Canonical Allele Identifier: CA1346226423

Gene: RAF1 MKRN2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584653A= , CM000665.2:g.12584653A=	GRCh38
NC_000003.11:g.12626152A= , CM000665.1:g.12626152A=	GRCh37
NC_000003.10:g.12601152A=	NCBI36
NG_007467.1:g.84527T= , LRG_413:g.84527T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1473T= (RAF1)	ENSP00000401088.1:n.*1473T=
ENST00000432427.3:c.1125T= (RAF1)
ENST00000460610.2:n.6120T= (RAF1)
ENST00000471449.2:n.618T= (RAF1)
ENST00000475353.2:n.4088T= (RAF1)
ENST00000684903.1:c.*1485T= (RAF1)	ENSP00000508612.1:n.*1485T=
ENST00000685348.1:c.*1519T= (RAF1)	ENSP00000510285.1:n.*1519T=
ENST00000685437.1:c.1709T= (RAF1)	ENSP00000508794.1:p.Leu570=
ENST00000685653.1:c.1808T= (RAF1)	ENSP00000509968.1:p.Leu603=
ENST00000685697.1:n.2543T= (RAF1)
ENST00000685738.1:c.*772T= (RAF1)	ENSP00000510156.1:n.*772T=
ENST00000686409.1:n.5217T= (RAF1)
ENST00000686455.1:n.4529T= (RAF1)
ENST00000686762.1:c.*367T= (RAF1)	ENSP00000509767.1:n.*367T=
ENST00000687257.1:n.4262T= (RAF1)
ENST00000687326.1:c.*3100T= (RAF1)	ENSP00000509665.1:n.*3100T=
ENST00000687505.1:n.1926T= (RAF1)
ENST00000687923.1:c.1697T= (RAF1)	ENSP00000510255.1:p.Leu566=
ENST00000688269.1:n.2404T= (RAF1)
ENST00000688444.1:n.3925T= (RAF1)
ENST00000688543.1:c.1709T= (RAF1)	ENSP00000509612.1:p.Leu570=
ENST00000688625.1:c.*3177T= (RAF1)	ENSP00000509522.1:n.*3177T=
ENST00000688803.1:n.3236T= (RAF1)
ENST00000689097.1:c.*1485T= (RAF1)	ENSP00000509756.1:n.*1485T=
ENST00000689389.1:c.1631T= (RAF1)	ENSP00000510213.1:p.Leu544=
ENST00000689418.1:c.*3703T= (RAF1)	ENSP00000509467.1:n.*3703T=
ENST00000689540.1:n.4176T= (RAF1)
ENST00000689876.1:c.*357T= (RAF1)	ENSP00000508535.1:n.*357T=
ENST00000689914.1:c.*742T= (RAF1)	ENSP00000509847.1:n.*742T=
ENST00000690397.1:c.1697T= (RAF1)	ENSP00000508730.1:p.Leu566=
ENST00000690460.1:c.1796T= (RAF1)	ENSP00000509106.1:p.Leu599=
ENST00000690585.1:c.534T= (RAF1)
ENST00000690625.1:n.2844T= (RAF1)
ENST00000691396.1:c.*1680T= (RAF1)	ENSP00000510712.1:n.*1680T=
ENST00000691643.1:n.2861T= (RAF1)
ENST00000691724.1:c.*765T= (RAF1)	ENSP00000509255.1:n.*765T=
ENST00000691779.1:c.*1386T= (RAF1)	ENSP00000508592.1:n.*1386T=
ENST00000691888.1:c.682T= (RAF1)
ENST00000691899.1:c.1808T= (RAF1)	ENSP00000508763.1:p.Leu603=
ENST00000692069.1:n.4732T= (RAF1)
ENST00000692093.1:c.1709T= (RAF1)	ENSP00000509669.1:p.Leu570=
ENST00000692311.1:n.2632T= (RAF1)
ENST00000692558.1:n.4391T= (RAF1)
ENST00000692773.1:c.*1545T= (RAF1)	ENSP00000509055.1:n.*1545T=
ENST00000692830.1:c.*1553T= (RAF1)	ENSP00000509461.1:n.*1553T=
ENST00000693312.1:c.1583T= (RAF1)	ENSP00000508686.1:p.Leu528=
ENST00000693664.1:c.*259T= (RAF1)	ENSP00000509614.1:n.*259T=
