Canonical Allele Identifier: CA351507218
Gene: RAF1 HGNC NCBI

Linked Data

dbSNP Id: rs2125377381

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12599704C>A , CM000665.2:g.12599704C>A GRCh38
NC_000003.11:g.12641203C>A , CM000665.1:g.12641203C>A GRCh37
NC_000003.10:g.12616203C>A NCBI36
NG_007467.1:g.69476G>T , LRG_413:g.69476G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000423275.6:c.*760G>T ENSP00000401088.1:n.*760G>T
ENST00000432427.3:c.415G>T
ENST00000465826.6:n.686G>T
ENST00000491290.2:n.1472G>T
ENST00000684903.1:c.*772G>T ENSP00000508612.1:n.*772G>T
ENST00000685348.1:c.*772G>T ENSP00000510285.1:n.*772G>T
ENST00000685437.1:c.996G>T ENSP00000508794.1:p.Lys332Asn
ENST00000685653.1:c.1095G>T ENSP00000509968.1:p.Lys365Asn
ENST00000685738.1:c.1095G>T ENSP00000510156.1:p.Lys365Asn
ENST00000686409.1:n.2146G>T
ENST00000686455.1:n.1458G>T
ENST00000686479.1:n.1466G>T
ENST00000686762.1:c.1095G>T ENSP00000509767.1:p.Lys365Asn
ENST00000687257.1:n.1331G>T
ENST00000687326.1:c.1095G>T ENSP00000509665.1:p.Lys365Asn
ENST00000687486.1:c.287G>T
ENST00000687505.1:n.1213G>T
ENST00000687923.1:c.996G>T ENSP00000510255.1:p.Lys332Asn
ENST00000687940.1:n.1472G>T
ENST00000688269.1:n.1691G>T
ENST00000688326.1:c.415G>T
ENST00000688444.1:n.1421G>T
ENST00000688543.1:c.996G>T ENSP00000509612.1:p.Lys332Asn
ENST00000688625.1:c.*673G>T ENSP00000509522.1:n.*673G>T
ENST00000688803.1:n.1326G>T
ENST00000688914.1:n.81G>T
ENST00000689097.1:c.*772G>T ENSP00000509756.1:n.*772G>T
ENST00000689389.1:c.1095G>T ENSP00000510213.1:p.Lys365Asn
ENST00000689418.1:c.*772G>T ENSP00000509467.1:n.*772G>T
ENST00000689481.1:c.*772G>T ENSP00000510248.1:n.*772G>T
ENST00000689540.1:n.1245G>T
ENST00000689876.1:c.1095G>T ENSP00000508535.1:p.Lys365Asn
ENST00000689914.1:c.1095G>T ENSP00000509847.1:p.Lys365Asn
ENST00000690397.1:c.984G>T ENSP00000508730.1:p.Lys328Asn
ENST00000690460.1:c.1083G>T ENSP00000509106.1:p.Lys361Asn
ENST00000690625.1:n.1398G>T
ENST00000691268.1:c.522G>T
ENST00000691396.1:c.*888G>T ENSP00000510712.1:n.*888G>T
ENST00000691724.1:c.*52G>T ENSP00000509255.1:n.*52G>T
ENST00000691779.1:c.*673G>T ENSP00000508592.1:n.*673G>T
ENST00000691899.1:c.1095G>T ENSP00000508763.1:p.Lys365Asn
ENST00000692069.1:n.1661G>T
ENST00000692093.1:c.996G>T ENSP00000509669.1:p.Lys332Asn
ENST00000692311.1:n.1919G>T
ENST00000692558.1:n.1460G>T
ENST00000692773.1:c.*832G>T ENSP00000509055.1:n.*832G>T
ENST00000692830.1:c.*840G>T ENSP00000509461.1:n.*840G>T
