Canonical Allele Identifier: CA351501639
Gene: RAF1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12590802T>C , CM000665.2:g.12590802T>C GRCh38
NC_000003.11:g.12632301T>C , CM000665.1:g.12632301T>C GRCh37
NC_000003.10:g.12607301T>C NCBI36
NG_007467.1:g.78378A>G , LRG_413:g.78378A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000423275.6:c.*1031A>G ENSP00000401088.1:n.*1031A>G
ENST00000432427.3:c.683A>G
ENST00000460610.2:n.160A>G
ENST00000465826.6:n.957A>G
ENST00000475353.2:n.1288A>G
ENST00000494557.2:n.1177A>G
ENST00000684903.1:c.*1043A>G ENSP00000508612.1:n.*1043A>G
ENST00000685348.1:c.*1043A>G ENSP00000510285.1:n.*1043A>G
ENST00000685437.1:c.1267A>G ENSP00000508794.1:p.Met423Val
ENST00000685653.1:c.1366A>G ENSP00000509968.1:p.Met456Val
ENST00000685738.1:c.*330A>G ENSP00000510156.1:n.*330A>G
ENST00000686409.1:n.2417A>G
ENST00000686455.1:n.1729A>G
ENST00000686762.1:c.1366A>G ENSP00000509767.1:p.Met456Val
ENST00000687257.1:n.1602A>G
ENST00000687326.1:c.*300A>G ENSP00000509665.1:n.*300A>G
ENST00000687505.1:n.1484A>G
ENST00000687923.1:c.1255A>G ENSP00000510255.1:p.Met419Val
ENST00000687940.1:n.1743A>G
ENST00000688269.1:n.1962A>G
ENST00000688326.1:c.799A>G
ENST00000688444.1:n.1692A>G
ENST00000688543.1:c.1267A>G ENSP00000509612.1:p.Met423Val
ENST00000688625.1:c.*944A>G ENSP00000509522.1:n.*944A>G
ENST00000688803.1:n.1597A>G
ENST00000688914.1:n.352A>G
ENST00000689097.1:c.*1043A>G ENSP00000509756.1:n.*1043A>G
ENST00000689389.1:c.1193+906A>G ENSP00000510213.1:n.1193+906A>G
ENST00000689418.1:c.*1043A>G ENSP00000509467.1:n.*1043A>G
ENST00000689481.1:c.*1043A>G ENSP00000510248.1:n.*1043A>G
ENST00000689540.1:n.1516A>G
ENST00000689876.1:c.1366A>G ENSP00000508535.1:p.Met456Val
ENST00000689914.1:c.*300A>G ENSP00000509847.1:n.*300A>G
ENST00000690397.1:c.1255A>G ENSP00000508730.1:p.Met419Val
ENST00000690460.1:c.1354A>G ENSP00000509106.1:p.Met452Val
ENST00000690585.1:c.258A>G
ENST00000690625.1:n.2402A>G
ENST00000691396.1:c.*1218A>G ENSP00000510712.1:n.*1218A>G
ENST00000691724.1:c.*323A>G ENSP00000509255.1:n.*323A>G
ENST00000691779.1:c.*944A>G ENSP00000508592.1:n.*944A>G
ENST00000691888.1:c.258A>G
ENST00000691899.1:c.1366A>G ENSP00000508763.1:p.Met456Val
ENST00000692069.1:n.1932A>G
ENST00000692093.1:c.1267A>G ENSP00000509669.1:p.Met423Val
ENST00000692311.1:n.2190A>G
ENST00000692558.1:n.1731A>G
ENST00000692773.1:c.*1103A>G ENSP00000509055.1:n.*1103A>G
ENST00000692830.1:c.*1111A>G ENSP00000509461.1:n.*1111A>G
ENST00000693069.1:c.*300A>G ENSP00000510072.1:n.*300A>G
