Canonical Allele Identifier: CA1346226903

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12584963G= , CM000665.2:g.12584963G= GRCh38
NC_000003.11:g.12626462G= , CM000665.1:g.12626462G= GRCh37
NC_000003.10:g.12601462G= NCBI36
NG_007467.1:g.84217C= , LRG_413:g.84217C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000423275.6:c.*1352C= (RAF1) ENSP00000401088.1:n.*1352C=
ENST00000432427.3:c.1004C= (RAF1)
ENST00000460610.2:n.5999C= (RAF1)
ENST00000471449.2:n.497C= (RAF1)
ENST00000475353.2:n.3967C= (RAF1)
ENST00000684903.1:c.*1364C= (RAF1) ENSP00000508612.1:n.*1364C=
ENST00000685348.1:c.*1398C= (RAF1) ENSP00000510285.1:n.*1398C=
ENST00000685437.1:c.1588C= (RAF1) ENSP00000508794.1:p.Arg530=
ENST00000685653.1:c.1687C= (RAF1) ENSP00000509968.1:p.Arg563=
ENST00000685697.1:n.2422C= (RAF1)
ENST00000685738.1:c.*651C= (RAF1) ENSP00000510156.1:n.*651C=
ENST00000686409.1:n.5096C= (RAF1)
ENST00000686455.1:n.4408C= (RAF1)
ENST00000686762.1:c.*246C= (RAF1) ENSP00000509767.1:n.*246C=
ENST00000687257.1:n.4141C= (RAF1)
ENST00000687326.1:c.*2979C= (RAF1) ENSP00000509665.1:n.*2979C=
ENST00000687505.1:n.1805C= (RAF1)
ENST00000687923.1:c.1576C= (RAF1) ENSP00000510255.1:p.Arg526=
ENST00000688269.1:n.2283C= (RAF1)
ENST00000688444.1:n.3804C= (RAF1)
ENST00000688543.1:c.1588C= (RAF1) ENSP00000509612.1:p.Arg530=
ENST00000688625.1:c.*3056C= (RAF1) ENSP00000509522.1:n.*3056C=
ENST00000688803.1:n.3115C= (RAF1)
ENST00000688914.1:n.1100C= (RAF1)
ENST00000689097.1:c.*1364C= (RAF1) ENSP00000509756.1:n.*1364C=
ENST00000689389.1:c.1510C= (RAF1) ENSP00000510213.1:p.Arg504=
ENST00000689418.1:c.*3582C= (RAF1) ENSP00000509467.1:n.*3582C=
ENST00000689540.1:n.4055C= (RAF1)
ENST00000689876.1:c.*236C= (RAF1) ENSP00000508535.1:n.*236C=
ENST00000689914.1:c.*621C= (RAF1) ENSP00000509847.1:n.*621C=
ENST00000690397.1:c.1576C= (RAF1) ENSP00000508730.1:p.Arg526=
ENST00000690460.1:c.1675C= (RAF1) ENSP00000509106.1:p.Arg559=
ENST00000690585.1:c.413C= (RAF1)
ENST00000690625.1:n.2723C= (RAF1)
ENST00000691396.1:c.*1559C= (RAF1) ENSP00000510712.1:n.*1559C=
ENST00000691643.1:n.2740C= (RAF1)
ENST00000691724.1:c.*644C= (RAF1) ENSP00000509255.1:n.*644C=
ENST00000691779.1:c.*1265C= (RAF1) ENSP00000508592.1:n.*1265C=
ENST00000691888.1:c.561C= (RAF1)
ENST00000691899.1:c.1687C= (RAF1) ENSP00000508763.1:p.Arg563=
ENST00000692069.1:n.4611C= (RAF1)
ENST00000692093.1:c.1588C= (RAF1) ENSP00000509669.1:p.Arg530=
ENST00000692311.1:n.2511C= (RAF1)
ENST00000692558.1:n.4270C= (RAF1)
ENST00000692773.1:c.*1424C= (RAF1) ENSP00000509055.1:n.*1424C=
ENST00000692830.1:c.*1432C= (RAF1) ENSP00000509461.1:n.*1432C=
ENST00000693312.1:c.1462C= (RAF1) ENSP00000508686.1:p.Arg488=
ENST00000693664.1:c.*138C= (RAF1) ENSP00000509614.1:n.*138C=
