Canonical Allele Identifier: CA351502222
Gene: RAF1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12590901A>C , CM000665.2:g.12590901A>C GRCh38
NC_000003.11:g.12632400A>C , CM000665.1:g.12632400A>C GRCh37
NC_000003.10:g.12607400A>C NCBI36
NG_007467.1:g.78279T>G , LRG_413:g.78279T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000423275.6:c.*932T>G ENSP00000401088.1:n.*932T>G
ENST00000432427.3:c.584T>G
ENST00000460610.2:n.61T>G
ENST00000465826.6:n.858T>G
ENST00000475353.2:n.1189T>G
ENST00000494557.2:n.1078T>G
ENST00000684903.1:c.*944T>G ENSP00000508612.1:n.*944T>G
ENST00000685348.1:c.*944T>G ENSP00000510285.1:n.*944T>G
ENST00000685437.1:c.1168T>G ENSP00000508794.1:p.Trp390Gly
ENST00000685653.1:c.1267T>G ENSP00000509968.1:p.Trp423Gly
ENST00000685738.1:c.*231T>G ENSP00000510156.1:n.*231T>G
ENST00000686409.1:n.2318T>G
ENST00000686455.1:n.1630T>G
ENST00000686762.1:c.1267T>G ENSP00000509767.1:p.Trp423Gly
ENST00000687257.1:n.1503T>G
ENST00000687326.1:c.*201T>G ENSP00000509665.1:n.*201T>G
ENST00000687505.1:n.1385T>G
ENST00000687923.1:c.1156T>G ENSP00000510255.1:p.Trp386Gly
ENST00000687940.1:n.1644T>G
ENST00000688269.1:n.1863T>G
ENST00000688326.1:c.700T>G
ENST00000688444.1:n.1593T>G
ENST00000688543.1:c.1168T>G ENSP00000509612.1:p.Trp390Gly
ENST00000688625.1:c.*845T>G ENSP00000509522.1:n.*845T>G
ENST00000688803.1:n.1498T>G
ENST00000688914.1:n.253T>G
ENST00000689097.1:c.*944T>G ENSP00000509756.1:n.*944T>G
ENST00000689389.1:c.1193+807T>G ENSP00000510213.1:n.1193+807T>G
ENST00000689418.1:c.*944T>G ENSP00000509467.1:n.*944T>G
ENST00000689481.1:c.*944T>G ENSP00000510248.1:n.*944T>G
ENST00000689540.1:n.1417T>G
ENST00000689876.1:c.1267T>G ENSP00000508535.1:p.Trp423Gly
ENST00000689914.1:c.*201T>G ENSP00000509847.1:n.*201T>G
ENST00000690397.1:c.1156T>G ENSP00000508730.1:p.Trp386Gly
ENST00000690460.1:c.1255T>G ENSP00000509106.1:p.Trp419Gly
ENST00000690585.1:c.159T>G
ENST00000690625.1:n.2303T>G
ENST00000691396.1:c.*1119T>G ENSP00000510712.1:n.*1119T>G
ENST00000691724.1:c.*224T>G ENSP00000509255.1:n.*224T>G
ENST00000691779.1:c.*845T>G ENSP00000508592.1:n.*845T>G
ENST00000691888.1:c.159T>G
ENST00000691899.1:c.1267T>G ENSP00000508763.1:p.Trp423Gly
ENST00000692069.1:n.1833T>G
ENST00000692093.1:c.1168T>G ENSP00000509669.1:p.Trp390Gly
ENST00000692311.1:n.2091T>G
ENST00000692558.1:n.1632T>G
ENST00000692773.1:c.*1004T>G ENSP00000509055.1:n.*1004T>G
ENST00000692830.1:c.*1012T>G ENSP00000509461.1:n.*1012T>G
ENST00000693069.1:c.*201T>G ENSP00000510072.1:n.*201T>G
