Canonical Allele Identifier: CA2702178704

Linked Data

dbSNP Id: rs2125314905

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12584434T>C , CM000665.2:g.12584434T>C GRCh38
NC_000003.11:g.12625933T>C , CM000665.1:g.12625933T>C GRCh37
NC_000003.10:g.12600933T>C NCBI36
NG_007467.1:g.84746A>G , LRG_413:g.84746A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000423275.6:c.*1692A>G (RAF1) ENSP00000401088.1:n.*1692A>G
ENST00000432427.3:c.1344A>G (RAF1)
ENST00000460610.2:n.6339A>G (RAF1)
ENST00000471449.2:n.837A>G (RAF1)
ENST00000475353.2:n.4307A>G (RAF1)
ENST00000684903.1:c.*1704A>G (RAF1) ENSP00000508612.1:n.*1704A>G
ENST00000685348.1:c.*1738A>G (RAF1) ENSP00000510285.1:n.*1738A>G
ENST00000685437.1:c.*80A>G (RAF1) ENSP00000508794.1:n.*80A>G
ENST00000685653.1:c.*80A>G (RAF1) ENSP00000509968.1:n.*80A>G
ENST00000685697.1:n.2762A>G (RAF1)
ENST00000685738.1:c.*991A>G (RAF1) ENSP00000510156.1:n.*991A>G
ENST00000686409.1:n.5436A>G (RAF1)
ENST00000686455.1:n.4748A>G (RAF1)
ENST00000686762.1:c.*586A>G (RAF1) ENSP00000509767.1:n.*586A>G
ENST00000687257.1:n.4481A>G (RAF1)
ENST00000687326.1:c.*3319A>G (RAF1) ENSP00000509665.1:n.*3319A>G
ENST00000687505.1:n.2145A>G (RAF1)
ENST00000687923.1:c.*80A>G (RAF1) ENSP00000510255.1:n.*80A>G
ENST00000688269.1:n.2623A>G (RAF1)
ENST00000688444.1:n.4144A>G (RAF1)
ENST00000688543.1:c.*80A>G (RAF1) ENSP00000509612.1:n.*80A>G
ENST00000688625.1:c.*3396A>G (RAF1) ENSP00000509522.1:n.*3396A>G
ENST00000688803.1:n.3455A>G (RAF1)
ENST00000689097.1:c.*1704A>G (RAF1) ENSP00000509756.1:n.*1704A>G
ENST00000689389.1:c.*80A>G (RAF1) ENSP00000510213.1:n.*80A>G
ENST00000689418.1:c.*3922A>G (RAF1) ENSP00000509467.1:n.*3922A>G
ENST00000689540.1:n.4395A>G (RAF1)
ENST00000689876.1:c.*576A>G (RAF1) ENSP00000508535.1:n.*576A>G
ENST00000689914.1:c.*961A>G (RAF1) ENSP00000509847.1:n.*961A>G
ENST00000690397.1:c.*80A>G (RAF1) ENSP00000508730.1:n.*80A>G
ENST00000690460.1:c.*80A>G (RAF1) ENSP00000509106.1:n.*80A>G
ENST00000690585.1:c.753A>G (RAF1)
ENST00000690625.1:n.3063A>G (RAF1)
ENST00000691396.1:c.*1899A>G (RAF1) ENSP00000510712.1:n.*1899A>G
ENST00000691643.1:n.3080A>G (RAF1)
ENST00000691724.1:c.*984A>G (RAF1) ENSP00000509255.1:n.*984A>G
ENST00000691779.1:c.*1605A>G (RAF1) ENSP00000508592.1:n.*1605A>G
ENST00000691888.1:c.901A>G (RAF1)
ENST00000691899.1:c.*80A>G (RAF1) ENSP00000508763.1:n.*80A>G
ENST00000692069.1:n.4951A>G (RAF1)
ENST00000692093.1:c.*80A>G (RAF1) ENSP00000509669.1:n.*80A>G
ENST00000692311.1:n.2851A>G (RAF1)
ENST00000692558.1:n.4610A>G (RAF1)
ENST00000692773.1:c.*1764A>G (RAF1) ENSP00000509055.1:n.*1764A>G
ENST00000692830.1:c.*1772A>G (RAF1) ENSP00000509461.1:n.*1772A>G
ENST00000693312.1:c.*80A>G (RAF1) ENSP00000508686.1:n.*80A>G
