Canonical Allele Identifier: CA432273758

Gene: RAF1

Linked Data

• MyVariant Identifiers: chr3:g.12641227T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12599728T>A , CM000665.2:g.12599728T>A	GRCh38
NC_000003.11:g.12641227T>A , CM000665.1:g.12641227T>A	GRCh37
NC_000003.10:g.12616227T>A	NCBI36
NG_007467.1:g.69452A>T , LRG_413:g.69452A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000423275.6:c.*736A>T	ENSP00000401088.1:n.*736A>T
ENST00000432427.3:c.391A>T
ENST00000465826.6:n.662A>T
ENST00000491290.2:n.1448A>T
ENST00000684903.1:c.*748A>T	ENSP00000508612.1:n.*748A>T
ENST00000685348.1:c.*748A>T	ENSP00000510285.1:n.*748A>T
ENST00000685437.1:c.972A>T	ENSP00000508794.1:p.Ser324=
ENST00000685653.1:c.1071A>T	ENSP00000509968.1:p.Ser357=
ENST00000685738.1:c.1071A>T	ENSP00000510156.1:p.Ser357=
ENST00000686409.1:n.2122A>T
ENST00000686455.1:n.1434A>T
ENST00000686479.1:n.1442A>T
ENST00000686762.1:c.1071A>T	ENSP00000509767.1:p.Ser357=
ENST00000687257.1:n.1307A>T
ENST00000687326.1:c.1071A>T	ENSP00000509665.1:p.Ser357=
ENST00000687486.1:c.263A>T
ENST00000687505.1:n.1189A>T
ENST00000687923.1:c.972A>T	ENSP00000510255.1:p.Ser324=
ENST00000687940.1:n.1448A>T
ENST00000688269.1:n.1667A>T
ENST00000688326.1:c.391A>T
ENST00000688444.1:n.1397A>T
ENST00000688543.1:c.972A>T	ENSP00000509612.1:p.Ser324=
ENST00000688625.1:c.*649A>T	ENSP00000509522.1:n.*649A>T
ENST00000688803.1:n.1302A>T
ENST00000688914.1:n.57A>T
ENST00000689097.1:c.*748A>T	ENSP00000509756.1:n.*748A>T
ENST00000689389.1:c.1071A>T	ENSP00000510213.1:p.Ser357=
ENST00000689418.1:c.*748A>T	ENSP00000509467.1:n.*748A>T
ENST00000689481.1:c.*748A>T	ENSP00000510248.1:n.*748A>T
ENST00000689540.1:n.1221A>T
ENST00000689876.1:c.1071A>T	ENSP00000508535.1:p.Ser357=
ENST00000689914.1:c.1071A>T	ENSP00000509847.1:p.Ser357=
ENST00000690397.1:c.960A>T	ENSP00000508730.1:p.Ser320=
ENST00000690460.1:c.1059A>T	ENSP00000509106.1:p.Ser353=
ENST00000690625.1:n.1374A>T
ENST00000691268.1:c.498A>T
ENST00000691396.1:c.*864A>T	ENSP00000510712.1:n.*864A>T
ENST00000691724.1:c.*28A>T	ENSP00000509255.1:n.*28A>T
ENST00000691779.1:c.*649A>T	ENSP00000508592.1:n.*649A>T
ENST00000691899.1:c.1071A>T	ENSP00000508763.1:p.Ser357=
ENST00000692069.1:n.1637A>T
ENST00000692093.1:c.972A>T	ENSP00000509669.1:p.Ser324=
ENST00000692311.1:n.1895A>T
ENST00000692558.1:n.1436A>T
ENST00000692773.1:c.*808A>T	ENSP00000509055.1:n.*808A>T
ENST00000692830.1:c.*816A>T	ENSP00000509461.1:n.*816A>T
