Canonical Allele Identifier: CA432273071
Gene: RAF1 HGNC NCBI

Linked Data

dbSNP Id: rs2125342690
MyVariant Identifiers: chr3:g.12632308A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12590809A>G , CM000665.2:g.12590809A>G GRCh38
NC_000003.11:g.12632308A>G , CM000665.1:g.12632308A>G GRCh37
NC_000003.10:g.12607308A>G NCBI36
NG_007467.1:g.78371T>C , LRG_413:g.78371T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000423275.6:c.*1024T>C ENSP00000401088.1:n.*1024T>C
ENST00000432427.3:c.676T>C
ENST00000460610.2:n.153T>C
ENST00000465826.6:n.950T>C
ENST00000475353.2:n.1281T>C
ENST00000494557.2:n.1170T>C
ENST00000684903.1:c.*1036T>C ENSP00000508612.1:n.*1036T>C
ENST00000685348.1:c.*1036T>C ENSP00000510285.1:n.*1036T>C
ENST00000685437.1:c.1260T>C ENSP00000508794.1:p.Ala420=
ENST00000685653.1:c.1359T>C ENSP00000509968.1:p.Ala453=
ENST00000685738.1:c.*323T>C ENSP00000510156.1:n.*323T>C
ENST00000686409.1:n.2410T>C
ENST00000686455.1:n.1722T>C
ENST00000686762.1:c.1359T>C ENSP00000509767.1:p.Ala453=
ENST00000687257.1:n.1595T>C
ENST00000687326.1:c.*293T>C ENSP00000509665.1:n.*293T>C
ENST00000687505.1:n.1477T>C
ENST00000687923.1:c.1248T>C ENSP00000510255.1:p.Ala416=
ENST00000687940.1:n.1736T>C
ENST00000688269.1:n.1955T>C
ENST00000688326.1:c.792T>C
ENST00000688444.1:n.1685T>C
ENST00000688543.1:c.1260T>C ENSP00000509612.1:p.Ala420=
ENST00000688625.1:c.*937T>C ENSP00000509522.1:n.*937T>C
ENST00000688803.1:n.1590T>C
ENST00000688914.1:n.345T>C
ENST00000689097.1:c.*1036T>C ENSP00000509756.1:n.*1036T>C
ENST00000689389.1:c.1193+899T>C ENSP00000510213.1:n.1193+899T>C
ENST00000689418.1:c.*1036T>C ENSP00000509467.1:n.*1036T>C
ENST00000689481.1:c.*1036T>C ENSP00000510248.1:n.*1036T>C
ENST00000689540.1:n.1509T>C
ENST00000689876.1:c.1359T>C ENSP00000508535.1:p.Ala453=
ENST00000689914.1:c.*293T>C ENSP00000509847.1:n.*293T>C
ENST00000690397.1:c.1248T>C ENSP00000508730.1:p.Ala416=
ENST00000690460.1:c.1347T>C ENSP00000509106.1:p.Ala449=
ENST00000690585.1:c.251T>C
ENST00000690625.1:n.2395T>C
ENST00000691396.1:c.*1211T>C ENSP00000510712.1:n.*1211T>C
ENST00000691724.1:c.*316T>C ENSP00000509255.1:n.*316T>C
ENST00000691779.1:c.*937T>C ENSP00000508592.1:n.*937T>C
ENST00000691888.1:c.251T>C
ENST00000691899.1:c.1359T>C ENSP00000508763.1:p.Ala453=
ENST00000692069.1:n.1925T>C
ENST00000692093.1:c.1260T>C ENSP00000509669.1:p.Ala420=
ENST00000692311.1:n.2183T>C
ENST00000692558.1:n.1724T>C
ENST00000692773.1:c.*1096T>C ENSP00000509055.1:n.*1096T>C
