Canonical Allele Identifier: CA69616788
Gene: RAF1 HGNC NCBI

Linked Data

dbSNP Id: rs563042465
gnomAD v4: 3-12600186-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12600186G>T , CM000665.2:g.12600186G>T GRCh38
NC_000003.11:g.12641685G>T , CM000665.1:g.12641685G>T GRCh37
NC_000003.10:g.12616685G>T NCBI36
NG_007467.1:g.68994C>A , LRG_413:g.68994C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000423275.6:c.*621C>A ENSP00000401088.1:n.*621C>A
ENST00000432427.3:c.276C>A
ENST00000465826.6:n.547C>A
ENST00000491290.2:n.1333C>A
ENST00000684903.1:c.*633C>A ENSP00000508612.1:n.*633C>A
ENST00000685348.1:c.*633C>A ENSP00000510285.1:n.*633C>A
ENST00000685437.1:c.857C>A ENSP00000508794.1:p.Ala286Glu
ENST00000685653.1:c.956C>A ENSP00000509968.1:p.Ala319Glu
ENST00000685738.1:c.956C>A ENSP00000510156.1:p.Ala319Glu
ENST00000686409.1:n.1664C>A
ENST00000686455.1:n.1319C>A
ENST00000686479.1:n.1327C>A
ENST00000686762.1:c.956C>A ENSP00000509767.1:p.Ala319Glu
ENST00000687257.1:n.1192C>A
ENST00000687326.1:c.956C>A ENSP00000509665.1:p.Ala319Glu
ENST00000687486.1:c.182+202C>A
ENST00000687505.1:n.1074C>A
ENST00000687923.1:c.857C>A ENSP00000510255.1:p.Ala286Glu
ENST00000687940.1:n.1333C>A
ENST00000688269.1:n.1552C>A
ENST00000688326.1:c.276C>A
ENST00000688444.1:n.1282C>A
ENST00000688543.1:c.857C>A ENSP00000509612.1:p.Ala286Glu
ENST00000688625.1:c.*534C>A ENSP00000509522.1:n.*534C>A
ENST00000688803.1:n.1187C>A
ENST00000689097.1:c.*633C>A ENSP00000509756.1:n.*633C>A
ENST00000689389.1:c.956C>A ENSP00000510213.1:p.Ala319Glu
ENST00000689418.1:c.*633C>A ENSP00000509467.1:n.*633C>A
ENST00000689481.1:c.*633C>A ENSP00000510248.1:n.*633C>A
ENST00000689540.1:n.1106C>A
ENST00000689876.1:c.956C>A ENSP00000508535.1:p.Ala319Glu
ENST00000689914.1:c.956C>A ENSP00000509847.1:p.Ala319Glu
ENST00000690397.1:c.845C>A ENSP00000508730.1:p.Ala282Glu
ENST00000690460.1:c.944C>A ENSP00000509106.1:p.Ala315Glu
ENST00000690625.1:n.1259C>A
ENST00000691268.1:c.383C>A
ENST00000691396.1:c.*749C>A ENSP00000510712.1:n.*749C>A
ENST00000691724.1:c.956C>A ENSP00000509255.1:p.Ala319Glu
ENST00000691779.1:c.*534C>A ENSP00000508592.1:n.*534C>A
ENST00000691899.1:c.956C>A ENSP00000508763.1:p.Ala319Glu
ENST00000692069.1:n.1179C>A
ENST00000692093.1:c.857C>A ENSP00000509669.1:p.Ala286Glu
ENST00000692311.1:n.1437C>A
ENST00000692558.1:n.1321C>A
ENST00000692773.1:c.*693C>A ENSP00000509055.1:n.*693C>A
ENST00000692830.1:c.*701C>A ENSP00000509461.1:n.*701C>A
