Canonical Allele Identifier: CA2586965630

Gene: RAF1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12590929dup , CM000665.2:g.12590929dup	GRCh38
NC_000003.11:g.12632428dup , CM000665.1:g.12632428dup	GRCh37
NC_000003.10:g.12607428dup	NCBI36
NG_007467.1:g.78253dup , LRG_413:g.78253dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*906dup	ENSP00000401088.1:n.*906dup
ENST00000432427.3:c.558dup
ENST00000460610.2:n.35dup
ENST00000465826.6:n.832dup
ENST00000475353.2:n.1163dup
ENST00000494557.2:n.1052dup
ENST00000684903.1:c.*918dup	ENSP00000508612.1:n.*918dup
ENST00000685348.1:c.*918dup	ENSP00000510285.1:n.*918dup
ENST00000685437.1:c.1142dup	ENSP00000508794.1:p.Asp382GlyfsTer?
ENST00000685653.1:c.1241dup	ENSP00000509968.1:p.Asp415GlyfsTer?
ENST00000685738.1:c.*205dup	ENSP00000510156.1:n.*205dup
ENST00000686409.1:n.2292dup
ENST00000686455.1:n.1604dup
ENST00000686762.1:c.1241dup	ENSP00000509767.1:p.Asp415GlyfsTer?
ENST00000687257.1:n.1477dup
ENST00000687326.1:c.*175dup	ENSP00000509665.1:n.*175dup
ENST00000687505.1:n.1359dup
ENST00000687923.1:c.1130dup	ENSP00000510255.1:p.Asp378GlyfsTer?
ENST00000687940.1:n.1618dup
ENST00000688269.1:n.1837dup
ENST00000688326.1:c.674dup
ENST00000688444.1:n.1567dup
ENST00000688543.1:c.1142dup	ENSP00000509612.1:p.Asp382GlyfsTer?
ENST00000688625.1:c.*819dup	ENSP00000509522.1:n.*819dup
ENST00000688803.1:n.1472dup
ENST00000688914.1:n.227dup
ENST00000689097.1:c.*918dup	ENSP00000509756.1:n.*918dup
ENST00000689389.1:c.1193+781dup	ENSP00000510213.1:n.1193+781dup
ENST00000689418.1:c.*918dup	ENSP00000509467.1:n.*918dup
ENST00000689481.1:c.*918dup	ENSP00000510248.1:n.*918dup
ENST00000689540.1:n.1391dup
ENST00000689876.1:c.1241dup	ENSP00000508535.1:p.Asp415GlyfsTer?
ENST00000689914.1:c.*175dup	ENSP00000509847.1:n.*175dup
ENST00000690397.1:c.1130dup	ENSP00000508730.1:p.Asp378GlyfsTer?
ENST00000690460.1:c.1229dup	ENSP00000509106.1:p.Asp411GlyfsTer?
ENST00000690585.1:c.133dup
ENST00000690625.1:n.2277dup
ENST00000691396.1:c.*1093dup	ENSP00000510712.1:n.*1093dup
ENST00000691724.1:c.*198dup	ENSP00000509255.1:n.*198dup
ENST00000691779.1:c.*819dup	ENSP00000508592.1:n.*819dup
ENST00000691888.1:c.133dup
ENST00000691899.1:c.1241dup	ENSP00000508763.1:p.Asp415GlyfsTer?
ENST00000692069.1:n.1807dup
ENST00000692093.1:c.1142dup	ENSP00000509669.1:p.Asp382GlyfsTer?
ENST00000692311.1:n.2065dup
ENST00000692558.1:n.1606dup
ENST00000692773.1:c.*978dup	ENSP00000509055.1:n.*978dup
ENST00000692830.1:c.*986dup	ENSP00000509461.1:n.*986dup
ENST00000693069.1:c.*175dup	ENSP00000510072.1:n.*175dup
ENST00000693312.1:c.1016dup	ENSP00000508686.1:p.Asp340GlyfsTer?
ENST00000693664.1:c.1241dup	ENSP00000509614.1:p.Asp415GlyfsTer?
ENST00000693705.1:c.*918dup	ENSP00000510697.1:n.*918dup
ENST00000251849.9:c.1241dup MANE Select	ENSP00000251849.4:p.Asp415GlyfsTer?
