Canonical Allele Identifier: CA351501778
Gene: RAF1 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000423275.6:c.*1002T>G ENSP00000401088.1:n.*1002T>G
ENST00000432427.3:c.654T>G
ENST00000460610.2:n.131T>G
ENST00000465826.6:n.928T>G
ENST00000475353.2:n.1259T>G
ENST00000494557.2:n.1148T>G
ENST00000684903.1:c.*1014T>G ENSP00000508612.1:n.*1014T>G
ENST00000685348.1:c.*1014T>G ENSP00000510285.1:n.*1014T>G
ENST00000685437.1:c.1238T>G ENSP00000508794.1:p.Ile413Ser
ENST00000685653.1:c.1337T>G ENSP00000509968.1:p.Ile446Ser
ENST00000685738.1:c.*301T>G ENSP00000510156.1:n.*301T>G
ENST00000686409.1:n.2388T>G
ENST00000686455.1:n.1700T>G
ENST00000686762.1:c.1337T>G ENSP00000509767.1:p.Ile446Ser
ENST00000687257.1:n.1573T>G
ENST00000687326.1:c.*271T>G ENSP00000509665.1:n.*271T>G
ENST00000687505.1:n.1455T>G
ENST00000687923.1:c.1226T>G ENSP00000510255.1:p.Ile409Ser
ENST00000687940.1:n.1714T>G
ENST00000688269.1:n.1933T>G
ENST00000688326.1:c.770T>G
ENST00000688444.1:n.1663T>G
ENST00000688543.1:c.1238T>G ENSP00000509612.1:p.Ile413Ser
ENST00000688625.1:c.*915T>G ENSP00000509522.1:n.*915T>G
ENST00000688803.1:n.1568T>G
ENST00000688914.1:n.323T>G
ENST00000689097.1:c.*1014T>G ENSP00000509756.1:n.*1014T>G
ENST00000689389.1:c.1193+877T>G ENSP00000510213.1:n.1193+877T>G
ENST00000689418.1:c.*1014T>G ENSP00000509467.1:n.*1014T>G
ENST00000689481.1:c.*1014T>G ENSP00000510248.1:n.*1014T>G
ENST00000689540.1:n.1487T>G
ENST00000689876.1:c.1337T>G ENSP00000508535.1:p.Ile446Ser
ENST00000689914.1:c.*271T>G ENSP00000509847.1:n.*271T>G
ENST00000690397.1:c.1226T>G ENSP00000508730.1:p.Ile409Ser
ENST00000690460.1:c.1325T>G ENSP00000509106.1:p.Ile442Ser
ENST00000690585.1:c.229T>G
ENST00000690625.1:n.2373T>G
ENST00000691396.1:c.*1189T>G ENSP00000510712.1:n.*1189T>G
ENST00000691724.1:c.*294T>G ENSP00000509255.1:n.*294T>G
ENST00000691779.1:c.*915T>G ENSP00000508592.1:n.*915T>G
ENST00000691888.1:c.229T>G
ENST00000691899.1:c.1337T>G ENSP00000508763.1:p.Ile446Ser
ENST00000692069.1:n.1903T>G
ENST00000692093.1:c.1238T>G ENSP00000509669.1:p.Ile413Ser
ENST00000692311.1:n.2161T>G
ENST00000692558.1:n.1702T>G
ENST00000692773.1:c.*1074T>G ENSP00000509055.1:n.*1074T>G
ENST00000692830.1:c.*1082T>G ENSP00000509461.1:n.*1082T>G
ENST00000693069.1:c.*271T>G ENSP00000510072.1:n.*271T>G
ENST00000693312.1:c.1112T>G ENSP00000508686.1:p.Ile371Ser
ENST00000693664.1:c.1337T>G ENSP00000509614.1:p.Ile446Ser
