Canonical Allele Identifier: CA432273769

Gene: RAF1

Linked Data

• dbSNP Id: rs2125377791
• gnomAD v4: 3-12599737-C-T
• MyVariant Identifiers: chr3:g.12641236C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12599737C>T , CM000665.2:g.12599737C>T	GRCh38
NC_000003.11:g.12641236C>T , CM000665.1:g.12641236C>T	GRCh37
NC_000003.10:g.12616236C>T	NCBI36
NG_007467.1:g.69443G>A , LRG_413:g.69443G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000423275.6:c.*727G>A	ENSP00000401088.1:n.*727G>A
ENST00000432427.3:c.382G>A
ENST00000465826.6:n.653G>A
ENST00000491290.2:n.1439G>A
ENST00000684903.1:c.*739G>A	ENSP00000508612.1:n.*739G>A
ENST00000685348.1:c.*739G>A	ENSP00000510285.1:n.*739G>A
ENST00000685437.1:c.963G>A	ENSP00000508794.1:p.Arg321=
ENST00000685653.1:c.1062G>A	ENSP00000509968.1:p.Arg354=
ENST00000685738.1:c.1062G>A	ENSP00000510156.1:p.Arg354=
ENST00000686409.1:n.2113G>A
ENST00000686455.1:n.1425G>A
ENST00000686479.1:n.1433G>A
ENST00000686762.1:c.1062G>A	ENSP00000509767.1:p.Arg354=
ENST00000687257.1:n.1298G>A
ENST00000687326.1:c.1062G>A	ENSP00000509665.1:p.Arg354=
ENST00000687486.1:c.254G>A
ENST00000687505.1:n.1180G>A
ENST00000687923.1:c.963G>A	ENSP00000510255.1:p.Arg321=
ENST00000687940.1:n.1439G>A
ENST00000688269.1:n.1658G>A
ENST00000688326.1:c.382G>A
ENST00000688444.1:n.1388G>A
ENST00000688543.1:c.963G>A	ENSP00000509612.1:p.Arg321=
ENST00000688625.1:c.*640G>A	ENSP00000509522.1:n.*640G>A
ENST00000688803.1:n.1293G>A
ENST00000688914.1:n.48G>A
ENST00000689097.1:c.*739G>A	ENSP00000509756.1:n.*739G>A
ENST00000689389.1:c.1062G>A	ENSP00000510213.1:p.Arg354=
ENST00000689418.1:c.*739G>A	ENSP00000509467.1:n.*739G>A
ENST00000689481.1:c.*739G>A	ENSP00000510248.1:n.*739G>A
ENST00000689540.1:n.1212G>A
ENST00000689876.1:c.1062G>A	ENSP00000508535.1:p.Arg354=
ENST00000689914.1:c.1062G>A	ENSP00000509847.1:p.Arg354=
ENST00000690397.1:c.951G>A	ENSP00000508730.1:p.Arg317=
ENST00000690460.1:c.1050G>A	ENSP00000509106.1:p.Arg350=
ENST00000690625.1:n.1365G>A
ENST00000691268.1:c.489G>A
ENST00000691396.1:c.*855G>A	ENSP00000510712.1:n.*855G>A
ENST00000691724.1:c.*19G>A	ENSP00000509255.1:n.*19G>A
ENST00000691779.1:c.*640G>A	ENSP00000508592.1:n.*640G>A
ENST00000691899.1:c.1062G>A	ENSP00000508763.1:p.Arg354=
ENST00000692069.1:n.1628G>A
ENST00000692093.1:c.963G>A	ENSP00000509669.1:p.Arg321=
ENST00000692311.1:n.1886G>A
ENST00000692558.1:n.1427G>A
ENST00000692773.1:c.*799G>A	ENSP00000509055.1:n.*799G>A