ENST00000693069.1:c.996G>T ENSP00000510072.1:p.Lys332Asn
ENST00000693312.1:c.870G>T ENSP00000508686.1:p.Lys290Asn
ENST00000693664.1:c.1095G>T ENSP00000509614.1:p.Lys365Asn
ENST00000693705.1:c.*772G>T ENSP00000510697.1:n.*772G>T
ENST00000251849.9:c.1095G>T MANE Select ENSP00000251849.4:p.Lys365Asn
ENST00000442415.7:c.1155G>T ENSP00000401888.2:p.Lys385Asn
ENST00000251849.8:c.1095G>T ENSP00000251849.4:p.Lys365Asn
ENST00000423275.5:c.*772G>T ENSP00000401088.1:n.*772G>T
ENST00000432427.2:c.732G>T ENSP00000398591.2:p.Lys244Asn
ENST00000442415.6:c.1155G>T ENSP00000401888.2:p.Lys385Asn
ENST00000460610.1:n.52G>T
ENST00000465826.5:n.339G>T
NM_002880.3:c.1095G>T , LRG_413t1:c.1095G>T NP_002871.1:p.Lys365Asn
XM_005265355.1:c.1095G>T XP_005265412.1:p.Lys365Asn
XM_005265357.1:c.996G>T XP_005265414.1:p.Lys332Asn
XM_005265358.3:c.852G>T XP_005265415.1:p.Lys284Asn
XM_005265359.3:c.753G>T XP_005265416.1:p.Lys251Asn
XM_005265360.1:c.1095G>T XP_005265417.1:p.Lys365Asn
XM_011533974.1:c.1095G>T XP_011532276.1:p.Lys365Asn
XM_011533975.1:c.852G>T XP_011532277.1:p.Lys284Asn
NM_001354689.1:c.1155G>T NP_001341618.1:p.Lys385Asn
NM_001354690.1:c.1095G>T NP_001341619.1:p.Lys365Asn
NM_001354691.1:c.852G>T NP_001341620.1:p.Lys284Asn
NM_001354692.1:c.852G>T NP_001341621.1:p.Lys284Asn
NM_001354693.1:c.996G>T NP_001341622.1:p.Lys332Asn
NM_001354694.1:c.912G>T NP_001341623.1:p.Lys304Asn
NM_001354695.1:c.753G>T NP_001341624.1:p.Lys251Asn
NR_148940.1:n.1510G>T
NR_148941.1:n.1510G>T
NR_148942.1:n.1508G>T
XM_011533974.3:c.1095G>T XP_011532276.1:p.Lys365Asn
XM_017006966.1:c.996G>T XP_016862455.1:p.Lys332Asn
XR_001740227.1:n.1327G>T
NM_001354689.3:c.1155G>T NP_001341618.1:p.Lys385Asn
NM_001354690.2:c.1095G>T NP_001341619.1:p.Lys365Asn
NM_001354691.2:c.852G>T NP_001341620.1:p.Lys284Asn
NM_001354692.2:c.852G>T NP_001341621.1:p.Lys284Asn
NM_001354693.2:c.996G>T NP_001341622.1:p.Lys332Asn
NM_001354694.2:c.912G>T NP_001341623.1:p.Lys304Asn
NM_001354695.2:c.753G>T NP_001341624.1:p.Lys251Asn
NR_148940.2:n.1426G>T
NR_148941.2:n.1426G>T
NR_148942.2:n.1424G>T
NM_001354690.3:c.1095G>T NP_001341619.1:p.Lys365Asn
NM_001354691.3:c.852G>T NP_001341620.1:p.Lys284Asn
NM_001354692.3:c.852G>T NP_001341621.1:p.Lys284Asn
NM_001354693.3:c.996G>T NP_001341622.1:p.Lys332Asn
NM_001354694.3:c.912G>T NP_001341623.1:p.Lys304Asn
NM_001354695.3:c.753G>T NP_001341624.1:p.Lys251Asn
NM_002880.4:c.1095G>T MANE Select NP_002871.1:p.Lys365Asn
NR_148940.3:n.1426G>T
NR_148941.3:n.1426G>T
NR_148942.3:n.1424G>T