Canonical Allele Identifier: CA1346226359

Gene: RAF1 MKRN2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584627A= , CM000665.2:g.12584627A=	GRCh38
NC_000003.11:g.12626126A= , CM000665.1:g.12626126A=	GRCh37
NC_000003.10:g.12601126A=	NCBI36
NG_007467.1:g.84553T= , LRG_413:g.84553T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000423275.6:c.*1499T= (RAF1)	ENSP00000401088.1:n.*1499T=
ENST00000432427.3:c.1151T= (RAF1)
ENST00000460610.2:n.6146T= (RAF1)
ENST00000471449.2:n.644T= (RAF1)
ENST00000475353.2:n.4114T= (RAF1)
ENST00000684903.1:c.*1511T= (RAF1)	ENSP00000508612.1:n.*1511T=
ENST00000685348.1:c.*1545T= (RAF1)	ENSP00000510285.1:n.*1545T=
ENST00000685437.1:c.1735T= (RAF1)	ENSP00000508794.1:p.Ser579=
ENST00000685653.1:c.1834T= (RAF1)	ENSP00000509968.1:p.Ser612=
ENST00000685697.1:n.2569T= (RAF1)
ENST00000685738.1:c.*798T= (RAF1)	ENSP00000510156.1:n.*798T=
ENST00000686409.1:n.5243T= (RAF1)
ENST00000686455.1:n.4555T= (RAF1)
ENST00000686762.1:c.*393T= (RAF1)	ENSP00000509767.1:n.*393T=
ENST00000687257.1:n.4288T= (RAF1)
ENST00000687326.1:c.*3126T= (RAF1)	ENSP00000509665.1:n.*3126T=
ENST00000687505.1:n.1952T= (RAF1)
ENST00000687923.1:c.1723T= (RAF1)	ENSP00000510255.1:p.Ser575=
ENST00000688269.1:n.2430T= (RAF1)
ENST00000688444.1:n.3951T= (RAF1)
ENST00000688543.1:c.1735T= (RAF1)	ENSP00000509612.1:p.Ser579=
ENST00000688625.1:c.*3203T= (RAF1)	ENSP00000509522.1:n.*3203T=
ENST00000688803.1:n.3262T= (RAF1)
ENST00000689097.1:c.*1511T= (RAF1)	ENSP00000509756.1:n.*1511T=
ENST00000689389.1:c.1657T= (RAF1)	ENSP00000510213.1:p.Ser553=
ENST00000689418.1:c.*3729T= (RAF1)	ENSP00000509467.1:n.*3729T=
ENST00000689540.1:n.4202T= (RAF1)
ENST00000689876.1:c.*383T= (RAF1)	ENSP00000508535.1:n.*383T=
ENST00000689914.1:c.*768T= (RAF1)	ENSP00000509847.1:n.*768T=
ENST00000690397.1:c.1723T= (RAF1)	ENSP00000508730.1:p.Ser575=
ENST00000690460.1:c.1822T= (RAF1)	ENSP00000509106.1:p.Ser608=
ENST00000690585.1:c.560T= (RAF1)
ENST00000690625.1:n.2870T= (RAF1)
ENST00000691396.1:c.*1706T= (RAF1)	ENSP00000510712.1:n.*1706T=
ENST00000691643.1:n.2887T= (RAF1)
ENST00000691724.1:c.*791T= (RAF1)	ENSP00000509255.1:n.*791T=
ENST00000691779.1:c.*1412T= (RAF1)	ENSP00000508592.1:n.*1412T=
ENST00000691888.1:c.708T= (RAF1)
ENST00000691899.1:c.1834T= (RAF1)	ENSP00000508763.1:p.Ser612=
ENST00000692069.1:n.4758T= (RAF1)
ENST00000692093.1:c.1735T= (RAF1)	ENSP00000509669.1:p.Ser579=
ENST00000692311.1:n.2658T= (RAF1)
ENST00000692558.1:n.4417T= (RAF1)
ENST00000692773.1:c.*1571T= (RAF1)	ENSP00000509055.1:n.*1571T=
ENST00000692830.1:c.*1579T= (RAF1)	ENSP00000509461.1:n.*1579T=
ENST00000693312.1:c.1609T= (RAF1)	ENSP00000508686.1:p.Ser537=
ENST00000693664.1:c.*285T= (RAF1)	ENSP00000509614.1:n.*285T=
