Canonical Allele Identifier: CA351502630

Gene: RAF1

Linked Data

• MyVariant Identifiers: chr3:g.12632455G>C (hg19) ; chr3:g.12590956G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12590956G>C , CM000665.2:g.12590956G>C	GRCh38
NC_000003.11:g.12632455G>C , CM000665.1:g.12632455G>C	GRCh37
NC_000003.10:g.12607455G>C	NCBI36
NG_007467.1:g.78224C>G , LRG_413:g.78224C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*877C>G	ENSP00000401088.1:n.*877C>G
ENST00000432427.3:c.529C>G
ENST00000460610.2:n.6C>G
ENST00000465826.6:n.803C>G
ENST00000475353.2:n.1134C>G
ENST00000494557.2:n.1023C>G
ENST00000684903.1:c.*889C>G	ENSP00000508612.1:n.*889C>G
ENST00000685348.1:c.*889C>G	ENSP00000510285.1:n.*889C>G
ENST00000685437.1:c.1113C>G	ENSP00000508794.1:p.Asn371Lys
ENST00000685653.1:c.1212C>G	ENSP00000509968.1:p.Asn404Lys
ENST00000685738.1:c.*176C>G	ENSP00000510156.1:n.*176C>G
ENST00000686409.1:n.2263C>G
ENST00000686455.1:n.1575C>G
ENST00000686762.1:c.1212C>G	ENSP00000509767.1:p.Asn404Lys
ENST00000687257.1:n.1448C>G
ENST00000687326.1:c.*146C>G	ENSP00000509665.1:n.*146C>G
ENST00000687505.1:n.1330C>G
ENST00000687923.1:c.1101C>G	ENSP00000510255.1:p.Asn367Lys
ENST00000687940.1:n.1589C>G
ENST00000688269.1:n.1808C>G
ENST00000688326.1:c.645C>G
ENST00000688444.1:n.1538C>G
ENST00000688543.1:c.1113C>G	ENSP00000509612.1:p.Asn371Lys
ENST00000688625.1:c.*790C>G	ENSP00000509522.1:n.*790C>G
ENST00000688803.1:n.1443C>G
ENST00000688914.1:n.198C>G
ENST00000689097.1:c.*889C>G	ENSP00000509756.1:n.*889C>G
ENST00000689389.1:c.1193+752C>G	ENSP00000510213.1:n.1193+752C>G
ENST00000689418.1:c.*889C>G	ENSP00000509467.1:n.*889C>G
ENST00000689481.1:c.*889C>G	ENSP00000510248.1:n.*889C>G
ENST00000689540.1:n.1362C>G
ENST00000689876.1:c.1212C>G	ENSP00000508535.1:p.Asn404Lys
ENST00000689914.1:c.*146C>G	ENSP00000509847.1:n.*146C>G
ENST00000690397.1:c.1101C>G	ENSP00000508730.1:p.Asn367Lys
ENST00000690460.1:c.1200C>G	ENSP00000509106.1:p.Asn400Lys
ENST00000690585.1:c.104C>G
ENST00000690625.1:n.2248C>G
ENST00000691396.1:c.*1064C>G	ENSP00000510712.1:n.*1064C>G
ENST00000691724.1:c.*169C>G	ENSP00000509255.1:n.*169C>G
ENST00000691779.1:c.*790C>G	ENSP00000508592.1:n.*790C>G
ENST00000691888.1:c.104C>G
ENST00000691899.1:c.1212C>G	ENSP00000508763.1:p.Asn404Lys
ENST00000692069.1:n.1778C>G
ENST00000692093.1:c.1113C>G	ENSP00000509669.1:p.Asn371Lys
ENST00000692311.1:n.2036C>G
ENST00000692558.1:n.1577C>G
ENST00000692773.1:c.*949C>G	ENSP00000509055.1:n.*949C>G
ENST00000692830.1:c.*957C>G	ENSP00000509461.1:n.*957C>G