ENST00000693705.1:c.*1187T= (RAF1)	ENSP00000510697.1:n.*1187T=
ENST00000251849.9:c.1808T= (RAF1) MANE Select	ENSP00000251849.4:p.Leu603=
ENST00000442415.7:c.1868T= (RAF1)	ENSP00000401888.2:p.Leu623=
ENST00000676541.1:c.*2400A= (MKRN2)	ENSP00000503730.1:n.*2400A=
ENST00000677142.1:c.*2400A= (MKRN2)	ENSP00000504455.1:n.*2400A=
ENST00000677816.1:c.*955A= (MKRN2)	ENSP00000502893.1:n.*955A=
ENST00000677941.1:n.2463A= (MKRN2)
ENST00000251849.8:c.1808T= (RAF1)	ENSP00000251849.4:p.Leu603=
ENST00000423275.5:c.*1485T= (RAF1)	ENSP00000401088.1:n.*1485T=
ENST00000432427.2:c.1445T= (RAF1)	ENSP00000398591.2:p.Leu482=
ENST00000442415.6:c.1868T= (RAF1)	ENSP00000401888.2:p.Leu623=
ENST00000471449.1:n.497T= (RAF1)
NM_002880.3:c.1808T= , LRG_413t1:c.1808T= (RAF1)	NP_002871.1:p.Leu603=
XM_005265355.1:c.1808T= (RAF1)	XP_005265412.1:p.Leu603=
XM_005265357.1:c.1709T= (RAF1)	XP_005265414.1:p.Leu570=
XM_005265358.3:c.1565T= (RAF1)	XP_005265415.1:p.Leu522=
XM_005265359.3:c.1466T= (RAF1)	XP_005265416.1:p.Leu489=
XM_011533974.1:c.1808T= (RAF1)	XP_011532276.1:p.Leu603=
XM_011533975.1:c.1565T= (RAF1)	XP_011532277.1:p.Leu522=
NM_001354689.1:c.1868T= (RAF1)	NP_001341618.1:p.Leu623=
NM_001354690.1:c.1808T= (RAF1)	NP_001341619.1:p.Leu603=
NM_001354691.1:c.1565T= (RAF1)	NP_001341620.1:p.Leu522=
NM_001354692.1:c.1565T= (RAF1)	NP_001341621.1:p.Leu522=
NM_001354693.1:c.1709T= (RAF1)	NP_001341622.1:p.Leu570=
NM_001354694.1:c.1625T= (RAF1)	NP_001341623.1:p.Leu542=
NM_001354695.1:c.1466T= (RAF1)	NP_001341624.1:p.Leu489=
NR_148940.1:n.2336T= (RAF1)
NR_148941.1:n.2282T= (RAF1)
NR_148942.1:n.2221T= (RAF1)
XM_011533974.3:c.1808T= (RAF1)	XP_011532276.1:p.Leu603=
XM_017006966.1:c.1709T= (RAF1)	XP_016862455.1:p.Leu570=
NM_001354689.3:c.1868T= (RAF1)	NP_001341618.1:p.Leu623=
NM_001354690.2:c.1808T= (RAF1)	NP_001341619.1:p.Leu603=
NM_001354691.2:c.1565T= (RAF1)	NP_001341620.1:p.Leu522=
NM_001354692.2:c.1565T= (RAF1)	NP_001341621.1:p.Leu522=
NM_001354693.2:c.1709T= (RAF1)	NP_001341622.1:p.Leu570=
NM_001354694.2:c.1625T= (RAF1)	NP_001341623.1:p.Leu542=
NM_001354695.2:c.1466T= (RAF1)	NP_001341624.1:p.Leu489=
NR_148940.2:n.2252T= (RAF1)
NR_148941.2:n.2198T= (RAF1)
NR_148942.2:n.2137T= (RAF1)
NM_001354690.3:c.1808T= (RAF1)	NP_001341619.1:p.Leu603=
NM_001354691.3:c.1565T= (RAF1)	NP_001341620.1:p.Leu522=
NM_001354692.3:c.1565T= (RAF1)	NP_001341621.1:p.Leu522=
NM_001354693.3:c.1709T= (RAF1)	NP_001341622.1:p.Leu570=
NM_001354694.3:c.1625T= (RAF1)	NP_001341623.1:p.Leu542=
NM_001354695.3:c.1466T= (RAF1)	NP_001341624.1:p.Leu489=
NM_002880.4:c.1808T= (RAF1) MANE Select	NP_002871.1:p.Leu603=
NR_148940.3:n.2252T= (RAF1)
NR_148941.3:n.2198T= (RAF1)
NR_148942.3:n.2137T= (RAF1)