Canonical Allele Identifier: CA351510162
Gene: RAF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1331356
dbSNP Id: rs2125381916

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12600413A>T , CM000665.2:g.12600413A>T GRCh38
NC_000003.11:g.12641912A>T , CM000665.1:g.12641912A>T GRCh37
NC_000003.10:g.12616912A>T NCBI36
NG_007467.1:g.68767T>A , LRG_413:g.68767T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000423275.6:c.*514T>A ENSP00000401088.1:n.*514T>A
ENST00000432427.3:c.157T>A
ENST00000465826.6:n.428T>A
ENST00000491290.2:n.1214T>A
ENST00000684903.1:c.*514T>A ENSP00000508612.1:n.*514T>A
ENST00000685348.1:c.*514T>A ENSP00000510285.1:n.*514T>A
ENST00000685437.1:c.738T>A ENSP00000508794.1:p.Asp246Glu
ENST00000685438.1:n.601T>A
ENST00000685653.1:c.837T>A ENSP00000509968.1:p.Asp279Glu
ENST00000685738.1:c.837T>A ENSP00000510156.1:p.Asp279Glu
ENST00000686409.1:n.1437T>A
ENST00000686455.1:n.1200T>A
ENST00000686479.1:n.1208T>A
ENST00000686762.1:c.837T>A ENSP00000509767.1:p.Asp279Glu
ENST00000687257.1:n.1073T>A
ENST00000687326.1:c.837T>A ENSP00000509665.1:p.Asp279Glu
ENST00000687486.1:c.157T>A
ENST00000687505.1:n.955T>A
ENST00000687923.1:c.738T>A ENSP00000510255.1:p.Asp246Glu
ENST00000687940.1:n.1214T>A
ENST00000688269.1:n.1445T>A
ENST00000688326.1:c.157T>A
ENST00000688444.1:n.1163T>A
ENST00000688543.1:c.738T>A ENSP00000509612.1:p.Asp246Glu
ENST00000688625.1:c.*415T>A ENSP00000509522.1:n.*415T>A
ENST00000688803.1:n.1068T>A
ENST00000689097.1:c.*514T>A ENSP00000509756.1:n.*514T>A
ENST00000689389.1:c.837T>A ENSP00000510213.1:p.Asp279Glu
ENST00000689418.1:c.*514T>A ENSP00000509467.1:n.*514T>A
ENST00000689481.1:c.*514T>A ENSP00000510248.1:n.*514T>A
ENST00000689540.1:n.987T>A
ENST00000689876.1:c.837T>A ENSP00000508535.1:p.Asp279Glu
ENST00000689914.1:c.837T>A ENSP00000509847.1:p.Asp279Glu
ENST00000690397.1:c.738T>A ENSP00000508730.1:p.Asp246Glu
ENST00000690460.1:c.837T>A ENSP00000509106.1:p.Asp279Glu
ENST00000690625.1:n.1140T>A
ENST00000691268.1:c.264T>A
ENST00000691396.1:c.*630T>A ENSP00000510712.1:n.*630T>A
ENST00000691724.1:c.837T>A ENSP00000509255.1:p.Asp279Glu
ENST00000691779.1:c.*415T>A ENSP00000508592.1:n.*415T>A
ENST00000691899.1:c.837T>A ENSP00000508763.1:p.Asp279Glu
ENST00000692069.1:n.952T>A
ENST00000692093.1:c.738T>A ENSP00000509669.1:p.Asp246Glu
ENST00000692311.1:n.1210T>A
ENST00000692558.1:n.1202T>A
ENST00000692773.1:c.*574T>A ENSP00000509055.1:n.*574T>A
ENST00000692830.1:c.*582T>A ENSP00000509461.1:n.*582T>A
