Canonical Allele Identifier: CA1346233954
Gene: RAF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12591708C= , CM000665.2:g.12591708C= GRCh38
NC_000003.11:g.12633207C= , CM000665.1:g.12633207C= GRCh37
NC_000003.10:g.12608207C= NCBI36
NG_007467.1:g.77472G= , LRG_413:g.77472G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000423275.6:c.*858G= ENSP00000401088.1:n.*858G=
ENST00000432427.3:c.510G=
ENST00000465826.6:n.784G=
ENST00000475353.2:n.1115G=
ENST00000491290.2:n.1553G=
ENST00000494557.2:n.1004G=
ENST00000684903.1:c.*870G= ENSP00000508612.1:n.*870G=
ENST00000685348.1:c.*870G= ENSP00000510285.1:n.*870G=
ENST00000685437.1:c.1094G= ENSP00000508794.1:p.Arg365=
ENST00000685653.1:c.1193G= ENSP00000509968.1:p.Arg398=
ENST00000685738.1:c.*157G= ENSP00000510156.1:n.*157G=
ENST00000686409.1:n.2244G=
ENST00000686455.1:n.1556G=
ENST00000686762.1:c.1193G= ENSP00000509767.1:p.Arg398=
ENST00000687257.1:n.1429G=
ENST00000687326.1:c.*127G= ENSP00000509665.1:n.*127G=
ENST00000687486.1:c.385G=
ENST00000687505.1:n.1311G=
ENST00000687923.1:c.1082G= ENSP00000510255.1:p.Arg361=
ENST00000687940.1:n.1570G=
ENST00000688269.1:n.1789G=
ENST00000688326.1:c.626G=
ENST00000688444.1:n.1519G=
ENST00000688543.1:c.1094G= ENSP00000509612.1:p.Arg365=
ENST00000688625.1:c.*771G= ENSP00000509522.1:n.*771G=
ENST00000688803.1:n.1424G=
ENST00000688914.1:n.179G=
ENST00000689097.1:c.*870G= ENSP00000509756.1:n.*870G=
ENST00000689389.1:c.1193G= ENSP00000510213.1:p.Arg398=
ENST00000689418.1:c.*870G= ENSP00000509467.1:n.*870G=
ENST00000689481.1:c.*870G= ENSP00000510248.1:n.*870G=
ENST00000689540.1:n.1343G=
ENST00000689876.1:c.1193G= ENSP00000508535.1:p.Arg398=
ENST00000689914.1:c.*127G= ENSP00000509847.1:n.*127G=
ENST00000690397.1:c.1082G= ENSP00000508730.1:p.Arg361=
ENST00000690460.1:c.1181G= ENSP00000509106.1:p.Arg394=
ENST00000690585.1:c.85G=
ENST00000690625.1:n.1496G=
ENST00000691396.1:c.*1045G= ENSP00000510712.1:n.*1045G=
ENST00000691724.1:c.*150G= ENSP00000509255.1:n.*150G=
ENST00000691779.1:c.*771G= ENSP00000508592.1:n.*771G=
ENST00000691888.1:c.85G=
ENST00000691899.1:c.1193G= ENSP00000508763.1:p.Arg398=
ENST00000692069.1:n.1759G=
ENST00000692093.1:c.1094G= ENSP00000509669.1:p.Arg365=
ENST00000692311.1:n.2017G=
ENST00000692558.1:n.1558G=
ENST00000692773.1:c.*930G= ENSP00000509055.1:n.*930G=
ENST00000692830.1:c.*938G= ENSP00000509461.1:n.*938G=
ENST00000693069.1:c.*127G= ENSP00000510072.1:n.*127G=
ENST00000693312.1:c.968G= ENSP00000508686.1:p.Arg323=
ENST00000693664.1:c.1193G= ENSP00000509614.1:p.Arg398=
ENST00000693705.1:c.*870G= ENSP00000510697.1:n.*870G=
ENST00000251849.9:c.1193G= MANE Select ENSP00000251849.4:p.Arg398=
ENST00000442415.7:c.1253G= ENSP00000401888.2:p.Arg418=
ENST00000251849.8:c.1193G= ENSP00000251849.4:p.Arg398=
ENST00000423275.5:c.*870G= ENSP00000401088.1:n.*870G=
ENST00000432427.2:c.830G= ENSP00000398591.2:p.Arg277=
ENST00000442415.6:c.1253G= ENSP00000401888.2:p.Arg418=
ENST00000460610.1:n.150G=
ENST00000465826.5:n.550G=
ENST00000475353.1:n.361G=
ENST00000494557.1:n.209G=
NM_002880.3:c.1193G= , LRG_413t1:c.1193G= NP_002871.1:p.Arg398=
XM_005265355.1:c.1193G= XP_005265412.1:p.Arg398=
XM_005265357.1:c.1094G= XP_005265414.1:p.Arg365=
XM_005265358.3:c.950G= XP_005265415.1:p.Arg317=
XM_005265359.3:c.851G= XP_005265416.1:p.Arg284=
XM_005265360.1:c.1193G= XP_005265417.1:p.Arg398=
XM_011533974.1:c.1193G= XP_011532276.1:p.Arg398=
XM_011533975.1:c.950G= XP_011532277.1:p.Arg317=
NM_001354689.1:c.1253G= NP_001341618.1:p.Arg418=
NM_001354690.1:c.1193G= NP_001341619.1:p.Arg398=
NM_001354691.1:c.950G= NP_001341620.1:p.Arg317=
NM_001354692.1:c.950G= NP_001341621.1:p.Arg317=
NM_001354693.1:c.1094G= NP_001341622.1:p.Arg365=
NM_001354694.1:c.1010G= NP_001341623.1:p.Arg337=
NM_001354695.1:c.851G= NP_001341624.1:p.Arg284=
NR_148940.1:n.1721G=
NR_148941.1:n.1667G=
NR_148942.1:n.1606G=
XM_011533974.3:c.1193G= XP_011532276.1:p.Arg398=
XM_017006966.1:c.1094G= XP_016862455.1:p.Arg365=
XR_001740227.1:n.1484G=
NM_001354689.3:c.1253G= NP_001341618.1:p.Arg418=
NM_001354690.2:c.1193G= NP_001341619.1:p.Arg398=
NM_001354691.2:c.950G= NP_001341620.1:p.Arg317=
NM_001354692.2:c.950G= NP_001341621.1:p.Arg317=
NM_001354693.2:c.1094G= NP_001341622.1:p.Arg365=
NM_001354694.2:c.1010G= NP_001341623.1:p.Arg337=
NM_001354695.2:c.851G= NP_001341624.1:p.Arg284=
NR_148940.2:n.1637G=
NR_148941.2:n.1583G=
NR_148942.2:n.1522G=
NM_001354690.3:c.1193G= NP_001341619.1:p.Arg398=
NM_001354691.3:c.950G= NP_001341620.1:p.Arg317=
NM_001354692.3:c.950G= NP_001341621.1:p.Arg317=
NM_001354693.3:c.1094G= NP_001341622.1:p.Arg365=
NM_001354694.3:c.1010G= NP_001341623.1:p.Arg337=
NM_001354695.3:c.851G= NP_001341624.1:p.Arg284=
NM_002880.4:c.1193G= MANE Select NP_002871.1:p.Arg398=
NR_148940.3:n.1637G=
NR_148941.3:n.1583G=
NR_148942.3:n.1522G=