Canonical Allele Identifier: CA351502431
Gene: RAF1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12590930G>A , CM000665.2:g.12590930G>A GRCh38
NC_000003.11:g.12632429G>A , CM000665.1:g.12632429G>A GRCh37
NC_000003.10:g.12607429G>A NCBI36
NG_007467.1:g.78250C>T , LRG_413:g.78250C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000423275.6:c.*903C>T ENSP00000401088.1:n.*903C>T
ENST00000432427.3:c.555C>T
ENST00000460610.2:n.32C>T
ENST00000465826.6:n.829C>T
ENST00000475353.2:n.1160C>T
ENST00000494557.2:n.1049C>T
ENST00000684903.1:c.*915C>T ENSP00000508612.1:n.*915C>T
ENST00000685348.1:c.*915C>T ENSP00000510285.1:n.*915C>T
ENST00000685437.1:c.1139C>T ENSP00000508794.1:p.Thr380Ile
ENST00000685653.1:c.1238C>T ENSP00000509968.1:p.Thr413Ile
ENST00000685738.1:c.*202C>T ENSP00000510156.1:n.*202C>T
ENST00000686409.1:n.2289C>T
ENST00000686455.1:n.1601C>T
ENST00000686762.1:c.1238C>T ENSP00000509767.1:p.Thr413Ile
ENST00000687257.1:n.1474C>T
ENST00000687326.1:c.*172C>T ENSP00000509665.1:n.*172C>T
ENST00000687505.1:n.1356C>T
ENST00000687923.1:c.1127C>T ENSP00000510255.1:p.Thr376Ile
ENST00000687940.1:n.1615C>T
ENST00000688269.1:n.1834C>T
ENST00000688326.1:c.671C>T
ENST00000688444.1:n.1564C>T
ENST00000688543.1:c.1139C>T ENSP00000509612.1:p.Thr380Ile
ENST00000688625.1:c.*816C>T ENSP00000509522.1:n.*816C>T
ENST00000688803.1:n.1469C>T
ENST00000688914.1:n.224C>T
ENST00000689097.1:c.*915C>T ENSP00000509756.1:n.*915C>T
ENST00000689389.1:c.1193+778C>T ENSP00000510213.1:n.1193+778C>T
ENST00000689418.1:c.*915C>T ENSP00000509467.1:n.*915C>T
ENST00000689481.1:c.*915C>T ENSP00000510248.1:n.*915C>T
ENST00000689540.1:n.1388C>T
ENST00000689876.1:c.1238C>T ENSP00000508535.1:p.Thr413Ile
ENST00000689914.1:c.*172C>T ENSP00000509847.1:n.*172C>T
ENST00000690397.1:c.1127C>T ENSP00000508730.1:p.Thr376Ile
ENST00000690460.1:c.1226C>T ENSP00000509106.1:p.Thr409Ile
ENST00000690585.1:c.130C>T
ENST00000690625.1:n.2274C>T
ENST00000691396.1:c.*1090C>T ENSP00000510712.1:n.*1090C>T
ENST00000691724.1:c.*195C>T ENSP00000509255.1:n.*195C>T
ENST00000691779.1:c.*816C>T ENSP00000508592.1:n.*816C>T
ENST00000691888.1:c.130C>T
ENST00000691899.1:c.1238C>T ENSP00000508763.1:p.Thr413Ile
ENST00000692069.1:n.1804C>T
ENST00000692093.1:c.1139C>T ENSP00000509669.1:p.Thr380Ile
ENST00000692311.1:n.2062C>T
ENST00000692558.1:n.1603C>T
ENST00000692773.1:c.*975C>T ENSP00000509055.1:n.*975C>T
ENST00000692830.1:c.*983C>T ENSP00000509461.1:n.*983C>T
ENST00000693069.1:c.*172C>T ENSP00000510072.1:n.*172C>T
