Canonical Allele Identifier: CA1346226277

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12584597C= , CM000665.2:g.12584597C= GRCh38
NC_000003.11:g.12626096C= , CM000665.1:g.12626096C= GRCh37
NC_000003.10:g.12601096C= NCBI36
NG_007467.1:g.84583G= , LRG_413:g.84583G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000423275.6:c.*1529G= (RAF1) ENSP00000401088.1:n.*1529G=
ENST00000432427.3:c.1181G= (RAF1)
ENST00000460610.2:n.6176G= (RAF1)
ENST00000471449.2:n.674G= (RAF1)
ENST00000475353.2:n.4144G= (RAF1)
ENST00000684903.1:c.*1541G= (RAF1) ENSP00000508612.1:n.*1541G=
ENST00000685348.1:c.*1575G= (RAF1) ENSP00000510285.1:n.*1575G=
ENST00000685437.1:c.1765G= (RAF1) ENSP00000508794.1:p.Glu589=
ENST00000685653.1:c.1864G= (RAF1) ENSP00000509968.1:p.Glu622=
ENST00000685697.1:n.2599G= (RAF1)
ENST00000685738.1:c.*828G= (RAF1) ENSP00000510156.1:n.*828G=
ENST00000686409.1:n.5273G= (RAF1)
ENST00000686455.1:n.4585G= (RAF1)
ENST00000686762.1:c.*423G= (RAF1) ENSP00000509767.1:n.*423G=
ENST00000687257.1:n.4318G= (RAF1)
ENST00000687326.1:c.*3156G= (RAF1) ENSP00000509665.1:n.*3156G=
ENST00000687505.1:n.1982G= (RAF1)
ENST00000687923.1:c.1753G= (RAF1) ENSP00000510255.1:p.Glu585=
ENST00000688269.1:n.2460G= (RAF1)
ENST00000688444.1:n.3981G= (RAF1)
ENST00000688543.1:c.1765G= (RAF1) ENSP00000509612.1:p.Glu589=
ENST00000688625.1:c.*3233G= (RAF1) ENSP00000509522.1:n.*3233G=
ENST00000688803.1:n.3292G= (RAF1)
ENST00000689097.1:c.*1541G= (RAF1) ENSP00000509756.1:n.*1541G=
ENST00000689389.1:c.1687G= (RAF1) ENSP00000510213.1:p.Glu563=
ENST00000689418.1:c.*3759G= (RAF1) ENSP00000509467.1:n.*3759G=
ENST00000689540.1:n.4232G= (RAF1)
ENST00000689876.1:c.*413G= (RAF1) ENSP00000508535.1:n.*413G=
ENST00000689914.1:c.*798G= (RAF1) ENSP00000509847.1:n.*798G=
ENST00000690397.1:c.1753G= (RAF1) ENSP00000508730.1:p.Glu585=
ENST00000690460.1:c.1852G= (RAF1) ENSP00000509106.1:p.Glu618=
ENST00000690585.1:c.590G= (RAF1)
ENST00000690625.1:n.2900G= (RAF1)
ENST00000691396.1:c.*1736G= (RAF1) ENSP00000510712.1:n.*1736G=
ENST00000691643.1:n.2917G= (RAF1)
ENST00000691724.1:c.*821G= (RAF1) ENSP00000509255.1:n.*821G=
ENST00000691779.1:c.*1442G= (RAF1) ENSP00000508592.1:n.*1442G=
ENST00000691888.1:c.738G= (RAF1)
ENST00000691899.1:c.1864G= (RAF1) ENSP00000508763.1:p.Glu622=
ENST00000692069.1:n.4788G= (RAF1)
ENST00000692093.1:c.1765G= (RAF1) ENSP00000509669.1:p.Glu589=
ENST00000692311.1:n.2688G= (RAF1)
ENST00000692558.1:n.4447G= (RAF1)
ENST00000692773.1:c.*1601G= (RAF1) ENSP00000509055.1:n.*1601G=
ENST00000692830.1:c.*1609G= (RAF1) ENSP00000509461.1:n.*1609G=
ENST00000693312.1:c.1639G= (RAF1) ENSP00000508686.1:p.Glu547=
ENST00000693664.1:c.*315G= (RAF1) ENSP00000509614.1:n.*315G=
