Canonical Allele Identifier: CA351496875

Gene: RAF1 MKRN2

Linked Data

• MyVariant Identifiers: chr3:g.12626443T>A (hg19) ; chr3:g.12584944T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584944T>A , CM000665.2:g.12584944T>A	GRCh38
NC_000003.11:g.12626443T>A , CM000665.1:g.12626443T>A	GRCh37
NC_000003.10:g.12601443T>A	NCBI36
NG_007467.1:g.84236A>T , LRG_413:g.84236A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1371A>T (RAF1)	ENSP00000401088.1:n.*1371A>T
ENST00000432427.3:c.1023A>T (RAF1)
ENST00000460610.2:n.6018A>T (RAF1)
ENST00000471449.2:n.516A>T (RAF1)
ENST00000475353.2:n.3986A>T (RAF1)
ENST00000684903.1:c.*1383A>T (RAF1)	ENSP00000508612.1:n.*1383A>T
ENST00000685348.1:c.*1417A>T (RAF1)	ENSP00000510285.1:n.*1417A>T
ENST00000685437.1:c.1607A>T (RAF1)	ENSP00000508794.1:p.Asp536Val
ENST00000685653.1:c.1706A>T (RAF1)	ENSP00000509968.1:p.Asp569Val
ENST00000685697.1:n.2441A>T (RAF1)
ENST00000685738.1:c.*670A>T (RAF1)	ENSP00000510156.1:n.*670A>T
ENST00000686409.1:n.5115A>T (RAF1)
ENST00000686455.1:n.4427A>T (RAF1)
ENST00000686762.1:c.*265A>T (RAF1)	ENSP00000509767.1:n.*265A>T
ENST00000687257.1:n.4160A>T (RAF1)
ENST00000687326.1:c.*2998A>T (RAF1)	ENSP00000509665.1:n.*2998A>T
ENST00000687505.1:n.1824A>T (RAF1)
ENST00000687923.1:c.1595A>T (RAF1)	ENSP00000510255.1:p.Asp532Val
ENST00000688269.1:n.2302A>T (RAF1)
ENST00000688444.1:n.3823A>T (RAF1)
ENST00000688543.1:c.1607A>T (RAF1)	ENSP00000509612.1:p.Asp536Val
ENST00000688625.1:c.*3075A>T (RAF1)	ENSP00000509522.1:n.*3075A>T
ENST00000688803.1:n.3134A>T (RAF1)
ENST00000688914.1:n.1119A>T (RAF1)
ENST00000689097.1:c.*1383A>T (RAF1)	ENSP00000509756.1:n.*1383A>T
ENST00000689389.1:c.1529A>T (RAF1)	ENSP00000510213.1:p.Asp510Val
ENST00000689418.1:c.*3601A>T (RAF1)	ENSP00000509467.1:n.*3601A>T
ENST00000689540.1:n.4074A>T (RAF1)
ENST00000689876.1:c.*255A>T (RAF1)	ENSP00000508535.1:n.*255A>T
ENST00000689914.1:c.*640A>T (RAF1)	ENSP00000509847.1:n.*640A>T
ENST00000690397.1:c.1595A>T (RAF1)	ENSP00000508730.1:p.Asp532Val
ENST00000690460.1:c.1694A>T (RAF1)	ENSP00000509106.1:p.Asp565Val
ENST00000690585.1:c.432A>T (RAF1)
ENST00000690625.1:n.2742A>T (RAF1)
ENST00000691396.1:c.*1578A>T (RAF1)	ENSP00000510712.1:n.*1578A>T
ENST00000691643.1:n.2759A>T (RAF1)
ENST00000691724.1:c.*663A>T (RAF1)	ENSP00000509255.1:n.*663A>T
ENST00000691779.1:c.*1284A>T (RAF1)	ENSP00000508592.1:n.*1284A>T
ENST00000691888.1:c.580A>T (RAF1)
ENST00000691899.1:c.1706A>T (RAF1)	ENSP00000508763.1:p.Asp569Val
ENST00000692069.1:n.4630A>T (RAF1)
ENST00000692093.1:c.1607A>T (RAF1)	ENSP00000509669.1:p.Asp536Val
ENST00000692311.1:n.2530A>T (RAF1)
ENST00000692558.1:n.4289A>T (RAF1)
ENST00000692773.1:c.*1443A>T (RAF1)	ENSP00000509055.1:n.*1443A>T
ENST00000692830.1:c.*1451A>T (RAF1)	ENSP00000509461.1:n.*1451A>T
ENST00000693312.1:c.1481A>T (RAF1)	ENSP00000508686.1:p.Asp494Val