ENST00000692830.1:c.*1104T>C ENSP00000509461.1:n.*1104T>C
ENST00000693069.1:c.*293T>C ENSP00000510072.1:n.*293T>C
ENST00000693312.1:c.1134T>C ENSP00000508686.1:p.Ala378=
ENST00000693664.1:c.1359T>C ENSP00000509614.1:p.Ala453=
ENST00000693705.1:c.*1036T>C ENSP00000510697.1:n.*1036T>C
ENST00000251849.9:c.1359T>C MANE Select ENSP00000251849.4:p.Ala453=
ENST00000442415.7:c.1419T>C ENSP00000401888.2:p.Ala473=
ENST00000251849.8:c.1359T>C ENSP00000251849.4:p.Ala453=
ENST00000423275.5:c.*1036T>C ENSP00000401088.1:n.*1036T>C
ENST00000432427.2:c.996T>C ENSP00000398591.2:p.Ala332=
ENST00000442415.6:c.1419T>C ENSP00000401888.2:p.Ala473=
ENST00000460610.1:n.316T>C
ENST00000465826.5:n.716T>C
ENST00000475353.1:n.527T>C
ENST00000494557.1:n.375T>C
NM_002880.3:c.1359T>C , LRG_413t1:c.1359T>C NP_002871.1:p.Ala453=
XM_005265355.1:c.1359T>C XP_005265412.1:p.Ala453=
XM_005265357.1:c.1260T>C XP_005265414.1:p.Ala420=
XM_005265358.3:c.1116T>C XP_005265415.1:p.Ala372=
XM_005265359.3:c.1017T>C XP_005265416.1:p.Ala339=
XM_005265360.1:c.1359T>C XP_005265417.1:p.Ala453=
XM_011533974.1:c.1359T>C XP_011532276.1:p.Ala453=
XM_011533975.1:c.1116T>C XP_011532277.1:p.Ala372=
NM_001354689.1:c.1419T>C NP_001341618.1:p.Ala473=
NM_001354690.1:c.1359T>C NP_001341619.1:p.Ala453=
NM_001354691.1:c.1116T>C NP_001341620.1:p.Ala372=
NM_001354692.1:c.1116T>C NP_001341621.1:p.Ala372=
NM_001354693.1:c.1260T>C NP_001341622.1:p.Ala420=
NM_001354694.1:c.1176T>C NP_001341623.1:p.Ala392=
NM_001354695.1:c.1017T>C NP_001341624.1:p.Ala339=
NR_148940.1:n.1887T>C
NR_148941.1:n.1833T>C
NR_148942.1:n.1772T>C
XM_011533974.3:c.1359T>C XP_011532276.1:p.Ala453=
XM_017006966.1:c.1260T>C XP_016862455.1:p.Ala420=
NM_001354689.3:c.1419T>C NP_001341618.1:p.Ala473=
NM_001354690.2:c.1359T>C NP_001341619.1:p.Ala453=
NM_001354691.2:c.1116T>C NP_001341620.1:p.Ala372=
NM_001354692.2:c.1116T>C NP_001341621.1:p.Ala372=
NM_001354693.2:c.1260T>C NP_001341622.1:p.Ala420=
NM_001354694.2:c.1176T>C NP_001341623.1:p.Ala392=
NM_001354695.2:c.1017T>C NP_001341624.1:p.Ala339=
NR_148940.2:n.1803T>C
NR_148941.2:n.1749T>C
NR_148942.2:n.1688T>C
NM_001354690.3:c.1359T>C NP_001341619.1:p.Ala453=
NM_001354691.3:c.1116T>C NP_001341620.1:p.Ala372=
NM_001354692.3:c.1116T>C NP_001341621.1:p.Ala372=
NM_001354693.3:c.1260T>C NP_001341622.1:p.Ala420=
NM_001354694.3:c.1176T>C NP_001341623.1:p.Ala392=
NM_001354695.3:c.1017T>C NP_001341624.1:p.Ala339=
NM_002880.4:c.1359T>C MANE Select NP_002871.1:p.Ala453=
NR_148940.3:n.1803T>C
NR_148941.3:n.1749T>C
NR_148942.3:n.1688T>C