Canonical Allele Identifier: CA1346226943

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12584977A= , CM000665.2:g.12584977A= GRCh38
NC_000003.11:g.12626476A= , CM000665.1:g.12626476A= GRCh37
NC_000003.10:g.12601476A= NCBI36
NG_007467.1:g.84203T= , LRG_413:g.84203T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000423275.6:c.*1338T= (RAF1) ENSP00000401088.1:n.*1338T=
ENST00000432427.3:c.990T= (RAF1)
ENST00000460610.2:n.5985T= (RAF1)
ENST00000471449.2:n.483T= (RAF1)
ENST00000475353.2:n.3953T= (RAF1)
ENST00000684903.1:c.*1350T= (RAF1) ENSP00000508612.1:n.*1350T=
ENST00000685348.1:c.*1384T= (RAF1) ENSP00000510285.1:n.*1384T=
ENST00000685437.1:c.1574T= (RAF1) ENSP00000508794.1:p.Ile525=
ENST00000685653.1:c.1673T= (RAF1) ENSP00000509968.1:p.Ile558=
ENST00000685697.1:n.2408T= (RAF1)
ENST00000685738.1:c.*637T= (RAF1) ENSP00000510156.1:n.*637T=
ENST00000686409.1:n.5082T= (RAF1)
ENST00000686455.1:n.4394T= (RAF1)
ENST00000686762.1:c.*232T= (RAF1) ENSP00000509767.1:n.*232T=
ENST00000687257.1:n.4127T= (RAF1)
ENST00000687326.1:c.*2965T= (RAF1) ENSP00000509665.1:n.*2965T=
ENST00000687505.1:n.1791T= (RAF1)
ENST00000687923.1:c.1562T= (RAF1) ENSP00000510255.1:p.Ile521=
ENST00000688269.1:n.2269T= (RAF1)
ENST00000688444.1:n.3790T= (RAF1)
ENST00000688543.1:c.1574T= (RAF1) ENSP00000509612.1:p.Ile525=
ENST00000688625.1:c.*3042T= (RAF1) ENSP00000509522.1:n.*3042T=
ENST00000688803.1:n.3101T= (RAF1)
ENST00000688914.1:n.1086T= (RAF1)
ENST00000689097.1:c.*1350T= (RAF1) ENSP00000509756.1:n.*1350T=
ENST00000689389.1:c.1496T= (RAF1) ENSP00000510213.1:p.Ile499=
ENST00000689418.1:c.*3568T= (RAF1) ENSP00000509467.1:n.*3568T=
ENST00000689540.1:n.4041T= (RAF1)
ENST00000689876.1:c.*222T= (RAF1) ENSP00000508535.1:n.*222T=
ENST00000689914.1:c.*607T= (RAF1) ENSP00000509847.1:n.*607T=
ENST00000690397.1:c.1562T= (RAF1) ENSP00000508730.1:p.Ile521=
ENST00000690460.1:c.1661T= (RAF1) ENSP00000509106.1:p.Ile554=
ENST00000690585.1:c.399T= (RAF1)
ENST00000690625.1:n.2709T= (RAF1)
ENST00000691396.1:c.*1545T= (RAF1) ENSP00000510712.1:n.*1545T=
ENST00000691643.1:n.2726T= (RAF1)
ENST00000691724.1:c.*630T= (RAF1) ENSP00000509255.1:n.*630T=
ENST00000691779.1:c.*1251T= (RAF1) ENSP00000508592.1:n.*1251T=
ENST00000691888.1:c.547T= (RAF1)
ENST00000691899.1:c.1673T= (RAF1) ENSP00000508763.1:p.Ile558=
ENST00000692069.1:n.4597T= (RAF1)
ENST00000692093.1:c.1574T= (RAF1) ENSP00000509669.1:p.Ile525=
ENST00000692311.1:n.2497T= (RAF1)
ENST00000692558.1:n.4256T= (RAF1)
ENST00000692773.1:c.*1410T= (RAF1) ENSP00000509055.1:n.*1410T=
ENST00000692830.1:c.*1418T= (RAF1) ENSP00000509461.1:n.*1418T=
ENST00000693312.1:c.1448T= (RAF1) ENSP00000508686.1:p.Ile483=
ENST00000693664.1:c.*124T= (RAF1) ENSP00000509614.1:n.*124T=