ENST00000693312.1:c.1042T>G ENSP00000508686.1:p.Trp348Gly
ENST00000693664.1:c.1267T>G ENSP00000509614.1:p.Trp423Gly
ENST00000693705.1:c.*944T>G ENSP00000510697.1:n.*944T>G
ENST00000251849.9:c.1267T>G MANE Select ENSP00000251849.4:p.Trp423Gly
ENST00000442415.7:c.1327T>G ENSP00000401888.2:p.Trp443Gly
ENST00000251849.8:c.1267T>G ENSP00000251849.4:p.Trp423Gly
ENST00000423275.5:c.*944T>G ENSP00000401088.1:n.*944T>G
ENST00000432427.2:c.904T>G ENSP00000398591.2:p.Trp302Gly
ENST00000442415.6:c.1327T>G ENSP00000401888.2:p.Trp443Gly
ENST00000460610.1:n.224T>G
ENST00000465826.5:n.624T>G
ENST00000475353.1:n.435T>G
ENST00000494557.1:n.283T>G
NM_002880.3:c.1267T>G , LRG_413t1:c.1267T>G NP_002871.1:p.Trp423Gly
XM_005265355.1:c.1267T>G XP_005265412.1:p.Trp423Gly
XM_005265357.1:c.1168T>G XP_005265414.1:p.Trp390Gly
XM_005265358.3:c.1024T>G XP_005265415.1:p.Trp342Gly
XM_005265359.3:c.925T>G XP_005265416.1:p.Trp309Gly
XM_005265360.1:c.1267T>G XP_005265417.1:p.Trp423Gly
XM_011533974.1:c.1267T>G XP_011532276.1:p.Trp423Gly
XM_011533975.1:c.1024T>G XP_011532277.1:p.Trp342Gly
NM_001354689.1:c.1327T>G NP_001341618.1:p.Trp443Gly
NM_001354690.1:c.1267T>G NP_001341619.1:p.Trp423Gly
NM_001354691.1:c.1024T>G NP_001341620.1:p.Trp342Gly
NM_001354692.1:c.1024T>G NP_001341621.1:p.Trp342Gly
NM_001354693.1:c.1168T>G NP_001341622.1:p.Trp390Gly
NM_001354694.1:c.1084T>G NP_001341623.1:p.Trp362Gly
NM_001354695.1:c.925T>G NP_001341624.1:p.Trp309Gly
NR_148940.1:n.1795T>G
NR_148941.1:n.1741T>G
NR_148942.1:n.1680T>G
XM_011533974.3:c.1267T>G XP_011532276.1:p.Trp423Gly
XM_017006966.1:c.1168T>G XP_016862455.1:p.Trp390Gly
NM_001354689.3:c.1327T>G NP_001341618.1:p.Trp443Gly
NM_001354690.2:c.1267T>G NP_001341619.1:p.Trp423Gly
NM_001354691.2:c.1024T>G NP_001341620.1:p.Trp342Gly
NM_001354692.2:c.1024T>G NP_001341621.1:p.Trp342Gly
NM_001354693.2:c.1168T>G NP_001341622.1:p.Trp390Gly
NM_001354694.2:c.1084T>G NP_001341623.1:p.Trp362Gly
NM_001354695.2:c.925T>G NP_001341624.1:p.Trp309Gly
NR_148940.2:n.1711T>G
NR_148941.2:n.1657T>G
NR_148942.2:n.1596T>G
NM_001354690.3:c.1267T>G NP_001341619.1:p.Trp423Gly
NM_001354691.3:c.1024T>G NP_001341620.1:p.Trp342Gly
NM_001354692.3:c.1024T>G NP_001341621.1:p.Trp342Gly
NM_001354693.3:c.1168T>G NP_001341622.1:p.Trp390Gly
NM_001354694.3:c.1084T>G NP_001341623.1:p.Trp362Gly
NM_001354695.3:c.925T>G NP_001341624.1:p.Trp309Gly
NM_002880.4:c.1267T>G MANE Select NP_002871.1:p.Trp423Gly
NR_148940.3:n.1711T>G
NR_148941.3:n.1657T>G
NR_148942.3:n.1596T>G