Canonical Allele Identifier: CA351496843

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12584937A>C , CM000665.2:g.12584937A>C GRCh38
NC_000003.11:g.12626436A>C , CM000665.1:g.12626436A>C GRCh37
NC_000003.10:g.12601436A>C NCBI36
NG_007467.1:g.84243T>G , LRG_413:g.84243T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000423275.6:c.*1378T>G (RAF1) ENSP00000401088.1:n.*1378T>G
ENST00000432427.3:c.1030T>G (RAF1)
ENST00000460610.2:n.6025T>G (RAF1)
ENST00000471449.2:n.523T>G (RAF1)
ENST00000475353.2:n.3993T>G (RAF1)
ENST00000684903.1:c.*1390T>G (RAF1) ENSP00000508612.1:n.*1390T>G
ENST00000685348.1:c.*1424T>G (RAF1) ENSP00000510285.1:n.*1424T>G
ENST00000685437.1:c.1614T>G (RAF1) ENSP00000508794.1:p.Ser538Arg
ENST00000685653.1:c.1713T>G (RAF1) ENSP00000509968.1:p.Ser571Arg
ENST00000685697.1:n.2448T>G (RAF1)
ENST00000685738.1:c.*677T>G (RAF1) ENSP00000510156.1:n.*677T>G
ENST00000686409.1:n.5122T>G (RAF1)
ENST00000686455.1:n.4434T>G (RAF1)
ENST00000686762.1:c.*272T>G (RAF1) ENSP00000509767.1:n.*272T>G
ENST00000687257.1:n.4167T>G (RAF1)
ENST00000687326.1:c.*3005T>G (RAF1) ENSP00000509665.1:n.*3005T>G
ENST00000687505.1:n.1831T>G (RAF1)
ENST00000687923.1:c.1602T>G (RAF1) ENSP00000510255.1:p.Ser534Arg
ENST00000688269.1:n.2309T>G (RAF1)
ENST00000688444.1:n.3830T>G (RAF1)
ENST00000688543.1:c.1614T>G (RAF1) ENSP00000509612.1:p.Ser538Arg
ENST00000688625.1:c.*3082T>G (RAF1) ENSP00000509522.1:n.*3082T>G
ENST00000688803.1:n.3141T>G (RAF1)
ENST00000688914.1:n.1126T>G (RAF1)
ENST00000689097.1:c.*1390T>G (RAF1) ENSP00000509756.1:n.*1390T>G
ENST00000689389.1:c.1536T>G (RAF1) ENSP00000510213.1:p.Ser512Arg
ENST00000689418.1:c.*3608T>G (RAF1) ENSP00000509467.1:n.*3608T>G
ENST00000689540.1:n.4081T>G (RAF1)
ENST00000689876.1:c.*262T>G (RAF1) ENSP00000508535.1:n.*262T>G
ENST00000689914.1:c.*647T>G (RAF1) ENSP00000509847.1:n.*647T>G
ENST00000690397.1:c.1602T>G (RAF1) ENSP00000508730.1:p.Ser534Arg
ENST00000690460.1:c.1701T>G (RAF1) ENSP00000509106.1:p.Ser567Arg
ENST00000690585.1:c.439T>G (RAF1)
ENST00000690625.1:n.2749T>G (RAF1)
ENST00000691396.1:c.*1585T>G (RAF1) ENSP00000510712.1:n.*1585T>G
ENST00000691643.1:n.2766T>G (RAF1)
ENST00000691724.1:c.*670T>G (RAF1) ENSP00000509255.1:n.*670T>G
ENST00000691779.1:c.*1291T>G (RAF1) ENSP00000508592.1:n.*1291T>G
ENST00000691888.1:c.587T>G (RAF1)
ENST00000691899.1:c.1713T>G (RAF1) ENSP00000508763.1:p.Ser571Arg
ENST00000692069.1:n.4637T>G (RAF1)
ENST00000692093.1:c.1614T>G (RAF1) ENSP00000509669.1:p.Ser538Arg
ENST00000692311.1:n.2537T>G (RAF1)
ENST00000692558.1:n.4296T>G (RAF1)
ENST00000692773.1:c.*1450T>G (RAF1) ENSP00000509055.1:n.*1450T>G
ENST00000692830.1:c.*1458T>G (RAF1) ENSP00000509461.1:n.*1458T>G
ENST00000693312.1:c.1488T>G (RAF1) ENSP00000508686.1:p.Ser496Arg
ENST00000693664.1:c.*164T>G (RAF1) ENSP00000509614.1:n.*164T>G