ENST00000693705.1:c.*1052T= (RAF1) ENSP00000510697.1:n.*1052T=
ENST00000251849.9:c.1673T= (RAF1) MANE Select ENSP00000251849.4:p.Ile558=
ENST00000442415.7:c.1733T= (RAF1) ENSP00000401888.2:p.Ile578=
ENST00000676541.1:c.*2724A= (MKRN2) ENSP00000503730.1:n.*2724A=
ENST00000677142.1:c.*2724A= (MKRN2) ENSP00000504455.1:n.*2724A=
ENST00000677816.1:c.*1279A= (MKRN2) ENSP00000502893.1:n.*1279A=
ENST00000677941.1:n.2787A= (MKRN2)
ENST00000251849.8:c.1673T= (RAF1) ENSP00000251849.4:p.Ile558=
ENST00000423275.5:c.*1350T= (RAF1) ENSP00000401088.1:n.*1350T=
ENST00000432427.2:c.1310T= (RAF1) ENSP00000398591.2:p.Ile437=
ENST00000442415.6:c.1733T= (RAF1) ENSP00000401888.2:p.Ile578=
ENST00000471449.1:n.362T= (RAF1)
NM_002880.3:c.1673T= , LRG_413t1:c.1673T= (RAF1) NP_002871.1:p.Ile558=
XM_005265355.1:c.1673T= (RAF1) XP_005265412.1:p.Ile558=
XM_005265357.1:c.1574T= (RAF1) XP_005265414.1:p.Ile525=
XM_005265358.3:c.1430T= (RAF1) XP_005265415.1:p.Ile477=
XM_005265359.3:c.1331T= (RAF1) XP_005265416.1:p.Ile444=
XM_011533974.1:c.1673T= (RAF1) XP_011532276.1:p.Ile558=
XM_011533975.1:c.1430T= (RAF1) XP_011532277.1:p.Ile477=
NM_001354689.1:c.1733T= (RAF1) NP_001341618.1:p.Ile578=
NM_001354690.1:c.1673T= (RAF1) NP_001341619.1:p.Ile558=
NM_001354691.1:c.1430T= (RAF1) NP_001341620.1:p.Ile477=
NM_001354692.1:c.1430T= (RAF1) NP_001341621.1:p.Ile477=
NM_001354693.1:c.1574T= (RAF1) NP_001341622.1:p.Ile525=
NM_001354694.1:c.1490T= (RAF1) NP_001341623.1:p.Ile497=
NM_001354695.1:c.1331T= (RAF1) NP_001341624.1:p.Ile444=
NR_148940.1:n.2201T= (RAF1)
NR_148941.1:n.2147T= (RAF1)
NR_148942.1:n.2086T= (RAF1)
XM_011533974.3:c.1673T= (RAF1) XP_011532276.1:p.Ile558=
XM_017006966.1:c.1574T= (RAF1) XP_016862455.1:p.Ile525=
NM_001354689.3:c.1733T= (RAF1) NP_001341618.1:p.Ile578=
NM_001354690.2:c.1673T= (RAF1) NP_001341619.1:p.Ile558=
NM_001354691.2:c.1430T= (RAF1) NP_001341620.1:p.Ile477=
NM_001354692.2:c.1430T= (RAF1) NP_001341621.1:p.Ile477=
NM_001354693.2:c.1574T= (RAF1) NP_001341622.1:p.Ile525=
NM_001354694.2:c.1490T= (RAF1) NP_001341623.1:p.Ile497=
NM_001354695.2:c.1331T= (RAF1) NP_001341624.1:p.Ile444=
NR_148940.2:n.2117T= (RAF1)
NR_148941.2:n.2063T= (RAF1)
NR_148942.2:n.2002T= (RAF1)
NM_001354690.3:c.1673T= (RAF1) NP_001341619.1:p.Ile558=
NM_001354691.3:c.1430T= (RAF1) NP_001341620.1:p.Ile477=
NM_001354692.3:c.1430T= (RAF1) NP_001341621.1:p.Ile477=
NM_001354693.3:c.1574T= (RAF1) NP_001341622.1:p.Ile525=
NM_001354694.3:c.1490T= (RAF1) NP_001341623.1:p.Ile497=
NM_001354695.3:c.1331T= (RAF1) NP_001341624.1:p.Ile444=
NM_002880.4:c.1673T= (RAF1) MANE Select NP_002871.1:p.Ile558=
NR_148940.3:n.2117T= (RAF1)
NR_148941.3:n.2063T= (RAF1)
NR_148942.3:n.2002T= (RAF1)