Canonical Allele Identifier: CA1346233253
Gene: RAF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12590890G= , CM000665.2:g.12590890G= GRCh38
NC_000003.11:g.12632389G= , CM000665.1:g.12632389G= GRCh37
NC_000003.10:g.12607389G= NCBI36
NG_007467.1:g.78290C= , LRG_413:g.78290C=

Transcript Alleles

HGVS Amino-acid change
ENST00000423275.6:c.*943C= ENSP00000401088.1:n.*943C=
ENST00000432427.3:c.595C=
ENST00000460610.2:n.72C=
ENST00000465826.6:n.869C=
ENST00000475353.2:n.1200C=
ENST00000494557.2:n.1089C=
ENST00000684903.1:c.*955C= ENSP00000508612.1:n.*955C=
ENST00000685348.1:c.*955C= ENSP00000510285.1:n.*955C=
ENST00000685437.1:c.1179C= ENSP00000508794.1:p.Gly393=
ENST00000685653.1:c.1278C= ENSP00000509968.1:p.Gly426=
ENST00000685738.1:c.*242C= ENSP00000510156.1:n.*242C=
ENST00000686409.1:n.2329C=
ENST00000686455.1:n.1641C=
ENST00000686762.1:c.1278C= ENSP00000509767.1:p.Gly426=
ENST00000687257.1:n.1514C=
ENST00000687326.1:c.*212C= ENSP00000509665.1:n.*212C=
ENST00000687505.1:n.1396C=
ENST00000687923.1:c.1167C= ENSP00000510255.1:p.Gly389=
ENST00000687940.1:n.1655C=
ENST00000688269.1:n.1874C=
ENST00000688326.1:c.711C=
ENST00000688444.1:n.1604C=
ENST00000688543.1:c.1179C= ENSP00000509612.1:p.Gly393=
ENST00000688625.1:c.*856C= ENSP00000509522.1:n.*856C=
ENST00000688803.1:n.1509C=
ENST00000688914.1:n.264C=
ENST00000689097.1:c.*955C= ENSP00000509756.1:n.*955C=
ENST00000689389.1:c.1193+818C= ENSP00000510213.1:n.1193+818C=
ENST00000689418.1:c.*955C= ENSP00000509467.1:n.*955C=
ENST00000689481.1:c.*955C= ENSP00000510248.1:n.*955C=
ENST00000689540.1:n.1428C=
ENST00000689876.1:c.1278C= ENSP00000508535.1:p.Gly426=
ENST00000689914.1:c.*212C= ENSP00000509847.1:n.*212C=
ENST00000690397.1:c.1167C= ENSP00000508730.1:p.Gly389=
ENST00000690460.1:c.1266C= ENSP00000509106.1:p.Gly422=
ENST00000690585.1:c.170C=
ENST00000690625.1:n.2314C=
ENST00000691396.1:c.*1130C= ENSP00000510712.1:n.*1130C=
ENST00000691724.1:c.*235C= ENSP00000509255.1:n.*235C=
ENST00000691779.1:c.*856C= ENSP00000508592.1:n.*856C=
ENST00000691888.1:c.170C=
ENST00000691899.1:c.1278C= ENSP00000508763.1:p.Gly426=
ENST00000692069.1:n.1844C=
ENST00000692093.1:c.1179C= ENSP00000509669.1:p.Gly393=
ENST00000692311.1:n.2102C=
ENST00000692558.1:n.1643C=
ENST00000692773.1:c.*1015C= ENSP00000509055.1:n.*1015C=
ENST00000692830.1:c.*1023C= ENSP00000509461.1:n.*1023C=
ENST00000693069.1:c.*212C= ENSP00000510072.1:n.*212C=
ENST00000693312.1:c.1053C= ENSP00000508686.1:p.Gly351=
ENST00000693664.1:c.1278C= ENSP00000509614.1:p.Gly426=
ENST00000693705.1:c.*955C= ENSP00000510697.1:n.*955C=
ENST00000251849.9:c.1278C= MANE Select ENSP00000251849.4:p.Gly426=
ENST00000442415.7:c.1338C= ENSP00000401888.2:p.Gly446=
ENST00000251849.8:c.1278C= ENSP00000251849.4:p.Gly426=
ENST00000423275.5:c.*955C= ENSP00000401088.1:n.*955C=
ENST00000432427.2:c.915C= ENSP00000398591.2:p.Gly305=
ENST00000442415.6:c.1338C= ENSP00000401888.2:p.Gly446=
ENST00000460610.1:n.235C=
ENST00000465826.5:n.635C=
ENST00000475353.1:n.446C=
ENST00000494557.1:n.294C=
NM_002880.3:c.1278C= , LRG_413t1:c.1278C= NP_002871.1:p.Gly426=
XM_005265355.1:c.1278C= XP_005265412.1:p.Gly426=
XM_005265357.1:c.1179C= XP_005265414.1:p.Gly393=
XM_005265358.3:c.1035C= XP_005265415.1:p.Gly345=
XM_005265359.3:c.936C= XP_005265416.1:p.Gly312=
XM_005265360.1:c.1278C= XP_005265417.1:p.Gly426=
XM_011533974.1:c.1278C= XP_011532276.1:p.Gly426=
XM_011533975.1:c.1035C= XP_011532277.1:p.Gly345=
NM_001354689.1:c.1338C= NP_001341618.1:p.Gly446=
NM_001354690.1:c.1278C= NP_001341619.1:p.Gly426=
NM_001354691.1:c.1035C= NP_001341620.1:p.Gly345=
NM_001354692.1:c.1035C= NP_001341621.1:p.Gly345=
NM_001354693.1:c.1179C= NP_001341622.1:p.Gly393=
NM_001354694.1:c.1095C= NP_001341623.1:p.Gly365=
NM_001354695.1:c.936C= NP_001341624.1:p.Gly312=
NR_148940.1:n.1806C=
NR_148941.1:n.1752C=
NR_148942.1:n.1691C=
XM_011533974.3:c.1278C= XP_011532276.1:p.Gly426=
XM_017006966.1:c.1179C= XP_016862455.1:p.Gly393=
NM_001354689.3:c.1338C= NP_001341618.1:p.Gly446=
NM_001354690.2:c.1278C= NP_001341619.1:p.Gly426=
NM_001354691.2:c.1035C= NP_001341620.1:p.Gly345=
NM_001354692.2:c.1035C= NP_001341621.1:p.Gly345=
NM_001354693.2:c.1179C= NP_001341622.1:p.Gly393=
NM_001354694.2:c.1095C= NP_001341623.1:p.Gly365=
NM_001354695.2:c.936C= NP_001341624.1:p.Gly312=
NR_148940.2:n.1722C=
NR_148941.2:n.1668C=
NR_148942.2:n.1607C=
NM_001354690.3:c.1278C= NP_001341619.1:p.Gly426=
NM_001354691.3:c.1035C= NP_001341620.1:p.Gly345=
NM_001354692.3:c.1035C= NP_001341621.1:p.Gly345=
NM_001354693.3:c.1179C= NP_001341622.1:p.Gly393=
NM_001354694.3:c.1095C= NP_001341623.1:p.Gly365=
NM_001354695.3:c.936C= NP_001341624.1:p.Gly312=
NM_002880.4:c.1278C= MANE Select NP_002871.1:p.Gly426=
NR_148940.3:n.1722C=
NR_148941.3:n.1668C=
NR_148942.3:n.1607C=