Canonical Allele Identifier: CA1346227904

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12585760T= , CM000665.2:g.12585760T= GRCh38
NC_000003.11:g.12627259T= , CM000665.1:g.12627259T= GRCh37
NC_000003.10:g.12602259T= NCBI36
NG_007467.1:g.83420A= , LRG_413:g.83420A=

Transcript Alleles

HGVS Amino-acid change
ENST00000423275.6:c.*1122A= (RAF1) ENSP00000401088.1:n.*1122A=
ENST00000432427.3:c.774A= (RAF1)
ENST00000460610.2:n.5202A= (RAF1)
ENST00000471449.2:n.267A= (RAF1)
ENST00000475353.2:n.3170A= (RAF1)
ENST00000684903.1:c.*1134A= (RAF1) ENSP00000508612.1:n.*1134A=
ENST00000685348.1:c.*1095-354A= (RAF1) ENSP00000510285.1:n.*1095-354A=
ENST00000685437.1:c.1358A= (RAF1) ENSP00000508794.1:p.Asp453=
ENST00000685653.1:c.1457A= (RAF1) ENSP00000509968.1:p.Asp486=
ENST00000685697.1:n.2192A= (RAF1)
ENST00000685738.1:c.*421A= (RAF1) ENSP00000510156.1:n.*421A=
ENST00000686409.1:n.4299A= (RAF1)
ENST00000686455.1:n.3611A= (RAF1)
ENST00000686762.1:c.*16A= (RAF1) ENSP00000509767.1:n.*16A=
ENST00000687257.1:n.3484A= (RAF1)
ENST00000687326.1:c.*2182A= (RAF1) ENSP00000509665.1:n.*2182A=
ENST00000687505.1:n.1575A= (RAF1)
ENST00000687923.1:c.1346A= (RAF1) ENSP00000510255.1:p.Asp449=
ENST00000688269.1:n.2053A= (RAF1)
ENST00000688444.1:n.3574A= (RAF1)
ENST00000688543.1:c.1358A= (RAF1) ENSP00000509612.1:p.Asp453=
ENST00000688625.1:c.*2826A= (RAF1) ENSP00000509522.1:n.*2826A=
ENST00000688803.1:n.2965-507A= (RAF1)
ENST00000688914.1:n.443A= (RAF1)
ENST00000689097.1:c.*1134A= (RAF1) ENSP00000509756.1:n.*1134A=
ENST00000689389.1:c.1280A= (RAF1) ENSP00000510213.1:p.Asp427=
ENST00000689418.1:c.*2925A= (RAF1) ENSP00000509467.1:n.*2925A=
ENST00000689540.1:n.3398A= (RAF1)
ENST00000689876.1:c.1418-354A= (RAF1) ENSP00000508535.1:n.1418-354A=
ENST00000689914.1:c.*391A= (RAF1) ENSP00000509847.1:n.*391A=
ENST00000690397.1:c.1346A= (RAF1) ENSP00000508730.1:p.Asp449=
ENST00000690460.1:c.1445A= (RAF1) ENSP00000509106.1:p.Asp482=
ENST00000690585.1:c.263-507A= (RAF1)
ENST00000690625.1:n.2493A= (RAF1)
ENST00000691396.1:c.*1329A= (RAF1) ENSP00000510712.1:n.*1329A=
ENST00000691643.1:n.2083A= (RAF1)
ENST00000691724.1:c.*414A= (RAF1) ENSP00000509255.1:n.*414A=
ENST00000691779.1:c.*1035A= (RAF1) ENSP00000508592.1:n.*1035A=
ENST00000691888.1:c.331A= (RAF1)
ENST00000691899.1:c.1457A= (RAF1) ENSP00000508763.1:p.Asp486=
ENST00000692069.1:n.3814A= (RAF1)
ENST00000692093.1:c.1358A= (RAF1) ENSP00000509669.1:p.Asp453=
ENST00000692311.1:n.2281A= (RAF1)
ENST00000692558.1:n.3613A= (RAF1)
ENST00000692773.1:c.*1194A= (RAF1) ENSP00000509055.1:n.*1194A=
ENST00000692830.1:c.*1202A= (RAF1) ENSP00000509461.1:n.*1202A=
ENST00000693312.1:c.1232A= (RAF1) ENSP00000508686.1:p.Asp411=
ENST00000693664.1:c.1488-507A= (RAF1) ENSP00000509614.1:n.1488-507A=
