Canonical Allele Identifier: CA351501921
Gene: RAF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2126217
ClinVar RCV Id: RCV003051546

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12590855G>T , CM000665.2:g.12590855G>T GRCh38
NC_000003.11:g.12632354G>T , CM000665.1:g.12632354G>T GRCh37
NC_000003.10:g.12607354G>T NCBI36
NG_007467.1:g.78325C>A , LRG_413:g.78325C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000423275.6:c.*978C>A ENSP00000401088.1:n.*978C>A
ENST00000432427.3:c.630C>A
ENST00000460610.2:n.107C>A
ENST00000465826.6:n.904C>A
ENST00000475353.2:n.1235C>A
ENST00000494557.2:n.1124C>A
ENST00000684903.1:c.*990C>A ENSP00000508612.1:n.*990C>A
ENST00000685348.1:c.*990C>A ENSP00000510285.1:n.*990C>A
ENST00000685437.1:c.1214C>A ENSP00000508794.1:p.Thr405Asn
ENST00000685653.1:c.1313C>A ENSP00000509968.1:p.Thr438Asn
ENST00000685738.1:c.*277C>A ENSP00000510156.1:n.*277C>A
ENST00000686409.1:n.2364C>A
ENST00000686455.1:n.1676C>A
ENST00000686762.1:c.1313C>A ENSP00000509767.1:p.Thr438Asn
ENST00000687257.1:n.1549C>A
ENST00000687326.1:c.*247C>A ENSP00000509665.1:n.*247C>A
ENST00000687505.1:n.1431C>A
ENST00000687923.1:c.1202C>A ENSP00000510255.1:p.Thr401Asn
ENST00000687940.1:n.1690C>A
ENST00000688269.1:n.1909C>A
ENST00000688326.1:c.746C>A
ENST00000688444.1:n.1639C>A
ENST00000688543.1:c.1214C>A ENSP00000509612.1:p.Thr405Asn
ENST00000688625.1:c.*891C>A ENSP00000509522.1:n.*891C>A
ENST00000688803.1:n.1544C>A
ENST00000688914.1:n.299C>A
ENST00000689097.1:c.*990C>A ENSP00000509756.1:n.*990C>A
ENST00000689389.1:c.1193+853C>A ENSP00000510213.1:n.1193+853C>A
ENST00000689418.1:c.*990C>A ENSP00000509467.1:n.*990C>A
ENST00000689481.1:c.*990C>A ENSP00000510248.1:n.*990C>A
ENST00000689540.1:n.1463C>A
ENST00000689876.1:c.1313C>A ENSP00000508535.1:p.Thr438Asn
ENST00000689914.1:c.*247C>A ENSP00000509847.1:n.*247C>A
ENST00000690397.1:c.1202C>A ENSP00000508730.1:p.Thr401Asn
ENST00000690460.1:c.1301C>A ENSP00000509106.1:p.Thr434Asn
ENST00000690585.1:c.205C>A
ENST00000690625.1:n.2349C>A
ENST00000691396.1:c.*1165C>A ENSP00000510712.1:n.*1165C>A
ENST00000691724.1:c.*270C>A ENSP00000509255.1:n.*270C>A
ENST00000691779.1:c.*891C>A ENSP00000508592.1:n.*891C>A
ENST00000691888.1:c.205C>A
ENST00000691899.1:c.1313C>A ENSP00000508763.1:p.Thr438Asn
ENST00000692069.1:n.1879C>A
ENST00000692093.1:c.1214C>A ENSP00000509669.1:p.Thr405Asn
ENST00000692311.1:n.2137C>A
ENST00000692558.1:n.1678C>A
ENST00000692773.1:c.*1050C>A ENSP00000509055.1:n.*1050C>A
ENST00000692830.1:c.*1058C>A ENSP00000509461.1:n.*1058C>A
