Canonical Allele Identifier: CA1346226849

Gene: RAF1 MKRN2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584951A= , CM000665.2:g.12584951A=	GRCh38
NC_000003.11:g.12626450A= , CM000665.1:g.12626450A=	GRCh37
NC_000003.10:g.12601450A=	NCBI36
NG_007467.1:g.84229T= , LRG_413:g.84229T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1364T= (RAF1)	ENSP00000401088.1:n.*1364T=
ENST00000432427.3:c.1016T= (RAF1)
ENST00000460610.2:n.6011T= (RAF1)
ENST00000471449.2:n.509T= (RAF1)
ENST00000475353.2:n.3979T= (RAF1)
ENST00000684903.1:c.*1376T= (RAF1)	ENSP00000508612.1:n.*1376T=
ENST00000685348.1:c.*1410T= (RAF1)	ENSP00000510285.1:n.*1410T=
ENST00000685437.1:c.1600T= (RAF1)	ENSP00000508794.1:p.Ser534=
ENST00000685653.1:c.1699T= (RAF1)	ENSP00000509968.1:p.Ser567=
ENST00000685697.1:n.2434T= (RAF1)
ENST00000685738.1:c.*663T= (RAF1)	ENSP00000510156.1:n.*663T=
ENST00000686409.1:n.5108T= (RAF1)
ENST00000686455.1:n.4420T= (RAF1)
ENST00000686762.1:c.*258T= (RAF1)	ENSP00000509767.1:n.*258T=
ENST00000687257.1:n.4153T= (RAF1)
ENST00000687326.1:c.*2991T= (RAF1)	ENSP00000509665.1:n.*2991T=
ENST00000687505.1:n.1817T= (RAF1)
ENST00000687923.1:c.1588T= (RAF1)	ENSP00000510255.1:p.Ser530=
ENST00000688269.1:n.2295T= (RAF1)
ENST00000688444.1:n.3816T= (RAF1)
ENST00000688543.1:c.1600T= (RAF1)	ENSP00000509612.1:p.Ser534=
ENST00000688625.1:c.*3068T= (RAF1)	ENSP00000509522.1:n.*3068T=
ENST00000688803.1:n.3127T= (RAF1)
ENST00000688914.1:n.1112T= (RAF1)
ENST00000689097.1:c.*1376T= (RAF1)	ENSP00000509756.1:n.*1376T=
ENST00000689389.1:c.1522T= (RAF1)	ENSP00000510213.1:p.Ser508=
ENST00000689418.1:c.*3594T= (RAF1)	ENSP00000509467.1:n.*3594T=
ENST00000689540.1:n.4067T= (RAF1)
ENST00000689876.1:c.*248T= (RAF1)	ENSP00000508535.1:n.*248T=
ENST00000689914.1:c.*633T= (RAF1)	ENSP00000509847.1:n.*633T=
ENST00000690397.1:c.1588T= (RAF1)	ENSP00000508730.1:p.Ser530=
ENST00000690460.1:c.1687T= (RAF1)	ENSP00000509106.1:p.Ser563=
ENST00000690585.1:c.425T= (RAF1)
ENST00000690625.1:n.2735T= (RAF1)
ENST00000691396.1:c.*1571T= (RAF1)	ENSP00000510712.1:n.*1571T=
ENST00000691643.1:n.2752T= (RAF1)
ENST00000691724.1:c.*656T= (RAF1)	ENSP00000509255.1:n.*656T=
ENST00000691779.1:c.*1277T= (RAF1)	ENSP00000508592.1:n.*1277T=
ENST00000691888.1:c.573T= (RAF1)
ENST00000691899.1:c.1699T= (RAF1)	ENSP00000508763.1:p.Ser567=
ENST00000692069.1:n.4623T= (RAF1)
ENST00000692093.1:c.1600T= (RAF1)	ENSP00000509669.1:p.Ser534=
ENST00000692311.1:n.2523T= (RAF1)
ENST00000692558.1:n.4282T= (RAF1)
ENST00000692773.1:c.*1436T= (RAF1)	ENSP00000509055.1:n.*1436T=
ENST00000692830.1:c.*1444T= (RAF1)	ENSP00000509461.1:n.*1444T=
ENST00000693312.1:c.1474T= (RAF1)	ENSP00000508686.1:p.Ser492=
ENST00000693664.1:c.*150T= (RAF1)	ENSP00000509614.1:n.*150T=
