Canonical Allele Identifier: CA351495728

Linked Data

ClinVar Variation Id: 2302043
ClinVar RCV Id: RCV004154375

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12584572T>C , CM000665.2:g.12584572T>C GRCh38
NC_000003.11:g.12626071T>C , CM000665.1:g.12626071T>C GRCh37
NC_000003.10:g.12601071T>C NCBI36
NG_007467.1:g.84608A>G , LRG_413:g.84608A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000423275.6:c.*1554A>G (RAF1) ENSP00000401088.1:n.*1554A>G
ENST00000432427.3:c.1206A>G (RAF1)
ENST00000460610.2:n.6201A>G (RAF1)
ENST00000471449.2:n.699A>G (RAF1)
ENST00000475353.2:n.4169A>G (RAF1)
ENST00000684903.1:c.*1566A>G (RAF1) ENSP00000508612.1:n.*1566A>G
ENST00000685348.1:c.*1600A>G (RAF1) ENSP00000510285.1:n.*1600A>G
ENST00000685437.1:c.1790A>G (RAF1) ENSP00000508794.1:p.His597Arg
ENST00000685653.1:c.1889A>G (RAF1) ENSP00000509968.1:p.His630Arg
ENST00000685697.1:n.2624A>G (RAF1)
ENST00000685738.1:c.*853A>G (RAF1) ENSP00000510156.1:n.*853A>G
ENST00000686409.1:n.5298A>G (RAF1)
ENST00000686455.1:n.4610A>G (RAF1)
ENST00000686762.1:c.*448A>G (RAF1) ENSP00000509767.1:n.*448A>G
ENST00000687257.1:n.4343A>G (RAF1)
ENST00000687326.1:c.*3181A>G (RAF1) ENSP00000509665.1:n.*3181A>G
ENST00000687505.1:n.2007A>G (RAF1)
ENST00000687923.1:c.1778A>G (RAF1) ENSP00000510255.1:p.His593Arg
ENST00000688269.1:n.2485A>G (RAF1)
ENST00000688444.1:n.4006A>G (RAF1)
ENST00000688543.1:c.1790A>G (RAF1) ENSP00000509612.1:p.His597Arg
ENST00000688625.1:c.*3258A>G (RAF1) ENSP00000509522.1:n.*3258A>G
ENST00000688803.1:n.3317A>G (RAF1)
ENST00000689097.1:c.*1566A>G (RAF1) ENSP00000509756.1:n.*1566A>G
ENST00000689389.1:c.1712A>G (RAF1) ENSP00000510213.1:p.His571Arg
ENST00000689418.1:c.*3784A>G (RAF1) ENSP00000509467.1:n.*3784A>G
ENST00000689540.1:n.4257A>G (RAF1)
ENST00000689876.1:c.*438A>G (RAF1) ENSP00000508535.1:n.*438A>G
ENST00000689914.1:c.*823A>G (RAF1) ENSP00000509847.1:n.*823A>G
ENST00000690397.1:c.1778A>G (RAF1) ENSP00000508730.1:p.His593Arg
ENST00000690460.1:c.1877A>G (RAF1) ENSP00000509106.1:p.His626Arg
ENST00000690585.1:c.615A>G (RAF1)
ENST00000690625.1:n.2925A>G (RAF1)
ENST00000691396.1:c.*1761A>G (RAF1) ENSP00000510712.1:n.*1761A>G
ENST00000691643.1:n.2942A>G (RAF1)
ENST00000691724.1:c.*846A>G (RAF1) ENSP00000509255.1:n.*846A>G
ENST00000691779.1:c.*1467A>G (RAF1) ENSP00000508592.1:n.*1467A>G
ENST00000691888.1:c.763A>G (RAF1)
ENST00000691899.1:c.1889A>G (RAF1) ENSP00000508763.1:p.His630Arg
ENST00000692069.1:n.4813A>G (RAF1)
ENST00000692093.1:c.1790A>G (RAF1) ENSP00000509669.1:p.His597Arg
ENST00000692311.1:n.2713A>G (RAF1)
ENST00000692558.1:n.4472A>G (RAF1)
ENST00000692773.1:c.*1626A>G (RAF1) ENSP00000509055.1:n.*1626A>G
ENST00000692830.1:c.*1634A>G (RAF1) ENSP00000509461.1:n.*1634A>G
ENST00000693312.1:c.1664A>G (RAF1) ENSP00000508686.1:p.His555Arg
ENST00000693664.1:c.*340A>G (RAF1) ENSP00000509614.1:n.*340A>G
