Canonical Allele Identifier: CA351507330

Gene: RAF1

Linked Data

• ClinVar Variation Id: 1061963
• ClinVar RCV Id: RCV001371630
• dbSNP Id: rs2125377494
• MyVariant Identifiers: chr3:g.12641213G>C (hg19) ; chr3:g.12599714G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12599714G>C , CM000665.2:g.12599714G>C	GRCh38
NC_000003.11:g.12641213G>C , CM000665.1:g.12641213G>C	GRCh37
NC_000003.10:g.12616213G>C	NCBI36
NG_007467.1:g.69466C>G , LRG_413:g.69466C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000423275.6:c.*750C>G	ENSP00000401088.1:n.*750C>G
ENST00000432427.3:c.405C>G
ENST00000465826.6:n.676C>G
ENST00000491290.2:n.1462C>G
ENST00000684903.1:c.*762C>G	ENSP00000508612.1:n.*762C>G
ENST00000685348.1:c.*762C>G	ENSP00000510285.1:n.*762C>G
ENST00000685437.1:c.986C>G	ENSP00000508794.1:p.Thr329Ser
ENST00000685653.1:c.1085C>G	ENSP00000509968.1:p.Thr362Ser
ENST00000685738.1:c.1085C>G	ENSP00000510156.1:p.Thr362Ser
ENST00000686409.1:n.2136C>G
ENST00000686455.1:n.1448C>G
ENST00000686479.1:n.1456C>G
ENST00000686762.1:c.1085C>G	ENSP00000509767.1:p.Thr362Ser
ENST00000687257.1:n.1321C>G
ENST00000687326.1:c.1085C>G	ENSP00000509665.1:p.Thr362Ser
ENST00000687486.1:c.277C>G
ENST00000687505.1:n.1203C>G
ENST00000687923.1:c.986C>G	ENSP00000510255.1:p.Thr329Ser
ENST00000687940.1:n.1462C>G
ENST00000688269.1:n.1681C>G
ENST00000688326.1:c.405C>G
ENST00000688444.1:n.1411C>G
ENST00000688543.1:c.986C>G	ENSP00000509612.1:p.Thr329Ser
ENST00000688625.1:c.*663C>G	ENSP00000509522.1:n.*663C>G
ENST00000688803.1:n.1316C>G
ENST00000688914.1:n.71C>G
ENST00000689097.1:c.*762C>G	ENSP00000509756.1:n.*762C>G
ENST00000689389.1:c.1085C>G	ENSP00000510213.1:p.Thr362Ser
ENST00000689418.1:c.*762C>G	ENSP00000509467.1:n.*762C>G
ENST00000689481.1:c.*762C>G	ENSP00000510248.1:n.*762C>G
ENST00000689540.1:n.1235C>G
ENST00000689876.1:c.1085C>G	ENSP00000508535.1:p.Thr362Ser
ENST00000689914.1:c.1085C>G	ENSP00000509847.1:p.Thr362Ser
ENST00000690397.1:c.974C>G	ENSP00000508730.1:p.Thr325Ser
ENST00000690460.1:c.1073C>G	ENSP00000509106.1:p.Thr358Ser
ENST00000690625.1:n.1388C>G
ENST00000691268.1:c.512C>G
ENST00000691396.1:c.*878C>G	ENSP00000510712.1:n.*878C>G
ENST00000691724.1:c.*42C>G	ENSP00000509255.1:n.*42C>G
ENST00000691779.1:c.*663C>G	ENSP00000508592.1:n.*663C>G
ENST00000691899.1:c.1085C>G	ENSP00000508763.1:p.Thr362Ser
ENST00000692069.1:n.1651C>G
ENST00000692093.1:c.986C>G	ENSP00000509669.1:p.Thr329Ser
ENST00000692311.1:n.1909C>G
ENST00000692558.1:n.1450C>G
ENST00000692773.1:c.*822C>G	ENSP00000509055.1:n.*822C>G