ENST00000693705.1:c.*1213T= (RAF1)	ENSP00000510697.1:n.*1213T=
ENST00000251849.9:c.1834T= (RAF1) MANE Select	ENSP00000251849.4:p.Ser612=
ENST00000442415.7:c.1894T= (RAF1)	ENSP00000401888.2:p.Ser632=
ENST00000676541.1:c.*2374A= (MKRN2)	ENSP00000503730.1:n.*2374A=
ENST00000677142.1:c.*2374A= (MKRN2)	ENSP00000504455.1:n.*2374A=
ENST00000677816.1:c.*929A= (MKRN2)	ENSP00000502893.1:n.*929A=
ENST00000677941.1:n.2437A= (MKRN2)
ENST00000251849.8:c.1834T= (RAF1)	ENSP00000251849.4:p.Ser612=
ENST00000423275.5:c.*1511T= (RAF1)	ENSP00000401088.1:n.*1511T=
ENST00000432427.2:c.1471T= (RAF1)	ENSP00000398591.2:p.Ser491=
ENST00000442415.6:c.1894T= (RAF1)	ENSP00000401888.2:p.Ser632=
ENST00000471449.1:n.523T= (RAF1)
NM_002880.3:c.1834T= , LRG_413t1:c.1834T= (RAF1)	NP_002871.1:p.Ser612=
XM_005265355.1:c.1834T= (RAF1)	XP_005265412.1:p.Ser612=
XM_005265357.1:c.1735T= (RAF1)	XP_005265414.1:p.Ser579=
XM_005265358.3:c.1591T= (RAF1)	XP_005265415.1:p.Ser531=
XM_005265359.3:c.1492T= (RAF1)	XP_005265416.1:p.Ser498=
XM_011533974.1:c.1834T= (RAF1)	XP_011532276.1:p.Ser612=
XM_011533975.1:c.1591T= (RAF1)	XP_011532277.1:p.Ser531=
NM_001354689.1:c.1894T= (RAF1)	NP_001341618.1:p.Ser632=
NM_001354690.1:c.1834T= (RAF1)	NP_001341619.1:p.Ser612=
NM_001354691.1:c.1591T= (RAF1)	NP_001341620.1:p.Ser531=
NM_001354692.1:c.1591T= (RAF1)	NP_001341621.1:p.Ser531=
NM_001354693.1:c.1735T= (RAF1)	NP_001341622.1:p.Ser579=
NM_001354694.1:c.1651T= (RAF1)	NP_001341623.1:p.Ser551=
NM_001354695.1:c.1492T= (RAF1)	NP_001341624.1:p.Ser498=
NR_148940.1:n.2362T= (RAF1)
NR_148941.1:n.2308T= (RAF1)
NR_148942.1:n.2247T= (RAF1)
XM_011533974.3:c.1834T= (RAF1)	XP_011532276.1:p.Ser612=
XM_017006966.1:c.1735T= (RAF1)	XP_016862455.1:p.Ser579=
NM_001354689.3:c.1894T= (RAF1)	NP_001341618.1:p.Ser632=
NM_001354690.2:c.1834T= (RAF1)	NP_001341619.1:p.Ser612=
NM_001354691.2:c.1591T= (RAF1)	NP_001341620.1:p.Ser531=
NM_001354692.2:c.1591T= (RAF1)	NP_001341621.1:p.Ser531=
NM_001354693.2:c.1735T= (RAF1)	NP_001341622.1:p.Ser579=
NM_001354694.2:c.1651T= (RAF1)	NP_001341623.1:p.Ser551=
NM_001354695.2:c.1492T= (RAF1)	NP_001341624.1:p.Ser498=
NR_148940.2:n.2278T= (RAF1)
NR_148941.2:n.2224T= (RAF1)
NR_148942.2:n.2163T= (RAF1)
NM_001354690.3:c.1834T= (RAF1)	NP_001341619.1:p.Ser612=
NM_001354691.3:c.1591T= (RAF1)	NP_001341620.1:p.Ser531=
NM_001354692.3:c.1591T= (RAF1)	NP_001341621.1:p.Ser531=
NM_001354693.3:c.1735T= (RAF1)	NP_001341622.1:p.Ser579=
NM_001354694.3:c.1651T= (RAF1)	NP_001341623.1:p.Ser551=
NM_001354695.3:c.1492T= (RAF1)	NP_001341624.1:p.Ser498=
NM_002880.4:c.1834T= (RAF1) MANE Select	NP_002871.1:p.Ser612=
NR_148940.3:n.2278T= (RAF1)
NR_148941.3:n.2224T= (RAF1)
NR_148942.3:n.2163T= (RAF1)