Canonical Allele Identifier: CA432273187

Gene: RAF1

Linked Data

• dbSNP Id: rs2125343614
• MyVariant Identifiers: chr3:g.12632464C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12590965C>G , CM000665.2:g.12590965C>G	GRCh38
NC_000003.11:g.12632464C>G , CM000665.1:g.12632464C>G	GRCh37
NC_000003.10:g.12607464C>G	NCBI36
NG_007467.1:g.78215G>C , LRG_413:g.78215G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*868G>C	ENSP00000401088.1:n.*868G>C
ENST00000432427.3:c.520G>C
ENST00000465826.6:n.794G>C
ENST00000475353.2:n.1125G>C
ENST00000494557.2:n.1014G>C
ENST00000684903.1:c.*880G>C	ENSP00000508612.1:n.*880G>C
ENST00000685348.1:c.*880G>C	ENSP00000510285.1:n.*880G>C
ENST00000685437.1:c.1104G>C	ENSP00000508794.1:p.Arg368=
ENST00000685653.1:c.1203G>C	ENSP00000509968.1:p.Arg401=
ENST00000685738.1:c.*167G>C	ENSP00000510156.1:n.*167G>C
ENST00000686409.1:n.2254G>C
ENST00000686455.1:n.1566G>C
ENST00000686762.1:c.1203G>C	ENSP00000509767.1:p.Arg401=
ENST00000687257.1:n.1439G>C
ENST00000687326.1:c.*137G>C	ENSP00000509665.1:n.*137G>C
ENST00000687505.1:n.1321G>C
ENST00000687923.1:c.1092G>C	ENSP00000510255.1:p.Arg364=
ENST00000687940.1:n.1580G>C
ENST00000688269.1:n.1799G>C
ENST00000688326.1:c.636G>C
ENST00000688444.1:n.1529G>C
ENST00000688543.1:c.1104G>C	ENSP00000509612.1:p.Arg368=
ENST00000688625.1:c.*781G>C	ENSP00000509522.1:n.*781G>C
ENST00000688803.1:n.1434G>C
ENST00000688914.1:n.189G>C
ENST00000689097.1:c.*880G>C	ENSP00000509756.1:n.*880G>C
ENST00000689389.1:c.1193+743G>C	ENSP00000510213.1:n.1193+743G>C
ENST00000689418.1:c.*880G>C	ENSP00000509467.1:n.*880G>C
ENST00000689481.1:c.*880G>C	ENSP00000510248.1:n.*880G>C
ENST00000689540.1:n.1353G>C
ENST00000689876.1:c.1203G>C	ENSP00000508535.1:p.Arg401=
ENST00000689914.1:c.*137G>C	ENSP00000509847.1:n.*137G>C
ENST00000690397.1:c.1092G>C	ENSP00000508730.1:p.Arg364=
ENST00000690460.1:c.1191G>C	ENSP00000509106.1:p.Arg397=
ENST00000690585.1:c.95G>C
ENST00000690625.1:n.2239G>C
ENST00000691396.1:c.*1055G>C	ENSP00000510712.1:n.*1055G>C
ENST00000691724.1:c.*160G>C	ENSP00000509255.1:n.*160G>C
ENST00000691779.1:c.*781G>C	ENSP00000508592.1:n.*781G>C
ENST00000691888.1:c.95G>C
ENST00000691899.1:c.1203G>C	ENSP00000508763.1:p.Arg401=
ENST00000692069.1:n.1769G>C
ENST00000692093.1:c.1104G>C	ENSP00000509669.1:p.Arg368=
ENST00000692311.1:n.2027G>C
ENST00000692558.1:n.1568G>C
ENST00000692773.1:c.*940G>C	ENSP00000509055.1:n.*940G>C
ENST00000692830.1:c.*948G>C	ENSP00000509461.1:n.*948G>C
