Canonical Allele Identifier: CA1346226938

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12584975A= , CM000665.2:g.12584975A= GRCh38
NC_000003.11:g.12626474A= , CM000665.1:g.12626474A= GRCh37
NC_000003.10:g.12601474A= NCBI36
NG_007467.1:g.84205T= , LRG_413:g.84205T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000423275.6:c.*1340T= (RAF1) ENSP00000401088.1:n.*1340T=
ENST00000432427.3:c.992T= (RAF1)
ENST00000460610.2:n.5987T= (RAF1)
ENST00000471449.2:n.485T= (RAF1)
ENST00000475353.2:n.3955T= (RAF1)
ENST00000684903.1:c.*1352T= (RAF1) ENSP00000508612.1:n.*1352T=
ENST00000685348.1:c.*1386T= (RAF1) ENSP00000510285.1:n.*1386T=
ENST00000685437.1:c.1576T= (RAF1) ENSP00000508794.1:p.Phe526=
ENST00000685653.1:c.1675T= (RAF1) ENSP00000509968.1:p.Phe559=
ENST00000685697.1:n.2410T= (RAF1)
ENST00000685738.1:c.*639T= (RAF1) ENSP00000510156.1:n.*639T=
ENST00000686409.1:n.5084T= (RAF1)
ENST00000686455.1:n.4396T= (RAF1)
ENST00000686762.1:c.*234T= (RAF1) ENSP00000509767.1:n.*234T=
ENST00000687257.1:n.4129T= (RAF1)
ENST00000687326.1:c.*2967T= (RAF1) ENSP00000509665.1:n.*2967T=
ENST00000687505.1:n.1793T= (RAF1)
ENST00000687923.1:c.1564T= (RAF1) ENSP00000510255.1:p.Phe522=
ENST00000688269.1:n.2271T= (RAF1)
ENST00000688444.1:n.3792T= (RAF1)
ENST00000688543.1:c.1576T= (RAF1) ENSP00000509612.1:p.Phe526=
ENST00000688625.1:c.*3044T= (RAF1) ENSP00000509522.1:n.*3044T=
ENST00000688803.1:n.3103T= (RAF1)
ENST00000688914.1:n.1088T= (RAF1)
ENST00000689097.1:c.*1352T= (RAF1) ENSP00000509756.1:n.*1352T=
ENST00000689389.1:c.1498T= (RAF1) ENSP00000510213.1:p.Phe500=
ENST00000689418.1:c.*3570T= (RAF1) ENSP00000509467.1:n.*3570T=
ENST00000689540.1:n.4043T= (RAF1)
ENST00000689876.1:c.*224T= (RAF1) ENSP00000508535.1:n.*224T=
ENST00000689914.1:c.*609T= (RAF1) ENSP00000509847.1:n.*609T=
ENST00000690397.1:c.1564T= (RAF1) ENSP00000508730.1:p.Phe522=
ENST00000690460.1:c.1663T= (RAF1) ENSP00000509106.1:p.Phe555=
ENST00000690585.1:c.401T= (RAF1)
ENST00000690625.1:n.2711T= (RAF1)
ENST00000691396.1:c.*1547T= (RAF1) ENSP00000510712.1:n.*1547T=
ENST00000691643.1:n.2728T= (RAF1)
ENST00000691724.1:c.*632T= (RAF1) ENSP00000509255.1:n.*632T=
ENST00000691779.1:c.*1253T= (RAF1) ENSP00000508592.1:n.*1253T=
ENST00000691888.1:c.549T= (RAF1)
ENST00000691899.1:c.1675T= (RAF1) ENSP00000508763.1:p.Phe559=
ENST00000692069.1:n.4599T= (RAF1)
ENST00000692093.1:c.1576T= (RAF1) ENSP00000509669.1:p.Phe526=
ENST00000692311.1:n.2499T= (RAF1)
ENST00000692558.1:n.4258T= (RAF1)
ENST00000692773.1:c.*1412T= (RAF1) ENSP00000509055.1:n.*1412T=
ENST00000692830.1:c.*1420T= (RAF1) ENSP00000509461.1:n.*1420T=
ENST00000693312.1:c.1450T= (RAF1) ENSP00000508686.1:p.Phe484=
ENST00000693664.1:c.*126T= (RAF1) ENSP00000509614.1:n.*126T=
