Canonical Allele Identifier: CA69616839

Gene: RAF1

Linked Data

• dbSNP Id: rs965966296
• MyVariant Identifiers: chr3:g.12641730C>A (hg19) ; chr3:g.12600231C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12600231C>A , CM000665.2:g.12600231C>A	GRCh38
NC_000003.11:g.12641730C>A , CM000665.1:g.12641730C>A	GRCh37
NC_000003.10:g.12616730C>A	NCBI36
NG_007467.1:g.68949G>T , LRG_413:g.68949G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*576G>T	ENSP00000401088.1:n.*576G>T
ENST00000432427.3:c.231G>T
ENST00000465826.6:n.502G>T
ENST00000491290.2:n.1288G>T
ENST00000684903.1:c.*588G>T	ENSP00000508612.1:n.*588G>T
ENST00000685348.1:c.*588G>T	ENSP00000510285.1:n.*588G>T
ENST00000685437.1:c.812G>T	ENSP00000508794.1:p.Gly271Val
ENST00000685438.1:n.675G>T
ENST00000685653.1:c.911G>T	ENSP00000509968.1:p.Gly304Val
ENST00000685738.1:c.911G>T	ENSP00000510156.1:p.Gly304Val
ENST00000686409.1:n.1619G>T
ENST00000686455.1:n.1274G>T
ENST00000686479.1:n.1282G>T
ENST00000686762.1:c.911G>T	ENSP00000509767.1:p.Gly304Val
ENST00000687257.1:n.1147G>T
ENST00000687326.1:c.911G>T	ENSP00000509665.1:p.Gly304Val
ENST00000687486.1:c.182+157G>T
ENST00000687505.1:n.1029G>T
ENST00000687923.1:c.812G>T	ENSP00000510255.1:p.Gly271Val
ENST00000687940.1:n.1288G>T
ENST00000688269.1:n.1507G>T
ENST00000688326.1:c.231G>T
ENST00000688444.1:n.1237G>T
ENST00000688543.1:c.812G>T	ENSP00000509612.1:p.Gly271Val
ENST00000688625.1:c.*489G>T	ENSP00000509522.1:n.*489G>T
ENST00000688803.1:n.1142G>T
ENST00000689097.1:c.*588G>T	ENSP00000509756.1:n.*588G>T
ENST00000689389.1:c.911G>T	ENSP00000510213.1:p.Gly304Val
ENST00000689418.1:c.*588G>T	ENSP00000509467.1:n.*588G>T
ENST00000689481.1:c.*588G>T	ENSP00000510248.1:n.*588G>T
ENST00000689540.1:n.1061G>T
ENST00000689876.1:c.911G>T	ENSP00000508535.1:p.Gly304Val
ENST00000689914.1:c.911G>T	ENSP00000509847.1:p.Gly304Val
ENST00000690397.1:c.800G>T	ENSP00000508730.1:p.Gly267Val
ENST00000690460.1:c.899G>T	ENSP00000509106.1:p.Gly300Val
ENST00000690625.1:n.1214G>T
ENST00000691268.1:c.338G>T
ENST00000691396.1:c.*704G>T	ENSP00000510712.1:n.*704G>T
ENST00000691724.1:c.911G>T	ENSP00000509255.1:p.Gly304Val
ENST00000691779.1:c.*489G>T	ENSP00000508592.1:n.*489G>T
ENST00000691899.1:c.911G>T	ENSP00000508763.1:p.Gly304Val
ENST00000692069.1:n.1134G>T
ENST00000692093.1:c.812G>T	ENSP00000509669.1:p.Gly271Val
ENST00000692311.1:n.1392G>T
ENST00000692558.1:n.1276G>T
ENST00000692773.1:c.*648G>T	ENSP00000509055.1:n.*648G>T
ENST00000692830.1:c.*656G>T	ENSP00000509461.1:n.*656G>T