ENST00000693069.1:c.857C>A ENSP00000510072.1:p.Ala286Glu
ENST00000693312.1:c.731C>A ENSP00000508686.1:p.Ala244Glu
ENST00000693664.1:c.956C>A ENSP00000509614.1:p.Ala319Glu
ENST00000693705.1:c.*633C>A ENSP00000510697.1:n.*633C>A
ENST00000251849.9:c.956C>A MANE Select ENSP00000251849.4:p.Ala319Glu
ENST00000442415.7:c.1016C>A ENSP00000401888.2:p.Ala339Glu
ENST00000251849.8:c.956C>A ENSP00000251849.4:p.Ala319Glu
ENST00000423275.5:c.*633C>A ENSP00000401088.1:n.*633C>A
ENST00000432427.2:c.593C>A ENSP00000398591.2:p.Ala198Glu
ENST00000442415.6:c.1016C>A ENSP00000401888.2:p.Ala339Glu
ENST00000465826.5:n.200C>A
NM_002880.3:c.956C>A , LRG_413t1:c.956C>A NP_002871.1:p.Ala319Glu
XM_005265355.1:c.956C>A XP_005265412.1:p.Ala319Glu
XM_005265357.1:c.857C>A XP_005265414.1:p.Ala286Glu
XM_005265358.3:c.713C>A XP_005265415.1:p.Ala238Glu
XM_005265359.3:c.614C>A XP_005265416.1:p.Ala205Glu
XM_005265360.1:c.956C>A XP_005265417.1:p.Ala319Glu
XM_011533974.1:c.956C>A XP_011532276.1:p.Ala319Glu
XM_011533975.1:c.713C>A XP_011532277.1:p.Ala238Glu
NM_001354689.1:c.1016C>A NP_001341618.1:p.Ala339Glu
NM_001354690.1:c.956C>A NP_001341619.1:p.Ala319Glu
NM_001354691.1:c.713C>A NP_001341620.1:p.Ala238Glu
NM_001354692.1:c.713C>A NP_001341621.1:p.Ala238Glu
NM_001354693.1:c.857C>A NP_001341622.1:p.Ala286Glu
NM_001354694.1:c.773C>A NP_001341623.1:p.Ala258Glu
NM_001354695.1:c.614C>A NP_001341624.1:p.Ala205Glu
NR_148940.1:n.1371C>A
NR_148941.1:n.1371C>A
NR_148942.1:n.1371C>A
XM_011533974.3:c.956C>A XP_011532276.1:p.Ala319Glu
XM_017006966.1:c.857C>A XP_016862455.1:p.Ala286Glu
XR_001740227.1:n.1188C>A
NM_001354689.3:c.1016C>A NP_001341618.1:p.Ala339Glu
NM_001354690.2:c.956C>A NP_001341619.1:p.Ala319Glu
NM_001354691.2:c.713C>A NP_001341620.1:p.Ala238Glu
NM_001354692.2:c.713C>A NP_001341621.1:p.Ala238Glu
NM_001354693.2:c.857C>A NP_001341622.1:p.Ala286Glu
NM_001354694.2:c.773C>A NP_001341623.1:p.Ala258Glu
NM_001354695.2:c.614C>A NP_001341624.1:p.Ala205Glu
NR_148940.2:n.1287C>A
NR_148941.2:n.1287C>A
NR_148942.2:n.1287C>A
NM_001354690.3:c.956C>A NP_001341619.1:p.Ala319Glu
NM_001354691.3:c.713C>A NP_001341620.1:p.Ala238Glu
NM_001354692.3:c.713C>A NP_001341621.1:p.Ala238Glu
NM_001354693.3:c.857C>A NP_001341622.1:p.Ala286Glu
NM_001354694.3:c.773C>A NP_001341623.1:p.Ala258Glu
NM_001354695.3:c.614C>A NP_001341624.1:p.Ala205Glu
NM_002880.4:c.956C>A MANE Select NP_002871.1:p.Ala319Glu
NR_148940.3:n.1287C>A
NR_148941.3:n.1287C>A
NR_148942.3:n.1287C>A