Canonical Allele Identifier: CA261620

Gene: RAF1

Linked Data

• ClinVar Variation Id: 44631
• ClinVar RCV Id: RCV000037699 ; RCV000550843 ; RCV002227051 ; RCV003450729
• dbSNP Id: rs397516825
• MyVariant Identifiers: chr3:g.12645703T>C (hg19) ; chr3:g.12604204T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12604204T>C , CM000665.2:g.12604204T>C	GRCh38
NC_000003.11:g.12645703T>C , CM000665.1:g.12645703T>C	GRCh37
NC_000003.10:g.12620703T>C	NCBI36
NG_007467.1:g.64976A>G , LRG_413:g.64976A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000416093.2:c.*443A>G	ENSP00000391265.2:n.*443A>G
ENST00000423275.6:c.*443A>G	ENSP00000401088.1:n.*443A>G
ENST00000432427.3:c.86A>G
ENST00000465826.6:n.357A>G
ENST00000491290.2:n.1143A>G
ENST00000684903.1:c.*443A>G	ENSP00000508612.1:n.*443A>G
ENST00000685348.1:c.*443A>G	ENSP00000510285.1:n.*443A>G
ENST00000685437.1:c.667A>G	ENSP00000508794.1:p.Arg223Gly
ENST00000685653.1:c.766A>G	ENSP00000509968.1:p.Arg256Gly
ENST00000685738.1:c.766A>G	ENSP00000510156.1:p.Arg256Gly
ENST00000685959.1:c.766A>G	ENSP00000510452.1:p.Arg256Gly
ENST00000686409.1:n.1366A>G
ENST00000686455.1:n.1129A>G
ENST00000686479.1:n.1137A>G
ENST00000686762.1:c.766A>G	ENSP00000509767.1:p.Arg256Gly
ENST00000687257.1:n.1002A>G
ENST00000687326.1:c.766A>G	ENSP00000509665.1:p.Arg256Gly
ENST00000687486.1:c.86A>G
ENST00000687505.1:n.884A>G
ENST00000687923.1:c.667A>G	ENSP00000510255.1:p.Arg223Gly
ENST00000687940.1:n.1143A>G
ENST00000688269.1:n.1374A>G
ENST00000688326.1:c.86A>G
ENST00000688444.1:n.1092A>G
ENST00000688543.1:c.667A>G	ENSP00000509612.1:p.Arg223Gly
ENST00000688625.1:c.*344A>G	ENSP00000509522.1:n.*344A>G
ENST00000688803.1:n.997A>G
ENST00000689033.1:c.766A>G	ENSP00000508983.1:p.Arg256Gly
ENST00000689097.1:c.*443A>G	ENSP00000509756.1:n.*443A>G
ENST00000689389.1:c.766A>G	ENSP00000510213.1:p.Arg256Gly
ENST00000689418.1:c.*443A>G	ENSP00000509467.1:n.*443A>G
ENST00000689481.1:c.*443A>G	ENSP00000510248.1:n.*443A>G
ENST00000689540.1:n.916A>G
ENST00000689876.1:c.766A>G	ENSP00000508535.1:p.Arg256Gly
ENST00000689914.1:c.766A>G	ENSP00000509847.1:p.Arg256Gly
ENST00000690397.1:c.667A>G	ENSP00000508730.1:p.Arg223Gly
ENST00000690460.1:c.766A>G	ENSP00000509106.1:p.Arg256Gly
ENST00000690625.1:n.1069A>G
ENST00000691268.1:c.262-3789A>G
ENST00000691396.1:c.*559A>G	ENSP00000510712.1:n.*559A>G
ENST00000691724.1:c.766A>G	ENSP00000509255.1:p.Arg256Gly
ENST00000691779.1:c.*344A>G	ENSP00000508592.1:n.*344A>G
ENST00000691899.1:c.766A>G	ENSP00000508763.1:p.Arg256Gly
ENST00000692093.1:c.667A>G	ENSP00000509669.1:p.Arg223Gly
ENST00000692311.1:n.1139A>G
ENST00000692558.1:n.1131A>G
