Canonical Allele Identifier: CA1346233273
Gene: RAF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12590902C= , CM000665.2:g.12590902C= GRCh38
NC_000003.11:g.12632401C= , CM000665.1:g.12632401C= GRCh37
NC_000003.10:g.12607401C= NCBI36
NG_007467.1:g.78278G= , LRG_413:g.78278G=

Transcript Alleles

HGVS Amino-acid change
ENST00000423275.6:c.*931G= ENSP00000401088.1:n.*931G=
ENST00000432427.3:c.583G=
ENST00000460610.2:n.60G=
ENST00000465826.6:n.857G=
ENST00000475353.2:n.1188G=
ENST00000494557.2:n.1077G=
ENST00000684903.1:c.*943G= ENSP00000508612.1:n.*943G=
ENST00000685348.1:c.*943G= ENSP00000510285.1:n.*943G=
ENST00000685437.1:c.1167G= ENSP00000508794.1:p.Gln389=
ENST00000685653.1:c.1266G= ENSP00000509968.1:p.Gln422=
ENST00000685738.1:c.*230G= ENSP00000510156.1:n.*230G=
ENST00000686409.1:n.2317G=
ENST00000686455.1:n.1629G=
ENST00000686762.1:c.1266G= ENSP00000509767.1:p.Gln422=
ENST00000687257.1:n.1502G=
ENST00000687326.1:c.*200G= ENSP00000509665.1:n.*200G=
ENST00000687505.1:n.1384G=
ENST00000687923.1:c.1155G= ENSP00000510255.1:p.Gln385=
ENST00000687940.1:n.1643G=
ENST00000688269.1:n.1862G=
ENST00000688326.1:c.699G=
ENST00000688444.1:n.1592G=
ENST00000688543.1:c.1167G= ENSP00000509612.1:p.Gln389=
ENST00000688625.1:c.*844G= ENSP00000509522.1:n.*844G=
ENST00000688803.1:n.1497G=
ENST00000688914.1:n.252G=
ENST00000689097.1:c.*943G= ENSP00000509756.1:n.*943G=
ENST00000689389.1:c.1193+806G= ENSP00000510213.1:n.1193+806G=
ENST00000689418.1:c.*943G= ENSP00000509467.1:n.*943G=
ENST00000689481.1:c.*943G= ENSP00000510248.1:n.*943G=
ENST00000689540.1:n.1416G=
ENST00000689876.1:c.1266G= ENSP00000508535.1:p.Gln422=
ENST00000689914.1:c.*200G= ENSP00000509847.1:n.*200G=
ENST00000690397.1:c.1155G= ENSP00000508730.1:p.Gln385=
ENST00000690460.1:c.1254G= ENSP00000509106.1:p.Gln418=
ENST00000690585.1:c.158G=
ENST00000690625.1:n.2302G=
ENST00000691396.1:c.*1118G= ENSP00000510712.1:n.*1118G=
ENST00000691724.1:c.*223G= ENSP00000509255.1:n.*223G=
ENST00000691779.1:c.*844G= ENSP00000508592.1:n.*844G=
ENST00000691888.1:c.158G=
ENST00000691899.1:c.1266G= ENSP00000508763.1:p.Gln422=
ENST00000692069.1:n.1832G=
ENST00000692093.1:c.1167G= ENSP00000509669.1:p.Gln389=
ENST00000692311.1:n.2090G=
ENST00000692558.1:n.1631G=
ENST00000692773.1:c.*1003G= ENSP00000509055.1:n.*1003G=
ENST00000692830.1:c.*1011G= ENSP00000509461.1:n.*1011G=
ENST00000693069.1:c.*200G= ENSP00000510072.1:n.*200G=
ENST00000693312.1:c.1041G= ENSP00000508686.1:p.Gln347=
ENST00000693664.1:c.1266G= ENSP00000509614.1:p.Gln422=
ENST00000693705.1:c.*943G= ENSP00000510697.1:n.*943G=
ENST00000251849.9:c.1266G= MANE Select ENSP00000251849.4:p.Gln422=
ENST00000442415.7:c.1326G= ENSP00000401888.2:p.Gln442=
ENST00000251849.8:c.1266G= ENSP00000251849.4:p.Gln422=
ENST00000423275.5:c.*943G= ENSP00000401088.1:n.*943G=
ENST00000432427.2:c.903G= ENSP00000398591.2:p.Gln301=
ENST00000442415.6:c.1326G= ENSP00000401888.2:p.Gln442=
ENST00000460610.1:n.223G=
ENST00000465826.5:n.623G=
ENST00000475353.1:n.434G=
ENST00000494557.1:n.282G=
NM_002880.3:c.1266G= , LRG_413t1:c.1266G= NP_002871.1:p.Gln422=
XM_005265355.1:c.1266G= XP_005265412.1:p.Gln422=
XM_005265357.1:c.1167G= XP_005265414.1:p.Gln389=
XM_005265358.3:c.1023G= XP_005265415.1:p.Gln341=
XM_005265359.3:c.924G= XP_005265416.1:p.Gln308=
XM_005265360.1:c.1266G= XP_005265417.1:p.Gln422=
XM_011533974.1:c.1266G= XP_011532276.1:p.Gln422=
XM_011533975.1:c.1023G= XP_011532277.1:p.Gln341=
NM_001354689.1:c.1326G= NP_001341618.1:p.Gln442=
NM_001354690.1:c.1266G= NP_001341619.1:p.Gln422=
NM_001354691.1:c.1023G= NP_001341620.1:p.Gln341=
NM_001354692.1:c.1023G= NP_001341621.1:p.Gln341=
NM_001354693.1:c.1167G= NP_001341622.1:p.Gln389=
NM_001354694.1:c.1083G= NP_001341623.1:p.Gln361=
NM_001354695.1:c.924G= NP_001341624.1:p.Gln308=
NR_148940.1:n.1794G=
NR_148941.1:n.1740G=
NR_148942.1:n.1679G=
XM_011533974.3:c.1266G= XP_011532276.1:p.Gln422=
XM_017006966.1:c.1167G= XP_016862455.1:p.Gln389=
NM_001354689.3:c.1326G= NP_001341618.1:p.Gln442=
NM_001354690.2:c.1266G= NP_001341619.1:p.Gln422=
NM_001354691.2:c.1023G= NP_001341620.1:p.Gln341=
NM_001354692.2:c.1023G= NP_001341621.1:p.Gln341=
NM_001354693.2:c.1167G= NP_001341622.1:p.Gln389=
NM_001354694.2:c.1083G= NP_001341623.1:p.Gln361=
NM_001354695.2:c.924G= NP_001341624.1:p.Gln308=
NR_148940.2:n.1710G=
NR_148941.2:n.1656G=
NR_148942.2:n.1595G=
NM_001354690.3:c.1266G= NP_001341619.1:p.Gln422=
NM_001354691.3:c.1023G= NP_001341620.1:p.Gln341=
NM_001354692.3:c.1023G= NP_001341621.1:p.Gln341=
NM_001354693.3:c.1167G= NP_001341622.1:p.Gln389=
NM_001354694.3:c.1083G= NP_001341623.1:p.Gln361=
NM_001354695.3:c.924G= NP_001341624.1:p.Gln308=
NM_002880.4:c.1266G= MANE Select NP_002871.1:p.Gln422=
NR_148940.3:n.1710G=
NR_148941.3:n.1656G=
NR_148942.3:n.1595G=