Canonical Allele Identifier: CA1346242381
Gene: RAF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12599947G= , CM000665.2:g.12599947G= GRCh38
NC_000003.11:g.12641446G= , CM000665.1:g.12641446G= GRCh37
NC_000003.10:g.12616446G= NCBI36
NG_007467.1:g.69233C= , LRG_413:g.69233C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000423275.6:c.*656-139C= ENSP00000401088.1:n.*656-139C=
ENST00000432427.3:c.311-139C=
ENST00000465826.6:n.582-139C=
ENST00000491290.2:n.1368-139C=
ENST00000684903.1:c.*668-139C= ENSP00000508612.1:n.*668-139C=
ENST00000685348.1:c.*668-139C= ENSP00000510285.1:n.*668-139C=
ENST00000685437.1:c.892-139C= ENSP00000508794.1:n.892-139C=
ENST00000685653.1:c.991-139C= ENSP00000509968.1:n.991-139C=
ENST00000685738.1:c.991-139C= ENSP00000510156.1:n.991-139C=
ENST00000686409.1:n.1903C=
ENST00000686455.1:n.1354-139C=
ENST00000686479.1:n.1362-139C=
ENST00000686762.1:c.991-139C= ENSP00000509767.1:n.991-139C=
ENST00000687257.1:n.1227-139C=
ENST00000687326.1:c.991-139C= ENSP00000509665.1:n.991-139C=
ENST00000687486.1:c.183-139C=
ENST00000687505.1:n.1109-139C=
ENST00000687923.1:c.892-139C= ENSP00000510255.1:n.892-139C=
ENST00000687940.1:n.1368-139C=
ENST00000688269.1:n.1587-139C=
ENST00000688326.1:c.311-139C=
ENST00000688444.1:n.1317-139C=
ENST00000688543.1:c.892-139C= ENSP00000509612.1:n.892-139C=
ENST00000688625.1:c.*569-139C= ENSP00000509522.1:n.*569-139C=
ENST00000688803.1:n.1222-139C=
ENST00000689097.1:c.*668-139C= ENSP00000509756.1:n.*668-139C=
ENST00000689389.1:c.991-139C= ENSP00000510213.1:n.991-139C=
ENST00000689418.1:c.*668-139C= ENSP00000509467.1:n.*668-139C=
ENST00000689481.1:c.*668-139C= ENSP00000510248.1:n.*668-139C=
ENST00000689540.1:n.1141-139C=
ENST00000689876.1:c.991-139C= ENSP00000508535.1:n.991-139C=
ENST00000689914.1:c.991-139C= ENSP00000509847.1:n.991-139C=
ENST00000690397.1:c.880-139C= ENSP00000508730.1:n.880-139C=
ENST00000690460.1:c.979-139C= ENSP00000509106.1:n.979-139C=
ENST00000690625.1:n.1294-139C=
ENST00000691268.1:c.418-139C=
ENST00000691396.1:c.*784-139C= ENSP00000510712.1:n.*784-139C=
ENST00000691724.1:c.991-141C= ENSP00000509255.1:n.991-141C=
ENST00000691779.1:c.*569-139C= ENSP00000508592.1:n.*569-139C=
ENST00000691899.1:c.991-139C= ENSP00000508763.1:n.991-139C=
ENST00000692069.1:n.1418C=
ENST00000692093.1:c.892-139C= ENSP00000509669.1:n.892-139C=
ENST00000692311.1:n.1676C=
ENST00000692558.1:n.1356-139C=
ENST00000692773.1:c.*728-139C= ENSP00000509055.1:n.*728-139C=
ENST00000692830.1:c.*736-139C= ENSP00000509461.1:n.*736-139C=
ENST00000693069.1:c.892-139C= ENSP00000510072.1:n.892-139C=
ENST00000693312.1:c.766-139C= ENSP00000508686.1:n.766-139C=
ENST00000693664.1:c.991-139C= ENSP00000509614.1:n.991-139C=
ENST00000693705.1:c.*668-139C= ENSP00000510697.1:n.*668-139C=
ENST00000251849.9:c.991-139C= MANE Select ENSP00000251849.4:n.991-139C=
ENST00000442415.7:c.1051-139C= ENSP00000401888.2:n.1051-139C=
ENST00000251849.8:c.991-139C= ENSP00000251849.4:n.991-139C=
ENST00000423275.5:c.*668-139C= ENSP00000401088.1:n.*668-139C=
ENST00000432427.2:c.628-139C= ENSP00000398591.2:n.628-139C=
ENST00000442415.6:c.1051-139C= ENSP00000401888.2:n.1051-139C=
ENST00000465826.5:n.235-139C=
NM_002880.3:c.991-139C= , LRG_413t1:c.991-139C= NP_002871.1:n.991-139C=
XM_005265355.1:c.991-139C= XP_005265412.1:n.991-139C=
XM_005265357.1:c.892-139C= XP_005265414.1:n.892-139C=
XM_005265358.3:c.748-139C= XP_005265415.1:n.748-139C=
XM_005265359.3:c.649-139C= XP_005265416.1:n.649-139C=
XM_005265360.1:c.991-139C= XP_005265417.1:n.991-139C=
XM_011533974.1:c.991-139C= XP_011532276.1:n.991-139C=
XM_011533975.1:c.748-139C= XP_011532277.1:n.748-139C=
NM_001354689.1:c.1051-139C= NP_001341618.1:n.1051-139C=
NM_001354690.1:c.991-139C= NP_001341619.1:n.991-139C=
NM_001354691.1:c.748-139C= NP_001341620.1:n.748-139C=
NM_001354692.1:c.748-139C= NP_001341621.1:n.748-139C=
NM_001354693.1:c.892-139C= NP_001341622.1:n.892-139C=
NM_001354694.1:c.808-139C= NP_001341623.1:n.808-139C=
NM_001354695.1:c.649-139C= NP_001341624.1:n.649-139C=
NR_148940.1:n.1406-139C=
NR_148941.1:n.1406-139C=
NR_148942.1:n.1406-141C=
XM_011533974.3:c.991-139C= XP_011532276.1:n.991-139C=
XM_017006966.1:c.892-139C= XP_016862455.1:n.892-139C=
XR_001740227.1:n.1223-139C=
NM_001354689.3:c.1051-139C= NP_001341618.1:n.1051-139C=
NM_001354690.2:c.991-139C= NP_001341619.1:n.991-139C=
NM_001354691.2:c.748-139C= NP_001341620.1:n.748-139C=
NM_001354692.2:c.748-139C= NP_001341621.1:n.748-139C=
NM_001354693.2:c.892-139C= NP_001341622.1:n.892-139C=
NM_001354694.2:c.808-139C= NP_001341623.1:n.808-139C=
NM_001354695.2:c.649-139C= NP_001341624.1:n.649-139C=
NR_148940.2:n.1322-139C=
NR_148941.2:n.1322-139C=
NR_148942.2:n.1322-141C=
NM_001354690.3:c.991-139C= NP_001341619.1:n.991-139C=
NM_001354691.3:c.748-139C= NP_001341620.1:n.748-139C=
NM_001354692.3:c.748-139C= NP_001341621.1:n.748-139C=
NM_001354693.3:c.892-139C= NP_001341622.1:n.892-139C=
NM_001354694.3:c.808-139C= NP_001341623.1:n.808-139C=
NM_001354695.3:c.649-139C= NP_001341624.1:n.649-139C=
NM_002880.4:c.991-139C= MANE Select NP_002871.1:n.991-139C=
NR_148940.3:n.1322-139C=
NR_148941.3:n.1322-139C=
NR_148942.3:n.1322-141C=