Canonical Allele Identifier: CA351499180

Linked Data

dbSNP Id: rs2058314665

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12585767T>A , CM000665.2:g.12585767T>A GRCh38
NC_000003.11:g.12627266T>A , CM000665.1:g.12627266T>A GRCh37
NC_000003.10:g.12602266T>A NCBI36
NG_007467.1:g.83413A>T , LRG_413:g.83413A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000423275.6:c.*1115A>T (RAF1) ENSP00000401088.1:n.*1115A>T
ENST00000432427.3:c.767A>T (RAF1)
ENST00000460610.2:n.5195A>T (RAF1)
ENST00000471449.2:n.260A>T (RAF1)
ENST00000475353.2:n.3163A>T (RAF1)
ENST00000684903.1:c.*1127A>T (RAF1) ENSP00000508612.1:n.*1127A>T
ENST00000685348.1:c.*1095-361A>T (RAF1) ENSP00000510285.1:n.*1095-361A>T
ENST00000685437.1:c.1351A>T (RAF1) ENSP00000508794.1:p.Ile451Phe
ENST00000685653.1:c.1450A>T (RAF1) ENSP00000509968.1:p.Ile484Phe
ENST00000685697.1:n.2185A>T (RAF1)
ENST00000685738.1:c.*414A>T (RAF1) ENSP00000510156.1:n.*414A>T
ENST00000686409.1:n.4292A>T (RAF1)
ENST00000686455.1:n.3604A>T (RAF1)
ENST00000686762.1:c.*9A>T (RAF1) ENSP00000509767.1:n.*9A>T
ENST00000687257.1:n.3477A>T (RAF1)
ENST00000687326.1:c.*2175A>T (RAF1) ENSP00000509665.1:n.*2175A>T
ENST00000687505.1:n.1568A>T (RAF1)
ENST00000687923.1:c.1339A>T (RAF1) ENSP00000510255.1:p.Ile447Phe
ENST00000688269.1:n.2046A>T (RAF1)
ENST00000688444.1:n.3567A>T (RAF1)
ENST00000688543.1:c.1351A>T (RAF1) ENSP00000509612.1:p.Ile451Phe
ENST00000688625.1:c.*2819A>T (RAF1) ENSP00000509522.1:n.*2819A>T
ENST00000688803.1:n.2964+508A>T (RAF1)
ENST00000688914.1:n.436A>T (RAF1)
ENST00000689097.1:c.*1127A>T (RAF1) ENSP00000509756.1:n.*1127A>T
ENST00000689389.1:c.1273A>T (RAF1) ENSP00000510213.1:p.Ile425Phe
ENST00000689418.1:c.*2918A>T (RAF1) ENSP00000509467.1:n.*2918A>T
ENST00000689540.1:n.3391A>T (RAF1)
ENST00000689876.1:c.1418-361A>T (RAF1) ENSP00000508535.1:n.1418-361A>T
ENST00000689914.1:c.*384A>T (RAF1) ENSP00000509847.1:n.*384A>T
ENST00000690397.1:c.1339A>T (RAF1) ENSP00000508730.1:p.Ile447Phe
ENST00000690460.1:c.1438A>T (RAF1) ENSP00000509106.1:p.Ile480Phe
ENST00000690585.1:c.263-514A>T (RAF1)
ENST00000690625.1:n.2486A>T (RAF1)
ENST00000691396.1:c.*1322A>T (RAF1) ENSP00000510712.1:n.*1322A>T
ENST00000691643.1:n.2076A>T (RAF1)
ENST00000691724.1:c.*407A>T (RAF1) ENSP00000509255.1:n.*407A>T
ENST00000691779.1:c.*1028A>T (RAF1) ENSP00000508592.1:n.*1028A>T
ENST00000691888.1:c.324A>T (RAF1)
ENST00000691899.1:c.1450A>T (RAF1) ENSP00000508763.1:p.Ile484Phe
ENST00000692069.1:n.3807A>T (RAF1)
ENST00000692093.1:c.1351A>T (RAF1) ENSP00000509669.1:p.Ile451Phe
ENST00000692311.1:n.2274A>T (RAF1)
ENST00000692558.1:n.3606A>T (RAF1)
ENST00000692773.1:c.*1187A>T (RAF1) ENSP00000509055.1:n.*1187A>T
ENST00000692830.1:c.*1195A>T (RAF1) ENSP00000509461.1:n.*1195A>T
ENST00000693312.1:c.1225A>T (RAF1) ENSP00000508686.1:p.Ile409Phe
ENST00000693664.1:c.1487+508A>T (RAF1) ENSP00000509614.1:n.1487+508A>T