ENST00000692830.1:c.*830C>G	ENSP00000509461.1:n.*830C>G
ENST00000693069.1:c.986C>G	ENSP00000510072.1:p.Thr329Ser
ENST00000693312.1:c.860C>G	ENSP00000508686.1:p.Thr287Ser
ENST00000693664.1:c.1085C>G	ENSP00000509614.1:p.Thr362Ser
ENST00000693705.1:c.*762C>G	ENSP00000510697.1:n.*762C>G
ENST00000251849.9:c.1085C>G MANE Select	ENSP00000251849.4:p.Thr362Ser
ENST00000442415.7:c.1145C>G	ENSP00000401888.2:p.Thr382Ser
ENST00000251849.8:c.1085C>G	ENSP00000251849.4:p.Thr362Ser
ENST00000423275.5:c.*762C>G	ENSP00000401088.1:n.*762C>G
ENST00000432427.2:c.722C>G	ENSP00000398591.2:p.Thr241Ser
ENST00000442415.6:c.1145C>G	ENSP00000401888.2:p.Thr382Ser
ENST00000460610.1:n.42C>G
ENST00000465826.5:n.329C>G
NM_002880.3:c.1085C>G , LRG_413t1:c.1085C>G	NP_002871.1:p.Thr362Ser
XM_005265355.1:c.1085C>G	XP_005265412.1:p.Thr362Ser
XM_005265357.1:c.986C>G	XP_005265414.1:p.Thr329Ser
XM_005265358.3:c.842C>G	XP_005265415.1:p.Thr281Ser
XM_005265359.3:c.743C>G	XP_005265416.1:p.Thr248Ser
XM_005265360.1:c.1085C>G	XP_005265417.1:p.Thr362Ser
XM_011533974.1:c.1085C>G	XP_011532276.1:p.Thr362Ser
XM_011533975.1:c.842C>G	XP_011532277.1:p.Thr281Ser
NM_001354689.1:c.1145C>G	NP_001341618.1:p.Thr382Ser
NM_001354690.1:c.1085C>G	NP_001341619.1:p.Thr362Ser
NM_001354691.1:c.842C>G	NP_001341620.1:p.Thr281Ser
NM_001354692.1:c.842C>G	NP_001341621.1:p.Thr281Ser
NM_001354693.1:c.986C>G	NP_001341622.1:p.Thr329Ser
NM_001354694.1:c.902C>G	NP_001341623.1:p.Thr301Ser
NM_001354695.1:c.743C>G	NP_001341624.1:p.Thr248Ser
NR_148940.1:n.1500C>G
NR_148941.1:n.1500C>G
NR_148942.1:n.1498C>G
XM_011533974.3:c.1085C>G	XP_011532276.1:p.Thr362Ser
XM_017006966.1:c.986C>G	XP_016862455.1:p.Thr329Ser
XR_001740227.1:n.1317C>G
NM_001354689.3:c.1145C>G	NP_001341618.1:p.Thr382Ser
NM_001354690.2:c.1085C>G	NP_001341619.1:p.Thr362Ser
NM_001354691.2:c.842C>G	NP_001341620.1:p.Thr281Ser
NM_001354692.2:c.842C>G	NP_001341621.1:p.Thr281Ser
NM_001354693.2:c.986C>G	NP_001341622.1:p.Thr329Ser
NM_001354694.2:c.902C>G	NP_001341623.1:p.Thr301Ser
NM_001354695.2:c.743C>G	NP_001341624.1:p.Thr248Ser
NR_148940.2:n.1416C>G
NR_148941.2:n.1416C>G
NR_148942.2:n.1414C>G
NM_001354690.3:c.1085C>G	NP_001341619.1:p.Thr362Ser
NM_001354691.3:c.842C>G	NP_001341620.1:p.Thr281Ser
NM_001354692.3:c.842C>G	NP_001341621.1:p.Thr281Ser
NM_001354693.3:c.986C>G	NP_001341622.1:p.Thr329Ser
NM_001354694.3:c.902C>G	NP_001341623.1:p.Thr301Ser
NM_001354695.3:c.743C>G	NP_001341624.1:p.Thr248Ser
NM_002880.4:c.1085C>G MANE Select	NP_002871.1:p.Thr362Ser
NR_148940.3:n.1416C>G
NR_148941.3:n.1416C>G
NR_148942.3:n.1414C>G