Canonical Allele Identifier: CA351502413

Gene: RAF1

Linked Data

• MyVariant Identifiers: chr3:g.12632426T>C (hg19) ; chr3:g.12590927T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12590927T>C , CM000665.2:g.12590927T>C	GRCh38
NC_000003.11:g.12632426T>C , CM000665.1:g.12632426T>C	GRCh37
NC_000003.10:g.12607426T>C	NCBI36
NG_007467.1:g.78253A>G , LRG_413:g.78253A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*906A>G	ENSP00000401088.1:n.*906A>G
ENST00000432427.3:c.558A>G
ENST00000460610.2:n.35A>G
ENST00000465826.6:n.832A>G
ENST00000475353.2:n.1163A>G
ENST00000494557.2:n.1052A>G
ENST00000684903.1:c.*918A>G	ENSP00000508612.1:n.*918A>G
ENST00000685348.1:c.*918A>G	ENSP00000510285.1:n.*918A>G
ENST00000685437.1:c.1142A>G	ENSP00000508794.1:p.Lys381Arg
ENST00000685653.1:c.1241A>G	ENSP00000509968.1:p.Lys414Arg
ENST00000685738.1:c.*205A>G	ENSP00000510156.1:n.*205A>G
ENST00000686409.1:n.2292A>G
ENST00000686455.1:n.1604A>G
ENST00000686762.1:c.1241A>G	ENSP00000509767.1:p.Lys414Arg
ENST00000687257.1:n.1477A>G
ENST00000687326.1:c.*175A>G	ENSP00000509665.1:n.*175A>G
ENST00000687505.1:n.1359A>G
ENST00000687923.1:c.1130A>G	ENSP00000510255.1:p.Lys377Arg
ENST00000687940.1:n.1618A>G
ENST00000688269.1:n.1837A>G
ENST00000688326.1:c.674A>G
ENST00000688444.1:n.1567A>G
ENST00000688543.1:c.1142A>G	ENSP00000509612.1:p.Lys381Arg
ENST00000688625.1:c.*819A>G	ENSP00000509522.1:n.*819A>G
ENST00000688803.1:n.1472A>G
ENST00000688914.1:n.227A>G
ENST00000689097.1:c.*918A>G	ENSP00000509756.1:n.*918A>G
ENST00000689389.1:c.1193+781A>G	ENSP00000510213.1:n.1193+781A>G
ENST00000689418.1:c.*918A>G	ENSP00000509467.1:n.*918A>G
ENST00000689481.1:c.*918A>G	ENSP00000510248.1:n.*918A>G
ENST00000689540.1:n.1391A>G
ENST00000689876.1:c.1241A>G	ENSP00000508535.1:p.Lys414Arg
ENST00000689914.1:c.*175A>G	ENSP00000509847.1:n.*175A>G
ENST00000690397.1:c.1130A>G	ENSP00000508730.1:p.Lys377Arg
ENST00000690460.1:c.1229A>G	ENSP00000509106.1:p.Lys410Arg
ENST00000690585.1:c.133A>G
ENST00000690625.1:n.2277A>G
ENST00000691396.1:c.*1093A>G	ENSP00000510712.1:n.*1093A>G
ENST00000691724.1:c.*198A>G	ENSP00000509255.1:n.*198A>G
ENST00000691779.1:c.*819A>G	ENSP00000508592.1:n.*819A>G
ENST00000691888.1:c.133A>G
ENST00000691899.1:c.1241A>G	ENSP00000508763.1:p.Lys414Arg
ENST00000692069.1:n.1807A>G
ENST00000692093.1:c.1142A>G	ENSP00000509669.1:p.Lys381Arg
ENST00000692311.1:n.2065A>G
ENST00000692558.1:n.1606A>G
ENST00000692773.1:c.*978A>G	ENSP00000509055.1:n.*978A>G
ENST00000692830.1:c.*986A>G	ENSP00000509461.1:n.*986A>G