ENST00000692773.1:c.*443A>G	ENSP00000509055.1:n.*443A>G
ENST00000692830.1:c.*511A>G	ENSP00000509461.1:n.*511A>G
ENST00000693069.1:c.667A>G	ENSP00000510072.1:p.Arg223Gly
ENST00000693312.1:c.541A>G	ENSP00000508686.1:p.Arg181Gly
ENST00000693664.1:c.766A>G	ENSP00000509614.1:p.Arg256Gly
ENST00000693705.1:c.*443A>G	ENSP00000510697.1:n.*443A>G
ENST00000251849.9:c.766A>G MANE Select	ENSP00000251849.4:p.Arg256Gly
ENST00000442415.7:c.766A>G	ENSP00000401888.2:p.Arg256Gly
ENST00000251849.8:c.766A>G	ENSP00000251849.4:p.Arg256Gly
ENST00000416093.1:c.*344A>G	ENSP00000391265.1:n.*344A>G
ENST00000423275.5:c.*443A>G	ENSP00000401088.1:n.*443A>G
ENST00000432427.2:c.403A>G	ENSP00000398591.2:p.Arg135Gly
ENST00000442415.6:c.766A>G	ENSP00000401888.2:p.Arg256Gly
ENST00000465826.5:n.10A>G
ENST00000491290.1:n.287A>G
NM_002880.3:c.766A>G , LRG_413t1:c.766A>G	NP_002871.1:p.Arg256Gly
XM_005265355.1:c.766A>G	XP_005265412.1:p.Arg256Gly
XM_005265357.1:c.667A>G	XP_005265414.1:p.Arg223Gly
XM_005265358.3:c.523A>G	XP_005265415.1:p.Arg175Gly
XM_005265359.3:c.424A>G	XP_005265416.1:p.Arg142Gly
XM_005265360.1:c.766A>G	XP_005265417.1:p.Arg256Gly
XM_011533974.1:c.766A>G	XP_011532276.1:p.Arg256Gly
XM_011533975.1:c.523A>G	XP_011532277.1:p.Arg175Gly
NM_001354689.1:c.766A>G	NP_001341618.1:p.Arg256Gly
NM_001354690.1:c.766A>G	NP_001341619.1:p.Arg256Gly
NM_001354691.1:c.523A>G	NP_001341620.1:p.Arg175Gly
NM_001354692.1:c.523A>G	NP_001341621.1:p.Arg175Gly
NM_001354693.1:c.667A>G	NP_001341622.1:p.Arg223Gly
NM_001354694.1:c.523A>G	NP_001341623.1:p.Arg175Gly
NM_001354695.1:c.424A>G	NP_001341624.1:p.Arg142Gly
NR_148940.1:n.1181A>G
NR_148941.1:n.1181A>G
NR_148942.1:n.1181A>G
XM_011533974.3:c.766A>G	XP_011532276.1:p.Arg256Gly
XM_017006966.1:c.667A>G	XP_016862455.1:p.Arg223Gly
XR_001740227.1:n.998A>G
NM_001354689.3:c.766A>G	NP_001341618.1:p.Arg256Gly
NM_001354690.2:c.766A>G	NP_001341619.1:p.Arg256Gly
NM_001354691.2:c.523A>G	NP_001341620.1:p.Arg175Gly
NM_001354692.2:c.523A>G	NP_001341621.1:p.Arg175Gly
NM_001354693.2:c.667A>G	NP_001341622.1:p.Arg223Gly
NM_001354694.2:c.523A>G	NP_001341623.1:p.Arg175Gly
NM_001354695.2:c.424A>G	NP_001341624.1:p.Arg142Gly
NR_148940.2:n.1097A>G
NR_148941.2:n.1097A>G
NR_148942.2:n.1097A>G
NM_001354690.3:c.766A>G	NP_001341619.1:p.Arg256Gly
NM_001354691.3:c.523A>G	NP_001341620.1:p.Arg175Gly
NM_001354692.3:c.523A>G	NP_001341621.1:p.Arg175Gly
NM_001354693.3:c.667A>G	NP_001341622.1:p.Arg223Gly
NM_001354694.3:c.523A>G	NP_001341623.1:p.Arg175Gly
NM_001354695.3:c.424A>G	NP_001341624.1:p.Arg142Gly
NM_002880.4:c.766A>G MANE Select	NP_002871.1:p.Arg256Gly
NR_148940.3:n.1097A>G
NR_148941.3:n.1097A>G
NR_148942.3:n.1097A>G