Canonical Allele Identifier: CA345872

Gene: RAF1

Linked Data

• ClinVar Variation Id: 155829
• ClinVar RCV Id: RCV000143944
• dbSNP Id: rs587782972
• MyVariant Identifiers: chr3:g.12633228C>A (hg19) ; chr3:g.12591729C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12591729C>A , CM000665.2:g.12591729C>A	GRCh38
NC_000003.11:g.12633228C>A , CM000665.1:g.12633228C>A	GRCh37
NC_000003.10:g.12608228C>A	NCBI36
NG_007467.1:g.77451G>T , LRG_413:g.77451G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*837G>T	ENSP00000401088.1:n.*837G>T
ENST00000432427.3:c.489G>T
ENST00000465826.6:n.763G>T
ENST00000475353.2:n.1094G>T
ENST00000491290.2:n.1532G>T
ENST00000494557.2:n.983G>T
ENST00000684903.1:c.*849G>T	ENSP00000508612.1:n.*849G>T
ENST00000685348.1:c.*849G>T	ENSP00000510285.1:n.*849G>T
ENST00000685437.1:c.1073G>T	ENSP00000508794.1:p.Arg358Met
ENST00000685653.1:c.1172G>T	ENSP00000509968.1:p.Arg391Met
ENST00000685738.1:c.*136G>T	ENSP00000510156.1:n.*136G>T
ENST00000686409.1:n.2223G>T
ENST00000686455.1:n.1535G>T
ENST00000686762.1:c.1172G>T	ENSP00000509767.1:p.Arg391Met
ENST00000687257.1:n.1408G>T
ENST00000687326.1:c.*106G>T	ENSP00000509665.1:n.*106G>T
ENST00000687486.1:c.364G>T
ENST00000687505.1:n.1290G>T
ENST00000687923.1:c.1061G>T	ENSP00000510255.1:p.Arg354Met
ENST00000687940.1:n.1549G>T
ENST00000688269.1:n.1768G>T
ENST00000688326.1:c.605G>T
ENST00000688444.1:n.1498G>T
ENST00000688543.1:c.1073G>T	ENSP00000509612.1:p.Arg358Met
ENST00000688625.1:c.*750G>T	ENSP00000509522.1:n.*750G>T
ENST00000688803.1:n.1403G>T
ENST00000688914.1:n.158G>T
ENST00000689097.1:c.*849G>T	ENSP00000509756.1:n.*849G>T
ENST00000689389.1:c.1172G>T	ENSP00000510213.1:p.Arg391Met
ENST00000689418.1:c.*849G>T	ENSP00000509467.1:n.*849G>T
ENST00000689481.1:c.*849G>T	ENSP00000510248.1:n.*849G>T
ENST00000689540.1:n.1322G>T
ENST00000689876.1:c.1172G>T	ENSP00000508535.1:p.Arg391Met
ENST00000689914.1:c.*106G>T	ENSP00000509847.1:n.*106G>T
ENST00000690397.1:c.1061G>T	ENSP00000508730.1:p.Arg354Met
ENST00000690460.1:c.1160G>T	ENSP00000509106.1:p.Arg387Met
ENST00000690585.1:c.64G>T
ENST00000690625.1:n.1475G>T
ENST00000691396.1:c.*1024G>T	ENSP00000510712.1:n.*1024G>T
ENST00000691724.1:c.*129G>T	ENSP00000509255.1:n.*129G>T
ENST00000691779.1:c.*750G>T	ENSP00000508592.1:n.*750G>T
ENST00000691888.1:c.64G>T
ENST00000691899.1:c.1172G>T	ENSP00000508763.1:p.Arg391Met
ENST00000692069.1:n.1738G>T
ENST00000692093.1:c.1073G>T	ENSP00000509669.1:p.Arg358Met
ENST00000692311.1:n.1996G>T
ENST00000692558.1:n.1537G>T
ENST00000692773.1:c.*909G>T	ENSP00000509055.1:n.*909G>T
