Canonical Allele Identifier: CA351507446

Gene: RAF1

Linked Data

• dbSNP Id: rs1205523835
• gnomAD v2: 3-12641220-A-C
• gnomAD v4: 3-12599721-A-C
• MyVariant Identifiers: chr3:g.12641220A>C (hg19) ; chr3:g.12599721A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12599721A>C , CM000665.2:g.12599721A>C	GRCh38
NC_000003.11:g.12641220A>C , CM000665.1:g.12641220A>C	GRCh37
NC_000003.10:g.12616220A>C	NCBI36
NG_007467.1:g.69459T>G , LRG_413:g.69459T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000423275.6:c.*743T>G	ENSP00000401088.1:n.*743T>G
ENST00000432427.3:c.398T>G
ENST00000465826.6:n.669T>G
ENST00000491290.2:n.1455T>G
ENST00000684903.1:c.*755T>G	ENSP00000508612.1:n.*755T>G
ENST00000685348.1:c.*755T>G	ENSP00000510285.1:n.*755T>G
ENST00000685437.1:c.979T>G	ENSP00000508794.1:p.Phe327Val
ENST00000685653.1:c.1078T>G	ENSP00000509968.1:p.Phe360Val
ENST00000685738.1:c.1078T>G	ENSP00000510156.1:p.Phe360Val
ENST00000686409.1:n.2129T>G
ENST00000686455.1:n.1441T>G
ENST00000686479.1:n.1449T>G
ENST00000686762.1:c.1078T>G	ENSP00000509767.1:p.Phe360Val
ENST00000687257.1:n.1314T>G
ENST00000687326.1:c.1078T>G	ENSP00000509665.1:p.Phe360Val
ENST00000687486.1:c.270T>G
ENST00000687505.1:n.1196T>G
ENST00000687923.1:c.979T>G	ENSP00000510255.1:p.Phe327Val
ENST00000687940.1:n.1455T>G
ENST00000688269.1:n.1674T>G
ENST00000688326.1:c.398T>G
ENST00000688444.1:n.1404T>G
ENST00000688543.1:c.979T>G	ENSP00000509612.1:p.Phe327Val
ENST00000688625.1:c.*656T>G	ENSP00000509522.1:n.*656T>G
ENST00000688803.1:n.1309T>G
ENST00000688914.1:n.64T>G
ENST00000689097.1:c.*755T>G	ENSP00000509756.1:n.*755T>G
ENST00000689389.1:c.1078T>G	ENSP00000510213.1:p.Phe360Val
ENST00000689418.1:c.*755T>G	ENSP00000509467.1:n.*755T>G
ENST00000689481.1:c.*755T>G	ENSP00000510248.1:n.*755T>G
ENST00000689540.1:n.1228T>G
ENST00000689876.1:c.1078T>G	ENSP00000508535.1:p.Phe360Val
ENST00000689914.1:c.1078T>G	ENSP00000509847.1:p.Phe360Val
ENST00000690397.1:c.967T>G	ENSP00000508730.1:p.Phe323Val
ENST00000690460.1:c.1066T>G	ENSP00000509106.1:p.Phe356Val
ENST00000690625.1:n.1381T>G
ENST00000691268.1:c.505T>G
ENST00000691396.1:c.*871T>G	ENSP00000510712.1:n.*871T>G
ENST00000691724.1:c.*35T>G	ENSP00000509255.1:n.*35T>G
ENST00000691779.1:c.*656T>G	ENSP00000508592.1:n.*656T>G
ENST00000691899.1:c.1078T>G	ENSP00000508763.1:p.Phe360Val
ENST00000692069.1:n.1644T>G
ENST00000692093.1:c.979T>G	ENSP00000509669.1:p.Phe327Val
ENST00000692311.1:n.1902T>G
ENST00000692558.1:n.1443T>G
ENST00000692773.1:c.*815T>G	ENSP00000509055.1:n.*815T>G
