Canonical Allele Identifier: CA1346233159
Gene: RAF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12590831A= , CM000665.2:g.12590831A= GRCh38
NC_000003.11:g.12632330A= , CM000665.1:g.12632330A= GRCh37
NC_000003.10:g.12607330A= NCBI36
NG_007467.1:g.78349T= , LRG_413:g.78349T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000423275.6:c.*1002T= ENSP00000401088.1:n.*1002T=
ENST00000432427.3:c.654T=
ENST00000460610.2:n.131T=
ENST00000465826.6:n.928T=
ENST00000475353.2:n.1259T=
ENST00000494557.2:n.1148T=
ENST00000684903.1:c.*1014T= ENSP00000508612.1:n.*1014T=
ENST00000685348.1:c.*1014T= ENSP00000510285.1:n.*1014T=
ENST00000685437.1:c.1238T= ENSP00000508794.1:p.Ile413=
ENST00000685653.1:c.1337T= ENSP00000509968.1:p.Ile446=
ENST00000685738.1:c.*301T= ENSP00000510156.1:n.*301T=
ENST00000686409.1:n.2388T=
ENST00000686455.1:n.1700T=
ENST00000686762.1:c.1337T= ENSP00000509767.1:p.Ile446=
ENST00000687257.1:n.1573T=
ENST00000687326.1:c.*271T= ENSP00000509665.1:n.*271T=
ENST00000687505.1:n.1455T=
ENST00000687923.1:c.1226T= ENSP00000510255.1:p.Ile409=
ENST00000687940.1:n.1714T=
ENST00000688269.1:n.1933T=
ENST00000688326.1:c.770T=
ENST00000688444.1:n.1663T=
ENST00000688543.1:c.1238T= ENSP00000509612.1:p.Ile413=
ENST00000688625.1:c.*915T= ENSP00000509522.1:n.*915T=
ENST00000688803.1:n.1568T=
ENST00000688914.1:n.323T=
ENST00000689097.1:c.*1014T= ENSP00000509756.1:n.*1014T=
ENST00000689389.1:c.1193+877T= ENSP00000510213.1:n.1193+877T=
ENST00000689418.1:c.*1014T= ENSP00000509467.1:n.*1014T=
ENST00000689481.1:c.*1014T= ENSP00000510248.1:n.*1014T=
ENST00000689540.1:n.1487T=
ENST00000689876.1:c.1337T= ENSP00000508535.1:p.Ile446=
ENST00000689914.1:c.*271T= ENSP00000509847.1:n.*271T=
ENST00000690397.1:c.1226T= ENSP00000508730.1:p.Ile409=
ENST00000690460.1:c.1325T= ENSP00000509106.1:p.Ile442=
ENST00000690585.1:c.229T=
ENST00000690625.1:n.2373T=
ENST00000691396.1:c.*1189T= ENSP00000510712.1:n.*1189T=
ENST00000691724.1:c.*294T= ENSP00000509255.1:n.*294T=
ENST00000691779.1:c.*915T= ENSP00000508592.1:n.*915T=
ENST00000691888.1:c.229T=
ENST00000691899.1:c.1337T= ENSP00000508763.1:p.Ile446=
ENST00000692069.1:n.1903T=
ENST00000692093.1:c.1238T= ENSP00000509669.1:p.Ile413=
ENST00000692311.1:n.2161T=
ENST00000692558.1:n.1702T=
ENST00000692773.1:c.*1074T= ENSP00000509055.1:n.*1074T=
ENST00000692830.1:c.*1082T= ENSP00000509461.1:n.*1082T=
ENST00000693069.1:c.*271T= ENSP00000510072.1:n.*271T=
ENST00000693312.1:c.1112T= ENSP00000508686.1:p.Ile371=
ENST00000693664.1:c.1337T= ENSP00000509614.1:p.Ile446=
ENST00000693705.1:c.*1014T= ENSP00000510697.1:n.*1014T=
ENST00000251849.9:c.1337T= MANE Select ENSP00000251849.4:p.Ile446=
ENST00000442415.7:c.1397T= ENSP00000401888.2:p.Ile466=
ENST00000251849.8:c.1337T= ENSP00000251849.4:p.Ile446=
ENST00000423275.5:c.*1014T= ENSP00000401088.1:n.*1014T=
ENST00000432427.2:c.974T= ENSP00000398591.2:p.Ile325=
ENST00000442415.6:c.1397T= ENSP00000401888.2:p.Ile466=
ENST00000460610.1:n.294T=
ENST00000465826.5:n.694T=
ENST00000475353.1:n.505T=
ENST00000494557.1:n.353T=
NM_002880.3:c.1337T= , LRG_413t1:c.1337T= NP_002871.1:p.Ile446=
XM_005265355.1:c.1337T= XP_005265412.1:p.Ile446=
XM_005265357.1:c.1238T= XP_005265414.1:p.Ile413=
XM_005265358.3:c.1094T= XP_005265415.1:p.Ile365=
XM_005265359.3:c.995T= XP_005265416.1:p.Ile332=
XM_005265360.1:c.1337T= XP_005265417.1:p.Ile446=
XM_011533974.1:c.1337T= XP_011532276.1:p.Ile446=
XM_011533975.1:c.1094T= XP_011532277.1:p.Ile365=
NM_001354689.1:c.1397T= NP_001341618.1:p.Ile466=
NM_001354690.1:c.1337T= NP_001341619.1:p.Ile446=
NM_001354691.1:c.1094T= NP_001341620.1:p.Ile365=
NM_001354692.1:c.1094T= NP_001341621.1:p.Ile365=
NM_001354693.1:c.1238T= NP_001341622.1:p.Ile413=
NM_001354694.1:c.1154T= NP_001341623.1:p.Ile385=
NM_001354695.1:c.995T= NP_001341624.1:p.Ile332=
NR_148940.1:n.1865T=
NR_148941.1:n.1811T=
NR_148942.1:n.1750T=
XM_011533974.3:c.1337T= XP_011532276.1:p.Ile446=
XM_017006966.1:c.1238T= XP_016862455.1:p.Ile413=
NM_001354689.3:c.1397T= NP_001341618.1:p.Ile466=
NM_001354690.2:c.1337T= NP_001341619.1:p.Ile446=
NM_001354691.2:c.1094T= NP_001341620.1:p.Ile365=
NM_001354692.2:c.1094T= NP_001341621.1:p.Ile365=
NM_001354693.2:c.1238T= NP_001341622.1:p.Ile413=
NM_001354694.2:c.1154T= NP_001341623.1:p.Ile385=
NM_001354695.2:c.995T= NP_001341624.1:p.Ile332=
NR_148940.2:n.1781T=
NR_148941.2:n.1727T=
NR_148942.2:n.1666T=
NM_001354690.3:c.1337T= NP_001341619.1:p.Ile446=
NM_001354691.3:c.1094T= NP_001341620.1:p.Ile365=
NM_001354692.3:c.1094T= NP_001341621.1:p.Ile365=
NM_001354693.3:c.1238T= NP_001341622.1:p.Ile413=
NM_001354694.3:c.1154T= NP_001341623.1:p.Ile385=
NM_001354695.3:c.995T= NP_001341624.1:p.Ile332=
NM_002880.4:c.1337T= MANE Select NP_002871.1:p.Ile446=
NR_148940.3:n.1781T=
NR_148941.3:n.1727T=
NR_148942.3:n.1666T=