ENST00000693705.1:c.*1243G= (RAF1) ENSP00000510697.1:n.*1243G=
ENST00000251849.9:c.1864G= (RAF1) MANE Select ENSP00000251849.4:p.Glu622=
ENST00000442415.7:c.1924G= (RAF1) ENSP00000401888.2:p.Glu642=
ENST00000676541.1:c.*2344C= (MKRN2) ENSP00000503730.1:n.*2344C=
ENST00000677142.1:c.*2344C= (MKRN2) ENSP00000504455.1:n.*2344C=
ENST00000677816.1:c.*899C= (MKRN2) ENSP00000502893.1:n.*899C=
ENST00000677941.1:n.2407C= (MKRN2)
ENST00000251849.8:c.1864G= (RAF1) ENSP00000251849.4:p.Glu622=
ENST00000423275.5:c.*1541G= (RAF1) ENSP00000401088.1:n.*1541G=
ENST00000432427.2:c.1501G= (RAF1) ENSP00000398591.2:p.Glu501=
ENST00000442415.6:c.1924G= (RAF1) ENSP00000401888.2:p.Glu642=
ENST00000471449.1:n.553G= (RAF1)
NM_002880.3:c.1864G= , LRG_413t1:c.1864G= (RAF1) NP_002871.1:p.Glu622=
XM_005265355.1:c.1864G= (RAF1) XP_005265412.1:p.Glu622=
XM_005265357.1:c.1765G= (RAF1) XP_005265414.1:p.Glu589=
XM_005265358.3:c.1621G= (RAF1) XP_005265415.1:p.Glu541=
XM_005265359.3:c.1522G= (RAF1) XP_005265416.1:p.Glu508=
XM_011533974.1:c.1864G= (RAF1) XP_011532276.1:p.Glu622=
XM_011533975.1:c.1621G= (RAF1) XP_011532277.1:p.Glu541=
NM_001354689.1:c.1924G= (RAF1) NP_001341618.1:p.Glu642=
NM_001354690.1:c.1864G= (RAF1) NP_001341619.1:p.Glu622=
NM_001354691.1:c.1621G= (RAF1) NP_001341620.1:p.Glu541=
NM_001354692.1:c.1621G= (RAF1) NP_001341621.1:p.Glu541=
NM_001354693.1:c.1765G= (RAF1) NP_001341622.1:p.Glu589=
NM_001354694.1:c.1681G= (RAF1) NP_001341623.1:p.Glu561=
NM_001354695.1:c.1522G= (RAF1) NP_001341624.1:p.Glu508=
NR_148940.1:n.2392G= (RAF1)
NR_148941.1:n.2338G= (RAF1)
NR_148942.1:n.2277G= (RAF1)
XM_011533974.3:c.1864G= (RAF1) XP_011532276.1:p.Glu622=
XM_017006966.1:c.1765G= (RAF1) XP_016862455.1:p.Glu589=
NM_001354689.3:c.1924G= (RAF1) NP_001341618.1:p.Glu642=
NM_001354690.2:c.1864G= (RAF1) NP_001341619.1:p.Glu622=
NM_001354691.2:c.1621G= (RAF1) NP_001341620.1:p.Glu541=
NM_001354692.2:c.1621G= (RAF1) NP_001341621.1:p.Glu541=
NM_001354693.2:c.1765G= (RAF1) NP_001341622.1:p.Glu589=
NM_001354694.2:c.1681G= (RAF1) NP_001341623.1:p.Glu561=
NM_001354695.2:c.1522G= (RAF1) NP_001341624.1:p.Glu508=
NR_148940.2:n.2308G= (RAF1)
NR_148941.2:n.2254G= (RAF1)
NR_148942.2:n.2193G= (RAF1)
NM_001354690.3:c.1864G= (RAF1) NP_001341619.1:p.Glu622=
NM_001354691.3:c.1621G= (RAF1) NP_001341620.1:p.Glu541=
NM_001354692.3:c.1621G= (RAF1) NP_001341621.1:p.Glu541=
NM_001354693.3:c.1765G= (RAF1) NP_001341622.1:p.Glu589=
NM_001354694.3:c.1681G= (RAF1) NP_001341623.1:p.Glu561=
NM_001354695.3:c.1522G= (RAF1) NP_001341624.1:p.Glu508=
NM_002880.4:c.1864G= (RAF1) MANE Select NP_002871.1:p.Glu622=
NR_148940.3:n.2308G= (RAF1)
NR_148941.3:n.2254G= (RAF1)
NR_148942.3:n.2193G= (RAF1)