ENST00000442415.7:c.1301dup	ENSP00000401888.2:p.Asp435GlyfsTer?
ENST00000251849.8:c.1241dup	ENSP00000251849.4:p.Asp415GlyfsTer?
ENST00000423275.5:c.*918dup	ENSP00000401088.1:n.*918dup
ENST00000432427.2:c.878dup	ENSP00000398591.2:p.Asp294GlyfsTer?
ENST00000442415.6:c.1301dup	ENSP00000401888.2:p.Asp435GlyfsTer?
ENST00000460610.1:n.198dup
ENST00000465826.5:n.598dup
ENST00000475353.1:n.409dup
ENST00000494557.1:n.257dup
NM_002880.3:c.1241dup , LRG_413t1:c.1241dup	NP_002871.1:p.Asp415GlyfsTer?
XM_005265355.1:c.1241dup	XP_005265412.1:p.Asp415GlyfsTer?
XM_005265357.1:c.1142dup	XP_005265414.1:p.Asp382GlyfsTer?
XM_005265358.3:c.998dup	XP_005265415.1:p.Asp334GlyfsTer?
XM_005265359.3:c.899dup	XP_005265416.1:p.Asp301GlyfsTer?
XM_005265360.1:c.1241dup	XP_005265417.1:p.Asp415GlyfsTer?
XM_011533974.1:c.1241dup	XP_011532276.1:p.Asp415GlyfsTer?
XM_011533975.1:c.998dup	XP_011532277.1:p.Asp334GlyfsTer?
NM_001354689.1:c.1301dup	NP_001341618.1:p.Asp435GlyfsTer?
NM_001354690.1:c.1241dup	NP_001341619.1:p.Asp415GlyfsTer?
NM_001354691.1:c.998dup	NP_001341620.1:p.Asp334GlyfsTer?
NM_001354692.1:c.998dup	NP_001341621.1:p.Asp334GlyfsTer?
NM_001354693.1:c.1142dup	NP_001341622.1:p.Asp382GlyfsTer?
NM_001354694.1:c.1058dup	NP_001341623.1:p.Asp354GlyfsTer?
NM_001354695.1:c.899dup	NP_001341624.1:p.Asp301GlyfsTer?
NR_148940.1:n.1769dup
NR_148941.1:n.1715dup
NR_148942.1:n.1654dup
XM_011533974.3:c.1241dup	XP_011532276.1:p.Asp415GlyfsTer?
XM_017006966.1:c.1142dup	XP_016862455.1:p.Asp382GlyfsTer?
NM_001354689.3:c.1301dup	NP_001341618.1:p.Asp435GlyfsTer?
NM_001354690.2:c.1241dup	NP_001341619.1:p.Asp415GlyfsTer?
NM_001354691.2:c.998dup	NP_001341620.1:p.Asp334GlyfsTer?
NM_001354692.2:c.998dup	NP_001341621.1:p.Asp334GlyfsTer?
NM_001354693.2:c.1142dup	NP_001341622.1:p.Asp382GlyfsTer?
NM_001354694.2:c.1058dup	NP_001341623.1:p.Asp354GlyfsTer?
NM_001354695.2:c.899dup	NP_001341624.1:p.Asp301GlyfsTer?
NR_148940.2:n.1685dup
NR_148941.2:n.1631dup
NR_148942.2:n.1570dup
NM_001354690.3:c.1241dup	NP_001341619.1:p.Asp415GlyfsTer?
NM_001354691.3:c.998dup	NP_001341620.1:p.Asp334GlyfsTer?
NM_001354692.3:c.998dup	NP_001341621.1:p.Asp334GlyfsTer?
NM_001354693.3:c.1142dup	NP_001341622.1:p.Asp382GlyfsTer?
NM_001354694.3:c.1058dup	NP_001341623.1:p.Asp354GlyfsTer?
NM_001354695.3:c.899dup	NP_001341624.1:p.Asp301GlyfsTer?
NM_002880.4:c.1241dup MANE Select	NP_002871.1:p.Asp415GlyfsTer?
NR_148940.3:n.1685dup
NR_148941.3:n.1631dup
NR_148942.3:n.1570dup