Canonical Allele Identifier: CA351496448

Linked Data

dbSNP Id: rs2058274541

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12584858G>T , CM000665.2:g.12584858G>T GRCh38
NC_000003.11:g.12626357G>T , CM000665.1:g.12626357G>T GRCh37
NC_000003.10:g.12601357G>T NCBI36
NG_007467.1:g.84322C>A , LRG_413:g.84322C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000423275.6:c.*1457C>A (RAF1) ENSP00000401088.1:n.*1457C>A
ENST00000432427.3:c.1109C>A (RAF1)
ENST00000460610.2:n.6104C>A (RAF1)
ENST00000471449.2:n.602C>A (RAF1)
ENST00000475353.2:n.4072C>A (RAF1)
ENST00000684903.1:c.*1469C>A (RAF1) ENSP00000508612.1:n.*1469C>A
ENST00000685348.1:c.*1503C>A (RAF1) ENSP00000510285.1:n.*1503C>A
ENST00000685437.1:c.1693C>A (RAF1) ENSP00000508794.1:p.Leu565Ile
ENST00000685653.1:c.1792C>A (RAF1) ENSP00000509968.1:p.Leu598Ile
ENST00000685697.1:n.2527C>A (RAF1)
ENST00000685738.1:c.*756C>A (RAF1) ENSP00000510156.1:n.*756C>A
ENST00000686409.1:n.5201C>A (RAF1)
ENST00000686455.1:n.4513C>A (RAF1)
ENST00000686762.1:c.*351C>A (RAF1) ENSP00000509767.1:n.*351C>A
ENST00000687257.1:n.4246C>A (RAF1)
ENST00000687326.1:c.*3084C>A (RAF1) ENSP00000509665.1:n.*3084C>A
ENST00000687505.1:n.1910C>A (RAF1)
ENST00000687923.1:c.1681C>A (RAF1) ENSP00000510255.1:p.Leu561Ile
ENST00000688269.1:n.2388C>A (RAF1)
ENST00000688444.1:n.3909C>A (RAF1)
ENST00000688543.1:c.1693C>A (RAF1) ENSP00000509612.1:p.Leu565Ile
ENST00000688625.1:c.*3161C>A (RAF1) ENSP00000509522.1:n.*3161C>A
ENST00000688803.1:n.3220C>A (RAF1)
ENST00000689097.1:c.*1469C>A (RAF1) ENSP00000509756.1:n.*1469C>A
ENST00000689389.1:c.1615C>A (RAF1) ENSP00000510213.1:p.Leu539Ile
ENST00000689418.1:c.*3687C>A (RAF1) ENSP00000509467.1:n.*3687C>A
ENST00000689540.1:n.4160C>A (RAF1)
ENST00000689876.1:c.*341C>A (RAF1) ENSP00000508535.1:n.*341C>A
ENST00000689914.1:c.*726C>A (RAF1) ENSP00000509847.1:n.*726C>A
ENST00000690397.1:c.1681C>A (RAF1) ENSP00000508730.1:p.Leu561Ile
ENST00000690460.1:c.1780C>A (RAF1) ENSP00000509106.1:p.Leu594Ile
ENST00000690585.1:c.518C>A (RAF1)
ENST00000690625.1:n.2828C>A (RAF1)
ENST00000691396.1:c.*1664C>A (RAF1) ENSP00000510712.1:n.*1664C>A
ENST00000691643.1:n.2845C>A (RAF1)
ENST00000691724.1:c.*749C>A (RAF1) ENSP00000509255.1:n.*749C>A
ENST00000691779.1:c.*1370C>A (RAF1) ENSP00000508592.1:n.*1370C>A
ENST00000691888.1:c.666C>A (RAF1)
ENST00000691899.1:c.1792C>A (RAF1) ENSP00000508763.1:p.Leu598Ile
ENST00000692069.1:n.4716C>A (RAF1)
ENST00000692093.1:c.1693C>A (RAF1) ENSP00000509669.1:p.Leu565Ile
ENST00000692311.1:n.2616C>A (RAF1)
ENST00000692558.1:n.4375C>A (RAF1)
ENST00000692773.1:c.*1529C>A (RAF1) ENSP00000509055.1:n.*1529C>A
ENST00000692830.1:c.*1537C>A (RAF1) ENSP00000509461.1:n.*1537C>A
ENST00000693312.1:c.1567C>A (RAF1) ENSP00000508686.1:p.Leu523Ile
ENST00000693664.1:c.*243C>A (RAF1) ENSP00000509614.1:n.*243C>A
