Canonical Allele Identifier: CA1346226370

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12584629T= , CM000665.2:g.12584629T= GRCh38
NC_000003.11:g.12626128T= , CM000665.1:g.12626128T= GRCh37
NC_000003.10:g.12601128T= NCBI36
NG_007467.1:g.84551A= , LRG_413:g.84551A=

Transcript Alleles

HGVS Amino-acid change
ENST00000423275.6:c.*1497A= (RAF1) ENSP00000401088.1:n.*1497A=
ENST00000432427.3:c.1149A= (RAF1)
ENST00000460610.2:n.6144A= (RAF1)
ENST00000471449.2:n.642A= (RAF1)
ENST00000475353.2:n.4112A= (RAF1)
ENST00000684903.1:c.*1509A= (RAF1) ENSP00000508612.1:n.*1509A=
ENST00000685348.1:c.*1543A= (RAF1) ENSP00000510285.1:n.*1543A=
ENST00000685437.1:c.1733A= (RAF1) ENSP00000508794.1:p.His578=
ENST00000685653.1:c.1832A= (RAF1) ENSP00000509968.1:p.His611=
ENST00000685697.1:n.2567A= (RAF1)
ENST00000685738.1:c.*796A= (RAF1) ENSP00000510156.1:n.*796A=
ENST00000686409.1:n.5241A= (RAF1)
ENST00000686455.1:n.4553A= (RAF1)
ENST00000686762.1:c.*391A= (RAF1) ENSP00000509767.1:n.*391A=
ENST00000687257.1:n.4286A= (RAF1)
ENST00000687326.1:c.*3124A= (RAF1) ENSP00000509665.1:n.*3124A=
ENST00000687505.1:n.1950A= (RAF1)
ENST00000687923.1:c.1721A= (RAF1) ENSP00000510255.1:p.His574=
ENST00000688269.1:n.2428A= (RAF1)
ENST00000688444.1:n.3949A= (RAF1)
ENST00000688543.1:c.1733A= (RAF1) ENSP00000509612.1:p.His578=
ENST00000688625.1:c.*3201A= (RAF1) ENSP00000509522.1:n.*3201A=
ENST00000688803.1:n.3260A= (RAF1)
ENST00000689097.1:c.*1509A= (RAF1) ENSP00000509756.1:n.*1509A=
ENST00000689389.1:c.1655A= (RAF1) ENSP00000510213.1:p.His552=
ENST00000689418.1:c.*3727A= (RAF1) ENSP00000509467.1:n.*3727A=
ENST00000689540.1:n.4200A= (RAF1)
ENST00000689876.1:c.*381A= (RAF1) ENSP00000508535.1:n.*381A=
ENST00000689914.1:c.*766A= (RAF1) ENSP00000509847.1:n.*766A=
ENST00000690397.1:c.1721A= (RAF1) ENSP00000508730.1:p.His574=
ENST00000690460.1:c.1820A= (RAF1) ENSP00000509106.1:p.His607=
ENST00000690585.1:c.558A= (RAF1)
ENST00000690625.1:n.2868A= (RAF1)
ENST00000691396.1:c.*1704A= (RAF1) ENSP00000510712.1:n.*1704A=
ENST00000691643.1:n.2885A= (RAF1)
ENST00000691724.1:c.*789A= (RAF1) ENSP00000509255.1:n.*789A=
ENST00000691779.1:c.*1410A= (RAF1) ENSP00000508592.1:n.*1410A=
ENST00000691888.1:c.706A= (RAF1)
ENST00000691899.1:c.1832A= (RAF1) ENSP00000508763.1:p.His611=
ENST00000692069.1:n.4756A= (RAF1)
ENST00000692093.1:c.1733A= (RAF1) ENSP00000509669.1:p.His578=
ENST00000692311.1:n.2656A= (RAF1)
ENST00000692558.1:n.4415A= (RAF1)
ENST00000692773.1:c.*1569A= (RAF1) ENSP00000509055.1:n.*1569A=
ENST00000692830.1:c.*1577A= (RAF1) ENSP00000509461.1:n.*1577A=
ENST00000693312.1:c.1607A= (RAF1) ENSP00000508686.1:p.His536=
ENST00000693664.1:c.*283A= (RAF1) ENSP00000509614.1:n.*283A=