ENST00000693705.1:c.*1268A>G (RAF1) ENSP00000510697.1:n.*1268A>G
ENST00000251849.9:c.1889A>G (RAF1) MANE Select ENSP00000251849.4:p.His630Arg
ENST00000442415.7:c.1949A>G (RAF1) ENSP00000401888.2:p.His650Arg
ENST00000676541.1:c.*2319T>C (MKRN2) ENSP00000503730.1:n.*2319T>C
ENST00000677142.1:c.*2319T>C (MKRN2) ENSP00000504455.1:n.*2319T>C
ENST00000677816.1:c.*874T>C (MKRN2) ENSP00000502893.1:n.*874T>C
ENST00000677941.1:n.2382T>C (MKRN2)
ENST00000251849.8:c.1889A>G (RAF1) ENSP00000251849.4:p.His630Arg
ENST00000423275.5:c.*1566A>G (RAF1) ENSP00000401088.1:n.*1566A>G
ENST00000432427.2:c.1526A>G (RAF1) ENSP00000398591.2:p.His509Arg
ENST00000442415.6:c.1949A>G (RAF1) ENSP00000401888.2:p.His650Arg
ENST00000471449.1:n.578A>G (RAF1)
NM_002880.3:c.1889A>G , LRG_413t1:c.1889A>G (RAF1) NP_002871.1:p.His630Arg
XM_005265355.1:c.1889A>G (RAF1) XP_005265412.1:p.His630Arg
XM_005265357.1:c.1790A>G (RAF1) XP_005265414.1:p.His597Arg
XM_005265358.3:c.1646A>G (RAF1) XP_005265415.1:p.His549Arg
XM_005265359.3:c.1547A>G (RAF1) XP_005265416.1:p.His516Arg
XM_011533974.1:c.1889A>G (RAF1) XP_011532276.1:p.His630Arg
XM_011533975.1:c.1646A>G (RAF1) XP_011532277.1:p.His549Arg
NM_001354689.1:c.1949A>G (RAF1) NP_001341618.1:p.His650Arg
NM_001354690.1:c.1889A>G (RAF1) NP_001341619.1:p.His630Arg
NM_001354691.1:c.1646A>G (RAF1) NP_001341620.1:p.His549Arg
NM_001354692.1:c.1646A>G (RAF1) NP_001341621.1:p.His549Arg
NM_001354693.1:c.1790A>G (RAF1) NP_001341622.1:p.His597Arg
NM_001354694.1:c.1706A>G (RAF1) NP_001341623.1:p.His569Arg
NM_001354695.1:c.1547A>G (RAF1) NP_001341624.1:p.His516Arg
NR_148940.1:n.2417A>G (RAF1)
NR_148941.1:n.2363A>G (RAF1)
NR_148942.1:n.2302A>G (RAF1)
XM_011533974.3:c.1889A>G (RAF1) XP_011532276.1:p.His630Arg
XM_017006966.1:c.1790A>G (RAF1) XP_016862455.1:p.His597Arg
NM_001354689.3:c.1949A>G (RAF1) NP_001341618.1:p.His650Arg
NM_001354690.2:c.1889A>G (RAF1) NP_001341619.1:p.His630Arg
NM_001354691.2:c.1646A>G (RAF1) NP_001341620.1:p.His549Arg
NM_001354692.2:c.1646A>G (RAF1) NP_001341621.1:p.His549Arg
NM_001354693.2:c.1790A>G (RAF1) NP_001341622.1:p.His597Arg
NM_001354694.2:c.1706A>G (RAF1) NP_001341623.1:p.His569Arg
NM_001354695.2:c.1547A>G (RAF1) NP_001341624.1:p.His516Arg
NR_148940.2:n.2333A>G (RAF1)
NR_148941.2:n.2279A>G (RAF1)
NR_148942.2:n.2218A>G (RAF1)
NM_001354690.3:c.1889A>G (RAF1) NP_001341619.1:p.His630Arg
NM_001354691.3:c.1646A>G (RAF1) NP_001341620.1:p.His549Arg
NM_001354692.3:c.1646A>G (RAF1) NP_001341621.1:p.His549Arg
NM_001354693.3:c.1790A>G (RAF1) NP_001341622.1:p.His597Arg
NM_001354694.3:c.1706A>G (RAF1) NP_001341623.1:p.His569Arg
NM_001354695.3:c.1547A>G (RAF1) NP_001341624.1:p.His516Arg
NM_002880.4:c.1889A>G (RAF1) MANE Select NP_002871.1:p.His630Arg
NR_148940.3:n.2333A>G (RAF1)
NR_148941.3:n.2279A>G (RAF1)
NR_148942.3:n.2218A>G (RAF1)