ENST00000693705.1:c.*1092T>G (RAF1) ENSP00000510697.1:n.*1092T>G
ENST00000251849.9:c.1713T>G (RAF1) MANE Select ENSP00000251849.4:p.Ser571Arg
ENST00000442415.7:c.1773T>G (RAF1) ENSP00000401888.2:p.Ser591Arg
ENST00000676541.1:c.*2684A>C (MKRN2) ENSP00000503730.1:n.*2684A>C
ENST00000677142.1:c.*2684A>C (MKRN2) ENSP00000504455.1:n.*2684A>C
ENST00000677816.1:c.*1239A>C (MKRN2) ENSP00000502893.1:n.*1239A>C
ENST00000677941.1:n.2747A>C (MKRN2)
ENST00000251849.8:c.1713T>G (RAF1) ENSP00000251849.4:p.Ser571Arg
ENST00000423275.5:c.*1390T>G (RAF1) ENSP00000401088.1:n.*1390T>G
ENST00000432427.2:c.1350T>G (RAF1) ENSP00000398591.2:p.Ser450Arg
ENST00000442415.6:c.1773T>G (RAF1) ENSP00000401888.2:p.Ser591Arg
ENST00000471449.1:n.402T>G (RAF1)
NM_002880.3:c.1713T>G , LRG_413t1:c.1713T>G (RAF1) NP_002871.1:p.Ser571Arg
XM_005265355.1:c.1713T>G (RAF1) XP_005265412.1:p.Ser571Arg
XM_005265357.1:c.1614T>G (RAF1) XP_005265414.1:p.Ser538Arg
XM_005265358.3:c.1470T>G (RAF1) XP_005265415.1:p.Ser490Arg
XM_005265359.3:c.1371T>G (RAF1) XP_005265416.1:p.Ser457Arg
XM_011533974.1:c.1713T>G (RAF1) XP_011532276.1:p.Ser571Arg
XM_011533975.1:c.1470T>G (RAF1) XP_011532277.1:p.Ser490Arg
NM_001354689.1:c.1773T>G (RAF1) NP_001341618.1:p.Ser591Arg
NM_001354690.1:c.1713T>G (RAF1) NP_001341619.1:p.Ser571Arg
NM_001354691.1:c.1470T>G (RAF1) NP_001341620.1:p.Ser490Arg
NM_001354692.1:c.1470T>G (RAF1) NP_001341621.1:p.Ser490Arg
NM_001354693.1:c.1614T>G (RAF1) NP_001341622.1:p.Ser538Arg
NM_001354694.1:c.1530T>G (RAF1) NP_001341623.1:p.Ser510Arg
NM_001354695.1:c.1371T>G (RAF1) NP_001341624.1:p.Ser457Arg
NR_148940.1:n.2241T>G (RAF1)
NR_148941.1:n.2187T>G (RAF1)
NR_148942.1:n.2126T>G (RAF1)
XM_011533974.3:c.1713T>G (RAF1) XP_011532276.1:p.Ser571Arg
XM_017006966.1:c.1614T>G (RAF1) XP_016862455.1:p.Ser538Arg
NM_001354689.3:c.1773T>G (RAF1) NP_001341618.1:p.Ser591Arg
NM_001354690.2:c.1713T>G (RAF1) NP_001341619.1:p.Ser571Arg
NM_001354691.2:c.1470T>G (RAF1) NP_001341620.1:p.Ser490Arg
NM_001354692.2:c.1470T>G (RAF1) NP_001341621.1:p.Ser490Arg
NM_001354693.2:c.1614T>G (RAF1) NP_001341622.1:p.Ser538Arg
NM_001354694.2:c.1530T>G (RAF1) NP_001341623.1:p.Ser510Arg
NM_001354695.2:c.1371T>G (RAF1) NP_001341624.1:p.Ser457Arg
NR_148940.2:n.2157T>G (RAF1)
NR_148941.2:n.2103T>G (RAF1)
NR_148942.2:n.2042T>G (RAF1)
NM_001354690.3:c.1713T>G (RAF1) NP_001341619.1:p.Ser571Arg
NM_001354691.3:c.1470T>G (RAF1) NP_001341620.1:p.Ser490Arg
NM_001354692.3:c.1470T>G (RAF1) NP_001341621.1:p.Ser490Arg
NM_001354693.3:c.1614T>G (RAF1) NP_001341622.1:p.Ser538Arg
NM_001354694.3:c.1530T>G (RAF1) NP_001341623.1:p.Ser510Arg
NM_001354695.3:c.1371T>G (RAF1) NP_001341624.1:p.Ser457Arg
NM_002880.4:c.1713T>G (RAF1) MANE Select NP_002871.1:p.Ser571Arg
NR_148940.3:n.2157T>G (RAF1)
NR_148941.3:n.2103T>G (RAF1)
NR_148942.3:n.2042T>G (RAF1)