Canonical Allele Identifier: CA351496878

Gene: RAF1 MKRN2

Linked Data

• dbSNP Id: rs2125319843
• MyVariant Identifiers: chr3:g.12626444C>T (hg19) ; chr3:g.12584945C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584945C>T , CM000665.2:g.12584945C>T	GRCh38
NC_000003.11:g.12626444C>T , CM000665.1:g.12626444C>T	GRCh37
NC_000003.10:g.12601444C>T	NCBI36
NG_007467.1:g.84235G>A , LRG_413:g.84235G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1370G>A (RAF1)	ENSP00000401088.1:n.*1370G>A
ENST00000432427.3:c.1022G>A (RAF1)
ENST00000460610.2:n.6017G>A (RAF1)
ENST00000471449.2:n.515G>A (RAF1)
ENST00000475353.2:n.3985G>A (RAF1)
ENST00000684903.1:c.*1382G>A (RAF1)	ENSP00000508612.1:n.*1382G>A
ENST00000685348.1:c.*1416G>A (RAF1)	ENSP00000510285.1:n.*1416G>A
ENST00000685437.1:c.1606G>A (RAF1)	ENSP00000508794.1:p.Asp536Asn
ENST00000685653.1:c.1705G>A (RAF1)	ENSP00000509968.1:p.Asp569Asn
ENST00000685697.1:n.2440G>A (RAF1)
ENST00000685738.1:c.*669G>A (RAF1)	ENSP00000510156.1:n.*669G>A
ENST00000686409.1:n.5114G>A (RAF1)
ENST00000686455.1:n.4426G>A (RAF1)
ENST00000686762.1:c.*264G>A (RAF1)	ENSP00000509767.1:n.*264G>A
ENST00000687257.1:n.4159G>A (RAF1)
ENST00000687326.1:c.*2997G>A (RAF1)	ENSP00000509665.1:n.*2997G>A
ENST00000687505.1:n.1823G>A (RAF1)
ENST00000687923.1:c.1594G>A (RAF1)	ENSP00000510255.1:p.Asp532Asn
ENST00000688269.1:n.2301G>A (RAF1)
ENST00000688444.1:n.3822G>A (RAF1)
ENST00000688543.1:c.1606G>A (RAF1)	ENSP00000509612.1:p.Asp536Asn
ENST00000688625.1:c.*3074G>A (RAF1)	ENSP00000509522.1:n.*3074G>A
ENST00000688803.1:n.3133G>A (RAF1)
ENST00000688914.1:n.1118G>A (RAF1)
ENST00000689097.1:c.*1382G>A (RAF1)	ENSP00000509756.1:n.*1382G>A
ENST00000689389.1:c.1528G>A (RAF1)	ENSP00000510213.1:p.Asp510Asn
ENST00000689418.1:c.*3600G>A (RAF1)	ENSP00000509467.1:n.*3600G>A
ENST00000689540.1:n.4073G>A (RAF1)
ENST00000689876.1:c.*254G>A (RAF1)	ENSP00000508535.1:n.*254G>A
ENST00000689914.1:c.*639G>A (RAF1)	ENSP00000509847.1:n.*639G>A
ENST00000690397.1:c.1594G>A (RAF1)	ENSP00000508730.1:p.Asp532Asn
ENST00000690460.1:c.1693G>A (RAF1)	ENSP00000509106.1:p.Asp565Asn
ENST00000690585.1:c.431G>A (RAF1)
ENST00000690625.1:n.2741G>A (RAF1)
ENST00000691396.1:c.*1577G>A (RAF1)	ENSP00000510712.1:n.*1577G>A
ENST00000691643.1:n.2758G>A (RAF1)
ENST00000691724.1:c.*662G>A (RAF1)	ENSP00000509255.1:n.*662G>A
ENST00000691779.1:c.*1283G>A (RAF1)	ENSP00000508592.1:n.*1283G>A
ENST00000691888.1:c.579G>A (RAF1)
ENST00000691899.1:c.1705G>A (RAF1)	ENSP00000508763.1:p.Asp569Asn
ENST00000692069.1:n.4629G>A (RAF1)
ENST00000692093.1:c.1606G>A (RAF1)	ENSP00000509669.1:p.Asp536Asn
ENST00000692311.1:n.2529G>A (RAF1)
ENST00000692558.1:n.4288G>A (RAF1)
ENST00000692773.1:c.*1442G>A (RAF1)	ENSP00000509055.1:n.*1442G>A
ENST00000692830.1:c.*1450G>A (RAF1)	ENSP00000509461.1:n.*1450G>A
ENST00000693312.1:c.1480G>A (RAF1)	ENSP00000508686.1:p.Asp494Asn
