Canonical Allele Identifier: CA1346226827

Gene: RAF1 MKRN2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584940A= , CM000665.2:g.12584940A=	GRCh38
NC_000003.11:g.12626439A= , CM000665.1:g.12626439A=	GRCh37
NC_000003.10:g.12601439A=	NCBI36
NG_007467.1:g.84240T= , LRG_413:g.84240T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1375T= (RAF1)	ENSP00000401088.1:n.*1375T=
ENST00000432427.3:c.1027T= (RAF1)
ENST00000460610.2:n.6022T= (RAF1)
ENST00000471449.2:n.520T= (RAF1)
ENST00000475353.2:n.3990T= (RAF1)
ENST00000684903.1:c.*1387T= (RAF1)	ENSP00000508612.1:n.*1387T=
ENST00000685348.1:c.*1421T= (RAF1)	ENSP00000510285.1:n.*1421T=
ENST00000685437.1:c.1611T= (RAF1)	ENSP00000508794.1:p.Leu537=
ENST00000685653.1:c.1710T= (RAF1)	ENSP00000509968.1:p.Leu570=
ENST00000685697.1:n.2445T= (RAF1)
ENST00000685738.1:c.*674T= (RAF1)	ENSP00000510156.1:n.*674T=
ENST00000686409.1:n.5119T= (RAF1)
ENST00000686455.1:n.4431T= (RAF1)
ENST00000686762.1:c.*269T= (RAF1)	ENSP00000509767.1:n.*269T=
ENST00000687257.1:n.4164T= (RAF1)
ENST00000687326.1:c.*3002T= (RAF1)	ENSP00000509665.1:n.*3002T=
ENST00000687505.1:n.1828T= (RAF1)
ENST00000687923.1:c.1599T= (RAF1)	ENSP00000510255.1:p.Leu533=
ENST00000688269.1:n.2306T= (RAF1)
ENST00000688444.1:n.3827T= (RAF1)
ENST00000688543.1:c.1611T= (RAF1)	ENSP00000509612.1:p.Leu537=
ENST00000688625.1:c.*3079T= (RAF1)	ENSP00000509522.1:n.*3079T=
ENST00000688803.1:n.3138T= (RAF1)
ENST00000688914.1:n.1123T= (RAF1)
ENST00000689097.1:c.*1387T= (RAF1)	ENSP00000509756.1:n.*1387T=
ENST00000689389.1:c.1533T= (RAF1)	ENSP00000510213.1:p.Leu511=
ENST00000689418.1:c.*3605T= (RAF1)	ENSP00000509467.1:n.*3605T=
ENST00000689540.1:n.4078T= (RAF1)
ENST00000689876.1:c.*259T= (RAF1)	ENSP00000508535.1:n.*259T=
ENST00000689914.1:c.*644T= (RAF1)	ENSP00000509847.1:n.*644T=
ENST00000690397.1:c.1599T= (RAF1)	ENSP00000508730.1:p.Leu533=
ENST00000690460.1:c.1698T= (RAF1)	ENSP00000509106.1:p.Leu566=
ENST00000690585.1:c.436T= (RAF1)
ENST00000690625.1:n.2746T= (RAF1)
ENST00000691396.1:c.*1582T= (RAF1)	ENSP00000510712.1:n.*1582T=
ENST00000691643.1:n.2763T= (RAF1)
ENST00000691724.1:c.*667T= (RAF1)	ENSP00000509255.1:n.*667T=
ENST00000691779.1:c.*1288T= (RAF1)	ENSP00000508592.1:n.*1288T=
ENST00000691888.1:c.584T= (RAF1)
ENST00000691899.1:c.1710T= (RAF1)	ENSP00000508763.1:p.Leu570=
ENST00000692069.1:n.4634T= (RAF1)
ENST00000692093.1:c.1611T= (RAF1)	ENSP00000509669.1:p.Leu537=
ENST00000692311.1:n.2534T= (RAF1)
ENST00000692558.1:n.4293T= (RAF1)
ENST00000692773.1:c.*1447T= (RAF1)	ENSP00000509055.1:n.*1447T=
ENST00000692830.1:c.*1455T= (RAF1)	ENSP00000509461.1:n.*1455T=
ENST00000693312.1:c.1485T= (RAF1)	ENSP00000508686.1:p.Leu495=
ENST00000693664.1:c.*161T= (RAF1)	ENSP00000509614.1:n.*161T=
