Canonical Allele Identifier: CA1346226690

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12584847C= , CM000665.2:g.12584847C= GRCh38
NC_000003.11:g.12626346C= , CM000665.1:g.12626346C= GRCh37
NC_000003.10:g.12601346C= NCBI36
NG_007467.1:g.84333G= , LRG_413:g.84333G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000423275.6:c.*1468G= (RAF1) ENSP00000401088.1:n.*1468G=
ENST00000432427.3:c.1120G= (RAF1)
ENST00000460610.2:n.6115G= (RAF1)
ENST00000471449.2:n.613G= (RAF1)
ENST00000475353.2:n.4083G= (RAF1)
ENST00000684903.1:c.*1480G= (RAF1) ENSP00000508612.1:n.*1480G=
ENST00000685348.1:c.*1514G= (RAF1) ENSP00000510285.1:n.*1514G=
ENST00000685437.1:c.1704G= (RAF1) ENSP00000508794.1:p.Gln568=
ENST00000685653.1:c.1803G= (RAF1) ENSP00000509968.1:p.Gln601=
ENST00000685697.1:n.2538G= (RAF1)
ENST00000685738.1:c.*767G= (RAF1) ENSP00000510156.1:n.*767G=
ENST00000686409.1:n.5212G= (RAF1)
ENST00000686455.1:n.4524G= (RAF1)
ENST00000686762.1:c.*362G= (RAF1) ENSP00000509767.1:n.*362G=
ENST00000687257.1:n.4257G= (RAF1)
ENST00000687326.1:c.*3095G= (RAF1) ENSP00000509665.1:n.*3095G=
ENST00000687505.1:n.1921G= (RAF1)
ENST00000687923.1:c.1692G= (RAF1) ENSP00000510255.1:p.Gln564=
ENST00000688269.1:n.2399G= (RAF1)
ENST00000688444.1:n.3920G= (RAF1)
ENST00000688543.1:c.1704G= (RAF1) ENSP00000509612.1:p.Gln568=
ENST00000688625.1:c.*3172G= (RAF1) ENSP00000509522.1:n.*3172G=
ENST00000688803.1:n.3231G= (RAF1)
ENST00000689097.1:c.*1480G= (RAF1) ENSP00000509756.1:n.*1480G=
ENST00000689389.1:c.1626G= (RAF1) ENSP00000510213.1:p.Gln542=
ENST00000689418.1:c.*3698G= (RAF1) ENSP00000509467.1:n.*3698G=
ENST00000689540.1:n.4171G= (RAF1)
ENST00000689876.1:c.*352G= (RAF1) ENSP00000508535.1:n.*352G=
ENST00000689914.1:c.*737G= (RAF1) ENSP00000509847.1:n.*737G=
ENST00000690397.1:c.1692G= (RAF1) ENSP00000508730.1:p.Gln564=
ENST00000690460.1:c.1791G= (RAF1) ENSP00000509106.1:p.Gln597=
ENST00000690585.1:c.529G= (RAF1)
ENST00000690625.1:n.2839G= (RAF1)
ENST00000691396.1:c.*1675G= (RAF1) ENSP00000510712.1:n.*1675G=
ENST00000691643.1:n.2856G= (RAF1)
ENST00000691724.1:c.*760G= (RAF1) ENSP00000509255.1:n.*760G=
ENST00000691779.1:c.*1381G= (RAF1) ENSP00000508592.1:n.*1381G=
ENST00000691888.1:c.677G= (RAF1)
ENST00000691899.1:c.1803G= (RAF1) ENSP00000508763.1:p.Gln601=
ENST00000692069.1:n.4727G= (RAF1)
ENST00000692093.1:c.1704G= (RAF1) ENSP00000509669.1:p.Gln568=
ENST00000692311.1:n.2627G= (RAF1)
ENST00000692558.1:n.4386G= (RAF1)
ENST00000692773.1:c.*1540G= (RAF1) ENSP00000509055.1:n.*1540G=
ENST00000692830.1:c.*1548G= (RAF1) ENSP00000509461.1:n.*1548G=
ENST00000693312.1:c.1578G= (RAF1) ENSP00000508686.1:p.Gln526=
ENST00000693664.1:c.*254G= (RAF1) ENSP00000509614.1:n.*254G=
