Canonical Allele Identifier: CA351496114

Gene: RAF1 MKRN2

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584629T>G , CM000665.2:g.12584629T>G	GRCh38
NC_000003.11:g.12626128T>G , CM000665.1:g.12626128T>G	GRCh37
NC_000003.10:g.12601128T>G	NCBI36
NG_007467.1:g.84551A>C , LRG_413:g.84551A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1497A>C (RAF1)	ENSP00000401088.1:n.*1497A>C
ENST00000432427.3:c.1149A>C (RAF1)
ENST00000460610.2:n.6144A>C (RAF1)
ENST00000471449.2:n.642A>C (RAF1)
ENST00000475353.2:n.4112A>C (RAF1)
ENST00000684903.1:c.*1509A>C (RAF1)	ENSP00000508612.1:n.*1509A>C
ENST00000685348.1:c.*1543A>C (RAF1)	ENSP00000510285.1:n.*1543A>C
ENST00000685437.1:c.1733A>C (RAF1)	ENSP00000508794.1:p.His578Pro
ENST00000685653.1:c.1832A>C (RAF1)	ENSP00000509968.1:p.His611Pro
ENST00000685697.1:n.2567A>C (RAF1)
ENST00000685738.1:c.*796A>C (RAF1)	ENSP00000510156.1:n.*796A>C
ENST00000686409.1:n.5241A>C (RAF1)
ENST00000686455.1:n.4553A>C (RAF1)
ENST00000686762.1:c.*391A>C (RAF1)	ENSP00000509767.1:n.*391A>C
ENST00000687257.1:n.4286A>C (RAF1)
ENST00000687326.1:c.*3124A>C (RAF1)	ENSP00000509665.1:n.*3124A>C
ENST00000687505.1:n.1950A>C (RAF1)
ENST00000687923.1:c.1721A>C (RAF1)	ENSP00000510255.1:p.His574Pro
ENST00000688269.1:n.2428A>C (RAF1)
ENST00000688444.1:n.3949A>C (RAF1)
ENST00000688543.1:c.1733A>C (RAF1)	ENSP00000509612.1:p.His578Pro
ENST00000688625.1:c.*3201A>C (RAF1)	ENSP00000509522.1:n.*3201A>C
ENST00000688803.1:n.3260A>C (RAF1)
ENST00000689097.1:c.*1509A>C (RAF1)	ENSP00000509756.1:n.*1509A>C
ENST00000689389.1:c.1655A>C (RAF1)	ENSP00000510213.1:p.His552Pro
ENST00000689418.1:c.*3727A>C (RAF1)	ENSP00000509467.1:n.*3727A>C
ENST00000689540.1:n.4200A>C (RAF1)
ENST00000689876.1:c.*381A>C (RAF1)	ENSP00000508535.1:n.*381A>C
ENST00000689914.1:c.*766A>C (RAF1)	ENSP00000509847.1:n.*766A>C
ENST00000690397.1:c.1721A>C (RAF1)	ENSP00000508730.1:p.His574Pro
ENST00000690460.1:c.1820A>C (RAF1)	ENSP00000509106.1:p.His607Pro
ENST00000690585.1:c.558A>C (RAF1)
ENST00000690625.1:n.2868A>C (RAF1)
ENST00000691396.1:c.*1704A>C (RAF1)	ENSP00000510712.1:n.*1704A>C
ENST00000691643.1:n.2885A>C (RAF1)
ENST00000691724.1:c.*789A>C (RAF1)	ENSP00000509255.1:n.*789A>C
ENST00000691779.1:c.*1410A>C (RAF1)	ENSP00000508592.1:n.*1410A>C
ENST00000691888.1:c.706A>C (RAF1)
ENST00000691899.1:c.1832A>C (RAF1)	ENSP00000508763.1:p.His611Pro
ENST00000692069.1:n.4756A>C (RAF1)
ENST00000692093.1:c.1733A>C (RAF1)	ENSP00000509669.1:p.His578Pro
ENST00000692311.1:n.2656A>C (RAF1)
ENST00000692558.1:n.4415A>C (RAF1)
ENST00000692773.1:c.*1569A>C (RAF1)	ENSP00000509055.1:n.*1569A>C
ENST00000692830.1:c.*1577A>C (RAF1)	ENSP00000509461.1:n.*1577A>C
ENST00000693312.1:c.1607A>C (RAF1)	ENSP00000508686.1:p.His536Pro
ENST00000693664.1:c.*283A>C (RAF1)	ENSP00000509614.1:n.*283A>C
