Canonical Allele Identifier: CA351501953

Gene: RAF1

Linked Data

• MyVariant Identifiers: chr3:g.12632358C>A (hg19) ; chr3:g.12590859C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12590859C>A , CM000665.2:g.12590859C>A	GRCh38
NC_000003.11:g.12632358C>A , CM000665.1:g.12632358C>A	GRCh37
NC_000003.10:g.12607358C>A	NCBI36
NG_007467.1:g.78321G>T , LRG_413:g.78321G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*974G>T	ENSP00000401088.1:n.*974G>T
ENST00000432427.3:c.626G>T
ENST00000460610.2:n.103G>T
ENST00000465826.6:n.900G>T
ENST00000475353.2:n.1231G>T
ENST00000494557.2:n.1120G>T
ENST00000684903.1:c.*986G>T	ENSP00000508612.1:n.*986G>T
ENST00000685348.1:c.*986G>T	ENSP00000510285.1:n.*986G>T
ENST00000685437.1:c.1210G>T	ENSP00000508794.1:p.Glu404Ter
ENST00000685653.1:c.1309G>T	ENSP00000509968.1:p.Glu437Ter
ENST00000685738.1:c.*273G>T	ENSP00000510156.1:n.*273G>T
ENST00000686409.1:n.2360G>T
ENST00000686455.1:n.1672G>T
ENST00000686762.1:c.1309G>T	ENSP00000509767.1:p.Glu437Ter
ENST00000687257.1:n.1545G>T
ENST00000687326.1:c.*243G>T	ENSP00000509665.1:n.*243G>T
ENST00000687505.1:n.1427G>T
ENST00000687923.1:c.1198G>T	ENSP00000510255.1:p.Glu400Ter
ENST00000687940.1:n.1686G>T
ENST00000688269.1:n.1905G>T
ENST00000688326.1:c.742G>T
ENST00000688444.1:n.1635G>T
ENST00000688543.1:c.1210G>T	ENSP00000509612.1:p.Glu404Ter
ENST00000688625.1:c.*887G>T	ENSP00000509522.1:n.*887G>T
ENST00000688803.1:n.1540G>T
ENST00000688914.1:n.295G>T
ENST00000689097.1:c.*986G>T	ENSP00000509756.1:n.*986G>T
ENST00000689389.1:c.1193+849G>T	ENSP00000510213.1:n.1193+849G>T
ENST00000689418.1:c.*986G>T	ENSP00000509467.1:n.*986G>T
ENST00000689481.1:c.*986G>T	ENSP00000510248.1:n.*986G>T
ENST00000689540.1:n.1459G>T
ENST00000689876.1:c.1309G>T	ENSP00000508535.1:p.Glu437Ter
ENST00000689914.1:c.*243G>T	ENSP00000509847.1:n.*243G>T
ENST00000690397.1:c.1198G>T	ENSP00000508730.1:p.Glu400Ter
ENST00000690460.1:c.1297G>T	ENSP00000509106.1:p.Glu433Ter
ENST00000690585.1:c.201G>T
ENST00000690625.1:n.2345G>T
ENST00000691396.1:c.*1161G>T	ENSP00000510712.1:n.*1161G>T
ENST00000691724.1:c.*266G>T	ENSP00000509255.1:n.*266G>T
ENST00000691779.1:c.*887G>T	ENSP00000508592.1:n.*887G>T
ENST00000691888.1:c.201G>T
ENST00000691899.1:c.1309G>T	ENSP00000508763.1:p.Glu437Ter
ENST00000692069.1:n.1875G>T
ENST00000692093.1:c.1210G>T	ENSP00000509669.1:p.Glu404Ter
ENST00000692311.1:n.2133G>T
ENST00000692558.1:n.1674G>T
ENST00000692773.1:c.*1046G>T	ENSP00000509055.1:n.*1046G>T
ENST00000692830.1:c.*1054G>T	ENSP00000509461.1:n.*1054G>T