ENST00000693312.1:c.1013C>T ENSP00000508686.1:p.Thr338Ile
ENST00000693664.1:c.1238C>T ENSP00000509614.1:p.Thr413Ile
ENST00000693705.1:c.*915C>T ENSP00000510697.1:n.*915C>T
ENST00000251849.9:c.1238C>T MANE Select ENSP00000251849.4:p.Thr413Ile
ENST00000442415.7:c.1298C>T ENSP00000401888.2:p.Thr433Ile
ENST00000251849.8:c.1238C>T ENSP00000251849.4:p.Thr413Ile
ENST00000423275.5:c.*915C>T ENSP00000401088.1:n.*915C>T
ENST00000432427.2:c.875C>T ENSP00000398591.2:p.Thr292Ile
ENST00000442415.6:c.1298C>T ENSP00000401888.2:p.Thr433Ile
ENST00000460610.1:n.195C>T
ENST00000465826.5:n.595C>T
ENST00000475353.1:n.406C>T
ENST00000494557.1:n.254C>T
NM_002880.3:c.1238C>T , LRG_413t1:c.1238C>T NP_002871.1:p.Thr413Ile
XM_005265355.1:c.1238C>T XP_005265412.1:p.Thr413Ile
XM_005265357.1:c.1139C>T XP_005265414.1:p.Thr380Ile
XM_005265358.3:c.995C>T XP_005265415.1:p.Thr332Ile
XM_005265359.3:c.896C>T XP_005265416.1:p.Thr299Ile
XM_005265360.1:c.1238C>T XP_005265417.1:p.Thr413Ile
XM_011533974.1:c.1238C>T XP_011532276.1:p.Thr413Ile
XM_011533975.1:c.995C>T XP_011532277.1:p.Thr332Ile
NM_001354689.1:c.1298C>T NP_001341618.1:p.Thr433Ile
NM_001354690.1:c.1238C>T NP_001341619.1:p.Thr413Ile
NM_001354691.1:c.995C>T NP_001341620.1:p.Thr332Ile
NM_001354692.1:c.995C>T NP_001341621.1:p.Thr332Ile
NM_001354693.1:c.1139C>T NP_001341622.1:p.Thr380Ile
NM_001354694.1:c.1055C>T NP_001341623.1:p.Thr352Ile
NM_001354695.1:c.896C>T NP_001341624.1:p.Thr299Ile
NR_148940.1:n.1766C>T
NR_148941.1:n.1712C>T
NR_148942.1:n.1651C>T
XM_011533974.3:c.1238C>T XP_011532276.1:p.Thr413Ile
XM_017006966.1:c.1139C>T XP_016862455.1:p.Thr380Ile
NM_001354689.3:c.1298C>T NP_001341618.1:p.Thr433Ile
NM_001354690.2:c.1238C>T NP_001341619.1:p.Thr413Ile
NM_001354691.2:c.995C>T NP_001341620.1:p.Thr332Ile
NM_001354692.2:c.995C>T NP_001341621.1:p.Thr332Ile
NM_001354693.2:c.1139C>T NP_001341622.1:p.Thr380Ile
NM_001354694.2:c.1055C>T NP_001341623.1:p.Thr352Ile
NM_001354695.2:c.896C>T NP_001341624.1:p.Thr299Ile
NR_148940.2:n.1682C>T
NR_148941.2:n.1628C>T
NR_148942.2:n.1567C>T
NM_001354690.3:c.1238C>T NP_001341619.1:p.Thr413Ile
NM_001354691.3:c.995C>T NP_001341620.1:p.Thr332Ile
NM_001354692.3:c.995C>T NP_001341621.1:p.Thr332Ile
NM_001354693.3:c.1139C>T NP_001341622.1:p.Thr380Ile
NM_001354694.3:c.1055C>T NP_001341623.1:p.Thr352Ile
NM_001354695.3:c.896C>T NP_001341624.1:p.Thr299Ile
NM_002880.4:c.1238C>T MANE Select NP_002871.1:p.Thr413Ile
NR_148940.3:n.1682C>T
NR_148941.3:n.1628C>T
NR_148942.3:n.1567C>T