Canonical Allele Identifier: CA351502387

Gene: RAF1

Linked Data

• MyVariant Identifiers: chr3:g.12632423T>C (hg19) ; chr3:g.12590924T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12590924T>C , CM000665.2:g.12590924T>C	GRCh38
NC_000003.11:g.12632423T>C , CM000665.1:g.12632423T>C	GRCh37
NC_000003.10:g.12607423T>C	NCBI36
NG_007467.1:g.78256A>G , LRG_413:g.78256A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*909A>G	ENSP00000401088.1:n.*909A>G
ENST00000432427.3:c.561A>G
ENST00000460610.2:n.38A>G
ENST00000465826.6:n.835A>G
ENST00000475353.2:n.1166A>G
ENST00000494557.2:n.1055A>G
ENST00000684903.1:c.*921A>G	ENSP00000508612.1:n.*921A>G
ENST00000685348.1:c.*921A>G	ENSP00000510285.1:n.*921A>G
ENST00000685437.1:c.1145A>G	ENSP00000508794.1:p.Asp382Gly
ENST00000685653.1:c.1244A>G	ENSP00000509968.1:p.Asp415Gly
ENST00000685738.1:c.*208A>G	ENSP00000510156.1:n.*208A>G
ENST00000686409.1:n.2295A>G
ENST00000686455.1:n.1607A>G
ENST00000686762.1:c.1244A>G	ENSP00000509767.1:p.Asp415Gly
ENST00000687257.1:n.1480A>G
ENST00000687326.1:c.*178A>G	ENSP00000509665.1:n.*178A>G
ENST00000687505.1:n.1362A>G
ENST00000687923.1:c.1133A>G	ENSP00000510255.1:p.Asp378Gly
ENST00000687940.1:n.1621A>G
ENST00000688269.1:n.1840A>G
ENST00000688326.1:c.677A>G
ENST00000688444.1:n.1570A>G
ENST00000688543.1:c.1145A>G	ENSP00000509612.1:p.Asp382Gly
ENST00000688625.1:c.*822A>G	ENSP00000509522.1:n.*822A>G
ENST00000688803.1:n.1475A>G
ENST00000688914.1:n.230A>G
ENST00000689097.1:c.*921A>G	ENSP00000509756.1:n.*921A>G
ENST00000689389.1:c.1193+784A>G	ENSP00000510213.1:n.1193+784A>G
ENST00000689418.1:c.*921A>G	ENSP00000509467.1:n.*921A>G
ENST00000689481.1:c.*921A>G	ENSP00000510248.1:n.*921A>G
ENST00000689540.1:n.1394A>G
ENST00000689876.1:c.1244A>G	ENSP00000508535.1:p.Asp415Gly
ENST00000689914.1:c.*178A>G	ENSP00000509847.1:n.*178A>G
ENST00000690397.1:c.1133A>G	ENSP00000508730.1:p.Asp378Gly
ENST00000690460.1:c.1232A>G	ENSP00000509106.1:p.Asp411Gly
ENST00000690585.1:c.136A>G
ENST00000690625.1:n.2280A>G
ENST00000691396.1:c.*1096A>G	ENSP00000510712.1:n.*1096A>G
ENST00000691724.1:c.*201A>G	ENSP00000509255.1:n.*201A>G
ENST00000691779.1:c.*822A>G	ENSP00000508592.1:n.*822A>G
ENST00000691888.1:c.136A>G
ENST00000691899.1:c.1244A>G	ENSP00000508763.1:p.Asp415Gly
ENST00000692069.1:n.1810A>G
ENST00000692093.1:c.1145A>G	ENSP00000509669.1:p.Asp382Gly
ENST00000692311.1:n.2068A>G
ENST00000692558.1:n.1609A>G
ENST00000692773.1:c.*981A>G	ENSP00000509055.1:n.*981A>G
ENST00000692830.1:c.*989A>G	ENSP00000509461.1:n.*989A>G