ENST00000693705.1:c.*1182G= (RAF1) ENSP00000510697.1:n.*1182G=
ENST00000251849.9:c.1803G= (RAF1) MANE Select ENSP00000251849.4:p.Gln601=
ENST00000442415.7:c.1863G= (RAF1) ENSP00000401888.2:p.Gln621=
ENST00000676541.1:c.*2594C= (MKRN2) ENSP00000503730.1:n.*2594C=
ENST00000677142.1:c.*2594C= (MKRN2) ENSP00000504455.1:n.*2594C=
ENST00000677816.1:c.*1149C= (MKRN2) ENSP00000502893.1:n.*1149C=
ENST00000677941.1:n.2657C= (MKRN2)
ENST00000251849.8:c.1803G= (RAF1) ENSP00000251849.4:p.Gln601=
ENST00000423275.5:c.*1480G= (RAF1) ENSP00000401088.1:n.*1480G=
ENST00000432427.2:c.1440G= (RAF1) ENSP00000398591.2:p.Gln480=
ENST00000442415.6:c.1863G= (RAF1) ENSP00000401888.2:p.Gln621=
ENST00000471449.1:n.492G= (RAF1)
NM_002880.3:c.1803G= , LRG_413t1:c.1803G= (RAF1) NP_002871.1:p.Gln601=
XM_005265355.1:c.1803G= (RAF1) XP_005265412.1:p.Gln601=
XM_005265357.1:c.1704G= (RAF1) XP_005265414.1:p.Gln568=
XM_005265358.3:c.1560G= (RAF1) XP_005265415.1:p.Gln520=
XM_005265359.3:c.1461G= (RAF1) XP_005265416.1:p.Gln487=
XM_011533974.1:c.1803G= (RAF1) XP_011532276.1:p.Gln601=
XM_011533975.1:c.1560G= (RAF1) XP_011532277.1:p.Gln520=
NM_001354689.1:c.1863G= (RAF1) NP_001341618.1:p.Gln621=
NM_001354690.1:c.1803G= (RAF1) NP_001341619.1:p.Gln601=
NM_001354691.1:c.1560G= (RAF1) NP_001341620.1:p.Gln520=
NM_001354692.1:c.1560G= (RAF1) NP_001341621.1:p.Gln520=
NM_001354693.1:c.1704G= (RAF1) NP_001341622.1:p.Gln568=
NM_001354694.1:c.1620G= (RAF1) NP_001341623.1:p.Gln540=
NM_001354695.1:c.1461G= (RAF1) NP_001341624.1:p.Gln487=
NR_148940.1:n.2331G= (RAF1)
NR_148941.1:n.2277G= (RAF1)
NR_148942.1:n.2216G= (RAF1)
XM_011533974.3:c.1803G= (RAF1) XP_011532276.1:p.Gln601=
XM_017006966.1:c.1704G= (RAF1) XP_016862455.1:p.Gln568=
NM_001354689.3:c.1863G= (RAF1) NP_001341618.1:p.Gln621=
NM_001354690.2:c.1803G= (RAF1) NP_001341619.1:p.Gln601=
NM_001354691.2:c.1560G= (RAF1) NP_001341620.1:p.Gln520=
NM_001354692.2:c.1560G= (RAF1) NP_001341621.1:p.Gln520=
NM_001354693.2:c.1704G= (RAF1) NP_001341622.1:p.Gln568=
NM_001354694.2:c.1620G= (RAF1) NP_001341623.1:p.Gln540=
NM_001354695.2:c.1461G= (RAF1) NP_001341624.1:p.Gln487=
NR_148940.2:n.2247G= (RAF1)
NR_148941.2:n.2193G= (RAF1)
NR_148942.2:n.2132G= (RAF1)
NM_001354690.3:c.1803G= (RAF1) NP_001341619.1:p.Gln601=
NM_001354691.3:c.1560G= (RAF1) NP_001341620.1:p.Gln520=
NM_001354692.3:c.1560G= (RAF1) NP_001341621.1:p.Gln520=
NM_001354693.3:c.1704G= (RAF1) NP_001341622.1:p.Gln568=
NM_001354694.3:c.1620G= (RAF1) NP_001341623.1:p.Gln540=
NM_001354695.3:c.1461G= (RAF1) NP_001341624.1:p.Gln487=
NM_002880.4:c.1803G= (RAF1) MANE Select NP_002871.1:p.Gln601=
NR_148940.3:n.2247G= (RAF1)
NR_148941.3:n.2193G= (RAF1)
NR_148942.3:n.2132G= (RAF1)