ENST00000693705.1:c.*1211A= (RAF1) ENSP00000510697.1:n.*1211A=
ENST00000251849.9:c.1832A= (RAF1) MANE Select ENSP00000251849.4:p.His611=
ENST00000442415.7:c.1892A= (RAF1) ENSP00000401888.2:p.His631=
ENST00000676541.1:c.*2376T= (MKRN2) ENSP00000503730.1:n.*2376T=
ENST00000677142.1:c.*2376T= (MKRN2) ENSP00000504455.1:n.*2376T=
ENST00000677816.1:c.*931T= (MKRN2) ENSP00000502893.1:n.*931T=
ENST00000677941.1:n.2439T= (MKRN2)
ENST00000251849.8:c.1832A= (RAF1) ENSP00000251849.4:p.His611=
ENST00000423275.5:c.*1509A= (RAF1) ENSP00000401088.1:n.*1509A=
ENST00000432427.2:c.1469A= (RAF1) ENSP00000398591.2:p.His490=
ENST00000442415.6:c.1892A= (RAF1) ENSP00000401888.2:p.His631=
ENST00000471449.1:n.521A= (RAF1)
NM_002880.3:c.1832A= , LRG_413t1:c.1832A= (RAF1) NP_002871.1:p.His611=
XM_005265355.1:c.1832A= (RAF1) XP_005265412.1:p.His611=
XM_005265357.1:c.1733A= (RAF1) XP_005265414.1:p.His578=
XM_005265358.3:c.1589A= (RAF1) XP_005265415.1:p.His530=
XM_005265359.3:c.1490A= (RAF1) XP_005265416.1:p.His497=
XM_011533974.1:c.1832A= (RAF1) XP_011532276.1:p.His611=
XM_011533975.1:c.1589A= (RAF1) XP_011532277.1:p.His530=
NM_001354689.1:c.1892A= (RAF1) NP_001341618.1:p.His631=
NM_001354690.1:c.1832A= (RAF1) NP_001341619.1:p.His611=
NM_001354691.1:c.1589A= (RAF1) NP_001341620.1:p.His530=
NM_001354692.1:c.1589A= (RAF1) NP_001341621.1:p.His530=
NM_001354693.1:c.1733A= (RAF1) NP_001341622.1:p.His578=
NM_001354694.1:c.1649A= (RAF1) NP_001341623.1:p.His550=
NM_001354695.1:c.1490A= (RAF1) NP_001341624.1:p.His497=
NR_148940.1:n.2360A= (RAF1)
NR_148941.1:n.2306A= (RAF1)
NR_148942.1:n.2245A= (RAF1)
XM_011533974.3:c.1832A= (RAF1) XP_011532276.1:p.His611=
XM_017006966.1:c.1733A= (RAF1) XP_016862455.1:p.His578=
NM_001354689.3:c.1892A= (RAF1) NP_001341618.1:p.His631=
NM_001354690.2:c.1832A= (RAF1) NP_001341619.1:p.His611=
NM_001354691.2:c.1589A= (RAF1) NP_001341620.1:p.His530=
NM_001354692.2:c.1589A= (RAF1) NP_001341621.1:p.His530=
NM_001354693.2:c.1733A= (RAF1) NP_001341622.1:p.His578=
NM_001354694.2:c.1649A= (RAF1) NP_001341623.1:p.His550=
NM_001354695.2:c.1490A= (RAF1) NP_001341624.1:p.His497=
NR_148940.2:n.2276A= (RAF1)
NR_148941.2:n.2222A= (RAF1)
NR_148942.2:n.2161A= (RAF1)
NM_001354690.3:c.1832A= (RAF1) NP_001341619.1:p.His611=
NM_001354691.3:c.1589A= (RAF1) NP_001341620.1:p.His530=
NM_001354692.3:c.1589A= (RAF1) NP_001341621.1:p.His530=
NM_001354693.3:c.1733A= (RAF1) NP_001341622.1:p.His578=
NM_001354694.3:c.1649A= (RAF1) NP_001341623.1:p.His550=
NM_001354695.3:c.1490A= (RAF1) NP_001341624.1:p.His497=
NM_002880.4:c.1832A= (RAF1) MANE Select NP_002871.1:p.His611=
NR_148940.3:n.2276A= (RAF1)
NR_148941.3:n.2222A= (RAF1)
NR_148942.3:n.2161A= (RAF1)