ENST00000693705.1:c.*1078T= (RAF1)	ENSP00000510697.1:n.*1078T=
ENST00000251849.9:c.1699T= (RAF1) MANE Select	ENSP00000251849.4:p.Ser567=
ENST00000442415.7:c.1759T= (RAF1)	ENSP00000401888.2:p.Ser587=
ENST00000676541.1:c.*2698A= (MKRN2)	ENSP00000503730.1:n.*2698A=
ENST00000677142.1:c.*2698A= (MKRN2)	ENSP00000504455.1:n.*2698A=
ENST00000677816.1:c.*1253A= (MKRN2)	ENSP00000502893.1:n.*1253A=
ENST00000677941.1:n.2761A= (MKRN2)
ENST00000251849.8:c.1699T= (RAF1)	ENSP00000251849.4:p.Ser567=
ENST00000423275.5:c.*1376T= (RAF1)	ENSP00000401088.1:n.*1376T=
ENST00000432427.2:c.1336T= (RAF1)	ENSP00000398591.2:p.Ser446=
ENST00000442415.6:c.1759T= (RAF1)	ENSP00000401888.2:p.Ser587=
ENST00000471449.1:n.388T= (RAF1)
NM_002880.3:c.1699T= , LRG_413t1:c.1699T= (RAF1)	NP_002871.1:p.Ser567=
XM_005265355.1:c.1699T= (RAF1)	XP_005265412.1:p.Ser567=
XM_005265357.1:c.1600T= (RAF1)	XP_005265414.1:p.Ser534=
XM_005265358.3:c.1456T= (RAF1)	XP_005265415.1:p.Ser486=
XM_005265359.3:c.1357T= (RAF1)	XP_005265416.1:p.Ser453=
XM_011533974.1:c.1699T= (RAF1)	XP_011532276.1:p.Ser567=
XM_011533975.1:c.1456T= (RAF1)	XP_011532277.1:p.Ser486=
NM_001354689.1:c.1759T= (RAF1)	NP_001341618.1:p.Ser587=
NM_001354690.1:c.1699T= (RAF1)	NP_001341619.1:p.Ser567=
NM_001354691.1:c.1456T= (RAF1)	NP_001341620.1:p.Ser486=
NM_001354692.1:c.1456T= (RAF1)	NP_001341621.1:p.Ser486=
NM_001354693.1:c.1600T= (RAF1)	NP_001341622.1:p.Ser534=
NM_001354694.1:c.1516T= (RAF1)	NP_001341623.1:p.Ser506=
NM_001354695.1:c.1357T= (RAF1)	NP_001341624.1:p.Ser453=
NR_148940.1:n.2227T= (RAF1)
NR_148941.1:n.2173T= (RAF1)
NR_148942.1:n.2112T= (RAF1)
XM_011533974.3:c.1699T= (RAF1)	XP_011532276.1:p.Ser567=
XM_017006966.1:c.1600T= (RAF1)	XP_016862455.1:p.Ser534=
NM_001354689.3:c.1759T= (RAF1)	NP_001341618.1:p.Ser587=
NM_001354690.2:c.1699T= (RAF1)	NP_001341619.1:p.Ser567=
NM_001354691.2:c.1456T= (RAF1)	NP_001341620.1:p.Ser486=
NM_001354692.2:c.1456T= (RAF1)	NP_001341621.1:p.Ser486=
NM_001354693.2:c.1600T= (RAF1)	NP_001341622.1:p.Ser534=
NM_001354694.2:c.1516T= (RAF1)	NP_001341623.1:p.Ser506=
NM_001354695.2:c.1357T= (RAF1)	NP_001341624.1:p.Ser453=
NR_148940.2:n.2143T= (RAF1)
NR_148941.2:n.2089T= (RAF1)
NR_148942.2:n.2028T= (RAF1)
NM_001354690.3:c.1699T= (RAF1)	NP_001341619.1:p.Ser567=
NM_001354691.3:c.1456T= (RAF1)	NP_001341620.1:p.Ser486=
NM_001354692.3:c.1456T= (RAF1)	NP_001341621.1:p.Ser486=
NM_001354693.3:c.1600T= (RAF1)	NP_001341622.1:p.Ser534=
NM_001354694.3:c.1516T= (RAF1)	NP_001341623.1:p.Ser506=
NM_001354695.3:c.1357T= (RAF1)	NP_001341624.1:p.Ser453=
NM_002880.4:c.1699T= (RAF1) MANE Select	NP_002871.1:p.Ser567=
NR_148940.3:n.2143T= (RAF1)
NR_148941.3:n.2089T= (RAF1)
NR_148942.3:n.2028T= (RAF1)