ENST00000693069.1:c.*137G>C	ENSP00000510072.1:n.*137G>C
ENST00000693312.1:c.978G>C	ENSP00000508686.1:p.Arg326=
ENST00000693664.1:c.1203G>C	ENSP00000509614.1:p.Arg401=
ENST00000693705.1:c.*880G>C	ENSP00000510697.1:n.*880G>C
ENST00000251849.9:c.1203G>C MANE Select	ENSP00000251849.4:p.Arg401=
ENST00000442415.7:c.1263G>C	ENSP00000401888.2:p.Arg421=
ENST00000251849.8:c.1203G>C	ENSP00000251849.4:p.Arg401=
ENST00000423275.5:c.*880G>C	ENSP00000401088.1:n.*880G>C
ENST00000432427.2:c.840G>C	ENSP00000398591.2:p.Arg280=
ENST00000442415.6:c.1263G>C	ENSP00000401888.2:p.Arg421=
ENST00000460610.1:n.160G>C
ENST00000465826.5:n.560G>C
ENST00000475353.1:n.371G>C
ENST00000494557.1:n.219G>C
NM_002880.3:c.1203G>C , LRG_413t1:c.1203G>C	NP_002871.1:p.Arg401=
XM_005265355.1:c.1203G>C	XP_005265412.1:p.Arg401=
XM_005265357.1:c.1104G>C	XP_005265414.1:p.Arg368=
XM_005265358.3:c.960G>C	XP_005265415.1:p.Arg320=
XM_005265359.3:c.861G>C	XP_005265416.1:p.Arg287=
XM_005265360.1:c.1203G>C	XP_005265417.1:p.Arg401=
XM_011533974.1:c.1203G>C	XP_011532276.1:p.Arg401=
XM_011533975.1:c.960G>C	XP_011532277.1:p.Arg320=
NM_001354689.1:c.1263G>C	NP_001341618.1:p.Arg421=
NM_001354690.1:c.1203G>C	NP_001341619.1:p.Arg401=
NM_001354691.1:c.960G>C	NP_001341620.1:p.Arg320=
NM_001354692.1:c.960G>C	NP_001341621.1:p.Arg320=
NM_001354693.1:c.1104G>C	NP_001341622.1:p.Arg368=
NM_001354694.1:c.1020G>C	NP_001341623.1:p.Arg340=
NM_001354695.1:c.861G>C	NP_001341624.1:p.Arg287=
NR_148940.1:n.1731G>C
NR_148941.1:n.1677G>C
NR_148942.1:n.1616G>C
XM_011533974.3:c.1203G>C	XP_011532276.1:p.Arg401=
XM_017006966.1:c.1104G>C	XP_016862455.1:p.Arg368=
XR_001740227.1:n.1494G>C
NM_001354689.3:c.1263G>C	NP_001341618.1:p.Arg421=
NM_001354690.2:c.1203G>C	NP_001341619.1:p.Arg401=
NM_001354691.2:c.960G>C	NP_001341620.1:p.Arg320=
NM_001354692.2:c.960G>C	NP_001341621.1:p.Arg320=
NM_001354693.2:c.1104G>C	NP_001341622.1:p.Arg368=
NM_001354694.2:c.1020G>C	NP_001341623.1:p.Arg340=
NM_001354695.2:c.861G>C	NP_001341624.1:p.Arg287=
NR_148940.2:n.1647G>C
NR_148941.2:n.1593G>C
NR_148942.2:n.1532G>C
NM_001354690.3:c.1203G>C	NP_001341619.1:p.Arg401=
NM_001354691.3:c.960G>C	NP_001341620.1:p.Arg320=
NM_001354692.3:c.960G>C	NP_001341621.1:p.Arg320=
NM_001354693.3:c.1104G>C	NP_001341622.1:p.Arg368=
NM_001354694.3:c.1020G>C	NP_001341623.1:p.Arg340=
NM_001354695.3:c.861G>C	NP_001341624.1:p.Arg287=
NM_002880.4:c.1203G>C MANE Select	NP_002871.1:p.Arg401=
NR_148940.3:n.1647G>C
NR_148941.3:n.1593G>C
NR_148942.3:n.1532G>C