ENST00000693312.1:c.1141A>G ENSP00000508686.1:p.Met381Val
ENST00000693664.1:c.1366A>G ENSP00000509614.1:p.Met456Val
ENST00000693705.1:c.*1043A>G ENSP00000510697.1:n.*1043A>G
ENST00000251849.9:c.1366A>G MANE Select ENSP00000251849.4:p.Met456Val
ENST00000442415.7:c.1426A>G ENSP00000401888.2:p.Met476Val
ENST00000251849.8:c.1366A>G ENSP00000251849.4:p.Met456Val
ENST00000423275.5:c.*1043A>G ENSP00000401088.1:n.*1043A>G
ENST00000432427.2:c.1003A>G ENSP00000398591.2:p.Met335Val
ENST00000442415.6:c.1426A>G ENSP00000401888.2:p.Met476Val
ENST00000460610.1:n.323A>G
ENST00000465826.5:n.723A>G
ENST00000475353.1:n.534A>G
ENST00000494557.1:n.382A>G
NM_002880.3:c.1366A>G , LRG_413t1:c.1366A>G NP_002871.1:p.Met456Val
XM_005265355.1:c.1366A>G XP_005265412.1:p.Met456Val
XM_005265357.1:c.1267A>G XP_005265414.1:p.Met423Val
XM_005265358.3:c.1123A>G XP_005265415.1:p.Met375Val
XM_005265359.3:c.1024A>G XP_005265416.1:p.Met342Val
XM_005265360.1:c.1366A>G XP_005265417.1:p.Met456Val
XM_011533974.1:c.1366A>G XP_011532276.1:p.Met456Val
XM_011533975.1:c.1123A>G XP_011532277.1:p.Met375Val
NM_001354689.1:c.1426A>G NP_001341618.1:p.Met476Val
NM_001354690.1:c.1366A>G NP_001341619.1:p.Met456Val
NM_001354691.1:c.1123A>G NP_001341620.1:p.Met375Val
NM_001354692.1:c.1123A>G NP_001341621.1:p.Met375Val
NM_001354693.1:c.1267A>G NP_001341622.1:p.Met423Val
NM_001354694.1:c.1183A>G NP_001341623.1:p.Met395Val
NM_001354695.1:c.1024A>G NP_001341624.1:p.Met342Val
NR_148940.1:n.1894A>G
NR_148941.1:n.1840A>G
NR_148942.1:n.1779A>G
XM_011533974.3:c.1366A>G XP_011532276.1:p.Met456Val
XM_017006966.1:c.1267A>G XP_016862455.1:p.Met423Val
NM_001354689.3:c.1426A>G NP_001341618.1:p.Met476Val
NM_001354690.2:c.1366A>G NP_001341619.1:p.Met456Val
NM_001354691.2:c.1123A>G NP_001341620.1:p.Met375Val
NM_001354692.2:c.1123A>G NP_001341621.1:p.Met375Val
NM_001354693.2:c.1267A>G NP_001341622.1:p.Met423Val
NM_001354694.2:c.1183A>G NP_001341623.1:p.Met395Val
NM_001354695.2:c.1024A>G NP_001341624.1:p.Met342Val
NR_148940.2:n.1810A>G
NR_148941.2:n.1756A>G
NR_148942.2:n.1695A>G
NM_001354690.3:c.1366A>G NP_001341619.1:p.Met456Val
NM_001354691.3:c.1123A>G NP_001341620.1:p.Met375Val
NM_001354692.3:c.1123A>G NP_001341621.1:p.Met375Val
NM_001354693.3:c.1267A>G NP_001341622.1:p.Met423Val
NM_001354694.3:c.1183A>G NP_001341623.1:p.Met395Val
NM_001354695.3:c.1024A>G NP_001341624.1:p.Met342Val
NM_002880.4:c.1366A>G MANE Select NP_002871.1:p.Met456Val
NR_148940.3:n.1810A>G
NR_148941.3:n.1756A>G
NR_148942.3:n.1695A>G