Canonical Allele Identifier: CA432273177

Gene: RAF1

Linked Data

• MyVariant Identifiers: chr3:g.12632449C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12590950C>A , CM000665.2:g.12590950C>A	GRCh38
NC_000003.11:g.12632449C>A , CM000665.1:g.12632449C>A	GRCh37
NC_000003.10:g.12607449C>A	NCBI36
NG_007467.1:g.78230G>T , LRG_413:g.78230G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*883G>T	ENSP00000401088.1:n.*883G>T
ENST00000432427.3:c.535G>T
ENST00000460610.2:n.12G>T
ENST00000465826.6:n.809G>T
ENST00000475353.2:n.1140G>T
ENST00000494557.2:n.1029G>T
ENST00000684903.1:c.*895G>T	ENSP00000508612.1:n.*895G>T
ENST00000685348.1:c.*895G>T	ENSP00000510285.1:n.*895G>T
ENST00000685437.1:c.1119G>T	ENSP00000508794.1:p.Leu373=
ENST00000685653.1:c.1218G>T	ENSP00000509968.1:p.Leu406=
ENST00000685738.1:c.*182G>T	ENSP00000510156.1:n.*182G>T
ENST00000686409.1:n.2269G>T
ENST00000686455.1:n.1581G>T
ENST00000686762.1:c.1218G>T	ENSP00000509767.1:p.Leu406=
ENST00000687257.1:n.1454G>T
ENST00000687326.1:c.*152G>T	ENSP00000509665.1:n.*152G>T
ENST00000687505.1:n.1336G>T
ENST00000687923.1:c.1107G>T	ENSP00000510255.1:p.Leu369=
ENST00000687940.1:n.1595G>T
ENST00000688269.1:n.1814G>T
ENST00000688326.1:c.651G>T
ENST00000688444.1:n.1544G>T
ENST00000688543.1:c.1119G>T	ENSP00000509612.1:p.Leu373=
ENST00000688625.1:c.*796G>T	ENSP00000509522.1:n.*796G>T
ENST00000688803.1:n.1449G>T
ENST00000688914.1:n.204G>T
ENST00000689097.1:c.*895G>T	ENSP00000509756.1:n.*895G>T
ENST00000689389.1:c.1193+758G>T	ENSP00000510213.1:n.1193+758G>T
ENST00000689418.1:c.*895G>T	ENSP00000509467.1:n.*895G>T
ENST00000689481.1:c.*895G>T	ENSP00000510248.1:n.*895G>T
ENST00000689540.1:n.1368G>T
ENST00000689876.1:c.1218G>T	ENSP00000508535.1:p.Leu406=
ENST00000689914.1:c.*152G>T	ENSP00000509847.1:n.*152G>T
ENST00000690397.1:c.1107G>T	ENSP00000508730.1:p.Leu369=
ENST00000690460.1:c.1206G>T	ENSP00000509106.1:p.Leu402=
ENST00000690585.1:c.110G>T
ENST00000690625.1:n.2254G>T
ENST00000691396.1:c.*1070G>T	ENSP00000510712.1:n.*1070G>T
ENST00000691724.1:c.*175G>T	ENSP00000509255.1:n.*175G>T
ENST00000691779.1:c.*796G>T	ENSP00000508592.1:n.*796G>T
ENST00000691888.1:c.110G>T
ENST00000691899.1:c.1218G>T	ENSP00000508763.1:p.Leu406=
ENST00000692069.1:n.1784G>T
ENST00000692093.1:c.1119G>T	ENSP00000509669.1:p.Leu373=
ENST00000692311.1:n.2042G>T
ENST00000692558.1:n.1583G>T
ENST00000692773.1:c.*955G>T	ENSP00000509055.1:n.*955G>T
ENST00000692830.1:c.*963G>T	ENSP00000509461.1:n.*963G>T