ENST00000693069.1:c.*146C>G	ENSP00000510072.1:n.*146C>G
ENST00000693312.1:c.987C>G	ENSP00000508686.1:p.Asn329Lys
ENST00000693664.1:c.1212C>G	ENSP00000509614.1:p.Asn404Lys
ENST00000693705.1:c.*889C>G	ENSP00000510697.1:n.*889C>G
ENST00000251849.9:c.1212C>G MANE Select	ENSP00000251849.4:p.Asn404Lys
ENST00000442415.7:c.1272C>G	ENSP00000401888.2:p.Asn424Lys
ENST00000251849.8:c.1212C>G	ENSP00000251849.4:p.Asn404Lys
ENST00000423275.5:c.*889C>G	ENSP00000401088.1:n.*889C>G
ENST00000432427.2:c.849C>G	ENSP00000398591.2:p.Asn283Lys
ENST00000442415.6:c.1272C>G	ENSP00000401888.2:p.Asn424Lys
ENST00000460610.1:n.169C>G
ENST00000465826.5:n.569C>G
ENST00000475353.1:n.380C>G
ENST00000494557.1:n.228C>G
NM_002880.3:c.1212C>G , LRG_413t1:c.1212C>G	NP_002871.1:p.Asn404Lys
XM_005265355.1:c.1212C>G	XP_005265412.1:p.Asn404Lys
XM_005265357.1:c.1113C>G	XP_005265414.1:p.Asn371Lys
XM_005265358.3:c.969C>G	XP_005265415.1:p.Asn323Lys
XM_005265359.3:c.870C>G	XP_005265416.1:p.Asn290Lys
XM_005265360.1:c.1212C>G	XP_005265417.1:p.Asn404Lys
XM_011533974.1:c.1212C>G	XP_011532276.1:p.Asn404Lys
XM_011533975.1:c.969C>G	XP_011532277.1:p.Asn323Lys
NM_001354689.1:c.1272C>G	NP_001341618.1:p.Asn424Lys
NM_001354690.1:c.1212C>G	NP_001341619.1:p.Asn404Lys
NM_001354691.1:c.969C>G	NP_001341620.1:p.Asn323Lys
NM_001354692.1:c.969C>G	NP_001341621.1:p.Asn323Lys
NM_001354693.1:c.1113C>G	NP_001341622.1:p.Asn371Lys
NM_001354694.1:c.1029C>G	NP_001341623.1:p.Asn343Lys
NM_001354695.1:c.870C>G	NP_001341624.1:p.Asn290Lys
NR_148940.1:n.1740C>G
NR_148941.1:n.1686C>G
NR_148942.1:n.1625C>G
XM_011533974.3:c.1212C>G	XP_011532276.1:p.Asn404Lys
XM_017006966.1:c.1113C>G	XP_016862455.1:p.Asn371Lys
XR_001740227.1:n.1503C>G
NM_001354689.3:c.1272C>G	NP_001341618.1:p.Asn424Lys
NM_001354690.2:c.1212C>G	NP_001341619.1:p.Asn404Lys
NM_001354691.2:c.969C>G	NP_001341620.1:p.Asn323Lys
NM_001354692.2:c.969C>G	NP_001341621.1:p.Asn323Lys
NM_001354693.2:c.1113C>G	NP_001341622.1:p.Asn371Lys
NM_001354694.2:c.1029C>G	NP_001341623.1:p.Asn343Lys
NM_001354695.2:c.870C>G	NP_001341624.1:p.Asn290Lys
NR_148940.2:n.1656C>G
NR_148941.2:n.1602C>G
NR_148942.2:n.1541C>G
NM_001354690.3:c.1212C>G	NP_001341619.1:p.Asn404Lys
NM_001354691.3:c.969C>G	NP_001341620.1:p.Asn323Lys
NM_001354692.3:c.969C>G	NP_001341621.1:p.Asn323Lys
NM_001354693.3:c.1113C>G	NP_001341622.1:p.Asn371Lys
NM_001354694.3:c.1029C>G	NP_001341623.1:p.Asn343Lys
NM_001354695.3:c.870C>G	NP_001341624.1:p.Asn290Lys
NM_002880.4:c.1212C>G MANE Select	NP_002871.1:p.Asn404Lys
NR_148940.3:n.1656C>G
NR_148941.3:n.1602C>G
NR_148942.3:n.1541C>G