Canonical Allele Identifier: CA1346225782

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12584346A= , CM000665.2:g.12584346A= GRCh38
NC_000003.11:g.12625845A= , CM000665.1:g.12625845A= GRCh37
NC_000003.10:g.12600845A= NCBI36
NG_007467.1:g.84834T= , LRG_413:g.84834T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000423275.6:c.*1780T= (RAF1) ENSP00000401088.1:n.*1780T=
ENST00000432427.3:c.1432T= (RAF1)
ENST00000460610.2:n.6427T= (RAF1)
ENST00000471449.2:n.925T= (RAF1)
ENST00000475353.2:n.4395T= (RAF1)
ENST00000684903.1:c.*1792T= (RAF1) ENSP00000508612.1:n.*1792T=
ENST00000685348.1:c.*1826T= (RAF1) ENSP00000510285.1:n.*1826T=
ENST00000685437.1:c.*168T= (RAF1) ENSP00000508794.1:n.*168T=
ENST00000685653.1:c.*168T= (RAF1) ENSP00000509968.1:n.*168T=
ENST00000685697.1:n.2850T= (RAF1)
ENST00000685738.1:c.*1079T= (RAF1) ENSP00000510156.1:n.*1079T=
ENST00000686409.1:n.5524T= (RAF1)
ENST00000686455.1:n.4836T= (RAF1)
ENST00000686762.1:c.*674T= (RAF1) ENSP00000509767.1:n.*674T=
ENST00000687257.1:n.4569T= (RAF1)
ENST00000687326.1:c.*3407T= (RAF1) ENSP00000509665.1:n.*3407T=
ENST00000687505.1:n.2233T= (RAF1)
ENST00000687923.1:c.*168T= (RAF1) ENSP00000510255.1:n.*168T=
ENST00000688269.1:n.2711T= (RAF1)
ENST00000688444.1:n.4232T= (RAF1)
ENST00000688543.1:c.*168T= (RAF1) ENSP00000509612.1:n.*168T=
ENST00000688625.1:c.*3484T= (RAF1) ENSP00000509522.1:n.*3484T=
ENST00000688803.1:n.3543T= (RAF1)
ENST00000689097.1:c.*1792T= (RAF1) ENSP00000509756.1:n.*1792T=
ENST00000689389.1:c.*168T= (RAF1) ENSP00000510213.1:n.*168T=
ENST00000689418.1:c.*4010T= (RAF1) ENSP00000509467.1:n.*4010T=
ENST00000689540.1:n.4483T= (RAF1)
ENST00000689876.1:c.*664T= (RAF1) ENSP00000508535.1:n.*664T=
ENST00000689914.1:c.*1049T= (RAF1) ENSP00000509847.1:n.*1049T=
ENST00000690397.1:c.*168T= (RAF1) ENSP00000508730.1:n.*168T=
ENST00000690460.1:c.*168T= (RAF1) ENSP00000509106.1:n.*168T=
ENST00000690585.1:c.841T= (RAF1)
ENST00000690625.1:n.3151T= (RAF1)
ENST00000691396.1:c.*1987T= (RAF1) ENSP00000510712.1:n.*1987T=
ENST00000691643.1:n.3168T= (RAF1)
ENST00000691724.1:c.*1072T= (RAF1) ENSP00000509255.1:n.*1072T=
ENST00000691779.1:c.*1693T= (RAF1) ENSP00000508592.1:n.*1693T=
ENST00000691888.1:c.989T= (RAF1)
ENST00000691899.1:c.*168T= (RAF1) ENSP00000508763.1:n.*168T=
ENST00000692069.1:n.5039T= (RAF1)
ENST00000692093.1:c.*168T= (RAF1) ENSP00000509669.1:n.*168T=
ENST00000692311.1:n.2939T= (RAF1)
ENST00000692558.1:n.4698T= (RAF1)
ENST00000692773.1:c.*1852T= (RAF1) ENSP00000509055.1:n.*1852T=
ENST00000692830.1:c.*1860T= (RAF1) ENSP00000509461.1:n.*1860T=
ENST00000693312.1:c.*168T= (RAF1) ENSP00000508686.1:n.*168T=
ENST00000693664.1:c.*566T= (RAF1) ENSP00000509614.1:n.*566T=
