Canonical Allele Identifier: CA1346226245

Gene: RAF1 MKRN2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584583A= , CM000665.2:g.12584583A=	GRCh38
NC_000003.11:g.12626082A= , CM000665.1:g.12626082A=	GRCh37
NC_000003.10:g.12601082A=	NCBI36
NG_007467.1:g.84597T= , LRG_413:g.84597T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1543T= (RAF1)	ENSP00000401088.1:n.*1543T=
ENST00000432427.3:c.1195T= (RAF1)
ENST00000460610.2:n.6190T= (RAF1)
ENST00000471449.2:n.688T= (RAF1)
ENST00000475353.2:n.4158T= (RAF1)
ENST00000684903.1:c.*1555T= (RAF1)	ENSP00000508612.1:n.*1555T=
ENST00000685348.1:c.*1589T= (RAF1)	ENSP00000510285.1:n.*1589T=
ENST00000685437.1:c.1779T= (RAF1)	ENSP00000508794.1:p.His593=
ENST00000685653.1:c.1878T= (RAF1)	ENSP00000509968.1:p.His626=
ENST00000685697.1:n.2613T= (RAF1)
ENST00000685738.1:c.*842T= (RAF1)	ENSP00000510156.1:n.*842T=
ENST00000686409.1:n.5287T= (RAF1)
ENST00000686455.1:n.4599T= (RAF1)
ENST00000686762.1:c.*437T= (RAF1)	ENSP00000509767.1:n.*437T=
ENST00000687257.1:n.4332T= (RAF1)
ENST00000687326.1:c.*3170T= (RAF1)	ENSP00000509665.1:n.*3170T=
ENST00000687505.1:n.1996T= (RAF1)
ENST00000687923.1:c.1767T= (RAF1)	ENSP00000510255.1:p.His589=
ENST00000688269.1:n.2474T= (RAF1)
ENST00000688444.1:n.3995T= (RAF1)
ENST00000688543.1:c.1779T= (RAF1)	ENSP00000509612.1:p.His593=
ENST00000688625.1:c.*3247T= (RAF1)	ENSP00000509522.1:n.*3247T=
ENST00000688803.1:n.3306T= (RAF1)
ENST00000689097.1:c.*1555T= (RAF1)	ENSP00000509756.1:n.*1555T=
ENST00000689389.1:c.1701T= (RAF1)	ENSP00000510213.1:p.His567=
ENST00000689418.1:c.*3773T= (RAF1)	ENSP00000509467.1:n.*3773T=
ENST00000689540.1:n.4246T= (RAF1)
ENST00000689876.1:c.*427T= (RAF1)	ENSP00000508535.1:n.*427T=
ENST00000689914.1:c.*812T= (RAF1)	ENSP00000509847.1:n.*812T=
ENST00000690397.1:c.1767T= (RAF1)	ENSP00000508730.1:p.His589=
ENST00000690460.1:c.1866T= (RAF1)	ENSP00000509106.1:p.His622=
ENST00000690585.1:c.604T= (RAF1)
ENST00000690625.1:n.2914T= (RAF1)
ENST00000691396.1:c.*1750T= (RAF1)	ENSP00000510712.1:n.*1750T=
ENST00000691643.1:n.2931T= (RAF1)
ENST00000691724.1:c.*835T= (RAF1)	ENSP00000509255.1:n.*835T=
ENST00000691779.1:c.*1456T= (RAF1)	ENSP00000508592.1:n.*1456T=
ENST00000691888.1:c.752T= (RAF1)
ENST00000691899.1:c.1878T= (RAF1)	ENSP00000508763.1:p.His626=
ENST00000692069.1:n.4802T= (RAF1)
ENST00000692093.1:c.1779T= (RAF1)	ENSP00000509669.1:p.His593=
ENST00000692311.1:n.2702T= (RAF1)
ENST00000692558.1:n.4461T= (RAF1)
ENST00000692773.1:c.*1615T= (RAF1)	ENSP00000509055.1:n.*1615T=
ENST00000692830.1:c.*1623T= (RAF1)	ENSP00000509461.1:n.*1623T=
ENST00000693312.1:c.1653T= (RAF1)	ENSP00000508686.1:p.His551=
ENST00000693664.1:c.*329T= (RAF1)	ENSP00000509614.1:n.*329T=