ENST00000693069.1:c.*247C>A ENSP00000510072.1:n.*247C>A
ENST00000693312.1:c.1088C>A ENSP00000508686.1:p.Thr363Asn
ENST00000693664.1:c.1313C>A ENSP00000509614.1:p.Thr438Asn
ENST00000693705.1:c.*990C>A ENSP00000510697.1:n.*990C>A
ENST00000251849.9:c.1313C>A MANE Select ENSP00000251849.4:p.Thr438Asn
ENST00000442415.7:c.1373C>A ENSP00000401888.2:p.Thr458Asn
ENST00000251849.8:c.1313C>A ENSP00000251849.4:p.Thr438Asn
ENST00000423275.5:c.*990C>A ENSP00000401088.1:n.*990C>A
ENST00000432427.2:c.950C>A ENSP00000398591.2:p.Thr317Asn
ENST00000442415.6:c.1373C>A ENSP00000401888.2:p.Thr458Asn
ENST00000460610.1:n.270C>A
ENST00000465826.5:n.670C>A
ENST00000475353.1:n.481C>A
ENST00000494557.1:n.329C>A
NM_002880.3:c.1313C>A , LRG_413t1:c.1313C>A NP_002871.1:p.Thr438Asn
XM_005265355.1:c.1313C>A XP_005265412.1:p.Thr438Asn
XM_005265357.1:c.1214C>A XP_005265414.1:p.Thr405Asn
XM_005265358.3:c.1070C>A XP_005265415.1:p.Thr357Asn
XM_005265359.3:c.971C>A XP_005265416.1:p.Thr324Asn
XM_005265360.1:c.1313C>A XP_005265417.1:p.Thr438Asn
XM_011533974.1:c.1313C>A XP_011532276.1:p.Thr438Asn
XM_011533975.1:c.1070C>A XP_011532277.1:p.Thr357Asn
NM_001354689.1:c.1373C>A NP_001341618.1:p.Thr458Asn
NM_001354690.1:c.1313C>A NP_001341619.1:p.Thr438Asn
NM_001354691.1:c.1070C>A NP_001341620.1:p.Thr357Asn
NM_001354692.1:c.1070C>A NP_001341621.1:p.Thr357Asn
NM_001354693.1:c.1214C>A NP_001341622.1:p.Thr405Asn
NM_001354694.1:c.1130C>A NP_001341623.1:p.Thr377Asn
NM_001354695.1:c.971C>A NP_001341624.1:p.Thr324Asn
NR_148940.1:n.1841C>A
NR_148941.1:n.1787C>A
NR_148942.1:n.1726C>A
XM_011533974.3:c.1313C>A XP_011532276.1:p.Thr438Asn
XM_017006966.1:c.1214C>A XP_016862455.1:p.Thr405Asn
NM_001354689.3:c.1373C>A NP_001341618.1:p.Thr458Asn
NM_001354690.2:c.1313C>A NP_001341619.1:p.Thr438Asn
NM_001354691.2:c.1070C>A NP_001341620.1:p.Thr357Asn
NM_001354692.2:c.1070C>A NP_001341621.1:p.Thr357Asn
NM_001354693.2:c.1214C>A NP_001341622.1:p.Thr405Asn
NM_001354694.2:c.1130C>A NP_001341623.1:p.Thr377Asn
NM_001354695.2:c.971C>A NP_001341624.1:p.Thr324Asn
NR_148940.2:n.1757C>A
NR_148941.2:n.1703C>A
NR_148942.2:n.1642C>A
NM_001354690.3:c.1313C>A NP_001341619.1:p.Thr438Asn
NM_001354691.3:c.1070C>A NP_001341620.1:p.Thr357Asn
NM_001354692.3:c.1070C>A NP_001341621.1:p.Thr357Asn
NM_001354693.3:c.1214C>A NP_001341622.1:p.Thr405Asn
NM_001354694.3:c.1130C>A NP_001341623.1:p.Thr377Asn
NM_001354695.3:c.971C>A NP_001341624.1:p.Thr324Asn
NM_002880.4:c.1313C>A MANE Select NP_002871.1:p.Thr438Asn
NR_148940.3:n.1757C>A
NR_148941.3:n.1703C>A
NR_148942.3:n.1642C>A