ENST00000693069.1:c.812G>T	ENSP00000510072.1:p.Gly271Val
ENST00000693312.1:c.686G>T	ENSP00000508686.1:p.Gly229Val
ENST00000693664.1:c.911G>T	ENSP00000509614.1:p.Gly304Val
ENST00000693705.1:c.*588G>T	ENSP00000510697.1:n.*588G>T
ENST00000251849.9:c.911G>T MANE Select	ENSP00000251849.4:p.Gly304Val
ENST00000442415.7:c.971G>T	ENSP00000401888.2:p.Gly324Val
ENST00000251849.8:c.911G>T	ENSP00000251849.4:p.Gly304Val
ENST00000423275.5:c.*588G>T	ENSP00000401088.1:n.*588G>T
ENST00000432427.2:c.548G>T	ENSP00000398591.2:p.Gly183Val
ENST00000442415.6:c.971G>T	ENSP00000401888.2:p.Gly324Val
ENST00000465826.5:n.155G>T
ENST00000491290.1:n.540G>T
NM_002880.3:c.911G>T , LRG_413t1:c.911G>T	NP_002871.1:p.Gly304Val
XM_005265355.1:c.911G>T	XP_005265412.1:p.Gly304Val
XM_005265357.1:c.812G>T	XP_005265414.1:p.Gly271Val
XM_005265358.3:c.668G>T	XP_005265415.1:p.Gly223Val
XM_005265359.3:c.569G>T	XP_005265416.1:p.Gly190Val
XM_005265360.1:c.911G>T	XP_005265417.1:p.Gly304Val
XM_011533974.1:c.911G>T	XP_011532276.1:p.Gly304Val
XM_011533975.1:c.668G>T	XP_011532277.1:p.Gly223Val
NM_001354689.1:c.971G>T	NP_001341618.1:p.Gly324Val
NM_001354690.1:c.911G>T	NP_001341619.1:p.Gly304Val
NM_001354691.1:c.668G>T	NP_001341620.1:p.Gly223Val
NM_001354692.1:c.668G>T	NP_001341621.1:p.Gly223Val
NM_001354693.1:c.812G>T	NP_001341622.1:p.Gly271Val
NM_001354694.1:c.728G>T	NP_001341623.1:p.Gly243Val
NM_001354695.1:c.569G>T	NP_001341624.1:p.Gly190Val
NR_148940.1:n.1326G>T
NR_148941.1:n.1326G>T
NR_148942.1:n.1326G>T
XM_011533974.3:c.911G>T	XP_011532276.1:p.Gly304Val
XM_017006966.1:c.812G>T	XP_016862455.1:p.Gly271Val
XR_001740227.1:n.1143G>T
NM_001354689.3:c.971G>T	NP_001341618.1:p.Gly324Val
NM_001354690.2:c.911G>T	NP_001341619.1:p.Gly304Val
NM_001354691.2:c.668G>T	NP_001341620.1:p.Gly223Val
NM_001354692.2:c.668G>T	NP_001341621.1:p.Gly223Val
NM_001354693.2:c.812G>T	NP_001341622.1:p.Gly271Val
NM_001354694.2:c.728G>T	NP_001341623.1:p.Gly243Val
NM_001354695.2:c.569G>T	NP_001341624.1:p.Gly190Val
NR_148940.2:n.1242G>T
NR_148941.2:n.1242G>T
NR_148942.2:n.1242G>T
NM_001354690.3:c.911G>T	NP_001341619.1:p.Gly304Val
NM_001354691.3:c.668G>T	NP_001341620.1:p.Gly223Val
NM_001354692.3:c.668G>T	NP_001341621.1:p.Gly223Val
NM_001354693.3:c.812G>T	NP_001341622.1:p.Gly271Val
NM_001354694.3:c.728G>T	NP_001341623.1:p.Gly243Val
NM_001354695.3:c.569G>T	NP_001341624.1:p.Gly190Val
NM_002880.4:c.911G>T MANE Select	NP_002871.1:p.Gly304Val
NR_148940.3:n.1242G>T
NR_148941.3:n.1242G>T
NR_148942.3:n.1242G>T