ENST00000693664.1:c.*157A>T (RAF1)	ENSP00000509614.1:n.*157A>T
ENST00000693705.1:c.*1085A>T (RAF1)	ENSP00000510697.1:n.*1085A>T
ENST00000251849.9:c.1706A>T (RAF1) MANE Select	ENSP00000251849.4:p.Asp569Val
ENST00000442415.7:c.1766A>T (RAF1)	ENSP00000401888.2:p.Asp589Val
ENST00000676541.1:c.*2691T>A (MKRN2)	ENSP00000503730.1:n.*2691T>A
ENST00000677142.1:c.*2691T>A (MKRN2)	ENSP00000504455.1:n.*2691T>A
ENST00000677816.1:c.*1246T>A (MKRN2)	ENSP00000502893.1:n.*1246T>A
ENST00000677941.1:n.2754T>A (MKRN2)
ENST00000251849.8:c.1706A>T (RAF1)	ENSP00000251849.4:p.Asp569Val
ENST00000423275.5:c.*1383A>T (RAF1)	ENSP00000401088.1:n.*1383A>T
ENST00000432427.2:c.1343A>T (RAF1)	ENSP00000398591.2:p.Asp448Val
ENST00000442415.6:c.1766A>T (RAF1)	ENSP00000401888.2:p.Asp589Val
ENST00000471449.1:n.395A>T (RAF1)
NM_002880.3:c.1706A>T , LRG_413t1:c.1706A>T (RAF1)	NP_002871.1:p.Asp569Val
XM_005265355.1:c.1706A>T (RAF1)	XP_005265412.1:p.Asp569Val
XM_005265357.1:c.1607A>T (RAF1)	XP_005265414.1:p.Asp536Val
XM_005265358.3:c.1463A>T (RAF1)	XP_005265415.1:p.Asp488Val
XM_005265359.3:c.1364A>T (RAF1)	XP_005265416.1:p.Asp455Val
XM_011533974.1:c.1706A>T (RAF1)	XP_011532276.1:p.Asp569Val
XM_011533975.1:c.1463A>T (RAF1)	XP_011532277.1:p.Asp488Val
NM_001354689.1:c.1766A>T (RAF1)	NP_001341618.1:p.Asp589Val
NM_001354690.1:c.1706A>T (RAF1)	NP_001341619.1:p.Asp569Val
NM_001354691.1:c.1463A>T (RAF1)	NP_001341620.1:p.Asp488Val
NM_001354692.1:c.1463A>T (RAF1)	NP_001341621.1:p.Asp488Val
NM_001354693.1:c.1607A>T (RAF1)	NP_001341622.1:p.Asp536Val
NM_001354694.1:c.1523A>T (RAF1)	NP_001341623.1:p.Asp508Val
NM_001354695.1:c.1364A>T (RAF1)	NP_001341624.1:p.Asp455Val
NR_148940.1:n.2234A>T (RAF1)
NR_148941.1:n.2180A>T (RAF1)
NR_148942.1:n.2119A>T (RAF1)
XM_011533974.3:c.1706A>T (RAF1)	XP_011532276.1:p.Asp569Val
XM_017006966.1:c.1607A>T (RAF1)	XP_016862455.1:p.Asp536Val
NM_001354689.3:c.1766A>T (RAF1)	NP_001341618.1:p.Asp589Val
NM_001354690.2:c.1706A>T (RAF1)	NP_001341619.1:p.Asp569Val
NM_001354691.2:c.1463A>T (RAF1)	NP_001341620.1:p.Asp488Val
NM_001354692.2:c.1463A>T (RAF1)	NP_001341621.1:p.Asp488Val
NM_001354693.2:c.1607A>T (RAF1)	NP_001341622.1:p.Asp536Val
NM_001354694.2:c.1523A>T (RAF1)	NP_001341623.1:p.Asp508Val
NM_001354695.2:c.1364A>T (RAF1)	NP_001341624.1:p.Asp455Val
NR_148940.2:n.2150A>T (RAF1)
NR_148941.2:n.2096A>T (RAF1)
NR_148942.2:n.2035A>T (RAF1)
NM_001354690.3:c.1706A>T (RAF1)	NP_001341619.1:p.Asp569Val
NM_001354691.3:c.1463A>T (RAF1)	NP_001341620.1:p.Asp488Val
NM_001354692.3:c.1463A>T (RAF1)	NP_001341621.1:p.Asp488Val
NM_001354693.3:c.1607A>T (RAF1)	NP_001341622.1:p.Asp536Val
NM_001354694.3:c.1523A>T (RAF1)	NP_001341623.1:p.Asp508Val
NM_001354695.3:c.1364A>T (RAF1)	NP_001341624.1:p.Asp455Val
NM_002880.4:c.1706A>T (RAF1) MANE Select	NP_002871.1:p.Asp569Val
NR_148940.3:n.2150A>T (RAF1)
NR_148941.3:n.2096A>T (RAF1)
NR_148942.3:n.2035A>T (RAF1)