c.1279A= NP_001341619.1:p.Ser427=
NM_001354691.2:c.1036A= NP_001341620.1:p.Ser346=
NM_001354692.2:c.1036A= NP_001341621.1:p.Ser346=
NM_001354693.2:c.1180A= NP_001341622.1:p.Ser394=
NM_001354694.2:c.1096A= NP_001341623.1:p.Ser366=
NM_001354695.2:c.937A= NP_001341624.1:p.Ser313=
NR_148940.2:n.1723A=
NR_148941.2:n.1669A=
NR_148942.2:n.1608A=
NM_001354690.3:c.1279A= NP_001341619.1:p.Ser427=
NM_001354691.3:c.1036A= NP_001341620.1:p.Ser346=
NM_001354692.3:c.1036A= NP_001341621.1:p.Ser346=
NM_001354693.3:c.1180A= NP_001341622.1:p.Ser394=
NM_001354694.3:c.1096A= NP_001341623.1:p.Ser366=
NM_001354695.3:c.937A= NP_001341624.1:p.Ser313=
NM_002880.4:c.1279A= MANE Select NP_002871.1:p.Ser427=
NR_148940.3:n.1723A=
NR_148941.3:n.1669A=
NR_148942.3:n.1608A=