Canonical Allele Identifier: CA2702178730

Gene: RAF1 MKRN2

Linked Data

• dbSNP Id: rs2125314911

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584435C>A , CM000665.2:g.12584435C>A	GRCh38
NC_000003.11:g.12625934C>A , CM000665.1:g.12625934C>A	GRCh37
NC_000003.10:g.12600934C>A	NCBI36
NG_007467.1:g.84745G>T , LRG_413:g.84745G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000423275.6:c.*1691G>T (RAF1)	ENSP00000401088.1:n.*1691G>T
ENST00000432427.3:c.1343G>T (RAF1)
ENST00000460610.2:n.6338G>T (RAF1)
ENST00000471449.2:n.836G>T (RAF1)
ENST00000475353.2:n.4306G>T (RAF1)
ENST00000684903.1:c.*1703G>T (RAF1)	ENSP00000508612.1:n.*1703G>T
ENST00000685348.1:c.*1737G>T (RAF1)	ENSP00000510285.1:n.*1737G>T
ENST00000685437.1:c.*79G>T (RAF1)	ENSP00000508794.1:n.*79G>T
ENST00000685653.1:c.*79G>T (RAF1)	ENSP00000509968.1:n.*79G>T
ENST00000685697.1:n.2761G>T (RAF1)
ENST00000685738.1:c.*990G>T (RAF1)	ENSP00000510156.1:n.*990G>T
ENST00000686409.1:n.5435G>T (RAF1)
ENST00000686455.1:n.4747G>T (RAF1)
ENST00000686762.1:c.*585G>T (RAF1)	ENSP00000509767.1:n.*585G>T
ENST00000687257.1:n.4480G>T (RAF1)
ENST00000687326.1:c.*3318G>T (RAF1)	ENSP00000509665.1:n.*3318G>T
ENST00000687505.1:n.2144G>T (RAF1)
ENST00000687923.1:c.*79G>T (RAF1)	ENSP00000510255.1:n.*79G>T
ENST00000688269.1:n.2622G>T (RAF1)
ENST00000688444.1:n.4143G>T (RAF1)
ENST00000688543.1:c.*79G>T (RAF1)	ENSP00000509612.1:n.*79G>T
ENST00000688625.1:c.*3395G>T (RAF1)	ENSP00000509522.1:n.*3395G>T
ENST00000688803.1:n.3454G>T (RAF1)
ENST00000689097.1:c.*1703G>T (RAF1)	ENSP00000509756.1:n.*1703G>T
ENST00000689389.1:c.*79G>T (RAF1)	ENSP00000510213.1:n.*79G>T
ENST00000689418.1:c.*3921G>T (RAF1)	ENSP00000509467.1:n.*3921G>T
ENST00000689540.1:n.4394G>T (RAF1)
ENST00000689876.1:c.*575G>T (RAF1)	ENSP00000508535.1:n.*575G>T
ENST00000689914.1:c.*960G>T (RAF1)	ENSP00000509847.1:n.*960G>T
ENST00000690397.1:c.*79G>T (RAF1)	ENSP00000508730.1:n.*79G>T
ENST00000690460.1:c.*79G>T (RAF1)	ENSP00000509106.1:n.*79G>T
ENST00000690585.1:c.752G>T (RAF1)
ENST00000690625.1:n.3062G>T (RAF1)
ENST00000691396.1:c.*1898G>T (RAF1)	ENSP00000510712.1:n.*1898G>T
ENST00000691643.1:n.3079G>T (RAF1)
ENST00000691724.1:c.*983G>T (RAF1)	ENSP00000509255.1:n.*983G>T
ENST00000691779.1:c.*1604G>T (RAF1)	ENSP00000508592.1:n.*1604G>T
ENST00000691888.1:c.900G>T (RAF1)
ENST00000691899.1:c.*79G>T (RAF1)	ENSP00000508763.1:n.*79G>T
ENST00000692069.1:n.4950G>T (RAF1)
ENST00000692093.1:c.*79G>T (RAF1)	ENSP00000509669.1:n.*79G>T
ENST00000692311.1:n.2850G>T (RAF1)
ENST00000692558.1:n.4609G>T (RAF1)
ENST00000692773.1:c.*1763G>T (RAF1)	ENSP00000509055.1:n.*1763G>T
ENST00000692830.1:c.*1771G>T (RAF1)	ENSP00000509461.1:n.*1771G>T
ENST00000693312.1:c.*79G>T (RAF1)	ENSP00000508686.1:n.*79G>T