ENST00000693705.1:c.*1066C= (RAF1) ENSP00000510697.1:n.*1066C=
ENST00000251849.9:c.1687C= (RAF1) MANE Select ENSP00000251849.4:p.Arg563=
ENST00000442415.7:c.1747C= (RAF1) ENSP00000401888.2:p.Arg583=
ENST00000676541.1:c.*2710G= (MKRN2) ENSP00000503730.1:n.*2710G=
ENST00000677142.1:c.*2710G= (MKRN2) ENSP00000504455.1:n.*2710G=
ENST00000677816.1:c.*1265G= (MKRN2) ENSP00000502893.1:n.*1265G=
ENST00000677941.1:n.2773G= (MKRN2)
ENST00000251849.8:c.1687C= (RAF1) ENSP00000251849.4:p.Arg563=
ENST00000423275.5:c.*1364C= (RAF1) ENSP00000401088.1:n.*1364C=
ENST00000432427.2:c.1324C= (RAF1) ENSP00000398591.2:p.Arg442=
ENST00000442415.6:c.1747C= (RAF1) ENSP00000401888.2:p.Arg583=
ENST00000471449.1:n.376C= (RAF1)
NM_002880.3:c.1687C= , LRG_413t1:c.1687C= (RAF1) NP_002871.1:p.Arg563=
XM_005265355.1:c.1687C= (RAF1) XP_005265412.1:p.Arg563=
XM_005265357.1:c.1588C= (RAF1) XP_005265414.1:p.Arg530=
XM_005265358.3:c.1444C= (RAF1) XP_005265415.1:p.Arg482=
XM_005265359.3:c.1345C= (RAF1) XP_005265416.1:p.Arg449=
XM_011533974.1:c.1687C= (RAF1) XP_011532276.1:p.Arg563=
XM_011533975.1:c.1444C= (RAF1) XP_011532277.1:p.Arg482=
NM_001354689.1:c.1747C= (RAF1) NP_001341618.1:p.Arg583=
NM_001354690.1:c.1687C= (RAF1) NP_001341619.1:p.Arg563=
NM_001354691.1:c.1444C= (RAF1) NP_001341620.1:p.Arg482=
NM_001354692.1:c.1444C= (RAF1) NP_001341621.1:p.Arg482=
NM_001354693.1:c.1588C= (RAF1) NP_001341622.1:p.Arg530=
NM_001354694.1:c.1504C= (RAF1) NP_001341623.1:p.Arg502=
NM_001354695.1:c.1345C= (RAF1) NP_001341624.1:p.Arg449=
NR_148940.1:n.2215C= (RAF1)
NR_148941.1:n.2161C= (RAF1)
NR_148942.1:n.2100C= (RAF1)
XM_011533974.3:c.1687C= (RAF1) XP_011532276.1:p.Arg563=
XM_017006966.1:c.1588C= (RAF1) XP_016862455.1:p.Arg530=
NM_001354689.3:c.1747C= (RAF1) NP_001341618.1:p.Arg583=
NM_001354690.2:c.1687C= (RAF1) NP_001341619.1:p.Arg563=
NM_001354691.2:c.1444C= (RAF1) NP_001341620.1:p.Arg482=
NM_001354692.2:c.1444C= (RAF1) NP_001341621.1:p.Arg482=
NM_001354693.2:c.1588C= (RAF1) NP_001341622.1:p.Arg530=
NM_001354694.2:c.1504C= (RAF1) NP_001341623.1:p.Arg502=
NM_001354695.2:c.1345C= (RAF1) NP_001341624.1:p.Arg449=
NR_148940.2:n.2131C= (RAF1)
NR_148941.2:n.2077C= (RAF1)
NR_148942.2:n.2016C= (RAF1)
NM_001354690.3:c.1687C= (RAF1) NP_001341619.1:p.Arg563=
NM_001354691.3:c.1444C= (RAF1) NP_001341620.1:p.Arg482=
NM_001354692.3:c.1444C= (RAF1) NP_001341621.1:p.Arg482=
NM_001354693.3:c.1588C= (RAF1) NP_001341622.1:p.Arg530=
NM_001354694.3:c.1504C= (RAF1) NP_001341623.1:p.Arg502=
NM_001354695.3:c.1345C= (RAF1) NP_001341624.1:p.Arg449=
NM_002880.4:c.1687C= (RAF1) MANE Select NP_002871.1:p.Arg563=
NR_148940.3:n.2131C= (RAF1)
NR_148941.3:n.2077C= (RAF1)
NR_148942.3:n.2016C= (RAF1)