ENST00000693705.1:c.*1048-786A>T (RAF1) ENSP00000510697.1:n.*1048-786A>T
ENST00000251849.9:c.1450A>T (RAF1) MANE Select ENSP00000251849.4:p.Ile484Phe
ENST00000442415.7:c.1510A>T (RAF1) ENSP00000401888.2:p.Ile504Phe
ENST00000676541.1:c.*3514T>A (MKRN2) ENSP00000503730.1:n.*3514T>A
ENST00000677142.1:c.*3514T>A (MKRN2) ENSP00000504455.1:n.*3514T>A
ENST00000677816.1:c.*2069T>A (MKRN2) ENSP00000502893.1:n.*2069T>A
ENST00000677941.1:n.3577T>A (MKRN2)
ENST00000251849.8:c.1450A>T (RAF1) ENSP00000251849.4:p.Ile484Phe
ENST00000423275.5:c.*1127A>T (RAF1) ENSP00000401088.1:n.*1127A>T
ENST00000432427.2:c.1087A>T (RAF1) ENSP00000398591.2:p.Ile363Phe
ENST00000442415.6:c.1510A>T (RAF1) ENSP00000401888.2:p.Ile504Phe
ENST00000471449.1:n.139A>T (RAF1)
NM_002880.3:c.1450A>T , LRG_413t1:c.1450A>T (RAF1) NP_002871.1:p.Ile484Phe
XM_005265355.1:c.1450A>T (RAF1) XP_005265412.1:p.Ile484Phe
XM_005265357.1:c.1351A>T (RAF1) XP_005265414.1:p.Ile451Phe
XM_005265358.3:c.1207A>T (RAF1) XP_005265415.1:p.Ile403Phe
XM_005265359.3:c.1108A>T (RAF1) XP_005265416.1:p.Ile370Phe
XM_005265360.1:c.1418-361A>T (RAF1) XP_005265417.1:n.1418-361A>T
XM_011533974.1:c.1450A>T (RAF1) XP_011532276.1:p.Ile484Phe
XM_011533975.1:c.1207A>T (RAF1) XP_011532277.1:p.Ile403Phe
NM_001354689.1:c.1510A>T (RAF1) NP_001341618.1:p.Ile504Phe
NM_001354690.1:c.1450A>T (RAF1) NP_001341619.1:p.Ile484Phe
NM_001354691.1:c.1207A>T (RAF1) NP_001341620.1:p.Ile403Phe
NM_001354692.1:c.1207A>T (RAF1) NP_001341621.1:p.Ile403Phe
NM_001354693.1:c.1351A>T (RAF1) NP_001341622.1:p.Ile451Phe
NM_001354694.1:c.1267A>T (RAF1) NP_001341623.1:p.Ile423Phe
NM_001354695.1:c.1108A>T (RAF1) NP_001341624.1:p.Ile370Phe
NR_148940.1:n.1978A>T (RAF1)
NR_148941.1:n.1924A>T (RAF1)
NR_148942.1:n.1863A>T (RAF1)
XM_011533974.3:c.1450A>T (RAF1) XP_011532276.1:p.Ile484Phe
XM_017006966.1:c.1351A>T (RAF1) XP_016862455.1:p.Ile451Phe
NM_001354689.3:c.1510A>T (RAF1) NP_001341618.1:p.Ile504Phe
NM_001354690.2:c.1450A>T (RAF1) NP_001341619.1:p.Ile484Phe
NM_001354691.2:c.1207A>T (RAF1) NP_001341620.1:p.Ile403Phe
NM_001354692.2:c.1207A>T (RAF1) NP_001341621.1:p.Ile403Phe
NM_001354693.2:c.1351A>T (RAF1) NP_001341622.1:p.Ile451Phe
NM_001354694.2:c.1267A>T (RAF1) NP_001341623.1:p.Ile423Phe
NM_001354695.2:c.1108A>T (RAF1) NP_001341624.1:p.Ile370Phe
NR_148940.2:n.1894A>T (RAF1)
NR_148941.2:n.1840A>T (RAF1)
NR_148942.2:n.1779A>T (RAF1)
NM_001354690.3:c.1450A>T (RAF1) NP_001341619.1:p.Ile484Phe
NM_001354691.3:c.1207A>T (RAF1) NP_001341620.1:p.Ile403Phe
NM_001354692.3:c.1207A>T (RAF1) NP_001341621.1:p.Ile403Phe
NM_001354693.3:c.1351A>T (RAF1) NP_001341622.1:p.Ile451Phe
NM_001354694.3:c.1267A>T (RAF1) NP_001341623.1:p.Ile423Phe
NM_001354695.3:c.1108A>T (RAF1) NP_001341624.1:p.Ile370Phe
NM_002880.4:c.1450A>T (RAF1) MANE Select NP_002871.1:p.Ile484Phe
NR_148940.3:n.1894A>T (RAF1)
NR_148941.3:n.1840A>T (RAF1)
NR_148942.3:n.1779A>T (RAF1)