ENST00000693705.1:c.*1211A>C (RAF1)	ENSP00000510697.1:n.*1211A>C
ENST00000251849.9:c.1832A>C (RAF1) MANE Select	ENSP00000251849.4:p.His611Pro
ENST00000442415.7:c.1892A>C (RAF1)	ENSP00000401888.2:p.His631Pro
ENST00000676541.1:c.*2376T>G (MKRN2)	ENSP00000503730.1:n.*2376T>G
ENST00000677142.1:c.*2376T>G (MKRN2)	ENSP00000504455.1:n.*2376T>G
ENST00000677816.1:c.*931T>G (MKRN2)	ENSP00000502893.1:n.*931T>G
ENST00000677941.1:n.2439T>G (MKRN2)
ENST00000251849.8:c.1832A>C (RAF1)	ENSP00000251849.4:p.His611Pro
ENST00000423275.5:c.*1509A>C (RAF1)	ENSP00000401088.1:n.*1509A>C
ENST00000432427.2:c.1469A>C (RAF1)	ENSP00000398591.2:p.His490Pro
ENST00000442415.6:c.1892A>C (RAF1)	ENSP00000401888.2:p.His631Pro
ENST00000471449.1:n.521A>C (RAF1)
NM_002880.3:c.1832A>C , LRG_413t1:c.1832A>C (RAF1)	NP_002871.1:p.His611Pro
XM_005265355.1:c.1832A>C (RAF1)	XP_005265412.1:p.His611Pro
XM_005265357.1:c.1733A>C (RAF1)	XP_005265414.1:p.His578Pro
XM_005265358.3:c.1589A>C (RAF1)	XP_005265415.1:p.His530Pro
XM_005265359.3:c.1490A>C (RAF1)	XP_005265416.1:p.His497Pro
XM_011533974.1:c.1832A>C (RAF1)	XP_011532276.1:p.His611Pro
XM_011533975.1:c.1589A>C (RAF1)	XP_011532277.1:p.His530Pro
NM_001354689.1:c.1892A>C (RAF1)	NP_001341618.1:p.His631Pro
NM_001354690.1:c.1832A>C (RAF1)	NP_001341619.1:p.His611Pro
NM_001354691.1:c.1589A>C (RAF1)	NP_001341620.1:p.His530Pro
NM_001354692.1:c.1589A>C (RAF1)	NP_001341621.1:p.His530Pro
NM_001354693.1:c.1733A>C (RAF1)	NP_001341622.1:p.His578Pro
NM_001354694.1:c.1649A>C (RAF1)	NP_001341623.1:p.His550Pro
NM_001354695.1:c.1490A>C (RAF1)	NP_001341624.1:p.His497Pro
NR_148940.1:n.2360A>C (RAF1)
NR_148941.1:n.2306A>C (RAF1)
NR_148942.1:n.2245A>C (RAF1)
XM_011533974.3:c.1832A>C (RAF1)	XP_011532276.1:p.His611Pro
XM_017006966.1:c.1733A>C (RAF1)	XP_016862455.1:p.His578Pro
NM_001354689.3:c.1892A>C (RAF1)	NP_001341618.1:p.His631Pro
NM_001354690.2:c.1832A>C (RAF1)	NP_001341619.1:p.His611Pro
NM_001354691.2:c.1589A>C (RAF1)	NP_001341620.1:p.His530Pro
NM_001354692.2:c.1589A>C (RAF1)	NP_001341621.1:p.His530Pro
NM_001354693.2:c.1733A>C (RAF1)	NP_001341622.1:p.His578Pro
NM_001354694.2:c.1649A>C (RAF1)	NP_001341623.1:p.His550Pro
NM_001354695.2:c.1490A>C (RAF1)	NP_001341624.1:p.His497Pro
NR_148940.2:n.2276A>C (RAF1)
NR_148941.2:n.2222A>C (RAF1)
NR_148942.2:n.2161A>C (RAF1)
NM_001354690.3:c.1832A>C (RAF1)	NP_001341619.1:p.His611Pro
NM_001354691.3:c.1589A>C (RAF1)	NP_001341620.1:p.His530Pro
NM_001354692.3:c.1589A>C (RAF1)	NP_001341621.1:p.His530Pro
NM_001354693.3:c.1733A>C (RAF1)	NP_001341622.1:p.His578Pro
NM_001354694.3:c.1649A>C (RAF1)	NP_001341623.1:p.His550Pro
NM_001354695.3:c.1490A>C (RAF1)	NP_001341624.1:p.His497Pro
NM_002880.4:c.1832A>C (RAF1) MANE Select	NP_002871.1:p.His611Pro
NR_148940.3:n.2276A>C (RAF1)
NR_148941.3:n.2222A>C (RAF1)
NR_148942.3:n.2161A>C (RAF1)