Canonical Allele Identifier: CA1346242584
Gene: RAF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12600168T= , CM000665.2:g.12600168T= GRCh38
NC_000003.11:g.12641667T= , CM000665.1:g.12641667T= GRCh37
NC_000003.10:g.12616667T= NCBI36
NG_007467.1:g.69012A= , LRG_413:g.69012A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000423275.6:c.*639A= ENSP00000401088.1:n.*639A=
ENST00000432427.3:c.294A=
ENST00000465826.6:n.565A=
ENST00000491290.2:n.1351A=
ENST00000684903.1:c.*651A= ENSP00000508612.1:n.*651A=
ENST00000685348.1:c.*651A= ENSP00000510285.1:n.*651A=
ENST00000685437.1:c.875A= ENSP00000508794.1:p.Gln292=
ENST00000685653.1:c.974A= ENSP00000509968.1:p.Gln325=
ENST00000685738.1:c.974A= ENSP00000510156.1:p.Gln325=
ENST00000686409.1:n.1682A=
ENST00000686455.1:n.1337A=
ENST00000686479.1:n.1345A=
ENST00000686762.1:c.974A= ENSP00000509767.1:p.Gln325=
ENST00000687257.1:n.1210A=
ENST00000687326.1:c.974A= ENSP00000509665.1:p.Gln325=
ENST00000687486.1:c.182+220A=
ENST00000687505.1:n.1092A=
ENST00000687923.1:c.875A= ENSP00000510255.1:p.Gln292=
ENST00000687940.1:n.1351A=
ENST00000688269.1:n.1570A=
ENST00000688326.1:c.294A=
ENST00000688444.1:n.1300A=
ENST00000688543.1:c.875A= ENSP00000509612.1:p.Gln292=
ENST00000688625.1:c.*552A= ENSP00000509522.1:n.*552A=
ENST00000688803.1:n.1205A=
ENST00000689097.1:c.*651A= ENSP00000509756.1:n.*651A=
ENST00000689389.1:c.974A= ENSP00000510213.1:p.Gln325=
ENST00000689418.1:c.*651A= ENSP00000509467.1:n.*651A=
ENST00000689481.1:c.*651A= ENSP00000510248.1:n.*651A=
ENST00000689540.1:n.1124A=
ENST00000689876.1:c.974A= ENSP00000508535.1:p.Gln325=
ENST00000689914.1:c.974A= ENSP00000509847.1:p.Gln325=
ENST00000690397.1:c.863A= ENSP00000508730.1:p.Gln288=
ENST00000690460.1:c.962A= ENSP00000509106.1:p.Gln321=
ENST00000690625.1:n.1277A=
ENST00000691268.1:c.401A=
ENST00000691396.1:c.*767A= ENSP00000510712.1:n.*767A=
ENST00000691724.1:c.974A= ENSP00000509255.1:p.Gln325=
ENST00000691779.1:c.*552A= ENSP00000508592.1:n.*552A=
ENST00000691899.1:c.974A= ENSP00000508763.1:p.Gln325=
ENST00000692069.1:n.1197A=
ENST00000692093.1:c.875A= ENSP00000509669.1:p.Gln292=
ENST00000692311.1:n.1455A=
ENST00000692558.1:n.1339A=
ENST00000692773.1:c.*711A= ENSP00000509055.1:n.*711A=
ENST00000692830.1:c.*719A= ENSP00000509461.1:n.*719A=
ENST00000693069.1:c.875A= ENSP00000510072.1:p.Gln292=
ENST00000693312.1:c.749A= ENSP00000508686.1:p.Gln250=
ENST00000693664.1:c.974A= ENSP00000509614.1:p.Gln325=
ENST00000693705.1:c.*651A= ENSP00000510697.1:n.*651A=
ENST00000251849.9:c.974A= MANE Select ENSP00000251849.4:p.Gln325=
ENST00000442415.7:c.1034A= ENSP00000401888.2:p.Gln345=
ENST00000251849.8:c.974A= ENSP00000251849.4:p.Gln325=
ENST00000423275.5:c.*651A= ENSP00000401088.1:n.*651A=
ENST00000432427.2:c.611A= ENSP00000398591.2:p.Gln204=
ENST00000442415.6:c.1034A= ENSP00000401888.2:p.Gln345=
ENST00000465826.5:n.218A=
NM_002880.3:c.974A= , LRG_413t1:c.974A= NP_002871.1:p.Gln325=
XM_005265355.1:c.974A= XP_005265412.1:p.Gln325=
XM_005265357.1:c.875A= XP_005265414.1:p.Gln292=
XM_005265358.3:c.731A= XP_005265415.1:p.Gln244=
XM_005265359.3:c.632A= XP_005265416.1:p.Gln211=
XM_005265360.1:c.974A= XP_005265417.1:p.Gln325=
XM_011533974.1:c.974A= XP_011532276.1:p.Gln325=
XM_011533975.1:c.731A= XP_011532277.1:p.Gln244=
NM_001354689.1:c.1034A= NP_001341618.1:p.Gln345=
NM_001354690.1:c.974A= NP_001341619.1:p.Gln325=
NM_001354691.1:c.731A= NP_001341620.1:p.Gln244=
NM_001354692.1:c.731A= NP_001341621.1:p.Gln244=
NM_001354693.1:c.875A= NP_001341622.1:p.Gln292=
NM_001354694.1:c.791A= NP_001341623.1:p.Gln264=
NM_001354695.1:c.632A= NP_001341624.1:p.Gln211=
NR_148940.1:n.1389A=
NR_148941.1:n.1389A=
NR_148942.1:n.1389A=
XM_011533974.3:c.974A= XP_011532276.1:p.Gln325=
XM_017006966.1:c.875A= XP_016862455.1:p.Gln292=
XR_001740227.1:n.1206A=
NM_001354689.3:c.1034A= NP_001341618.1:p.Gln345=
NM_001354690.2:c.974A= NP_001341619.1:p.Gln325=
NM_001354691.2:c.731A= NP_001341620.1:p.Gln244=
NM_001354692.2:c.731A= NP_001341621.1:p.Gln244=
NM_001354693.2:c.875A= NP_001341622.1:p.Gln292=
NM_001354694.2:c.791A= NP_001341623.1:p.Gln264=
NM_001354695.2:c.632A= NP_001341624.1:p.Gln211=
NR_148940.2:n.1305A=
NR_148941.2:n.1305A=
NR_148942.2:n.1305A=
NM_001354690.3:c.974A= NP_001341619.1:p.Gln325=
NM_001354691.3:c.731A= NP_001341620.1:p.Gln244=
NM_001354692.3:c.731A= NP_001341621.1:p.Gln244=
NM_001354693.3:c.875A= NP_001341622.1:p.Gln292=
NM_001354694.3:c.791A= NP_001341623.1:p.Gln264=
NM_001354695.3:c.632A= NP_001341624.1:p.Gln211=
NM_002880.4:c.974A= MANE Select NP_002871.1:p.Gln325=
NR_148940.3:n.1305A=
NR_148941.3:n.1305A=
NR_148942.3:n.1305A=