Canonical Allele Identifier: CA351512238
Gene: RAF1 HGNC NCBI

Linked Data

dbSNP Id: rs2125397342

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12604171T>A , CM000665.2:g.12604171T>A GRCh38
NC_000003.11:g.12645670T>A , CM000665.1:g.12645670T>A GRCh37
NC_000003.10:g.12620670T>A NCBI36
NG_007467.1:g.65009A>T , LRG_413:g.65009A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000416093.2:c.*476A>T ENSP00000391265.2:n.*476A>T
ENST00000423275.6:c.*476A>T ENSP00000401088.1:n.*476A>T
ENST00000432427.3:c.119A>T
ENST00000465826.6:n.390A>T
ENST00000491290.2:n.1176A>T
ENST00000684903.1:c.*476A>T ENSP00000508612.1:n.*476A>T
ENST00000685348.1:c.*476A>T ENSP00000510285.1:n.*476A>T
ENST00000685437.1:c.700A>T ENSP00000508794.1:p.Ser234Cys
ENST00000685653.1:c.799A>T ENSP00000509968.1:p.Ser267Cys
ENST00000685738.1:c.799A>T ENSP00000510156.1:p.Ser267Cys
ENST00000685959.1:c.799A>T ENSP00000510452.1:p.Ser267Cys
ENST00000686409.1:n.1399A>T
ENST00000686455.1:n.1162A>T
ENST00000686479.1:n.1170A>T
ENST00000686762.1:c.799A>T ENSP00000509767.1:p.Ser267Cys
ENST00000687257.1:n.1035A>T
ENST00000687326.1:c.799A>T ENSP00000509665.1:p.Ser267Cys
ENST00000687486.1:c.119A>T
ENST00000687505.1:n.917A>T
ENST00000687923.1:c.700A>T ENSP00000510255.1:p.Ser234Cys
ENST00000687940.1:n.1176A>T
ENST00000688269.1:n.1407A>T
ENST00000688326.1:c.119A>T
ENST00000688444.1:n.1125A>T
ENST00000688543.1:c.700A>T ENSP00000509612.1:p.Ser234Cys
ENST00000688625.1:c.*377A>T ENSP00000509522.1:n.*377A>T
ENST00000688803.1:n.1030A>T
ENST00000689033.1:c.799A>T ENSP00000508983.1:p.Ser267Cys
ENST00000689097.1:c.*476A>T ENSP00000509756.1:n.*476A>T
ENST00000689389.1:c.799A>T ENSP00000510213.1:p.Ser267Cys
ENST00000689418.1:c.*476A>T ENSP00000509467.1:n.*476A>T
ENST00000689481.1:c.*476A>T ENSP00000510248.1:n.*476A>T
ENST00000689540.1:n.949A>T
ENST00000689876.1:c.799A>T ENSP00000508535.1:p.Ser267Cys
ENST00000689914.1:c.799A>T ENSP00000509847.1:p.Ser267Cys
ENST00000690397.1:c.700A>T ENSP00000508730.1:p.Ser234Cys
ENST00000690460.1:c.799A>T ENSP00000509106.1:p.Ser267Cys
ENST00000690625.1:n.1102A>T
ENST00000691268.1:c.262-3756A>T
ENST00000691396.1:c.*592A>T ENSP00000510712.1:n.*592A>T
ENST00000691724.1:c.799A>T ENSP00000509255.1:p.Ser267Cys
ENST00000691779.1:c.*377A>T ENSP00000508592.1:n.*377A>T
ENST00000691899.1:c.799A>T ENSP00000508763.1:p.Ser267Cys
ENST00000692093.1:c.700A>T ENSP00000509669.1:p.Ser234Cys
ENST00000692311.1:n.1172A>T
ENST00000692558.1:n.1164A>T
ENST00000692773.1:c.*476A>T ENSP00000509055.1:n.*476A>T
ENST00000692830.1:c.*544A>T ENSP00000509461.1:n.*544A>T
