Canonical Allele Identifier: CA351498767

Linked Data

dbSNP Id: rs2125325450

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12585684C>A , CM000665.2:g.12585684C>A GRCh38
NC_000003.11:g.12627183C>A , CM000665.1:g.12627183C>A GRCh37
NC_000003.10:g.12602183C>A NCBI36
NG_007467.1:g.83496G>T , LRG_413:g.83496G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000423275.6:c.*1198G>T (RAF1) ENSP00000401088.1:n.*1198G>T
ENST00000432427.3:c.850G>T (RAF1)
ENST00000460610.2:n.5278G>T (RAF1)
ENST00000471449.2:n.343G>T (RAF1)
ENST00000475353.2:n.3246G>T (RAF1)
ENST00000684903.1:c.*1210G>T (RAF1) ENSP00000508612.1:n.*1210G>T
ENST00000685348.1:c.*1095-278G>T (RAF1) ENSP00000510285.1:n.*1095-278G>T
ENST00000685437.1:c.1434G>T (RAF1) ENSP00000508794.1:p.Trp478Cys
ENST00000685653.1:c.1533G>T (RAF1) ENSP00000509968.1:p.Trp511Cys
ENST00000685697.1:n.2268G>T (RAF1)
ENST00000685738.1:c.*497G>T (RAF1) ENSP00000510156.1:n.*497G>T
ENST00000686409.1:n.4375G>T (RAF1)
ENST00000686455.1:n.3687G>T (RAF1)
ENST00000686762.1:c.*92G>T (RAF1) ENSP00000509767.1:n.*92G>T
ENST00000687257.1:n.3560G>T (RAF1)
ENST00000687326.1:c.*2258G>T (RAF1) ENSP00000509665.1:n.*2258G>T
ENST00000687505.1:n.1651G>T (RAF1)
ENST00000687923.1:c.1422G>T (RAF1) ENSP00000510255.1:p.Trp474Cys
ENST00000688269.1:n.2129G>T (RAF1)
ENST00000688444.1:n.3650G>T (RAF1)
ENST00000688543.1:c.1434G>T (RAF1) ENSP00000509612.1:p.Trp478Cys
ENST00000688625.1:c.*2902G>T (RAF1) ENSP00000509522.1:n.*2902G>T
ENST00000688803.1:n.2965-431G>T (RAF1)
ENST00000688914.1:n.519G>T (RAF1)
ENST00000689097.1:c.*1210G>T (RAF1) ENSP00000509756.1:n.*1210G>T
ENST00000689389.1:c.1356G>T (RAF1) ENSP00000510213.1:p.Trp452Cys
ENST00000689418.1:c.*3001G>T (RAF1) ENSP00000509467.1:n.*3001G>T
ENST00000689540.1:n.3474G>T (RAF1)
ENST00000689876.1:c.1418-278G>T (RAF1) ENSP00000508535.1:n.1418-278G>T
ENST00000689914.1:c.*467G>T (RAF1) ENSP00000509847.1:n.*467G>T
ENST00000690397.1:c.1422G>T (RAF1) ENSP00000508730.1:p.Trp474Cys
ENST00000690460.1:c.1521G>T (RAF1) ENSP00000509106.1:p.Trp507Cys
ENST00000690585.1:c.263-431G>T (RAF1)
ENST00000690625.1:n.2569G>T (RAF1)
ENST00000691396.1:c.*1405G>T (RAF1) ENSP00000510712.1:n.*1405G>T
ENST00000691643.1:n.2159G>T (RAF1)
ENST00000691724.1:c.*490G>T (RAF1) ENSP00000509255.1:n.*490G>T
ENST00000691779.1:c.*1111G>T (RAF1) ENSP00000508592.1:n.*1111G>T
ENST00000691888.1:c.407G>T (RAF1)
ENST00000691899.1:c.1533G>T (RAF1) ENSP00000508763.1:p.Trp511Cys
ENST00000692069.1:n.3890G>T (RAF1)
ENST00000692093.1:c.1434G>T (RAF1) ENSP00000509669.1:p.Trp478Cys
ENST00000692311.1:n.2357G>T (RAF1)
ENST00000692558.1:n.3689G>T (RAF1)
ENST00000692773.1:c.*1270G>T (RAF1) ENSP00000509055.1:n.*1270G>T
ENST00000692830.1:c.*1278G>T (RAF1) ENSP00000509461.1:n.*1278G>T
ENST00000693312.1:c.1308G>T (RAF1) ENSP00000508686.1:p.Trp436Cys
ENST00000693664.1:c.1488-431G>T (RAF1) ENSP00000509614.1:n.1488-431G>T
