Canonical Allele Identifier: CA1346226401

Gene: RAF1 MKRN2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584640C= , CM000665.2:g.12584640C=	GRCh38
NC_000003.11:g.12626139C= , CM000665.1:g.12626139C=	GRCh37
NC_000003.10:g.12601139C=	NCBI36
NG_007467.1:g.84540G= , LRG_413:g.84540G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000423275.6:c.*1486G= (RAF1)	ENSP00000401088.1:n.*1486G=
ENST00000432427.3:c.1138G= (RAF1)
ENST00000460610.2:n.6133G= (RAF1)
ENST00000471449.2:n.631G= (RAF1)
ENST00000475353.2:n.4101G= (RAF1)
ENST00000684903.1:c.*1498G= (RAF1)	ENSP00000508612.1:n.*1498G=
ENST00000685348.1:c.*1532G= (RAF1)	ENSP00000510285.1:n.*1532G=
ENST00000685437.1:c.1722G= (RAF1)	ENSP00000508794.1:p.Glu574=
ENST00000685653.1:c.1821G= (RAF1)	ENSP00000509968.1:p.Glu607=
ENST00000685697.1:n.2556G= (RAF1)
ENST00000685738.1:c.*785G= (RAF1)	ENSP00000510156.1:n.*785G=
ENST00000686409.1:n.5230G= (RAF1)
ENST00000686455.1:n.4542G= (RAF1)
ENST00000686762.1:c.*380G= (RAF1)	ENSP00000509767.1:n.*380G=
ENST00000687257.1:n.4275G= (RAF1)
ENST00000687326.1:c.*3113G= (RAF1)	ENSP00000509665.1:n.*3113G=
ENST00000687505.1:n.1939G= (RAF1)
ENST00000687923.1:c.1710G= (RAF1)	ENSP00000510255.1:p.Glu570=
ENST00000688269.1:n.2417G= (RAF1)
ENST00000688444.1:n.3938G= (RAF1)
ENST00000688543.1:c.1722G= (RAF1)	ENSP00000509612.1:p.Glu574=
ENST00000688625.1:c.*3190G= (RAF1)	ENSP00000509522.1:n.*3190G=
ENST00000688803.1:n.3249G= (RAF1)
ENST00000689097.1:c.*1498G= (RAF1)	ENSP00000509756.1:n.*1498G=
ENST00000689389.1:c.1644G= (RAF1)	ENSP00000510213.1:p.Glu548=
ENST00000689418.1:c.*3716G= (RAF1)	ENSP00000509467.1:n.*3716G=
ENST00000689540.1:n.4189G= (RAF1)
ENST00000689876.1:c.*370G= (RAF1)	ENSP00000508535.1:n.*370G=
ENST00000689914.1:c.*755G= (RAF1)	ENSP00000509847.1:n.*755G=
ENST00000690397.1:c.1710G= (RAF1)	ENSP00000508730.1:p.Glu570=
ENST00000690460.1:c.1809G= (RAF1)	ENSP00000509106.1:p.Glu603=
ENST00000690585.1:c.547G= (RAF1)
ENST00000690625.1:n.2857G= (RAF1)
ENST00000691396.1:c.*1693G= (RAF1)	ENSP00000510712.1:n.*1693G=
ENST00000691643.1:n.2874G= (RAF1)
ENST00000691724.1:c.*778G= (RAF1)	ENSP00000509255.1:n.*778G=
ENST00000691779.1:c.*1399G= (RAF1)	ENSP00000508592.1:n.*1399G=
ENST00000691888.1:c.695G= (RAF1)
ENST00000691899.1:c.1821G= (RAF1)	ENSP00000508763.1:p.Glu607=
ENST00000692069.1:n.4745G= (RAF1)
ENST00000692093.1:c.1722G= (RAF1)	ENSP00000509669.1:p.Glu574=
ENST00000692311.1:n.2645G= (RAF1)
ENST00000692558.1:n.4404G= (RAF1)
ENST00000692773.1:c.*1558G= (RAF1)	ENSP00000509055.1:n.*1558G=
ENST00000692830.1:c.*1566G= (RAF1)	ENSP00000509461.1:n.*1566G=
ENST00000693312.1:c.1596G= (RAF1)	ENSP00000508686.1:p.Glu532=
ENST00000693664.1:c.*272G= (RAF1)	ENSP00000509614.1:n.*272G=