ENST00000692830.1:c.*807G>A	ENSP00000509461.1:n.*807G>A
ENST00000693069.1:c.963G>A	ENSP00000510072.1:p.Arg321=
ENST00000693312.1:c.837G>A	ENSP00000508686.1:p.Arg279=
ENST00000693664.1:c.1062G>A	ENSP00000509614.1:p.Arg354=
ENST00000693705.1:c.*739G>A	ENSP00000510697.1:n.*739G>A
ENST00000251849.9:c.1062G>A MANE Select	ENSP00000251849.4:p.Arg354=
ENST00000442415.7:c.1122G>A	ENSP00000401888.2:p.Arg374=
ENST00000251849.8:c.1062G>A	ENSP00000251849.4:p.Arg354=
ENST00000423275.5:c.*739G>A	ENSP00000401088.1:n.*739G>A
ENST00000432427.2:c.699G>A	ENSP00000398591.2:p.Arg233=
ENST00000442415.6:c.1122G>A	ENSP00000401888.2:p.Arg374=
ENST00000460610.1:n.19G>A
ENST00000465826.5:n.306G>A
NM_002880.3:c.1062G>A , LRG_413t1:c.1062G>A	NP_002871.1:p.Arg354=
XM_005265355.1:c.1062G>A	XP_005265412.1:p.Arg354=
XM_005265357.1:c.963G>A	XP_005265414.1:p.Arg321=
XM_005265358.3:c.819G>A	XP_005265415.1:p.Arg273=
XM_005265359.3:c.720G>A	XP_005265416.1:p.Arg240=
XM_005265360.1:c.1062G>A	XP_005265417.1:p.Arg354=
XM_011533974.1:c.1062G>A	XP_011532276.1:p.Arg354=
XM_011533975.1:c.819G>A	XP_011532277.1:p.Arg273=
NM_001354689.1:c.1122G>A	NP_001341618.1:p.Arg374=
NM_001354690.1:c.1062G>A	NP_001341619.1:p.Arg354=
NM_001354691.1:c.819G>A	NP_001341620.1:p.Arg273=
NM_001354692.1:c.819G>A	NP_001341621.1:p.Arg273=
NM_001354693.1:c.963G>A	NP_001341622.1:p.Arg321=
NM_001354694.1:c.879G>A	NP_001341623.1:p.Arg293=
NM_001354695.1:c.720G>A	NP_001341624.1:p.Arg240=
NR_148940.1:n.1477G>A
NR_148941.1:n.1477G>A
NR_148942.1:n.1475G>A
XM_011533974.3:c.1062G>A	XP_011532276.1:p.Arg354=
XM_017006966.1:c.963G>A	XP_016862455.1:p.Arg321=
XR_001740227.1:n.1294G>A
NM_001354689.3:c.1122G>A	NP_001341618.1:p.Arg374=
NM_001354690.2:c.1062G>A	NP_001341619.1:p.Arg354=
NM_001354691.2:c.819G>A	NP_001341620.1:p.Arg273=
NM_001354692.2:c.819G>A	NP_001341621.1:p.Arg273=
NM_001354693.2:c.963G>A	NP_001341622.1:p.Arg321=
NM_001354694.2:c.879G>A	NP_001341623.1:p.Arg293=
NM_001354695.2:c.720G>A	NP_001341624.1:p.Arg240=
NR_148940.2:n.1393G>A
NR_148941.2:n.1393G>A
NR_148942.2:n.1391G>A
NM_001354690.3:c.1062G>A	NP_001341619.1:p.Arg354=
NM_001354691.3:c.819G>A	NP_001341620.1:p.Arg273=
NM_001354692.3:c.819G>A	NP_001341621.1:p.Arg273=
NM_001354693.3:c.963G>A	NP_001341622.1:p.Arg321=
NM_001354694.3:c.879G>A	NP_001341623.1:p.Arg293=
NM_001354695.3:c.720G>A	NP_001341624.1:p.Arg240=
NM_002880.4:c.1062G>A MANE Select	NP_002871.1:p.Arg354=
NR_148940.3:n.1393G>A
NR_148941.3:n.1393G>A
NR_148942.3:n.1391G>A