ENST00000693705.1:c.*1494T= (RAF1) ENSP00000510697.1:n.*1494T=
ENST00000251849.9:c.*168T= (RAF1) MANE Select ENSP00000251849.4:n.*168T=
ENST00000442415.7:c.*168T= (RAF1) ENSP00000401888.2:n.*168T=
ENST00000676541.1:c.*2093A= (MKRN2) ENSP00000503730.1:n.*2093A=
ENST00000677142.1:c.*2093A= (MKRN2) ENSP00000504455.1:n.*2093A=
ENST00000677816.1:c.*648A= (MKRN2) ENSP00000502893.1:n.*648A=
ENST00000677941.1:n.2156A= (MKRN2)
ENST00000251849.8:c.*168T= (RAF1) ENSP00000251849.4:n.*168T=
ENST00000423275.5:c.*1792T= (RAF1) ENSP00000401088.1:n.*1792T=
ENST00000432427.2:c.1752T= (RAF1) ENSP00000398591.2:n.1752T=
ENST00000442415.6:c.*168T= (RAF1) ENSP00000401888.2:n.*168T=
ENST00000471449.1:n.804T= (RAF1)
NM_002880.3:c.*168T= , LRG_413t1:c.*168T= (RAF1) NP_002871.1:n.*168T=
XM_005265355.1:c.*168T= (RAF1) XP_005265412.1:n.*168T=
XM_005265357.1:c.*168T= (RAF1) XP_005265414.1:n.*168T=
XM_005265358.3:c.*168T= (RAF1) XP_005265415.1:n.*168T=
XM_005265359.3:c.*168T= (RAF1) XP_005265416.1:n.*168T=
XM_011533974.1:c.*168T= (RAF1) XP_011532276.1:n.*168T=
XM_011533975.1:c.*168T= (RAF1) XP_011532277.1:n.*168T=
NM_001354689.1:c.*168T= (RAF1) NP_001341618.1:n.*168T=
NM_001354690.1:c.*168T= (RAF1) NP_001341619.1:n.*168T=
NM_001354691.1:c.*168T= (RAF1) NP_001341620.1:n.*168T=
NM_001354692.1:c.*168T= (RAF1) NP_001341621.1:n.*168T=
NM_001354693.1:c.*168T= (RAF1) NP_001341622.1:n.*168T=
NM_001354694.1:c.*168T= (RAF1) NP_001341623.1:n.*168T=
NM_001354695.1:c.*168T= (RAF1) NP_001341624.1:n.*168T=
NR_148940.1:n.2643T= (RAF1)
NR_148941.1:n.2589T= (RAF1)
NR_148942.1:n.2528T= (RAF1)
XM_011533974.3:c.*168T= (RAF1) XP_011532276.1:n.*168T=
XM_017006966.1:c.*168T= (RAF1) XP_016862455.1:n.*168T=
NM_001354689.3:c.*168T= (RAF1) NP_001341618.1:n.*168T=
NM_001354690.2:c.*168T= (RAF1) NP_001341619.1:n.*168T=
NM_001354691.2:c.*168T= (RAF1) NP_001341620.1:n.*168T=
NM_001354692.2:c.*168T= (RAF1) NP_001341621.1:n.*168T=
NM_001354693.2:c.*168T= (RAF1) NP_001341622.1:n.*168T=
NM_001354694.2:c.*168T= (RAF1) NP_001341623.1:n.*168T=
NM_001354695.2:c.*168T= (RAF1) NP_001341624.1:n.*168T=
NR_148940.2:n.2559T= (RAF1)
NR_148941.2:n.2505T= (RAF1)
NR_148942.2:n.2444T= (RAF1)
NM_001354690.3:c.*168T= (RAF1) NP_001341619.1:n.*168T=
NM_001354691.3:c.*168T= (RAF1) NP_001341620.1:n.*168T=
NM_001354692.3:c.*168T= (RAF1) NP_001341621.1:n.*168T=
NM_001354693.3:c.*168T= (RAF1) NP_001341622.1:n.*168T=
NM_001354694.3:c.*168T= (RAF1) NP_001341623.1:n.*168T=
NM_001354695.3:c.*168T= (RAF1) NP_001341624.1:n.*168T=
NM_002880.4:c.*168T= (RAF1) MANE Select NP_002871.1:n.*168T=
NR_148940.3:n.2559T= (RAF1)
NR_148941.3:n.2505T= (RAF1)
NR_148942.3:n.2444T= (RAF1)