ENST00000693664.1:c.*156G>A (RAF1)	ENSP00000509614.1:n.*156G>A
ENST00000693705.1:c.*1084G>A (RAF1)	ENSP00000510697.1:n.*1084G>A
ENST00000251849.9:c.1705G>A (RAF1) MANE Select	ENSP00000251849.4:p.Asp569Asn
ENST00000442415.7:c.1765G>A (RAF1)	ENSP00000401888.2:p.Asp589Asn
ENST00000676541.1:c.*2692C>T (MKRN2)	ENSP00000503730.1:n.*2692C>T
ENST00000677142.1:c.*2692C>T (MKRN2)	ENSP00000504455.1:n.*2692C>T
ENST00000677816.1:c.*1247C>T (MKRN2)	ENSP00000502893.1:n.*1247C>T
ENST00000677941.1:n.2755C>T (MKRN2)
ENST00000251849.8:c.1705G>A (RAF1)	ENSP00000251849.4:p.Asp569Asn
ENST00000423275.5:c.*1382G>A (RAF1)	ENSP00000401088.1:n.*1382G>A
ENST00000432427.2:c.1342G>A (RAF1)	ENSP00000398591.2:p.Asp448Asn
ENST00000442415.6:c.1765G>A (RAF1)	ENSP00000401888.2:p.Asp589Asn
ENST00000471449.1:n.394G>A (RAF1)
NM_002880.3:c.1705G>A , LRG_413t1:c.1705G>A (RAF1)	NP_002871.1:p.Asp569Asn
XM_005265355.1:c.1705G>A (RAF1)	XP_005265412.1:p.Asp569Asn
XM_005265357.1:c.1606G>A (RAF1)	XP_005265414.1:p.Asp536Asn
XM_005265358.3:c.1462G>A (RAF1)	XP_005265415.1:p.Asp488Asn
XM_005265359.3:c.1363G>A (RAF1)	XP_005265416.1:p.Asp455Asn
XM_011533974.1:c.1705G>A (RAF1)	XP_011532276.1:p.Asp569Asn
XM_011533975.1:c.1462G>A (RAF1)	XP_011532277.1:p.Asp488Asn
NM_001354689.1:c.1765G>A (RAF1)	NP_001341618.1:p.Asp589Asn
NM_001354690.1:c.1705G>A (RAF1)	NP_001341619.1:p.Asp569Asn
NM_001354691.1:c.1462G>A (RAF1)	NP_001341620.1:p.Asp488Asn
NM_001354692.1:c.1462G>A (RAF1)	NP_001341621.1:p.Asp488Asn
NM_001354693.1:c.1606G>A (RAF1)	NP_001341622.1:p.Asp536Asn
NM_001354694.1:c.1522G>A (RAF1)	NP_001341623.1:p.Asp508Asn
NM_001354695.1:c.1363G>A (RAF1)	NP_001341624.1:p.Asp455Asn
NR_148940.1:n.2233G>A (RAF1)
NR_148941.1:n.2179G>A (RAF1)
NR_148942.1:n.2118G>A (RAF1)
XM_011533974.3:c.1705G>A (RAF1)	XP_011532276.1:p.Asp569Asn
XM_017006966.1:c.1606G>A (RAF1)	XP_016862455.1:p.Asp536Asn
NM_001354689.3:c.1765G>A (RAF1)	NP_001341618.1:p.Asp589Asn
NM_001354690.2:c.1705G>A (RAF1)	NP_001341619.1:p.Asp569Asn
NM_001354691.2:c.1462G>A (RAF1)	NP_001341620.1:p.Asp488Asn
NM_001354692.2:c.1462G>A (RAF1)	NP_001341621.1:p.Asp488Asn
NM_001354693.2:c.1606G>A (RAF1)	NP_001341622.1:p.Asp536Asn
NM_001354694.2:c.1522G>A (RAF1)	NP_001341623.1:p.Asp508Asn
NM_001354695.2:c.1363G>A (RAF1)	NP_001341624.1:p.Asp455Asn
NR_148940.2:n.2149G>A (RAF1)
NR_148941.2:n.2095G>A (RAF1)
NR_148942.2:n.2034G>A (RAF1)
NM_001354690.3:c.1705G>A (RAF1)	NP_001341619.1:p.Asp569Asn
NM_001354691.3:c.1462G>A (RAF1)	NP_001341620.1:p.Asp488Asn
NM_001354692.3:c.1462G>A (RAF1)	NP_001341621.1:p.Asp488Asn
NM_001354693.3:c.1606G>A (RAF1)	NP_001341622.1:p.Asp536Asn
NM_001354694.3:c.1522G>A (RAF1)	NP_001341623.1:p.Asp508Asn
NM_001354695.3:c.1363G>A (RAF1)	NP_001341624.1:p.Asp455Asn
NM_002880.4:c.1705G>A (RAF1) MANE Select	NP_002871.1:p.Asp569Asn
NR_148940.3:n.2149G>A (RAF1)
NR_148941.3:n.2095G>A (RAF1)
NR_148942.3:n.2034G>A (RAF1)