ENST00000693705.1:c.*1048-779A= (RAF1) ENSP00000510697.1:n.*1048-779A=
ENST00000251849.9:c.1457A= (RAF1) MANE Select ENSP00000251849.4:p.Asp486=
ENST00000442415.7:c.1517A= (RAF1) ENSP00000401888.2:p.Asp506=
ENST00000676541.1:c.*3507T= (MKRN2) ENSP00000503730.1:n.*3507T=
ENST00000677142.1:c.*3507T= (MKRN2) ENSP00000504455.1:n.*3507T=
ENST00000677816.1:c.*2062T= (MKRN2) ENSP00000502893.1:n.*2062T=
ENST00000677941.1:n.3570T= (MKRN2)
ENST00000251849.8:c.1457A= (RAF1) ENSP00000251849.4:p.Asp486=
ENST00000423275.5:c.*1134A= (RAF1) ENSP00000401088.1:n.*1134A=
ENST00000432427.2:c.1094A= (RAF1) ENSP00000398591.2:p.Asp365=
ENST00000442415.6:c.1517A= (RAF1) ENSP00000401888.2:p.Asp506=
ENST00000471449.1:n.146A= (RAF1)
NM_002880.3:c.1457A= , LRG_413t1:c.1457A= (RAF1) NP_002871.1:p.Asp486=
XM_005265355.1:c.1457A= (RAF1) XP_005265412.1:p.Asp486=
XM_005265357.1:c.1358A= (RAF1) XP_005265414.1:p.Asp453=
XM_005265358.3:c.1214A= (RAF1) XP_005265415.1:p.Asp405=
XM_005265359.3:c.1115A= (RAF1) XP_005265416.1:p.Asp372=
XM_005265360.1:c.1418-354A= (RAF1) XP_005265417.1:n.1418-354A=
XM_011533974.1:c.1457A= (RAF1) XP_011532276.1:p.Asp486=
XM_011533975.1:c.1214A= (RAF1) XP_011532277.1:p.Asp405=
NM_001354689.1:c.1517A= (RAF1) NP_001341618.1:p.Asp506=
NM_001354690.1:c.1457A= (RAF1) NP_001341619.1:p.Asp486=
NM_001354691.1:c.1214A= (RAF1) NP_001341620.1:p.Asp405=
NM_001354692.1:c.1214A= (RAF1) NP_001341621.1:p.Asp405=
NM_001354693.1:c.1358A= (RAF1) NP_001341622.1:p.Asp453=
NM_001354694.1:c.1274A= (RAF1) NP_001341623.1:p.Asp425=
NM_001354695.1:c.1115A= (RAF1) NP_001341624.1:p.Asp372=
NR_148940.1:n.1985A= (RAF1)
NR_148941.1:n.1931A= (RAF1)
NR_148942.1:n.1870A= (RAF1)
XM_011533974.3:c.1457A= (RAF1) XP_011532276.1:p.Asp486=
XM_017006966.1:c.1358A= (RAF1) XP_016862455.1:p.Asp453=
NM_001354689.3:c.1517A= (RAF1) NP_001341618.1:p.Asp506=
NM_001354690.2:c.1457A= (RAF1) NP_001341619.1:p.Asp486=
NM_001354691.2:c.1214A= (RAF1) NP_001341620.1:p.Asp405=
NM_001354692.2:c.1214A= (RAF1) NP_001341621.1:p.Asp405=
NM_001354693.2:c.1358A= (RAF1) NP_001341622.1:p.Asp453=
NM_001354694.2:c.1274A= (RAF1) NP_001341623.1:p.Asp425=
NM_001354695.2:c.1115A= (RAF1) NP_001341624.1:p.Asp372=
NR_148940.2:n.1901A= (RAF1)
NR_148941.2:n.1847A= (RAF1)
NR_148942.2:n.1786A= (RAF1)
NM_001354690.3:c.1457A= (RAF1) NP_001341619.1:p.Asp486=
NM_001354691.3:c.1214A= (RAF1) NP_001341620.1:p.Asp405=
NM_001354692.3:c.1214A= (RAF1) NP_001341621.1:p.Asp405=
NM_001354693.3:c.1358A= (RAF1) NP_001341622.1:p.Asp453=
NM_001354694.3:c.1274A= (RAF1) NP_001341623.1:p.Asp425=
NM_001354695.3:c.1115A= (RAF1) NP_001341624.1:p.Asp372=
NM_002880.4:c.1457A= (RAF1) MANE Select NP_002871.1:p.Asp486=
NR_148940.3:n.1901A= (RAF1)
NR_148941.3:n.1847A= (RAF1)
NR_148942.3:n.1786A= (RAF1)