ENST00000693664.1:c.*477G>T (RAF1)	ENSP00000509614.1:n.*477G>T
ENST00000693705.1:c.*1405G>T (RAF1)	ENSP00000510697.1:n.*1405G>T
ENST00000251849.9:c.*79G>T (RAF1) MANE Select	ENSP00000251849.4:n.*79G>T
ENST00000442415.7:c.*79G>T (RAF1)	ENSP00000401888.2:n.*79G>T
ENST00000676541.1:c.*2182C>A (MKRN2)	ENSP00000503730.1:n.*2182C>A
ENST00000677142.1:c.*2182C>A (MKRN2)	ENSP00000504455.1:n.*2182C>A
ENST00000677816.1:c.*737C>A (MKRN2)	ENSP00000502893.1:n.*737C>A
ENST00000677941.1:n.2245C>A (MKRN2)
ENST00000251849.8:c.*79G>T (RAF1)	ENSP00000251849.4:n.*79G>T
ENST00000423275.5:c.*1703G>T (RAF1)	ENSP00000401088.1:n.*1703G>T
ENST00000432427.2:c.1663G>T (RAF1)	ENSP00000398591.2:n.1663G>T
ENST00000442415.6:c.*79G>T (RAF1)	ENSP00000401888.2:n.*79G>T
ENST00000471449.1:n.715G>T (RAF1)
NM_002880.3:c.*79G>T , LRG_413t1:c.*79G>T (RAF1)	NP_002871.1:n.*79G>T
XM_005265355.1:c.*79G>T (RAF1)	XP_005265412.1:n.*79G>T
XM_005265357.1:c.*79G>T (RAF1)	XP_005265414.1:n.*79G>T
XM_005265358.3:c.*79G>T (RAF1)	XP_005265415.1:n.*79G>T
XM_005265359.3:c.*79G>T (RAF1)	XP_005265416.1:n.*79G>T
XM_011533974.1:c.*79G>T (RAF1)	XP_011532276.1:n.*79G>T
XM_011533975.1:c.*79G>T (RAF1)	XP_011532277.1:n.*79G>T
NM_001354689.1:c.*79G>T (RAF1)	NP_001341618.1:n.*79G>T
NM_001354690.1:c.*79G>T (RAF1)	NP_001341619.1:n.*79G>T
NM_001354691.1:c.*79G>T (RAF1)	NP_001341620.1:n.*79G>T
NM_001354692.1:c.*79G>T (RAF1)	NP_001341621.1:n.*79G>T
NM_001354693.1:c.*79G>T (RAF1)	NP_001341622.1:n.*79G>T
NM_001354694.1:c.*79G>T (RAF1)	NP_001341623.1:n.*79G>T
NM_001354695.1:c.*79G>T (RAF1)	NP_001341624.1:n.*79G>T
NR_148940.1:n.2554G>T (RAF1)
NR_148941.1:n.2500G>T (RAF1)
NR_148942.1:n.2439G>T (RAF1)
XM_011533974.3:c.*79G>T (RAF1)	XP_011532276.1:n.*79G>T
XM_017006966.1:c.*79G>T (RAF1)	XP_016862455.1:n.*79G>T
NM_001354689.3:c.*79G>T (RAF1)	NP_001341618.1:n.*79G>T
NM_001354690.2:c.*79G>T (RAF1)	NP_001341619.1:n.*79G>T
NM_001354691.2:c.*79G>T (RAF1)	NP_001341620.1:n.*79G>T
NM_001354692.2:c.*79G>T (RAF1)	NP_001341621.1:n.*79G>T
NM_001354693.2:c.*79G>T (RAF1)	NP_001341622.1:n.*79G>T
NM_001354694.2:c.*79G>T (RAF1)	NP_001341623.1:n.*79G>T
NM_001354695.2:c.*79G>T (RAF1)	NP_001341624.1:n.*79G>T
NR_148940.2:n.2470G>T (RAF1)
NR_148941.2:n.2416G>T (RAF1)
NR_148942.2:n.2355G>T (RAF1)
NM_001354690.3:c.*79G>T (RAF1)	NP_001341619.1:n.*79G>T
NM_001354691.3:c.*79G>T (RAF1)	NP_001341620.1:n.*79G>T
NM_001354692.3:c.*79G>T (RAF1)	NP_001341621.1:n.*79G>T
NM_001354693.3:c.*79G>T (RAF1)	NP_001341622.1:n.*79G>T
NM_001354694.3:c.*79G>T (RAF1)	NP_001341623.1:n.*79G>T
NM_001354695.3:c.*79G>T (RAF1)	NP_001341624.1:n.*79G>T
NM_002880.4:c.*79G>T (RAF1) MANE Select	NP_002871.1:n.*79G>T
NR_148940.3:n.2470G>T (RAF1)
NR_148941.3:n.2416G>T (RAF1)
NR_148942.3:n.2355G>T (RAF1)