ENST00000693069.1:c.*178A>G	ENSP00000510072.1:n.*178A>G
ENST00000693312.1:c.1019A>G	ENSP00000508686.1:p.Asp340Gly
ENST00000693664.1:c.1244A>G	ENSP00000509614.1:p.Asp415Gly
ENST00000693705.1:c.*921A>G	ENSP00000510697.1:n.*921A>G
ENST00000251849.9:c.1244A>G MANE Select	ENSP00000251849.4:p.Asp415Gly
ENST00000442415.7:c.1304A>G	ENSP00000401888.2:p.Asp435Gly
ENST00000251849.8:c.1244A>G	ENSP00000251849.4:p.Asp415Gly
ENST00000423275.5:c.*921A>G	ENSP00000401088.1:n.*921A>G
ENST00000432427.2:c.881A>G	ENSP00000398591.2:p.Asp294Gly
ENST00000442415.6:c.1304A>G	ENSP00000401888.2:p.Asp435Gly
ENST00000460610.1:n.201A>G
ENST00000465826.5:n.601A>G
ENST00000475353.1:n.412A>G
ENST00000494557.1:n.260A>G
NM_002880.3:c.1244A>G , LRG_413t1:c.1244A>G	NP_002871.1:p.Asp415Gly
XM_005265355.1:c.1244A>G	XP_005265412.1:p.Asp415Gly
XM_005265357.1:c.1145A>G	XP_005265414.1:p.Asp382Gly
XM_005265358.3:c.1001A>G	XP_005265415.1:p.Asp334Gly
XM_005265359.3:c.902A>G	XP_005265416.1:p.Asp301Gly
XM_005265360.1:c.1244A>G	XP_005265417.1:p.Asp415Gly
XM_011533974.1:c.1244A>G	XP_011532276.1:p.Asp415Gly
XM_011533975.1:c.1001A>G	XP_011532277.1:p.Asp334Gly
NM_001354689.1:c.1304A>G	NP_001341618.1:p.Asp435Gly
NM_001354690.1:c.1244A>G	NP_001341619.1:p.Asp415Gly
NM_001354691.1:c.1001A>G	NP_001341620.1:p.Asp334Gly
NM_001354692.1:c.1001A>G	NP_001341621.1:p.Asp334Gly
NM_001354693.1:c.1145A>G	NP_001341622.1:p.Asp382Gly
NM_001354694.1:c.1061A>G	NP_001341623.1:p.Asp354Gly
NM_001354695.1:c.902A>G	NP_001341624.1:p.Asp301Gly
NR_148940.1:n.1772A>G
NR_148941.1:n.1718A>G
NR_148942.1:n.1657A>G
XM_011533974.3:c.1244A>G	XP_011532276.1:p.Asp415Gly
XM_017006966.1:c.1145A>G	XP_016862455.1:p.Asp382Gly
NM_001354689.3:c.1304A>G	NP_001341618.1:p.Asp435Gly
NM_001354690.2:c.1244A>G	NP_001341619.1:p.Asp415Gly
NM_001354691.2:c.1001A>G	NP_001341620.1:p.Asp334Gly
NM_001354692.2:c.1001A>G	NP_001341621.1:p.Asp334Gly
NM_001354693.2:c.1145A>G	NP_001341622.1:p.Asp382Gly
NM_001354694.2:c.1061A>G	NP_001341623.1:p.Asp354Gly
NM_001354695.2:c.902A>G	NP_001341624.1:p.Asp301Gly
NR_148940.2:n.1688A>G
NR_148941.2:n.1634A>G
NR_148942.2:n.1573A>G
NM_001354690.3:c.1244A>G	NP_001341619.1:p.Asp415Gly
NM_001354691.3:c.1001A>G	NP_001341620.1:p.Asp334Gly
NM_001354692.3:c.1001A>G	NP_001341621.1:p.Asp334Gly
NM_001354693.3:c.1145A>G	NP_001341622.1:p.Asp382Gly
NM_001354694.3:c.1061A>G	NP_001341623.1:p.Asp354Gly
NM_001354695.3:c.902A>G	NP_001341624.1:p.Asp301Gly
NM_002880.4:c.1244A>G MANE Select	NP_002871.1:p.Asp415Gly
NR_148940.3:n.1688A>G
NR_148941.3:n.1634A>G
NR_148942.3:n.1573A>G