ENST00000693705.1:c.*1089T= (RAF1)	ENSP00000510697.1:n.*1089T=
ENST00000251849.9:c.1710T= (RAF1) MANE Select	ENSP00000251849.4:p.Leu570=
ENST00000442415.7:c.1770T= (RAF1)	ENSP00000401888.2:p.Leu590=
ENST00000676541.1:c.*2687A= (MKRN2)	ENSP00000503730.1:n.*2687A=
ENST00000677142.1:c.*2687A= (MKRN2)	ENSP00000504455.1:n.*2687A=
ENST00000677816.1:c.*1242A= (MKRN2)	ENSP00000502893.1:n.*1242A=
ENST00000677941.1:n.2750A= (MKRN2)
ENST00000251849.8:c.1710T= (RAF1)	ENSP00000251849.4:p.Leu570=
ENST00000423275.5:c.*1387T= (RAF1)	ENSP00000401088.1:n.*1387T=
ENST00000432427.2:c.1347T= (RAF1)	ENSP00000398591.2:p.Leu449=
ENST00000442415.6:c.1770T= (RAF1)	ENSP00000401888.2:p.Leu590=
ENST00000471449.1:n.399T= (RAF1)
NM_002880.3:c.1710T= , LRG_413t1:c.1710T= (RAF1)	NP_002871.1:p.Leu570=
XM_005265355.1:c.1710T= (RAF1)	XP_005265412.1:p.Leu570=
XM_005265357.1:c.1611T= (RAF1)	XP_005265414.1:p.Leu537=
XM_005265358.3:c.1467T= (RAF1)	XP_005265415.1:p.Leu489=
XM_005265359.3:c.1368T= (RAF1)	XP_005265416.1:p.Leu456=
XM_011533974.1:c.1710T= (RAF1)	XP_011532276.1:p.Leu570=
XM_011533975.1:c.1467T= (RAF1)	XP_011532277.1:p.Leu489=
NM_001354689.1:c.1770T= (RAF1)	NP_001341618.1:p.Leu590=
NM_001354690.1:c.1710T= (RAF1)	NP_001341619.1:p.Leu570=
NM_001354691.1:c.1467T= (RAF1)	NP_001341620.1:p.Leu489=
NM_001354692.1:c.1467T= (RAF1)	NP_001341621.1:p.Leu489=
NM_001354693.1:c.1611T= (RAF1)	NP_001341622.1:p.Leu537=
NM_001354694.1:c.1527T= (RAF1)	NP_001341623.1:p.Leu509=
NM_001354695.1:c.1368T= (RAF1)	NP_001341624.1:p.Leu456=
NR_148940.1:n.2238T= (RAF1)
NR_148941.1:n.2184T= (RAF1)
NR_148942.1:n.2123T= (RAF1)
XM_011533974.3:c.1710T= (RAF1)	XP_011532276.1:p.Leu570=
XM_017006966.1:c.1611T= (RAF1)	XP_016862455.1:p.Leu537=
NM_001354689.3:c.1770T= (RAF1)	NP_001341618.1:p.Leu590=
NM_001354690.2:c.1710T= (RAF1)	NP_001341619.1:p.Leu570=
NM_001354691.2:c.1467T= (RAF1)	NP_001341620.1:p.Leu489=
NM_001354692.2:c.1467T= (RAF1)	NP_001341621.1:p.Leu489=
NM_001354693.2:c.1611T= (RAF1)	NP_001341622.1:p.Leu537=
NM_001354694.2:c.1527T= (RAF1)	NP_001341623.1:p.Leu509=
NM_001354695.2:c.1368T= (RAF1)	NP_001341624.1:p.Leu456=
NR_148940.2:n.2154T= (RAF1)
NR_148941.2:n.2100T= (RAF1)
NR_148942.2:n.2039T= (RAF1)
NM_001354690.3:c.1710T= (RAF1)	NP_001341619.1:p.Leu570=
NM_001354691.3:c.1467T= (RAF1)	NP_001341620.1:p.Leu489=
NM_001354692.3:c.1467T= (RAF1)	NP_001341621.1:p.Leu489=
NM_001354693.3:c.1611T= (RAF1)	NP_001341622.1:p.Leu537=
NM_001354694.3:c.1527T= (RAF1)	NP_001341623.1:p.Leu509=
NM_001354695.3:c.1368T= (RAF1)	NP_001341624.1:p.Leu456=
NM_002880.4:c.1710T= (RAF1) MANE Select	NP_002871.1:p.Leu570=
NR_148940.3:n.2154T= (RAF1)
NR_148941.3:n.2100T= (RAF1)
NR_148942.3:n.2039T= (RAF1)