ENST00000693705.1:c.*1048-703G>T (RAF1) ENSP00000510697.1:n.*1048-703G>T
ENST00000251849.9:c.1533G>T (RAF1) MANE Select ENSP00000251849.4:p.Trp511Cys
ENST00000442415.7:c.1593G>T (RAF1) ENSP00000401888.2:p.Trp531Cys
ENST00000676541.1:c.*3431C>A (MKRN2) ENSP00000503730.1:n.*3431C>A
ENST00000677142.1:c.*3431C>A (MKRN2) ENSP00000504455.1:n.*3431C>A
ENST00000677816.1:c.*1986C>A (MKRN2) ENSP00000502893.1:n.*1986C>A
ENST00000677941.1:n.3494C>A (MKRN2)
ENST00000251849.8:c.1533G>T (RAF1) ENSP00000251849.4:p.Trp511Cys
ENST00000423275.5:c.*1210G>T (RAF1) ENSP00000401088.1:n.*1210G>T
ENST00000432427.2:c.1170G>T (RAF1) ENSP00000398591.2:p.Trp390Cys
ENST00000442415.6:c.1593G>T (RAF1) ENSP00000401888.2:p.Trp531Cys
ENST00000471449.1:n.222G>T (RAF1)
NM_002880.3:c.1533G>T , LRG_413t1:c.1533G>T (RAF1) NP_002871.1:p.Trp511Cys
XM_005265355.1:c.1533G>T (RAF1) XP_005265412.1:p.Trp511Cys
XM_005265357.1:c.1434G>T (RAF1) XP_005265414.1:p.Trp478Cys
XM_005265358.3:c.1290G>T (RAF1) XP_005265415.1:p.Trp430Cys
XM_005265359.3:c.1191G>T (RAF1) XP_005265416.1:p.Trp397Cys
XM_005265360.1:c.1418-278G>T (RAF1) XP_005265417.1:n.1418-278G>T
XM_011533974.1:c.1533G>T (RAF1) XP_011532276.1:p.Trp511Cys
XM_011533975.1:c.1290G>T (RAF1) XP_011532277.1:p.Trp430Cys
NM_001354689.1:c.1593G>T (RAF1) NP_001341618.1:p.Trp531Cys
NM_001354690.1:c.1533G>T (RAF1) NP_001341619.1:p.Trp511Cys
NM_001354691.1:c.1290G>T (RAF1) NP_001341620.1:p.Trp430Cys
NM_001354692.1:c.1290G>T (RAF1) NP_001341621.1:p.Trp430Cys
NM_001354693.1:c.1434G>T (RAF1) NP_001341622.1:p.Trp478Cys
NM_001354694.1:c.1350G>T (RAF1) NP_001341623.1:p.Trp450Cys
NM_001354695.1:c.1191G>T (RAF1) NP_001341624.1:p.Trp397Cys
NR_148940.1:n.2061G>T (RAF1)
NR_148941.1:n.2007G>T (RAF1)
NR_148942.1:n.1946G>T (RAF1)
XM_011533974.3:c.1533G>T (RAF1) XP_011532276.1:p.Trp511Cys
XM_017006966.1:c.1434G>T (RAF1) XP_016862455.1:p.Trp478Cys
NM_001354689.3:c.1593G>T (RAF1) NP_001341618.1:p.Trp531Cys
NM_001354690.2:c.1533G>T (RAF1) NP_001341619.1:p.Trp511Cys
NM_001354691.2:c.1290G>T (RAF1) NP_001341620.1:p.Trp430Cys
NM_001354692.2:c.1290G>T (RAF1) NP_001341621.1:p.Trp430Cys
NM_001354693.2:c.1434G>T (RAF1) NP_001341622.1:p.Trp478Cys
NM_001354694.2:c.1350G>T (RAF1) NP_001341623.1:p.Trp450Cys
NM_001354695.2:c.1191G>T (RAF1) NP_001341624.1:p.Trp397Cys
NR_148940.2:n.1977G>T (RAF1)
NR_148941.2:n.1923G>T (RAF1)
NR_148942.2:n.1862G>T (RAF1)
NM_001354690.3:c.1533G>T (RAF1) NP_001341619.1:p.Trp511Cys
NM_001354691.3:c.1290G>T (RAF1) NP_001341620.1:p.Trp430Cys
NM_001354692.3:c.1290G>T (RAF1) NP_001341621.1:p.Trp430Cys
NM_001354693.3:c.1434G>T (RAF1) NP_001341622.1:p.Trp478Cys
NM_001354694.3:c.1350G>T (RAF1) NP_001341623.1:p.Trp450Cys
NM_001354695.3:c.1191G>T (RAF1) NP_001341624.1:p.Trp397Cys
NM_002880.4:c.1533G>T (RAF1) MANE Select NP_002871.1:p.Trp511Cys
NR_148940.3:n.1977G>T (RAF1)
NR_148941.3:n.1923G>T (RAF1)
NR_148942.3:n.1862G>T (RAF1)