Canonical Allele Identifier: CA351501670
Gene: RAF1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12590808G>C , CM000665.2:g.12590808G>C GRCh38
NC_000003.11:g.12632307G>C , CM000665.1:g.12632307G>C GRCh37
NC_000003.10:g.12607307G>C NCBI36
NG_007467.1:g.78372C>G , LRG_413:g.78372C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000423275.6:c.*1025C>G ENSP00000401088.1:n.*1025C>G
ENST00000432427.3:c.677C>G
ENST00000460610.2:n.154C>G
ENST00000465826.6:n.951C>G
ENST00000475353.2:n.1282C>G
ENST00000494557.2:n.1171C>G
ENST00000684903.1:c.*1037C>G ENSP00000508612.1:n.*1037C>G
ENST00000685348.1:c.*1037C>G ENSP00000510285.1:n.*1037C>G
ENST00000685437.1:c.1261C>G ENSP00000508794.1:p.Gln421Glu
ENST00000685653.1:c.1360C>G ENSP00000509968.1:p.Gln454Glu
ENST00000685738.1:c.*324C>G ENSP00000510156.1:n.*324C>G
ENST00000686409.1:n.2411C>G
ENST00000686455.1:n.1723C>G
ENST00000686762.1:c.1360C>G ENSP00000509767.1:p.Gln454Glu
ENST00000687257.1:n.1596C>G
ENST00000687326.1:c.*294C>G ENSP00000509665.1:n.*294C>G
ENST00000687505.1:n.1478C>G
ENST00000687923.1:c.1249C>G ENSP00000510255.1:p.Gln417Glu
ENST00000687940.1:n.1737C>G
ENST00000688269.1:n.1956C>G
ENST00000688326.1:c.793C>G
ENST00000688444.1:n.1686C>G
ENST00000688543.1:c.1261C>G ENSP00000509612.1:p.Gln421Glu
ENST00000688625.1:c.*938C>G ENSP00000509522.1:n.*938C>G
ENST00000688803.1:n.1591C>G
ENST00000688914.1:n.346C>G
ENST00000689097.1:c.*1037C>G ENSP00000509756.1:n.*1037C>G
ENST00000689389.1:c.1193+900C>G ENSP00000510213.1:n.1193+900C>G
ENST00000689418.1:c.*1037C>G ENSP00000509467.1:n.*1037C>G
ENST00000689481.1:c.*1037C>G ENSP00000510248.1:n.*1037C>G
ENST00000689540.1:n.1510C>G
ENST00000689876.1:c.1360C>G ENSP00000508535.1:p.Gln454Glu
ENST00000689914.1:c.*294C>G ENSP00000509847.1:n.*294C>G
ENST00000690397.1:c.1249C>G ENSP00000508730.1:p.Gln417Glu
ENST00000690460.1:c.1348C>G ENSP00000509106.1:p.Gln450Glu
ENST00000690585.1:c.252C>G
ENST00000690625.1:n.2396C>G
ENST00000691396.1:c.*1212C>G ENSP00000510712.1:n.*1212C>G
ENST00000691724.1:c.*317C>G ENSP00000509255.1:n.*317C>G
ENST00000691779.1:c.*938C>G ENSP00000508592.1:n.*938C>G
ENST00000691888.1:c.252C>G
ENST00000691899.1:c.1360C>G ENSP00000508763.1:p.Gln454Glu
ENST00000692069.1:n.1926C>G
ENST00000692093.1:c.1261C>G ENSP00000509669.1:p.Gln421Glu
ENST00000692311.1:n.2184C>G
ENST00000692558.1:n.1725C>G
ENST00000692773.1:c.*1097C>G ENSP00000509055.1:n.*1097C>G
ENST00000692830.1:c.*1105C>G ENSP00000509461.1:n.*1105C>G
ENST00000693069.1:c.*294C>G ENSP00000510072.1:n.*294C>G
