Canonical Allele Identifier: CA1346233212
Gene: RAF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12590869C= , CM000665.2:g.12590869C= GRCh38
NC_000003.11:g.12632368C= , CM000665.1:g.12632368C= GRCh37
NC_000003.10:g.12607368C= NCBI36
NG_007467.1:g.78311G= , LRG_413:g.78311G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000423275.6:c.*964G= ENSP00000401088.1:n.*964G=
ENST00000432427.3:c.616G=
ENST00000460610.2:n.93G=
ENST00000465826.6:n.890G=
ENST00000475353.2:n.1221G=
ENST00000494557.2:n.1110G=
ENST00000684903.1:c.*976G= ENSP00000508612.1:n.*976G=
ENST00000685348.1:c.*976G= ENSP00000510285.1:n.*976G=
ENST00000685437.1:c.1200G= ENSP00000508794.1:p.Leu400=
ENST00000685653.1:c.1299G= ENSP00000509968.1:p.Leu433=
ENST00000685738.1:c.*263G= ENSP00000510156.1:n.*263G=
ENST00000686409.1:n.2350G=
ENST00000686455.1:n.1662G=
ENST00000686762.1:c.1299G= ENSP00000509767.1:p.Leu433=
ENST00000687257.1:n.1535G=
ENST00000687326.1:c.*233G= ENSP00000509665.1:n.*233G=
ENST00000687505.1:n.1417G=
ENST00000687923.1:c.1188G= ENSP00000510255.1:p.Leu396=
ENST00000687940.1:n.1676G=
ENST00000688269.1:n.1895G=
ENST00000688326.1:c.732G=
ENST00000688444.1:n.1625G=
ENST00000688543.1:c.1200G= ENSP00000509612.1:p.Leu400=
ENST00000688625.1:c.*877G= ENSP00000509522.1:n.*877G=
ENST00000688803.1:n.1530G=
ENST00000688914.1:n.285G=
ENST00000689097.1:c.*976G= ENSP00000509756.1:n.*976G=
ENST00000689389.1:c.1193+839G= ENSP00000510213.1:n.1193+839G=
ENST00000689418.1:c.*976G= ENSP00000509467.1:n.*976G=
ENST00000689481.1:c.*976G= ENSP00000510248.1:n.*976G=
ENST00000689540.1:n.1449G=
ENST00000689876.1:c.1299G= ENSP00000508535.1:p.Leu433=
ENST00000689914.1:c.*233G= ENSP00000509847.1:n.*233G=
ENST00000690397.1:c.1188G= ENSP00000508730.1:p.Leu396=
ENST00000690460.1:c.1287G= ENSP00000509106.1:p.Leu429=
ENST00000690585.1:c.191G=
ENST00000690625.1:n.2335G=
ENST00000691396.1:c.*1151G= ENSP00000510712.1:n.*1151G=
ENST00000691724.1:c.*256G= ENSP00000509255.1:n.*256G=
ENST00000691779.1:c.*877G= ENSP00000508592.1:n.*877G=
ENST00000691888.1:c.191G=
ENST00000691899.1:c.1299G= ENSP00000508763.1:p.Leu433=
ENST00000692069.1:n.1865G=
ENST00000692093.1:c.1200G= ENSP00000509669.1:p.Leu400=
ENST00000692311.1:n.2123G=
ENST00000692558.1:n.1664G=
ENST00000692773.1:c.*1036G= ENSP00000509055.1:n.*1036G=
ENST00000692830.1:c.*1044G= ENSP00000509461.1:n.*1044G=
ENST00000693069.1:c.*233G= ENSP00000510072.1:n.*233G=
ENST00000693312.1:c.1074G= ENSP00000508686.1:p.Leu358=
ENST00000693664.1:c.1299G= ENSP00000509614.1:p.Leu433=
ENST00000693705.1:c.*976G= ENSP00000510697.1:n.*976G=
ENST00000251849.9:c.1299G= MANE Select ENSP00000251849.4:p.Leu433=
ENST00000442415.7:c.1359G= ENSP00000401888.2:p.Leu453=
ENST00000251849.8:c.1299G= ENSP00000251849.4:p.Leu433=
ENST00000423275.5:c.*976G= ENSP00000401088.1:n.*976G=
ENST00000432427.2:c.936G= ENSP00000398591.2:p.Leu312=
ENST00000442415.6:c.1359G= ENSP00000401888.2:p.Leu453=
ENST00000460610.1:n.256G=
ENST00000465826.5:n.656G=
ENST00000475353.1:n.467G=
ENST00000494557.1:n.315G=
NM_002880.3:c.1299G= , LRG_413t1:c.1299G= NP_002871.1:p.Leu433=
XM_005265355.1:c.1299G= XP_005265412.1:p.Leu433=
XM_005265357.1:c.1200G= XP_005265414.1:p.Leu400=
XM_005265358.3:c.1056G= XP_005265415.1:p.Leu352=
XM_005265359.3:c.957G= XP_005265416.1:p.Leu319=
XM_005265360.1:c.1299G= XP_005265417.1:p.Leu433=
XM_011533974.1:c.1299G= XP_011532276.1:p.Leu433=
XM_011533975.1:c.1056G= XP_011532277.1:p.Leu352=
NM_001354689.1:c.1359G= NP_001341618.1:p.Leu453=
NM_001354690.1:c.1299G= NP_001341619.1:p.Leu433=
NM_001354691.1:c.1056G= NP_001341620.1:p.Leu352=
NM_001354692.1:c.1056G= NP_001341621.1:p.Leu352=
NM_001354693.1:c.1200G= NP_001341622.1:p.Leu400=
NM_001354694.1:c.1116G= NP_001341623.1:p.Leu372=
NM_001354695.1:c.957G= NP_001341624.1:p.Leu319=
NR_148940.1:n.1827G=
NR_148941.1:n.1773G=
NR_148942.1:n.1712G=
XM_011533974.3:c.1299G= XP_011532276.1:p.Leu433=
XM_017006966.1:c.1200G= XP_016862455.1:p.Leu400=
NM_001354689.3:c.1359G= NP_001341618.1:p.Leu453=
NM_001354690.2:c.1299G= NP_001341619.1:p.Leu433=
NM_001354691.2:c.1056G= NP_001341620.1:p.Leu352=
NM_001354692.2:c.1056G= NP_001341621.1:p.Leu352=
NM_001354693.2:c.1200G= NP_001341622.1:p.Leu400=
NM_001354694.2:c.1116G= NP_001341623.1:p.Leu372=
NM_001354695.2:c.957G= NP_001341624.1:p.Leu319=
NR_148940.2:n.1743G=
NR_148941.2:n.1689G=
NR_148942.2:n.1628G=
NM_001354690.3:c.1299G= NP_001341619.1:p.Leu433=
NM_001354691.3:c.1056G= NP_001341620.1:p.Leu352=
NM_001354692.3:c.1056G= NP_001341621.1:p.Leu352=
NM_001354693.3:c.1200G= NP_001341622.1:p.Leu400=
NM_001354694.3:c.1116G= NP_001341623.1:p.Leu372=
NM_001354695.3:c.957G= NP_001341624.1:p.Leu319=
NM_002880.4:c.1299G= MANE Select NP_002871.1:p.Leu433=
NR_148940.3:n.1743G=
NR_148941.3:n.1689G=
NR_148942.3:n.1628G=