Canonical Allele Identifier: CA261626

Gene: RAF1

Linked Data

• ClinVar Variation Id: 40605
• ClinVar RCV Id: RCV000208199 ; RCV000211848 ; RCV000354359 ; RCV000763094 ; RCV001217833
• dbSNP Id: rs121434594
• MyVariant Identifiers: chr3:g.12645688G>C (hg19) ; chr3:g.12604189G>C (hg38)
• PubMed: PMID:17603482 ; PMID:17603486 ; PMID:23885229

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12604189G>C , CM000665.2:g.12604189G>C	GRCh38
NC_000003.11:g.12645688G>C , CM000665.1:g.12645688G>C	GRCh37
NC_000003.10:g.12620688G>C	NCBI36
NG_007467.1:g.64991C>G , LRG_413:g.64991C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000416093.2:c.*458C>G	ENSP00000391265.2:n.*458C>G
ENST00000423275.6:c.*458C>G	ENSP00000401088.1:n.*458C>G
ENST00000432427.3:c.101C>G
ENST00000465826.6:n.372C>G
ENST00000491290.2:n.1158C>G
ENST00000684903.1:c.*458C>G	ENSP00000508612.1:n.*458C>G
ENST00000685348.1:c.*458C>G	ENSP00000510285.1:n.*458C>G
ENST00000685437.1:c.682C>G	ENSP00000508794.1:p.Pro228Ala
ENST00000685653.1:c.781C>G	ENSP00000509968.1:p.Pro261Ala
ENST00000685738.1:c.781C>G	ENSP00000510156.1:p.Pro261Ala
ENST00000685959.1:c.781C>G	ENSP00000510452.1:p.Pro261Ala
ENST00000686409.1:n.1381C>G
ENST00000686455.1:n.1144C>G
ENST00000686479.1:n.1152C>G
ENST00000686762.1:c.781C>G	ENSP00000509767.1:p.Pro261Ala
ENST00000687257.1:n.1017C>G
ENST00000687326.1:c.781C>G	ENSP00000509665.1:p.Pro261Ala
ENST00000687486.1:c.101C>G
ENST00000687505.1:n.899C>G
ENST00000687923.1:c.682C>G	ENSP00000510255.1:p.Pro228Ala
ENST00000687940.1:n.1158C>G
ENST00000688269.1:n.1389C>G
ENST00000688326.1:c.101C>G
ENST00000688444.1:n.1107C>G
ENST00000688543.1:c.682C>G	ENSP00000509612.1:p.Pro228Ala
ENST00000688625.1:c.*359C>G	ENSP00000509522.1:n.*359C>G
ENST00000688803.1:n.1012C>G
ENST00000689033.1:c.781C>G	ENSP00000508983.1:p.Pro261Ala
ENST00000689097.1:c.*458C>G	ENSP00000509756.1:n.*458C>G
ENST00000689389.1:c.781C>G	ENSP00000510213.1:p.Pro261Ala
ENST00000689418.1:c.*458C>G	ENSP00000509467.1:n.*458C>G
ENST00000689481.1:c.*458C>G	ENSP00000510248.1:n.*458C>G
ENST00000689540.1:n.931C>G
ENST00000689876.1:c.781C>G	ENSP00000508535.1:p.Pro261Ala
ENST00000689914.1:c.781C>G	ENSP00000509847.1:p.Pro261Ala
ENST00000690397.1:c.682C>G	ENSP00000508730.1:p.Pro228Ala
ENST00000690460.1:c.781C>G	ENSP00000509106.1:p.Pro261Ala
ENST00000690625.1:n.1084C>G
ENST00000691268.1:c.262-3774C>G
ENST00000691396.1:c.*574C>G	ENSP00000510712.1:n.*574C>G
ENST00000691724.1:c.781C>G	ENSP00000509255.1:p.Pro261Ala
ENST00000691779.1:c.*359C>G	ENSP00000508592.1:n.*359C>G
ENST00000691899.1:c.781C>G	ENSP00000508763.1:p.Pro261Ala
ENST00000692093.1:c.682C>G	ENSP00000509669.1:p.Pro228Ala
ENST00000692311.1:n.1154C>G