ENST00000693312.1:c.1135C>G ENSP00000508686.1:p.Gln379Glu
ENST00000693664.1:c.1360C>G ENSP00000509614.1:p.Gln454Glu
ENST00000693705.1:c.*1037C>G ENSP00000510697.1:n.*1037C>G
ENST00000251849.9:c.1360C>G MANE Select ENSP00000251849.4:p.Gln454Glu
ENST00000442415.7:c.1420C>G ENSP00000401888.2:p.Gln474Glu
ENST00000251849.8:c.1360C>G ENSP00000251849.4:p.Gln454Glu
ENST00000423275.5:c.*1037C>G ENSP00000401088.1:n.*1037C>G
ENST00000432427.2:c.997C>G ENSP00000398591.2:p.Gln333Glu
ENST00000442415.6:c.1420C>G ENSP00000401888.2:p.Gln474Glu
ENST00000460610.1:n.317C>G
ENST00000465826.5:n.717C>G
ENST00000475353.1:n.528C>G
ENST00000494557.1:n.376C>G
NM_002880.3:c.1360C>G , LRG_413t1:c.1360C>G NP_002871.1:p.Gln454Glu
XM_005265355.1:c.1360C>G XP_005265412.1:p.Gln454Glu
XM_005265357.1:c.1261C>G XP_005265414.1:p.Gln421Glu
XM_005265358.3:c.1117C>G XP_005265415.1:p.Gln373Glu
XM_005265359.3:c.1018C>G XP_005265416.1:p.Gln340Glu
XM_005265360.1:c.1360C>G XP_005265417.1:p.Gln454Glu
XM_011533974.1:c.1360C>G XP_011532276.1:p.Gln454Glu
XM_011533975.1:c.1117C>G XP_011532277.1:p.Gln373Glu
NM_001354689.1:c.1420C>G NP_001341618.1:p.Gln474Glu
NM_001354690.1:c.1360C>G NP_001341619.1:p.Gln454Glu
NM_001354691.1:c.1117C>G NP_001341620.1:p.Gln373Glu
NM_001354692.1:c.1117C>G NP_001341621.1:p.Gln373Glu
NM_001354693.1:c.1261C>G NP_001341622.1:p.Gln421Glu
NM_001354694.1:c.1177C>G NP_001341623.1:p.Gln393Glu
NM_001354695.1:c.1018C>G NP_001341624.1:p.Gln340Glu
NR_148940.1:n.1888C>G
NR_148941.1:n.1834C>G
NR_148942.1:n.1773C>G
XM_011533974.3:c.1360C>G XP_011532276.1:p.Gln454Glu
XM_017006966.1:c.1261C>G XP_016862455.1:p.Gln421Glu
NM_001354689.3:c.1420C>G NP_001341618.1:p.Gln474Glu
NM_001354690.2:c.1360C>G NP_001341619.1:p.Gln454Glu
NM_001354691.2:c.1117C>G NP_001341620.1:p.Gln373Glu
NM_001354692.2:c.1117C>G NP_001341621.1:p.Gln373Glu
NM_001354693.2:c.1261C>G NP_001341622.1:p.Gln421Glu
NM_001354694.2:c.1177C>G NP_001341623.1:p.Gln393Glu
NM_001354695.2:c.1018C>G NP_001341624.1:p.Gln340Glu
NR_148940.2:n.1804C>G
NR_148941.2:n.1750C>G
NR_148942.2:n.1689C>G
NM_001354690.3:c.1360C>G NP_001341619.1:p.Gln454Glu
NM_001354691.3:c.1117C>G NP_001341620.1:p.Gln373Glu
NM_001354692.3:c.1117C>G NP_001341621.1:p.Gln373Glu
NM_001354693.3:c.1261C>G NP_001341622.1:p.Gln421Glu
NM_001354694.3:c.1177C>G NP_001341623.1:p.Gln393Glu
NM_001354695.3:c.1018C>G NP_001341624.1:p.Gln340Glu
NM_002880.4:c.1360C>G MANE Select NP_002871.1:p.Gln454Glu
NR_148940.3:n.1804C>G
NR_148941.3:n.1750C>G
NR_148942.3:n.1689C>G