ENST00000693705.1:c.*1014T>G ENSP00000510697.1:n.*1014T>G
ENST00000251849.9:c.1337T>G MANE Select ENSP00000251849.4:p.Ile446Ser
ENST00000442415.7:c.1397T>G ENSP00000401888.2:p.Ile466Ser
ENST00000251849.8:c.1337T>G ENSP00000251849.4:p.Ile446Ser
ENST00000423275.5:c.*1014T>G ENSP00000401088.1:n.*1014T>G
ENST00000432427.2:c.974T>G ENSP00000398591.2:p.Ile325Ser
ENST00000442415.6:c.1397T>G ENSP00000401888.2:p.Ile466Ser
ENST00000460610.1:n.294T>G
ENST00000465826.5:n.694T>G
ENST00000475353.1:n.505T>G
ENST00000494557.1:n.353T>G
NM_002880.3:c.1337T>G , LRG_413t1:c.1337T>G NP_002871.1:p.Ile446Ser
XM_005265355.1:c.1337T>G XP_005265412.1:p.Ile446Ser
XM_005265357.1:c.1238T>G XP_005265414.1:p.Ile413Ser
XM_005265358.3:c.1094T>G XP_005265415.1:p.Ile365Ser
XM_005265359.3:c.995T>G XP_005265416.1:p.Ile332Ser
XM_005265360.1:c.1337T>G XP_005265417.1:p.Ile446Ser
XM_011533974.1:c.1337T>G XP_011532276.1:p.Ile446Ser
XM_011533975.1:c.1094T>G XP_011532277.1:p.Ile365Ser
NM_001354689.1:c.1397T>G NP_001341618.1:p.Ile466Ser
NM_001354690.1:c.1337T>G NP_001341619.1:p.Ile446Ser
NM_001354691.1:c.1094T>G NP_001341620.1:p.Ile365Ser
NM_001354692.1:c.1094T>G NP_001341621.1:p.Ile365Ser
NM_001354693.1:c.1238T>G NP_001341622.1:p.Ile413Ser
NM_001354694.1:c.1154T>G NP_001341623.1:p.Ile385Ser
NM_001354695.1:c.995T>G NP_001341624.1:p.Ile332Ser
NR_148940.1:n.1865T>G
NR_148941.1:n.1811T>G
NR_148942.1:n.1750T>G
XM_011533974.3:c.1337T>G XP_011532276.1:p.Ile446Ser
XM_017006966.1:c.1238T>G XP_016862455.1:p.Ile413Ser
NM_001354689.3:c.1397T>G NP_001341618.1:p.Ile466Ser
NM_001354690.2:c.1337T>G NP_001341619.1:p.Ile446Ser
NM_001354691.2:c.1094T>G NP_001341620.1:p.Ile365Ser
NM_001354692.2:c.1094T>G NP_001341621.1:p.Ile365Ser
NM_001354693.2:c.1238T>G NP_001341622.1:p.Ile413Ser
NM_001354694.2:c.1154T>G NP_001341623.1:p.Ile385Ser
NM_001354695.2:c.995T>G NP_001341624.1:p.Ile332Ser
NR_148940.2:n.1781T>G
NR_148941.2:n.1727T>G
NR_148942.2:n.1666T>G
NM_001354690.3:c.1337T>G NP_001341619.1:p.Ile446Ser
NM_001354691.3:c.1094T>G NP_001341620.1:p.Ile365Ser
NM_001354692.3:c.1094T>G NP_001341621.1:p.Ile365Ser
NM_001354693.3:c.1238T>G NP_001341622.1:p.Ile413Ser
NM_001354694.3:c.1154T>G NP_001341623.1:p.Ile385Ser
NM_001354695.3:c.995T>G NP_001341624.1:p.Ile332Ser
NM_002880.4:c.1337T>G MANE Select NP_002871.1:p.Ile446Ser
NR_148940.3:n.1781T>G
NR_148941.3:n.1727T>G
NR_148942.3:n.1666T>G