ENST00000693069.1:c.*175A>G	ENSP00000510072.1:n.*175A>G
ENST00000693312.1:c.1016A>G	ENSP00000508686.1:p.Lys339Arg
ENST00000693664.1:c.1241A>G	ENSP00000509614.1:p.Lys414Arg
ENST00000693705.1:c.*918A>G	ENSP00000510697.1:n.*918A>G
ENST00000251849.9:c.1241A>G MANE Select	ENSP00000251849.4:p.Lys414Arg
ENST00000442415.7:c.1301A>G	ENSP00000401888.2:p.Lys434Arg
ENST00000251849.8:c.1241A>G	ENSP00000251849.4:p.Lys414Arg
ENST00000423275.5:c.*918A>G	ENSP00000401088.1:n.*918A>G
ENST00000432427.2:c.878A>G	ENSP00000398591.2:p.Lys293Arg
ENST00000442415.6:c.1301A>G	ENSP00000401888.2:p.Lys434Arg
ENST00000460610.1:n.198A>G
ENST00000465826.5:n.598A>G
ENST00000475353.1:n.409A>G
ENST00000494557.1:n.257A>G
NM_002880.3:c.1241A>G , LRG_413t1:c.1241A>G	NP_002871.1:p.Lys414Arg
XM_005265355.1:c.1241A>G	XP_005265412.1:p.Lys414Arg
XM_005265357.1:c.1142A>G	XP_005265414.1:p.Lys381Arg
XM_005265358.3:c.998A>G	XP_005265415.1:p.Lys333Arg
XM_005265359.3:c.899A>G	XP_005265416.1:p.Lys300Arg
XM_005265360.1:c.1241A>G	XP_005265417.1:p.Lys414Arg
XM_011533974.1:c.1241A>G	XP_011532276.1:p.Lys414Arg
XM_011533975.1:c.998A>G	XP_011532277.1:p.Lys333Arg
NM_001354689.1:c.1301A>G	NP_001341618.1:p.Lys434Arg
NM_001354690.1:c.1241A>G	NP_001341619.1:p.Lys414Arg
NM_001354691.1:c.998A>G	NP_001341620.1:p.Lys333Arg
NM_001354692.1:c.998A>G	NP_001341621.1:p.Lys333Arg
NM_001354693.1:c.1142A>G	NP_001341622.1:p.Lys381Arg
NM_001354694.1:c.1058A>G	NP_001341623.1:p.Lys353Arg
NM_001354695.1:c.899A>G	NP_001341624.1:p.Lys300Arg
NR_148940.1:n.1769A>G
NR_148941.1:n.1715A>G
NR_148942.1:n.1654A>G
XM_011533974.3:c.1241A>G	XP_011532276.1:p.Lys414Arg
XM_017006966.1:c.1142A>G	XP_016862455.1:p.Lys381Arg
NM_001354689.3:c.1301A>G	NP_001341618.1:p.Lys434Arg
NM_001354690.2:c.1241A>G	NP_001341619.1:p.Lys414Arg
NM_001354691.2:c.998A>G	NP_001341620.1:p.Lys333Arg
NM_001354692.2:c.998A>G	NP_001341621.1:p.Lys333Arg
NM_001354693.2:c.1142A>G	NP_001341622.1:p.Lys381Arg
NM_001354694.2:c.1058A>G	NP_001341623.1:p.Lys353Arg
NM_001354695.2:c.899A>G	NP_001341624.1:p.Lys300Arg
NR_148940.2:n.1685A>G
NR_148941.2:n.1631A>G
NR_148942.2:n.1570A>G
NM_001354690.3:c.1241A>G	NP_001341619.1:p.Lys414Arg
NM_001354691.3:c.998A>G	NP_001341620.1:p.Lys333Arg
NM_001354692.3:c.998A>G	NP_001341621.1:p.Lys333Arg
NM_001354693.3:c.1142A>G	NP_001341622.1:p.Lys381Arg
NM_001354694.3:c.1058A>G	NP_001341623.1:p.Lys353Arg
NM_001354695.3:c.899A>G	NP_001341624.1:p.Lys300Arg
NM_002880.4:c.1241A>G MANE Select	NP_002871.1:p.Lys414Arg
NR_148940.3:n.1685A>G
NR_148941.3:n.1631A>G
NR_148942.3:n.1570A>G