ENST00000693705.1:c.*1171C>A (RAF1) ENSP00000510697.1:n.*1171C>A
ENST00000251849.9:c.1792C>A (RAF1) MANE Select ENSP00000251849.4:p.Leu598Ile
ENST00000442415.7:c.1852C>A (RAF1) ENSP00000401888.2:p.Leu618Ile
ENST00000676541.1:c.*2605G>T (MKRN2) ENSP00000503730.1:n.*2605G>T
ENST00000677142.1:c.*2605G>T (MKRN2) ENSP00000504455.1:n.*2605G>T
ENST00000677816.1:c.*1160G>T (MKRN2) ENSP00000502893.1:n.*1160G>T
ENST00000677941.1:n.2668G>T (MKRN2)
ENST00000251849.8:c.1792C>A (RAF1) ENSP00000251849.4:p.Leu598Ile
ENST00000423275.5:c.*1469C>A (RAF1) ENSP00000401088.1:n.*1469C>A
ENST00000432427.2:c.1429C>A (RAF1) ENSP00000398591.2:p.Leu477Ile
ENST00000442415.6:c.1852C>A (RAF1) ENSP00000401888.2:p.Leu618Ile
ENST00000471449.1:n.481C>A (RAF1)
NM_002880.3:c.1792C>A , LRG_413t1:c.1792C>A (RAF1) NP_002871.1:p.Leu598Ile
XM_005265355.1:c.1792C>A (RAF1) XP_005265412.1:p.Leu598Ile
XM_005265357.1:c.1693C>A (RAF1) XP_005265414.1:p.Leu565Ile
XM_005265358.3:c.1549C>A (RAF1) XP_005265415.1:p.Leu517Ile
XM_005265359.3:c.1450C>A (RAF1) XP_005265416.1:p.Leu484Ile
XM_011533974.1:c.1792C>A (RAF1) XP_011532276.1:p.Leu598Ile
XM_011533975.1:c.1549C>A (RAF1) XP_011532277.1:p.Leu517Ile
NM_001354689.1:c.1852C>A (RAF1) NP_001341618.1:p.Leu618Ile
NM_001354690.1:c.1792C>A (RAF1) NP_001341619.1:p.Leu598Ile
NM_001354691.1:c.1549C>A (RAF1) NP_001341620.1:p.Leu517Ile
NM_001354692.1:c.1549C>A (RAF1) NP_001341621.1:p.Leu517Ile
NM_001354693.1:c.1693C>A (RAF1) NP_001341622.1:p.Leu565Ile
NM_001354694.1:c.1609C>A (RAF1) NP_001341623.1:p.Leu537Ile
NM_001354695.1:c.1450C>A (RAF1) NP_001341624.1:p.Leu484Ile
NR_148940.1:n.2320C>A (RAF1)
NR_148941.1:n.2266C>A (RAF1)
NR_148942.1:n.2205C>A (RAF1)
XM_011533974.3:c.1792C>A (RAF1) XP_011532276.1:p.Leu598Ile
XM_017006966.1:c.1693C>A (RAF1) XP_016862455.1:p.Leu565Ile
NM_001354689.3:c.1852C>A (RAF1) NP_001341618.1:p.Leu618Ile
NM_001354690.2:c.1792C>A (RAF1) NP_001341619.1:p.Leu598Ile
NM_001354691.2:c.1549C>A (RAF1) NP_001341620.1:p.Leu517Ile
NM_001354692.2:c.1549C>A (RAF1) NP_001341621.1:p.Leu517Ile
NM_001354693.2:c.1693C>A (RAF1) NP_001341622.1:p.Leu565Ile
NM_001354694.2:c.1609C>A (RAF1) NP_001341623.1:p.Leu537Ile
NM_001354695.2:c.1450C>A (RAF1) NP_001341624.1:p.Leu484Ile
NR_148940.2:n.2236C>A (RAF1)
NR_148941.2:n.2182C>A (RAF1)
NR_148942.2:n.2121C>A (RAF1)
NM_001354690.3:c.1792C>A (RAF1) NP_001341619.1:p.Leu598Ile
NM_001354691.3:c.1549C>A (RAF1) NP_001341620.1:p.Leu517Ile
NM_001354692.3:c.1549C>A (RAF1) NP_001341621.1:p.Leu517Ile
NM_001354693.3:c.1693C>A (RAF1) NP_001341622.1:p.Leu565Ile
NM_001354694.3:c.1609C>A (RAF1) NP_001341623.1:p.Leu537Ile
NM_001354695.3:c.1450C>A (RAF1) NP_001341624.1:p.Leu484Ile
NM_002880.4:c.1792C>A (RAF1) MANE Select NP_002871.1:p.Leu598Ile
NR_148940.3:n.2236C>A (RAF1)
NR_148941.3:n.2182C>A (RAF1)
NR_148942.3:n.2121C>A (RAF1)