Canonical Allele Identifier: CA351499170

Gene: RAF1 MKRN2

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12585764C>T , CM000665.2:g.12585764C>T	GRCh38
NC_000003.11:g.12627263C>T , CM000665.1:g.12627263C>T	GRCh37
NC_000003.10:g.12602263C>T	NCBI36
NG_007467.1:g.83416G>A , LRG_413:g.83416G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1118G>A (RAF1)	ENSP00000401088.1:n.*1118G>A
ENST00000432427.3:c.770G>A (RAF1)
ENST00000460610.2:n.5198G>A (RAF1)
ENST00000471449.2:n.263G>A (RAF1)
ENST00000475353.2:n.3166G>A (RAF1)
ENST00000684903.1:c.*1130G>A (RAF1)	ENSP00000508612.1:n.*1130G>A
ENST00000685348.1:c.*1095-358G>A (RAF1)	ENSP00000510285.1:n.*1095-358G>A
ENST00000685437.1:c.1354G>A (RAF1)	ENSP00000508794.1:p.Gly452Arg
ENST00000685653.1:c.1453G>A (RAF1)	ENSP00000509968.1:p.Gly485Arg
ENST00000685697.1:n.2188G>A (RAF1)
ENST00000685738.1:c.*417G>A (RAF1)	ENSP00000510156.1:n.*417G>A
ENST00000686409.1:n.4295G>A (RAF1)
ENST00000686455.1:n.3607G>A (RAF1)
ENST00000686762.1:c.*12G>A (RAF1)	ENSP00000509767.1:n.*12G>A
ENST00000687257.1:n.3480G>A (RAF1)
ENST00000687326.1:c.*2178G>A (RAF1)	ENSP00000509665.1:n.*2178G>A
ENST00000687505.1:n.1571G>A (RAF1)
ENST00000687923.1:c.1342G>A (RAF1)	ENSP00000510255.1:p.Gly448Arg
ENST00000688269.1:n.2049G>A (RAF1)
ENST00000688444.1:n.3570G>A (RAF1)
ENST00000688543.1:c.1354G>A (RAF1)	ENSP00000509612.1:p.Gly452Arg
ENST00000688625.1:c.*2822G>A (RAF1)	ENSP00000509522.1:n.*2822G>A
ENST00000688803.1:n.2965-511G>A (RAF1)
ENST00000688914.1:n.439G>A (RAF1)
ENST00000689097.1:c.*1130G>A (RAF1)	ENSP00000509756.1:n.*1130G>A
ENST00000689389.1:c.1276G>A (RAF1)	ENSP00000510213.1:p.Gly426Arg
ENST00000689418.1:c.*2921G>A (RAF1)	ENSP00000509467.1:n.*2921G>A
ENST00000689540.1:n.3394G>A (RAF1)
ENST00000689876.1:c.1418-358G>A (RAF1)	ENSP00000508535.1:n.1418-358G>A
ENST00000689914.1:c.*387G>A (RAF1)	ENSP00000509847.1:n.*387G>A
ENST00000690397.1:c.1342G>A (RAF1)	ENSP00000508730.1:p.Gly448Arg
ENST00000690460.1:c.1441G>A (RAF1)	ENSP00000509106.1:p.Gly481Arg
ENST00000690585.1:c.263-511G>A (RAF1)
ENST00000690625.1:n.2489G>A (RAF1)
ENST00000691396.1:c.*1325G>A (RAF1)	ENSP00000510712.1:n.*1325G>A
ENST00000691643.1:n.2079G>A (RAF1)
ENST00000691724.1:c.*410G>A (RAF1)	ENSP00000509255.1:n.*410G>A
ENST00000691779.1:c.*1031G>A (RAF1)	ENSP00000508592.1:n.*1031G>A
ENST00000691888.1:c.327G>A (RAF1)
ENST00000691899.1:c.1453G>A (RAF1)	ENSP00000508763.1:p.Gly485Arg
ENST00000692069.1:n.3810G>A (RAF1)
ENST00000692093.1:c.1354G>A (RAF1)	ENSP00000509669.1:p.Gly452Arg
ENST00000692311.1:n.2277G>A (RAF1)
ENST00000692558.1:n.3609G>A (RAF1)
ENST00000692773.1:c.*1190G>A (RAF1)	ENSP00000509055.1:n.*1190G>A
ENST00000692830.1:c.*1198G>A (RAF1)	ENSP00000509461.1:n.*1198G>A
ENST00000693312.1:c.1228G>A (RAF1)	ENSP00000508686.1:p.Gly410Arg
ENST00000693664.1:c.1488-511G>A (RAF1)	ENSP00000509614.1:n.1488-511G>A