ENST00000692558.1:n.1146C>G
ENST00000692773.1:c.*458C>G	ENSP00000509055.1:n.*458C>G
ENST00000692830.1:c.*526C>G	ENSP00000509461.1:n.*526C>G
ENST00000693069.1:c.682C>G	ENSP00000510072.1:p.Pro228Ala
ENST00000693312.1:c.556C>G	ENSP00000508686.1:p.Pro186Ala
ENST00000693664.1:c.781C>G	ENSP00000509614.1:p.Pro261Ala
ENST00000693705.1:c.*458C>G	ENSP00000510697.1:n.*458C>G
ENST00000251849.9:c.781C>G MANE Select	ENSP00000251849.4:p.Pro261Ala
ENST00000442415.7:c.781C>G	ENSP00000401888.2:p.Pro261Ala
ENST00000251849.8:c.781C>G	ENSP00000251849.4:p.Pro261Ala
ENST00000416093.1:c.*359C>G	ENSP00000391265.1:n.*359C>G
ENST00000423275.5:c.*458C>G	ENSP00000401088.1:n.*458C>G
ENST00000432427.2:c.418C>G	ENSP00000398591.2:p.Pro140Ala
ENST00000442415.6:c.781C>G	ENSP00000401888.2:p.Pro261Ala
ENST00000465826.5:n.25C>G
ENST00000491290.1:n.302C>G
NM_002880.3:c.781C>G , LRG_413t1:c.781C>G	NP_002871.1:p.Pro261Ala
XM_005265355.1:c.781C>G	XP_005265412.1:p.Pro261Ala
XM_005265357.1:c.682C>G	XP_005265414.1:p.Pro228Ala
XM_005265358.3:c.538C>G	XP_005265415.1:p.Pro180Ala
XM_005265359.3:c.439C>G	XP_005265416.1:p.Pro147Ala
XM_005265360.1:c.781C>G	XP_005265417.1:p.Pro261Ala
XM_011533974.1:c.781C>G	XP_011532276.1:p.Pro261Ala
XM_011533975.1:c.538C>G	XP_011532277.1:p.Pro180Ala
NM_001354689.1:c.781C>G	NP_001341618.1:p.Pro261Ala
NM_001354690.1:c.781C>G	NP_001341619.1:p.Pro261Ala
NM_001354691.1:c.538C>G	NP_001341620.1:p.Pro180Ala
NM_001354692.1:c.538C>G	NP_001341621.1:p.Pro180Ala
NM_001354693.1:c.682C>G	NP_001341622.1:p.Pro228Ala
NM_001354694.1:c.538C>G	NP_001341623.1:p.Pro180Ala
NM_001354695.1:c.439C>G	NP_001341624.1:p.Pro147Ala
NR_148940.1:n.1196C>G
NR_148941.1:n.1196C>G
NR_148942.1:n.1196C>G
XM_011533974.3:c.781C>G	XP_011532276.1:p.Pro261Ala
XM_017006966.1:c.682C>G	XP_016862455.1:p.Pro228Ala
XR_001740227.1:n.1013C>G
NM_001354689.3:c.781C>G	NP_001341618.1:p.Pro261Ala
NM_001354690.2:c.781C>G	NP_001341619.1:p.Pro261Ala
NM_001354691.2:c.538C>G	NP_001341620.1:p.Pro180Ala
NM_001354692.2:c.538C>G	NP_001341621.1:p.Pro180Ala
NM_001354693.2:c.682C>G	NP_001341622.1:p.Pro228Ala
NM_001354694.2:c.538C>G	NP_001341623.1:p.Pro180Ala
NM_001354695.2:c.439C>G	NP_001341624.1:p.Pro147Ala
NR_148940.2:n.1112C>G
NR_148941.2:n.1112C>G
NR_148942.2:n.1112C>G
NM_001354690.3:c.781C>G	NP_001341619.1:p.Pro261Ala
NM_001354691.3:c.538C>G	NP_001341620.1:p.Pro180Ala
NM_001354692.3:c.538C>G	NP_001341621.1:p.Pro180Ala
NM_001354693.3:c.682C>G	NP_001341622.1:p.Pro228Ala
NM_001354694.3:c.538C>G	NP_001341623.1:p.Pro180Ala
NM_001354695.3:c.439C>G	NP_001341624.1:p.Pro147Ala
NM_002880.4:c.781C>G MANE Select	NP_002871.1:p.Pro261Ala
NR_148940.3:n.1112C>G
NR_148941.3:n.1112C>G
NR_148942.3:n.1112C>G