ENST00000692830.1:c.*823T>G	ENSP00000509461.1:n.*823T>G
ENST00000693069.1:c.979T>G	ENSP00000510072.1:p.Phe327Val
ENST00000693312.1:c.853T>G	ENSP00000508686.1:p.Phe285Val
ENST00000693664.1:c.1078T>G	ENSP00000509614.1:p.Phe360Val
ENST00000693705.1:c.*755T>G	ENSP00000510697.1:n.*755T>G
ENST00000251849.9:c.1078T>G MANE Select	ENSP00000251849.4:p.Phe360Val
ENST00000442415.7:c.1138T>G	ENSP00000401888.2:p.Phe380Val
ENST00000251849.8:c.1078T>G	ENSP00000251849.4:p.Phe360Val
ENST00000423275.5:c.*755T>G	ENSP00000401088.1:n.*755T>G
ENST00000432427.2:c.715T>G	ENSP00000398591.2:p.Phe239Val
ENST00000442415.6:c.1138T>G	ENSP00000401888.2:p.Phe380Val
ENST00000460610.1:n.35T>G
ENST00000465826.5:n.322T>G
NM_002880.3:c.1078T>G , LRG_413t1:c.1078T>G	NP_002871.1:p.Phe360Val
XM_005265355.1:c.1078T>G	XP_005265412.1:p.Phe360Val
XM_005265357.1:c.979T>G	XP_005265414.1:p.Phe327Val
XM_005265358.3:c.835T>G	XP_005265415.1:p.Phe279Val
XM_005265359.3:c.736T>G	XP_005265416.1:p.Phe246Val
XM_005265360.1:c.1078T>G	XP_005265417.1:p.Phe360Val
XM_011533974.1:c.1078T>G	XP_011532276.1:p.Phe360Val
XM_011533975.1:c.835T>G	XP_011532277.1:p.Phe279Val
NM_001354689.1:c.1138T>G	NP_001341618.1:p.Phe380Val
NM_001354690.1:c.1078T>G	NP_001341619.1:p.Phe360Val
NM_001354691.1:c.835T>G	NP_001341620.1:p.Phe279Val
NM_001354692.1:c.835T>G	NP_001341621.1:p.Phe279Val
NM_001354693.1:c.979T>G	NP_001341622.1:p.Phe327Val
NM_001354694.1:c.895T>G	NP_001341623.1:p.Phe299Val
NM_001354695.1:c.736T>G	NP_001341624.1:p.Phe246Val
NR_148940.1:n.1493T>G
NR_148941.1:n.1493T>G
NR_148942.1:n.1491T>G
XM_011533974.3:c.1078T>G	XP_011532276.1:p.Phe360Val
XM_017006966.1:c.979T>G	XP_016862455.1:p.Phe327Val
XR_001740227.1:n.1310T>G
NM_001354689.3:c.1138T>G	NP_001341618.1:p.Phe380Val
NM_001354690.2:c.1078T>G	NP_001341619.1:p.Phe360Val
NM_001354691.2:c.835T>G	NP_001341620.1:p.Phe279Val
NM_001354692.2:c.835T>G	NP_001341621.1:p.Phe279Val
NM_001354693.2:c.979T>G	NP_001341622.1:p.Phe327Val
NM_001354694.2:c.895T>G	NP_001341623.1:p.Phe299Val
NM_001354695.2:c.736T>G	NP_001341624.1:p.Phe246Val
NR_148940.2:n.1409T>G
NR_148941.2:n.1409T>G
NR_148942.2:n.1407T>G
NM_001354690.3:c.1078T>G	NP_001341619.1:p.Phe360Val
NM_001354691.3:c.835T>G	NP_001341620.1:p.Phe279Val
NM_001354692.3:c.835T>G	NP_001341621.1:p.Phe279Val
NM_001354693.3:c.979T>G	NP_001341622.1:p.Phe327Val
NM_001354694.3:c.895T>G	NP_001341623.1:p.Phe299Val
NM_001354695.3:c.736T>G	NP_001341624.1:p.Phe246Val
NM_002880.4:c.1078T>G MANE Select	NP_002871.1:p.Phe360Val
NR_148940.3:n.1409T>G
NR_148941.3:n.1409T>G
NR_148942.3:n.1407T>G