ENST00000692830.1:c.*917G>T	ENSP00000509461.1:n.*917G>T
ENST00000693069.1:c.*106G>T	ENSP00000510072.1:n.*106G>T
ENST00000693312.1:c.947G>T	ENSP00000508686.1:p.Arg316Met
ENST00000693664.1:c.1172G>T	ENSP00000509614.1:p.Arg391Met
ENST00000693705.1:c.*849G>T	ENSP00000510697.1:n.*849G>T
ENST00000251849.9:c.1172G>T MANE Select	ENSP00000251849.4:p.Arg391Met
ENST00000442415.7:c.1232G>T	ENSP00000401888.2:p.Arg411Met
ENST00000251849.8:c.1172G>T	ENSP00000251849.4:p.Arg391Met
ENST00000423275.5:c.*849G>T	ENSP00000401088.1:n.*849G>T
ENST00000432427.2:c.809G>T	ENSP00000398591.2:p.Arg270Met
ENST00000442415.6:c.1232G>T	ENSP00000401888.2:p.Arg411Met
ENST00000460610.1:n.129G>T
ENST00000465826.5:n.529G>T
ENST00000475353.1:n.340G>T
ENST00000494557.1:n.188G>T
NM_002880.3:c.1172G>T , LRG_413t1:c.1172G>T	NP_002871.1:p.Arg391Met
XM_005265355.1:c.1172G>T	XP_005265412.1:p.Arg391Met
XM_005265357.1:c.1073G>T	XP_005265414.1:p.Arg358Met
XM_005265358.3:c.929G>T	XP_005265415.1:p.Arg310Met
XM_005265359.3:c.830G>T	XP_005265416.1:p.Arg277Met
XM_005265360.1:c.1172G>T	XP_005265417.1:p.Arg391Met
XM_011533974.1:c.1172G>T	XP_011532276.1:p.Arg391Met
XM_011533975.1:c.929G>T	XP_011532277.1:p.Arg310Met
NM_001354689.1:c.1232G>T	NP_001341618.1:p.Arg411Met
NM_001354690.1:c.1172G>T	NP_001341619.1:p.Arg391Met
NM_001354691.1:c.929G>T	NP_001341620.1:p.Arg310Met
NM_001354692.1:c.929G>T	NP_001341621.1:p.Arg310Met
NM_001354693.1:c.1073G>T	NP_001341622.1:p.Arg358Met
NM_001354694.1:c.989G>T	NP_001341623.1:p.Arg330Met
NM_001354695.1:c.830G>T	NP_001341624.1:p.Arg277Met
NR_148940.1:n.1700G>T
NR_148941.1:n.1646G>T
NR_148942.1:n.1585G>T
XM_011533974.3:c.1172G>T	XP_011532276.1:p.Arg391Met
XM_017006966.1:c.1073G>T	XP_016862455.1:p.Arg358Met
XR_001740227.1:n.1463G>T
NM_001354689.3:c.1232G>T	NP_001341618.1:p.Arg411Met
NM_001354690.2:c.1172G>T	NP_001341619.1:p.Arg391Met
NM_001354691.2:c.929G>T	NP_001341620.1:p.Arg310Met
NM_001354692.2:c.929G>T	NP_001341621.1:p.Arg310Met
NM_001354693.2:c.1073G>T	NP_001341622.1:p.Arg358Met
NM_001354694.2:c.989G>T	NP_001341623.1:p.Arg330Met
NM_001354695.2:c.830G>T	NP_001341624.1:p.Arg277Met
NR_148940.2:n.1616G>T
NR_148941.2:n.1562G>T
NR_148942.2:n.1501G>T
NM_001354690.3:c.1172G>T	NP_001341619.1:p.Arg391Met
NM_001354691.3:c.929G>T	NP_001341620.1:p.Arg310Met
NM_001354692.3:c.929G>T	NP_001341621.1:p.Arg310Met
NM_001354693.3:c.1073G>T	NP_001341622.1:p.Arg358Met
NM_001354694.3:c.989G>T	NP_001341623.1:p.Arg330Met
NM_001354695.3:c.830G>T	NP_001341624.1:p.Arg277Met
NM_002880.4:c.1172G>T MANE Select	NP_002871.1:p.Arg391Met
NR_148940.3:n.1616G>T
NR_148941.3:n.1562G>T
NR_148942.3:n.1501G>T