ENST00000693069.1:c.*243G>T	ENSP00000510072.1:n.*243G>T
ENST00000693312.1:c.1084G>T	ENSP00000508686.1:p.Glu362Ter
ENST00000693664.1:c.1309G>T	ENSP00000509614.1:p.Glu437Ter
ENST00000693705.1:c.*986G>T	ENSP00000510697.1:n.*986G>T
ENST00000251849.9:c.1309G>T MANE Select	ENSP00000251849.4:p.Glu437Ter
ENST00000442415.7:c.1369G>T	ENSP00000401888.2:p.Glu457Ter
ENST00000251849.8:c.1309G>T	ENSP00000251849.4:p.Glu437Ter
ENST00000423275.5:c.*986G>T	ENSP00000401088.1:n.*986G>T
ENST00000432427.2:c.946G>T	ENSP00000398591.2:p.Glu316Ter
ENST00000442415.6:c.1369G>T	ENSP00000401888.2:p.Glu457Ter
ENST00000460610.1:n.266G>T
ENST00000465826.5:n.666G>T
ENST00000475353.1:n.477G>T
ENST00000494557.1:n.325G>T
NM_002880.3:c.1309G>T , LRG_413t1:c.1309G>T	NP_002871.1:p.Glu437Ter
XM_005265355.1:c.1309G>T	XP_005265412.1:p.Glu437Ter
XM_005265357.1:c.1210G>T	XP_005265414.1:p.Glu404Ter
XM_005265358.3:c.1066G>T	XP_005265415.1:p.Glu356Ter
XM_005265359.3:c.967G>T	XP_005265416.1:p.Glu323Ter
XM_005265360.1:c.1309G>T	XP_005265417.1:p.Glu437Ter
XM_011533974.1:c.1309G>T	XP_011532276.1:p.Glu437Ter
XM_011533975.1:c.1066G>T	XP_011532277.1:p.Glu356Ter
NM_001354689.1:c.1369G>T	NP_001341618.1:p.Glu457Ter
NM_001354690.1:c.1309G>T	NP_001341619.1:p.Glu437Ter
NM_001354691.1:c.1066G>T	NP_001341620.1:p.Glu356Ter
NM_001354692.1:c.1066G>T	NP_001341621.1:p.Glu356Ter
NM_001354693.1:c.1210G>T	NP_001341622.1:p.Glu404Ter
NM_001354694.1:c.1126G>T	NP_001341623.1:p.Glu376Ter
NM_001354695.1:c.967G>T	NP_001341624.1:p.Glu323Ter
NR_148940.1:n.1837G>T
NR_148941.1:n.1783G>T
NR_148942.1:n.1722G>T
XM_011533974.3:c.1309G>T	XP_011532276.1:p.Glu437Ter
XM_017006966.1:c.1210G>T	XP_016862455.1:p.Glu404Ter
NM_001354689.3:c.1369G>T	NP_001341618.1:p.Glu457Ter
NM_001354690.2:c.1309G>T	NP_001341619.1:p.Glu437Ter
NM_001354691.2:c.1066G>T	NP_001341620.1:p.Glu356Ter
NM_001354692.2:c.1066G>T	NP_001341621.1:p.Glu356Ter
NM_001354693.2:c.1210G>T	NP_001341622.1:p.Glu404Ter
NM_001354694.2:c.1126G>T	NP_001341623.1:p.Glu376Ter
NM_001354695.2:c.967G>T	NP_001341624.1:p.Glu323Ter
NR_148940.2:n.1753G>T
NR_148941.2:n.1699G>T
NR_148942.2:n.1638G>T
NM_001354690.3:c.1309G>T	NP_001341619.1:p.Glu437Ter
NM_001354691.3:c.1066G>T	NP_001341620.1:p.Glu356Ter
NM_001354692.3:c.1066G>T	NP_001341621.1:p.Glu356Ter
NM_001354693.3:c.1210G>T	NP_001341622.1:p.Glu404Ter
NM_001354694.3:c.1126G>T	NP_001341623.1:p.Glu376Ter
NM_001354695.3:c.967G>T	NP_001341624.1:p.Glu323Ter
NM_002880.4:c.1309G>T MANE Select	NP_002871.1:p.Glu437Ter
NR_148940.3:n.1753G>T
NR_148941.3:n.1699G>T
NR_148942.3:n.1638G>T