ENST00000693664.1:c.*478A>G (RAF1) ENSP00000509614.1:n.*478A>G
ENST00000693705.1:c.*1406A>G (RAF1) ENSP00000510697.1:n.*1406A>G
ENST00000251849.9:c.*80A>G (RAF1) MANE Select ENSP00000251849.4:n.*80A>G
ENST00000442415.7:c.*80A>G (RAF1) ENSP00000401888.2:n.*80A>G
ENST00000676541.1:c.*2181T>C (MKRN2) ENSP00000503730.1:n.*2181T>C
ENST00000677142.1:c.*2181T>C (MKRN2) ENSP00000504455.1:n.*2181T>C
ENST00000677816.1:c.*736T>C (MKRN2) ENSP00000502893.1:n.*736T>C
ENST00000677941.1:n.2244T>C (MKRN2)
ENST00000251849.8:c.*80A>G (RAF1) ENSP00000251849.4:n.*80A>G
ENST00000423275.5:c.*1704A>G (RAF1) ENSP00000401088.1:n.*1704A>G
ENST00000432427.2:c.1664A>G (RAF1) ENSP00000398591.2:n.1664A>G
ENST00000442415.6:c.*80A>G (RAF1) ENSP00000401888.2:n.*80A>G
ENST00000471449.1:n.716A>G (RAF1)
NM_002880.3:c.*80A>G , LRG_413t1:c.*80A>G (RAF1) NP_002871.1:n.*80A>G
XM_005265355.1:c.*80A>G (RAF1) XP_005265412.1:n.*80A>G
XM_005265357.1:c.*80A>G (RAF1) XP_005265414.1:n.*80A>G
XM_005265358.3:c.*80A>G (RAF1) XP_005265415.1:n.*80A>G
XM_005265359.3:c.*80A>G (RAF1) XP_005265416.1:n.*80A>G
XM_011533974.1:c.*80A>G (RAF1) XP_011532276.1:n.*80A>G
XM_011533975.1:c.*80A>G (RAF1) XP_011532277.1:n.*80A>G
NM_001354689.1:c.*80A>G (RAF1) NP_001341618.1:n.*80A>G
NM_001354690.1:c.*80A>G (RAF1) NP_001341619.1:n.*80A>G
NM_001354691.1:c.*80A>G (RAF1) NP_001341620.1:n.*80A>G
NM_001354692.1:c.*80A>G (RAF1) NP_001341621.1:n.*80A>G
NM_001354693.1:c.*80A>G (RAF1) NP_001341622.1:n.*80A>G
NM_001354694.1:c.*80A>G (RAF1) NP_001341623.1:n.*80A>G
NM_001354695.1:c.*80A>G (RAF1) NP_001341624.1:n.*80A>G
NR_148940.1:n.2555A>G (RAF1)
NR_148941.1:n.2501A>G (RAF1)
NR_148942.1:n.2440A>G (RAF1)
XM_011533974.3:c.*80A>G (RAF1) XP_011532276.1:n.*80A>G
XM_017006966.1:c.*80A>G (RAF1) XP_016862455.1:n.*80A>G
NM_001354689.3:c.*80A>G (RAF1) NP_001341618.1:n.*80A>G
NM_001354690.2:c.*80A>G (RAF1) NP_001341619.1:n.*80A>G
NM_001354691.2:c.*80A>G (RAF1) NP_001341620.1:n.*80A>G
NM_001354692.2:c.*80A>G (RAF1) NP_001341621.1:n.*80A>G
NM_001354693.2:c.*80A>G (RAF1) NP_001341622.1:n.*80A>G
NM_001354694.2:c.*80A>G (RAF1) NP_001341623.1:n.*80A>G
NM_001354695.2:c.*80A>G (RAF1) NP_001341624.1:n.*80A>G
NR_148940.2:n.2471A>G (RAF1)
NR_148941.2:n.2417A>G (RAF1)
NR_148942.2:n.2356A>G (RAF1)
NM_001354690.3:c.*80A>G (RAF1) NP_001341619.1:n.*80A>G
NM_001354691.3:c.*80A>G (RAF1) NP_001341620.1:n.*80A>G
NM_001354692.3:c.*80A>G (RAF1) NP_001341621.1:n.*80A>G
NM_001354693.3:c.*80A>G (RAF1) NP_001341622.1:n.*80A>G
NM_001354694.3:c.*80A>G (RAF1) NP_001341623.1:n.*80A>G
NM_001354695.3:c.*80A>G (RAF1) NP_001341624.1:n.*80A>G
NM_002880.4:c.*80A>G (RAF1) MANE Select NP_002871.1:n.*80A>G
NR_148940.3:n.2471A>G (RAF1)
NR_148941.3:n.2417A>G (RAF1)
NR_148942.3:n.2356A>G (RAF1)