ENST00000693705.1:c.*1054T= (RAF1) ENSP00000510697.1:n.*1054T=
ENST00000251849.9:c.1675T= (RAF1) MANE Select ENSP00000251849.4:p.Phe559=
ENST00000442415.7:c.1735T= (RAF1) ENSP00000401888.2:p.Phe579=
ENST00000676541.1:c.*2722A= (MKRN2) ENSP00000503730.1:n.*2722A=
ENST00000677142.1:c.*2722A= (MKRN2) ENSP00000504455.1:n.*2722A=
ENST00000677816.1:c.*1277A= (MKRN2) ENSP00000502893.1:n.*1277A=
ENST00000677941.1:n.2785A= (MKRN2)
ENST00000251849.8:c.1675T= (RAF1) ENSP00000251849.4:p.Phe559=
ENST00000423275.5:c.*1352T= (RAF1) ENSP00000401088.1:n.*1352T=
ENST00000432427.2:c.1312T= (RAF1) ENSP00000398591.2:p.Phe438=
ENST00000442415.6:c.1735T= (RAF1) ENSP00000401888.2:p.Phe579=
ENST00000471449.1:n.364T= (RAF1)
NM_002880.3:c.1675T= , LRG_413t1:c.1675T= (RAF1) NP_002871.1:p.Phe559=
XM_005265355.1:c.1675T= (RAF1) XP_005265412.1:p.Phe559=
XM_005265357.1:c.1576T= (RAF1) XP_005265414.1:p.Phe526=
XM_005265358.3:c.1432T= (RAF1) XP_005265415.1:p.Phe478=
XM_005265359.3:c.1333T= (RAF1) XP_005265416.1:p.Phe445=
XM_011533974.1:c.1675T= (RAF1) XP_011532276.1:p.Phe559=
XM_011533975.1:c.1432T= (RAF1) XP_011532277.1:p.Phe478=
NM_001354689.1:c.1735T= (RAF1) NP_001341618.1:p.Phe579=
NM_001354690.1:c.1675T= (RAF1) NP_001341619.1:p.Phe559=
NM_001354691.1:c.1432T= (RAF1) NP_001341620.1:p.Phe478=
NM_001354692.1:c.1432T= (RAF1) NP_001341621.1:p.Phe478=
NM_001354693.1:c.1576T= (RAF1) NP_001341622.1:p.Phe526=
NM_001354694.1:c.1492T= (RAF1) NP_001341623.1:p.Phe498=
NM_001354695.1:c.1333T= (RAF1) NP_001341624.1:p.Phe445=
NR_148940.1:n.2203T= (RAF1)
NR_148941.1:n.2149T= (RAF1)
NR_148942.1:n.2088T= (RAF1)
XM_011533974.3:c.1675T= (RAF1) XP_011532276.1:p.Phe559=
XM_017006966.1:c.1576T= (RAF1) XP_016862455.1:p.Phe526=
NM_001354689.3:c.1735T= (RAF1) NP_001341618.1:p.Phe579=
NM_001354690.2:c.1675T= (RAF1) NP_001341619.1:p.Phe559=
NM_001354691.2:c.1432T= (RAF1) NP_001341620.1:p.Phe478=
NM_001354692.2:c.1432T= (RAF1) NP_001341621.1:p.Phe478=
NM_001354693.2:c.1576T= (RAF1) NP_001341622.1:p.Phe526=
NM_001354694.2:c.1492T= (RAF1) NP_001341623.1:p.Phe498=
NM_001354695.2:c.1333T= (RAF1) NP_001341624.1:p.Phe445=
NR_148940.2:n.2119T= (RAF1)
NR_148941.2:n.2065T= (RAF1)
NR_148942.2:n.2004T= (RAF1)
NM_001354690.3:c.1675T= (RAF1) NP_001341619.1:p.Phe559=
NM_001354691.3:c.1432T= (RAF1) NP_001341620.1:p.Phe478=
NM_001354692.3:c.1432T= (RAF1) NP_001341621.1:p.Phe478=
NM_001354693.3:c.1576T= (RAF1) NP_001341622.1:p.Phe526=
NM_001354694.3:c.1492T= (RAF1) NP_001341623.1:p.Phe498=
NM_001354695.3:c.1333T= (RAF1) NP_001341624.1:p.Phe445=
NM_002880.4:c.1675T= (RAF1) MANE Select NP_002871.1:p.Phe559=
NR_148940.3:n.2119T= (RAF1)
NR_148941.3:n.2065T= (RAF1)
NR_148942.3:n.2004T= (RAF1)