Canonical Allele Identifier: CA351501880

Gene: RAF1

Linked Data

• MyVariant Identifiers: chr3:g.12632348A>G (hg19) ; chr3:g.12590849A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12590849A>G , CM000665.2:g.12590849A>G	GRCh38
NC_000003.11:g.12632348A>G , CM000665.1:g.12632348A>G	GRCh37
NC_000003.10:g.12607348A>G	NCBI36
NG_007467.1:g.78331T>C , LRG_413:g.78331T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*984T>C	ENSP00000401088.1:n.*984T>C
ENST00000432427.3:c.636T>C
ENST00000460610.2:n.113T>C
ENST00000465826.6:n.910T>C
ENST00000475353.2:n.1241T>C
ENST00000494557.2:n.1130T>C
ENST00000684903.1:c.*996T>C	ENSP00000508612.1:n.*996T>C
ENST00000685348.1:c.*996T>C	ENSP00000510285.1:n.*996T>C
ENST00000685437.1:c.1220T>C	ENSP00000508794.1:p.Phe407Ser
ENST00000685653.1:c.1319T>C	ENSP00000509968.1:p.Phe440Ser
ENST00000685738.1:c.*283T>C	ENSP00000510156.1:n.*283T>C
ENST00000686409.1:n.2370T>C
ENST00000686455.1:n.1682T>C
ENST00000686762.1:c.1319T>C	ENSP00000509767.1:p.Phe440Ser
ENST00000687257.1:n.1555T>C
ENST00000687326.1:c.*253T>C	ENSP00000509665.1:n.*253T>C
ENST00000687505.1:n.1437T>C
ENST00000687923.1:c.1208T>C	ENSP00000510255.1:p.Phe403Ser
ENST00000687940.1:n.1696T>C
ENST00000688269.1:n.1915T>C
ENST00000688326.1:c.752T>C
ENST00000688444.1:n.1645T>C
ENST00000688543.1:c.1220T>C	ENSP00000509612.1:p.Phe407Ser
ENST00000688625.1:c.*897T>C	ENSP00000509522.1:n.*897T>C
ENST00000688803.1:n.1550T>C
ENST00000688914.1:n.305T>C
ENST00000689097.1:c.*996T>C	ENSP00000509756.1:n.*996T>C
ENST00000689389.1:c.1193+859T>C	ENSP00000510213.1:n.1193+859T>C
ENST00000689418.1:c.*996T>C	ENSP00000509467.1:n.*996T>C
ENST00000689481.1:c.*996T>C	ENSP00000510248.1:n.*996T>C
ENST00000689540.1:n.1469T>C
ENST00000689876.1:c.1319T>C	ENSP00000508535.1:p.Phe440Ser
ENST00000689914.1:c.*253T>C	ENSP00000509847.1:n.*253T>C
ENST00000690397.1:c.1208T>C	ENSP00000508730.1:p.Phe403Ser
ENST00000690460.1:c.1307T>C	ENSP00000509106.1:p.Phe436Ser
ENST00000690585.1:c.211T>C
ENST00000690625.1:n.2355T>C
ENST00000691396.1:c.*1171T>C	ENSP00000510712.1:n.*1171T>C
ENST00000691724.1:c.*276T>C	ENSP00000509255.1:n.*276T>C
ENST00000691779.1:c.*897T>C	ENSP00000508592.1:n.*897T>C
ENST00000691888.1:c.211T>C
ENST00000691899.1:c.1319T>C	ENSP00000508763.1:p.Phe440Ser
ENST00000692069.1:n.1885T>C
ENST00000692093.1:c.1220T>C	ENSP00000509669.1:p.Phe407Ser
ENST00000692311.1:n.2143T>C
ENST00000692558.1:n.1684T>C
ENST00000692773.1:c.*1056T>C	ENSP00000509055.1:n.*1056T>C
ENST00000692830.1:c.*1064T>C	ENSP00000509461.1:n.*1064T>C