ENST00000693069.1:c.738T>A ENSP00000510072.1:p.Asp246Glu
ENST00000693312.1:c.612T>A ENSP00000508686.1:p.Asp204Glu
ENST00000693664.1:c.837T>A ENSP00000509614.1:p.Asp279Glu
ENST00000693705.1:c.*514T>A ENSP00000510697.1:n.*514T>A
ENST00000251849.9:c.837T>A MANE Select ENSP00000251849.4:p.Asp279Glu
ENST00000442415.7:c.897T>A ENSP00000401888.2:p.Asp299Glu
ENST00000251849.8:c.837T>A ENSP00000251849.4:p.Asp279Glu
ENST00000423275.5:c.*514T>A ENSP00000401088.1:n.*514T>A
ENST00000432427.2:c.474T>A ENSP00000398591.2:p.Asp158Glu
ENST00000442415.6:c.897T>A ENSP00000401888.2:p.Asp299Glu
ENST00000465826.5:n.81T>A
ENST00000491290.1:n.358T>A
NM_002880.3:c.837T>A , LRG_413t1:c.837T>A NP_002871.1:p.Asp279Glu
XM_005265355.1:c.837T>A XP_005265412.1:p.Asp279Glu
XM_005265357.1:c.738T>A XP_005265414.1:p.Asp246Glu
XM_005265358.3:c.594T>A XP_005265415.1:p.Asp198Glu
XM_005265359.3:c.495T>A XP_005265416.1:p.Asp165Glu
XM_005265360.1:c.837T>A XP_005265417.1:p.Asp279Glu
XM_011533974.1:c.837T>A XP_011532276.1:p.Asp279Glu
XM_011533975.1:c.594T>A XP_011532277.1:p.Asp198Glu
NM_001354689.1:c.897T>A NP_001341618.1:p.Asp299Glu
NM_001354690.1:c.837T>A NP_001341619.1:p.Asp279Glu
NM_001354691.1:c.594T>A NP_001341620.1:p.Asp198Glu
NM_001354692.1:c.594T>A NP_001341621.1:p.Asp198Glu
NM_001354693.1:c.738T>A NP_001341622.1:p.Asp246Glu
NM_001354694.1:c.654T>A NP_001341623.1:p.Asp218Glu
NM_001354695.1:c.495T>A NP_001341624.1:p.Asp165Glu
NR_148940.1:n.1252T>A
NR_148941.1:n.1252T>A
NR_148942.1:n.1252T>A
XM_011533974.3:c.837T>A XP_011532276.1:p.Asp279Glu
XM_017006966.1:c.738T>A XP_016862455.1:p.Asp246Glu
XR_001740227.1:n.1069T>A
NM_001354689.3:c.897T>A NP_001341618.1:p.Asp299Glu
NM_001354690.2:c.837T>A NP_001341619.1:p.Asp279Glu
NM_001354691.2:c.594T>A NP_001341620.1:p.Asp198Glu
NM_001354692.2:c.594T>A NP_001341621.1:p.Asp198Glu
NM_001354693.2:c.738T>A NP_001341622.1:p.Asp246Glu
NM_001354694.2:c.654T>A NP_001341623.1:p.Asp218Glu
NM_001354695.2:c.495T>A NP_001341624.1:p.Asp165Glu
NR_148940.2:n.1168T>A
NR_148941.2:n.1168T>A
NR_148942.2:n.1168T>A
NM_001354690.3:c.837T>A NP_001341619.1:p.Asp279Glu
NM_001354691.3:c.594T>A NP_001341620.1:p.Asp198Glu
NM_001354692.3:c.594T>A NP_001341621.1:p.Asp198Glu
NM_001354693.3:c.738T>A NP_001341622.1:p.Asp246Glu
NM_001354694.3:c.654T>A NP_001341623.1:p.Asp218Glu
NM_001354695.3:c.495T>A NP_001341624.1:p.Asp165Glu
NM_002880.4:c.837T>A MANE Select NP_002871.1:p.Asp279Glu
NR_148940.3:n.1168T>A
NR_148941.3:n.1168T>A
NR_148942.3:n.1168T>A