ENST00000693705.1:c.*1048-783G>A (RAF1)	ENSP00000510697.1:n.*1048-783G>A
ENST00000251849.9:c.1453G>A (RAF1) MANE Select	ENSP00000251849.4:p.Gly485Arg
ENST00000442415.7:c.1513G>A (RAF1)	ENSP00000401888.2:p.Gly505Arg
ENST00000676541.1:c.*3511C>T (MKRN2)	ENSP00000503730.1:n.*3511C>T
ENST00000677142.1:c.*3511C>T (MKRN2)	ENSP00000504455.1:n.*3511C>T
ENST00000677816.1:c.*2066C>T (MKRN2)	ENSP00000502893.1:n.*2066C>T
ENST00000677941.1:n.3574C>T (MKRN2)
ENST00000251849.8:c.1453G>A (RAF1)	ENSP00000251849.4:p.Gly485Arg
ENST00000423275.5:c.*1130G>A (RAF1)	ENSP00000401088.1:n.*1130G>A
ENST00000432427.2:c.1090G>A (RAF1)	ENSP00000398591.2:p.Gly364Arg
ENST00000442415.6:c.1513G>A (RAF1)	ENSP00000401888.2:p.Gly505Arg
ENST00000471449.1:n.142G>A (RAF1)
NM_002880.3:c.1453G>A , LRG_413t1:c.1453G>A (RAF1)	NP_002871.1:p.Gly485Arg
XM_005265355.1:c.1453G>A (RAF1)	XP_005265412.1:p.Gly485Arg
XM_005265357.1:c.1354G>A (RAF1)	XP_005265414.1:p.Gly452Arg
XM_005265358.3:c.1210G>A (RAF1)	XP_005265415.1:p.Gly404Arg
XM_005265359.3:c.1111G>A (RAF1)	XP_005265416.1:p.Gly371Arg
XM_005265360.1:c.1418-358G>A (RAF1)	XP_005265417.1:n.1418-358G>A
XM_011533974.1:c.1453G>A (RAF1)	XP_011532276.1:p.Gly485Arg
XM_011533975.1:c.1210G>A (RAF1)	XP_011532277.1:p.Gly404Arg
NM_001354689.1:c.1513G>A (RAF1)	NP_001341618.1:p.Gly505Arg
NM_001354690.1:c.1453G>A (RAF1)	NP_001341619.1:p.Gly485Arg
NM_001354691.1:c.1210G>A (RAF1)	NP_001341620.1:p.Gly404Arg
NM_001354692.1:c.1210G>A (RAF1)	NP_001341621.1:p.Gly404Arg
NM_001354693.1:c.1354G>A (RAF1)	NP_001341622.1:p.Gly452Arg
NM_001354694.1:c.1270G>A (RAF1)	NP_001341623.1:p.Gly424Arg
NM_001354695.1:c.1111G>A (RAF1)	NP_001341624.1:p.Gly371Arg
NR_148940.1:n.1981G>A (RAF1)
NR_148941.1:n.1927G>A (RAF1)
NR_148942.1:n.1866G>A (RAF1)
XM_011533974.3:c.1453G>A (RAF1)	XP_011532276.1:p.Gly485Arg
XM_017006966.1:c.1354G>A (RAF1)	XP_016862455.1:p.Gly452Arg
NM_001354689.3:c.1513G>A (RAF1)	NP_001341618.1:p.Gly505Arg
NM_001354690.2:c.1453G>A (RAF1)	NP_001341619.1:p.Gly485Arg
NM_001354691.2:c.1210G>A (RAF1)	NP_001341620.1:p.Gly404Arg
NM_001354692.2:c.1210G>A (RAF1)	NP_001341621.1:p.Gly404Arg
NM_001354693.2:c.1354G>A (RAF1)	NP_001341622.1:p.Gly452Arg
NM_001354694.2:c.1270G>A (RAF1)	NP_001341623.1:p.Gly424Arg
NM_001354695.2:c.1111G>A (RAF1)	NP_001341624.1:p.Gly371Arg
NR_148940.2:n.1897G>A (RAF1)
NR_148941.2:n.1843G>A (RAF1)
NR_148942.2:n.1782G>A (RAF1)
NM_001354690.3:c.1453G>A (RAF1)	NP_001341619.1:p.Gly485Arg
NM_001354691.3:c.1210G>A (RAF1)	NP_001341620.1:p.Gly404Arg
NM_001354692.3:c.1210G>A (RAF1)	NP_001341621.1:p.Gly404Arg
NM_001354693.3:c.1354G>A (RAF1)	NP_001341622.1:p.Gly452Arg
NM_001354694.3:c.1270G>A (RAF1)	NP_001341623.1:p.Gly424Arg
NM_001354695.3:c.1111G>A (RAF1)	NP_001341624.1:p.Gly371Arg
NM_002880.4:c.1453G>A (RAF1) MANE Select	NP_002871.1:p.Gly485Arg
NR_148940.3:n.1897G>A (RAF1)
NR_148941.3:n.1843G>A (RAF1)
NR_148942.3:n.1782G>A (RAF1)