ENST00000693069.1:c.*253T>C	ENSP00000510072.1:n.*253T>C
ENST00000693312.1:c.1094T>C	ENSP00000508686.1:p.Phe365Ser
ENST00000693664.1:c.1319T>C	ENSP00000509614.1:p.Phe440Ser
ENST00000693705.1:c.*996T>C	ENSP00000510697.1:n.*996T>C
ENST00000251849.9:c.1319T>C MANE Select	ENSP00000251849.4:p.Phe440Ser
ENST00000442415.7:c.1379T>C	ENSP00000401888.2:p.Phe460Ser
ENST00000251849.8:c.1319T>C	ENSP00000251849.4:p.Phe440Ser
ENST00000423275.5:c.*996T>C	ENSP00000401088.1:n.*996T>C
ENST00000432427.2:c.956T>C	ENSP00000398591.2:p.Phe319Ser
ENST00000442415.6:c.1379T>C	ENSP00000401888.2:p.Phe460Ser
ENST00000460610.1:n.276T>C
ENST00000465826.5:n.676T>C
ENST00000475353.1:n.487T>C
ENST00000494557.1:n.335T>C
NM_002880.3:c.1319T>C , LRG_413t1:c.1319T>C	NP_002871.1:p.Phe440Ser
XM_005265355.1:c.1319T>C	XP_005265412.1:p.Phe440Ser
XM_005265357.1:c.1220T>C	XP_005265414.1:p.Phe407Ser
XM_005265358.3:c.1076T>C	XP_005265415.1:p.Phe359Ser
XM_005265359.3:c.977T>C	XP_005265416.1:p.Phe326Ser
XM_005265360.1:c.1319T>C	XP_005265417.1:p.Phe440Ser
XM_011533974.1:c.1319T>C	XP_011532276.1:p.Phe440Ser
XM_011533975.1:c.1076T>C	XP_011532277.1:p.Phe359Ser
NM_001354689.1:c.1379T>C	NP_001341618.1:p.Phe460Ser
NM_001354690.1:c.1319T>C	NP_001341619.1:p.Phe440Ser
NM_001354691.1:c.1076T>C	NP_001341620.1:p.Phe359Ser
NM_001354692.1:c.1076T>C	NP_001341621.1:p.Phe359Ser
NM_001354693.1:c.1220T>C	NP_001341622.1:p.Phe407Ser
NM_001354694.1:c.1136T>C	NP_001341623.1:p.Phe379Ser
NM_001354695.1:c.977T>C	NP_001341624.1:p.Phe326Ser
NR_148940.1:n.1847T>C
NR_148941.1:n.1793T>C
NR_148942.1:n.1732T>C
XM_011533974.3:c.1319T>C	XP_011532276.1:p.Phe440Ser
XM_017006966.1:c.1220T>C	XP_016862455.1:p.Phe407Ser
NM_001354689.3:c.1379T>C	NP_001341618.1:p.Phe460Ser
NM_001354690.2:c.1319T>C	NP_001341619.1:p.Phe440Ser
NM_001354691.2:c.1076T>C	NP_001341620.1:p.Phe359Ser
NM_001354692.2:c.1076T>C	NP_001341621.1:p.Phe359Ser
NM_001354693.2:c.1220T>C	NP_001341622.1:p.Phe407Ser
NM_001354694.2:c.1136T>C	NP_001341623.1:p.Phe379Ser
NM_001354695.2:c.977T>C	NP_001341624.1:p.Phe326Ser
NR_148940.2:n.1763T>C
NR_148941.2:n.1709T>C
NR_148942.2:n.1648T>C
NM_001354690.3:c.1319T>C	NP_001341619.1:p.Phe440Ser
NM_001354691.3:c.1076T>C	NP_001341620.1:p.Phe359Ser
NM_001354692.3:c.1076T>C	NP_001341621.1:p.Phe359Ser
NM_001354693.3:c.1220T>C	NP_001341622.1:p.Phe407Ser
NM_001354694.3:c.1136T>C	NP_001341623.1:p.Phe379Ser
NM_001354695.3:c.977T>C	NP_001341624.1:p.Phe326Ser
NM_002880.4:c.1319T>C MANE Select	NP_002871.1:p.Phe440Ser
NR_148940.3:n.1763T>C
NR_148941.3:n.1709T>C
NR_148942.3:n.1648T>C