ENST00000693705.1:c.*1257T= (RAF1)	ENSP00000510697.1:n.*1257T=
ENST00000251849.9:c.1878T= (RAF1) MANE Select	ENSP00000251849.4:p.His626=
ENST00000442415.7:c.1938T= (RAF1)	ENSP00000401888.2:p.His646=
ENST00000676541.1:c.*2330A= (MKRN2)	ENSP00000503730.1:n.*2330A=
ENST00000677142.1:c.*2330A= (MKRN2)	ENSP00000504455.1:n.*2330A=
ENST00000677816.1:c.*885A= (MKRN2)	ENSP00000502893.1:n.*885A=
ENST00000677941.1:n.2393A= (MKRN2)
ENST00000251849.8:c.1878T= (RAF1)	ENSP00000251849.4:p.His626=
ENST00000423275.5:c.*1555T= (RAF1)	ENSP00000401088.1:n.*1555T=
ENST00000432427.2:c.1515T= (RAF1)	ENSP00000398591.2:p.His505=
ENST00000442415.6:c.1938T= (RAF1)	ENSP00000401888.2:p.His646=
ENST00000471449.1:n.567T= (RAF1)
NM_002880.3:c.1878T= , LRG_413t1:c.1878T= (RAF1)	NP_002871.1:p.His626=
XM_005265355.1:c.1878T= (RAF1)	XP_005265412.1:p.His626=
XM_005265357.1:c.1779T= (RAF1)	XP_005265414.1:p.His593=
XM_005265358.3:c.1635T= (RAF1)	XP_005265415.1:p.His545=
XM_005265359.3:c.1536T= (RAF1)	XP_005265416.1:p.His512=
XM_011533974.1:c.1878T= (RAF1)	XP_011532276.1:p.His626=
XM_011533975.1:c.1635T= (RAF1)	XP_011532277.1:p.His545=
NM_001354689.1:c.1938T= (RAF1)	NP_001341618.1:p.His646=
NM_001354690.1:c.1878T= (RAF1)	NP_001341619.1:p.His626=
NM_001354691.1:c.1635T= (RAF1)	NP_001341620.1:p.His545=
NM_001354692.1:c.1635T= (RAF1)	NP_001341621.1:p.His545=
NM_001354693.1:c.1779T= (RAF1)	NP_001341622.1:p.His593=
NM_001354694.1:c.1695T= (RAF1)	NP_001341623.1:p.His565=
NM_001354695.1:c.1536T= (RAF1)	NP_001341624.1:p.His512=
NR_148940.1:n.2406T= (RAF1)
NR_148941.1:n.2352T= (RAF1)
NR_148942.1:n.2291T= (RAF1)
XM_011533974.3:c.1878T= (RAF1)	XP_011532276.1:p.His626=
XM_017006966.1:c.1779T= (RAF1)	XP_016862455.1:p.His593=
NM_001354689.3:c.1938T= (RAF1)	NP_001341618.1:p.His646=
NM_001354690.2:c.1878T= (RAF1)	NP_001341619.1:p.His626=
NM_001354691.2:c.1635T= (RAF1)	NP_001341620.1:p.His545=
NM_001354692.2:c.1635T= (RAF1)	NP_001341621.1:p.His545=
NM_001354693.2:c.1779T= (RAF1)	NP_001341622.1:p.His593=
NM_001354694.2:c.1695T= (RAF1)	NP_001341623.1:p.His565=
NM_001354695.2:c.1536T= (RAF1)	NP_001341624.1:p.His512=
NR_148940.2:n.2322T= (RAF1)
NR_148941.2:n.2268T= (RAF1)
NR_148942.2:n.2207T= (RAF1)
NM_001354690.3:c.1878T= (RAF1)	NP_001341619.1:p.His626=
NM_001354691.3:c.1635T= (RAF1)	NP_001341620.1:p.His545=
NM_001354692.3:c.1635T= (RAF1)	NP_001341621.1:p.His545=
NM_001354693.3:c.1779T= (RAF1)	NP_001341622.1:p.His593=
NM_001354694.3:c.1695T= (RAF1)	NP_001341623.1:p.His565=
NM_001354695.3:c.1536T= (RAF1)	NP_001341624.1:p.His512=
NM_002880.4:c.1878T= (RAF1) MANE Select	NP_002871.1:p.His626=
NR_148940.3:n.2322T= (RAF1)
NR_148941.3:n.2268T= (RAF1)
NR_148942.3:n.2207T= (RAF1)