ENST00000693069.1:c.972A>T	ENSP00000510072.1:p.Ser324=
ENST00000693312.1:c.846A>T	ENSP00000508686.1:p.Ser282=
ENST00000693664.1:c.1071A>T	ENSP00000509614.1:p.Ser357=
ENST00000693705.1:c.*748A>T	ENSP00000510697.1:n.*748A>T
ENST00000251849.9:c.1071A>T MANE Select	ENSP00000251849.4:p.Ser357=
ENST00000442415.7:c.1131A>T	ENSP00000401888.2:p.Ser377=
ENST00000251849.8:c.1071A>T	ENSP00000251849.4:p.Ser357=
ENST00000423275.5:c.*748A>T	ENSP00000401088.1:n.*748A>T
ENST00000432427.2:c.708A>T	ENSP00000398591.2:p.Ser236=
ENST00000442415.6:c.1131A>T	ENSP00000401888.2:p.Ser377=
ENST00000460610.1:n.28A>T
ENST00000465826.5:n.315A>T
NM_002880.3:c.1071A>T , LRG_413t1:c.1071A>T	NP_002871.1:p.Ser357=
XM_005265355.1:c.1071A>T	XP_005265412.1:p.Ser357=
XM_005265357.1:c.972A>T	XP_005265414.1:p.Ser324=
XM_005265358.3:c.828A>T	XP_005265415.1:p.Ser276=
XM_005265359.3:c.729A>T	XP_005265416.1:p.Ser243=
XM_005265360.1:c.1071A>T	XP_005265417.1:p.Ser357=
XM_011533974.1:c.1071A>T	XP_011532276.1:p.Ser357=
XM_011533975.1:c.828A>T	XP_011532277.1:p.Ser276=
NM_001354689.1:c.1131A>T	NP_001341618.1:p.Ser377=
NM_001354690.1:c.1071A>T	NP_001341619.1:p.Ser357=
NM_001354691.1:c.828A>T	NP_001341620.1:p.Ser276=
NM_001354692.1:c.828A>T	NP_001341621.1:p.Ser276=
NM_001354693.1:c.972A>T	NP_001341622.1:p.Ser324=
NM_001354694.1:c.888A>T	NP_001341623.1:p.Ser296=
NM_001354695.1:c.729A>T	NP_001341624.1:p.Ser243=
NR_148940.1:n.1486A>T
NR_148941.1:n.1486A>T
NR_148942.1:n.1484A>T
XM_011533974.3:c.1071A>T	XP_011532276.1:p.Ser357=
XM_017006966.1:c.972A>T	XP_016862455.1:p.Ser324=
XR_001740227.1:n.1303A>T
NM_001354689.3:c.1131A>T	NP_001341618.1:p.Ser377=
NM_001354690.2:c.1071A>T	NP_001341619.1:p.Ser357=
NM_001354691.2:c.828A>T	NP_001341620.1:p.Ser276=
NM_001354692.2:c.828A>T	NP_001341621.1:p.Ser276=
NM_001354693.2:c.972A>T	NP_001341622.1:p.Ser324=
NM_001354694.2:c.888A>T	NP_001341623.1:p.Ser296=
NM_001354695.2:c.729A>T	NP_001341624.1:p.Ser243=
NR_148940.2:n.1402A>T
NR_148941.2:n.1402A>T
NR_148942.2:n.1400A>T
NM_001354690.3:c.1071A>T	NP_001341619.1:p.Ser357=
NM_001354691.3:c.828A>T	NP_001341620.1:p.Ser276=
NM_001354692.3:c.828A>T	NP_001341621.1:p.Ser276=
NM_001354693.3:c.972A>T	NP_001341622.1:p.Ser324=
NM_001354694.3:c.888A>T	NP_001341623.1:p.Ser296=
NM_001354695.3:c.729A>T	NP_001341624.1:p.Ser243=
NM_002880.4:c.1071A>T MANE Select	NP_002871.1:p.Ser357=
NR_148940.3:n.1402A>T
NR_148941.3:n.1402A>T
NR_148942.3:n.1400A>T