ENST00000693069.1:c.*152G>T	ENSP00000510072.1:n.*152G>T
ENST00000693312.1:c.993G>T	ENSP00000508686.1:p.Leu331=
ENST00000693664.1:c.1218G>T	ENSP00000509614.1:p.Leu406=
ENST00000693705.1:c.*895G>T	ENSP00000510697.1:n.*895G>T
ENST00000251849.9:c.1218G>T MANE Select	ENSP00000251849.4:p.Leu406=
ENST00000442415.7:c.1278G>T	ENSP00000401888.2:p.Leu426=
ENST00000251849.8:c.1218G>T	ENSP00000251849.4:p.Leu406=
ENST00000423275.5:c.*895G>T	ENSP00000401088.1:n.*895G>T
ENST00000432427.2:c.855G>T	ENSP00000398591.2:p.Leu285=
ENST00000442415.6:c.1278G>T	ENSP00000401888.2:p.Leu426=
ENST00000460610.1:n.175G>T
ENST00000465826.5:n.575G>T
ENST00000475353.1:n.386G>T
ENST00000494557.1:n.234G>T
NM_002880.3:c.1218G>T , LRG_413t1:c.1218G>T	NP_002871.1:p.Leu406=
XM_005265355.1:c.1218G>T	XP_005265412.1:p.Leu406=
XM_005265357.1:c.1119G>T	XP_005265414.1:p.Leu373=
XM_005265358.3:c.975G>T	XP_005265415.1:p.Leu325=
XM_005265359.3:c.876G>T	XP_005265416.1:p.Leu292=
XM_005265360.1:c.1218G>T	XP_005265417.1:p.Leu406=
XM_011533974.1:c.1218G>T	XP_011532276.1:p.Leu406=
XM_011533975.1:c.975G>T	XP_011532277.1:p.Leu325=
NM_001354689.1:c.1278G>T	NP_001341618.1:p.Leu426=
NM_001354690.1:c.1218G>T	NP_001341619.1:p.Leu406=
NM_001354691.1:c.975G>T	NP_001341620.1:p.Leu325=
NM_001354692.1:c.975G>T	NP_001341621.1:p.Leu325=
NM_001354693.1:c.1119G>T	NP_001341622.1:p.Leu373=
NM_001354694.1:c.1035G>T	NP_001341623.1:p.Leu345=
NM_001354695.1:c.876G>T	NP_001341624.1:p.Leu292=
NR_148940.1:n.1746G>T
NR_148941.1:n.1692G>T
NR_148942.1:n.1631G>T
XM_011533974.3:c.1218G>T	XP_011532276.1:p.Leu406=
XM_017006966.1:c.1119G>T	XP_016862455.1:p.Leu373=
XR_001740227.1:n.1509G>T
NM_001354689.3:c.1278G>T	NP_001341618.1:p.Leu426=
NM_001354690.2:c.1218G>T	NP_001341619.1:p.Leu406=
NM_001354691.2:c.975G>T	NP_001341620.1:p.Leu325=
NM_001354692.2:c.975G>T	NP_001341621.1:p.Leu325=
NM_001354693.2:c.1119G>T	NP_001341622.1:p.Leu373=
NM_001354694.2:c.1035G>T	NP_001341623.1:p.Leu345=
NM_001354695.2:c.876G>T	NP_001341624.1:p.Leu292=
NR_148940.2:n.1662G>T
NR_148941.2:n.1608G>T
NR_148942.2:n.1547G>T
NM_001354690.3:c.1218G>T	NP_001341619.1:p.Leu406=
NM_001354691.3:c.975G>T	NP_001341620.1:p.Leu325=
NM_001354692.3:c.975G>T	NP_001341621.1:p.Leu325=
NM_001354693.3:c.1119G>T	NP_001341622.1:p.Leu373=
NM_001354694.3:c.1035G>T	NP_001341623.1:p.Leu345=
NM_001354695.3:c.876G>T	NP_001341624.1:p.Leu292=
NM_002880.4:c.1218G>T MANE Select	NP_002871.1:p.Leu406=
NR_148940.3:n.1662G>T
NR_148941.3:n.1608G>T
NR_148942.3:n.1547G>T