ENST00000693705.1:c.*1200G= (RAF1)	ENSP00000510697.1:n.*1200G=
ENST00000251849.9:c.1821G= (RAF1) MANE Select	ENSP00000251849.4:p.Glu607=
ENST00000442415.7:c.1881G= (RAF1)	ENSP00000401888.2:p.Glu627=
ENST00000676541.1:c.*2387C= (MKRN2)	ENSP00000503730.1:n.*2387C=
ENST00000677142.1:c.*2387C= (MKRN2)	ENSP00000504455.1:n.*2387C=
ENST00000677816.1:c.*942C= (MKRN2)	ENSP00000502893.1:n.*942C=
ENST00000677941.1:n.2450C= (MKRN2)
ENST00000251849.8:c.1821G= (RAF1)	ENSP00000251849.4:p.Glu607=
ENST00000423275.5:c.*1498G= (RAF1)	ENSP00000401088.1:n.*1498G=
ENST00000432427.2:c.1458G= (RAF1)	ENSP00000398591.2:p.Glu486=
ENST00000442415.6:c.1881G= (RAF1)	ENSP00000401888.2:p.Glu627=
ENST00000471449.1:n.510G= (RAF1)
NM_002880.3:c.1821G= , LRG_413t1:c.1821G= (RAF1)	NP_002871.1:p.Glu607=
XM_005265355.1:c.1821G= (RAF1)	XP_005265412.1:p.Glu607=
XM_005265357.1:c.1722G= (RAF1)	XP_005265414.1:p.Glu574=
XM_005265358.3:c.1578G= (RAF1)	XP_005265415.1:p.Glu526=
XM_005265359.3:c.1479G= (RAF1)	XP_005265416.1:p.Glu493=
XM_011533974.1:c.1821G= (RAF1)	XP_011532276.1:p.Glu607=
XM_011533975.1:c.1578G= (RAF1)	XP_011532277.1:p.Glu526=
NM_001354689.1:c.1881G= (RAF1)	NP_001341618.1:p.Glu627=
NM_001354690.1:c.1821G= (RAF1)	NP_001341619.1:p.Glu607=
NM_001354691.1:c.1578G= (RAF1)	NP_001341620.1:p.Glu526=
NM_001354692.1:c.1578G= (RAF1)	NP_001341621.1:p.Glu526=
NM_001354693.1:c.1722G= (RAF1)	NP_001341622.1:p.Glu574=
NM_001354694.1:c.1638G= (RAF1)	NP_001341623.1:p.Glu546=
NM_001354695.1:c.1479G= (RAF1)	NP_001341624.1:p.Glu493=
NR_148940.1:n.2349G= (RAF1)
NR_148941.1:n.2295G= (RAF1)
NR_148942.1:n.2234G= (RAF1)
XM_011533974.3:c.1821G= (RAF1)	XP_011532276.1:p.Glu607=
XM_017006966.1:c.1722G= (RAF1)	XP_016862455.1:p.Glu574=
NM_001354689.3:c.1881G= (RAF1)	NP_001341618.1:p.Glu627=
NM_001354690.2:c.1821G= (RAF1)	NP_001341619.1:p.Glu607=
NM_001354691.2:c.1578G= (RAF1)	NP_001341620.1:p.Glu526=
NM_001354692.2:c.1578G= (RAF1)	NP_001341621.1:p.Glu526=
NM_001354693.2:c.1722G= (RAF1)	NP_001341622.1:p.Glu574=
NM_001354694.2:c.1638G= (RAF1)	NP_001341623.1:p.Glu546=
NM_001354695.2:c.1479G= (RAF1)	NP_001341624.1:p.Glu493=
NR_148940.2:n.2265G= (RAF1)
NR_148941.2:n.2211G= (RAF1)
NR_148942.2:n.2150G= (RAF1)
NM_001354690.3:c.1821G= (RAF1)	NP_001341619.1:p.Glu607=
NM_001354691.3:c.1578G= (RAF1)	NP_001341620.1:p.Glu526=
NM_001354692.3:c.1578G= (RAF1)	NP_001341621.1:p.Glu526=
NM_001354693.3:c.1722G= (RAF1)	NP_001341622.1:p.Glu574=
NM_001354694.3:c.1638G= (RAF1)	NP_001341623.1:p.Glu546=
NM_001354695.3:c.1479G= (RAF1)	NP_001341624.1:p.Glu493=
NM_002880.4:c.1821G= (RAF1) MANE Select	NP_002871.1:p.Glu607=
NR_148940.3:n.2265G= (RAF1)
NR_148941.3:n.2211G= (RAF1)
NR_148942.3:n.2150G= (RAF1)