ENST00000693069.1:c.700A>T ENSP00000510072.1:p.Ser234Cys
ENST00000693312.1:c.574A>T ENSP00000508686.1:p.Ser192Cys
ENST00000693664.1:c.799A>T ENSP00000509614.1:p.Ser267Cys
ENST00000693705.1:c.*476A>T ENSP00000510697.1:n.*476A>T
ENST00000251849.9:c.799A>T MANE Select ENSP00000251849.4:p.Ser267Cys
ENST00000442415.7:c.799A>T ENSP00000401888.2:p.Ser267Cys
ENST00000251849.8:c.799A>T ENSP00000251849.4:p.Ser267Cys
ENST00000416093.1:c.*377A>T ENSP00000391265.1:n.*377A>T
ENST00000423275.5:c.*476A>T ENSP00000401088.1:n.*476A>T
ENST00000432427.2:c.436A>T ENSP00000398591.2:p.Ser146Cys
ENST00000442415.6:c.799A>T ENSP00000401888.2:p.Ser267Cys
ENST00000465826.5:n.43A>T
ENST00000491290.1:n.320A>T
NM_002880.3:c.799A>T , LRG_413t1:c.799A>T NP_002871.1:p.Ser267Cys
XM_005265355.1:c.799A>T XP_005265412.1:p.Ser267Cys
XM_005265357.1:c.700A>T XP_005265414.1:p.Ser234Cys
XM_005265358.3:c.556A>T XP_005265415.1:p.Ser186Cys
XM_005265359.3:c.457A>T XP_005265416.1:p.Ser153Cys
XM_005265360.1:c.799A>T XP_005265417.1:p.Ser267Cys
XM_011533974.1:c.799A>T XP_011532276.1:p.Ser267Cys
XM_011533975.1:c.556A>T XP_011532277.1:p.Ser186Cys
NM_001354689.1:c.799A>T NP_001341618.1:p.Ser267Cys
NM_001354690.1:c.799A>T NP_001341619.1:p.Ser267Cys
NM_001354691.1:c.556A>T NP_001341620.1:p.Ser186Cys
NM_001354692.1:c.556A>T NP_001341621.1:p.Ser186Cys
NM_001354693.1:c.700A>T NP_001341622.1:p.Ser234Cys
NM_001354694.1:c.556A>T NP_001341623.1:p.Ser186Cys
NM_001354695.1:c.457A>T NP_001341624.1:p.Ser153Cys
NR_148940.1:n.1214A>T
NR_148941.1:n.1214A>T
NR_148942.1:n.1214A>T
XM_011533974.3:c.799A>T XP_011532276.1:p.Ser267Cys
XM_017006966.1:c.700A>T XP_016862455.1:p.Ser234Cys
XR_001740227.1:n.1031A>T
NM_001354689.3:c.799A>T NP_001341618.1:p.Ser267Cys
NM_001354690.2:c.799A>T NP_001341619.1:p.Ser267Cys
NM_001354691.2:c.556A>T NP_001341620.1:p.Ser186Cys
NM_001354692.2:c.556A>T NP_001341621.1:p.Ser186Cys
NM_001354693.2:c.700A>T NP_001341622.1:p.Ser234Cys
NM_001354694.2:c.556A>T NP_001341623.1:p.Ser186Cys
NM_001354695.2:c.457A>T NP_001341624.1:p.Ser153Cys
NR_148940.2:n.1130A>T
NR_148941.2:n.1130A>T
NR_148942.2:n.1130A>T
NM_001354690.3:c.799A>T NP_001341619.1:p.Ser267Cys
NM_001354691.3:c.556A>T NP_001341620.1:p.Ser186Cys
NM_001354692.3:c.556A>T NP_001341621.1:p.Ser186Cys
NM_001354693.3:c.700A>T NP_001341622.1:p.Ser234Cys
NM_001354694.3:c.556A>T NP_001341623.1:p.Ser186Cys
NM_001354695.3:c.457A>T NP_001341624.1:p.Ser153Cys
NM_002880.4:c.799A>T MANE Select NP_002871.1:p.Ser267Cys
NR_148940.3:n.1130A>T
NR_148941.3:n.1130A>T
NR_148942.3:n.1130A>T