Canonical Allele Identifier: CA2259463

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12585181C>T , CM000665.2:g.12585181C>T GRCh38
NC_000003.11:g.12626680C>T , CM000665.1:g.12626680C>T GRCh37
NC_000003.10:g.12601680C>T NCBI36
NG_007467.1:g.83999G>A , LRG_413:g.83999G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000423275.6:c.*1274G>A (RAF1) ENSP00000401088.1:n.*1274G>A
ENST00000432427.3:c.926G>A (RAF1)
ENST00000460610.2:n.5781G>A (RAF1)
ENST00000471449.2:n.419G>A (RAF1)
ENST00000475353.2:n.3749G>A (RAF1)
ENST00000684903.1:c.*1286G>A (RAF1) ENSP00000508612.1:n.*1286G>A
ENST00000685348.1:c.*1320G>A (RAF1) ENSP00000510285.1:n.*1320G>A
ENST00000685437.1:c.1510G>A (RAF1) ENSP00000508794.1:p.Val504Ile
ENST00000685653.1:c.1609G>A (RAF1) ENSP00000509968.1:p.Val537Ile
ENST00000685697.1:n.2344G>A (RAF1)
ENST00000685738.1:c.*573G>A (RAF1) ENSP00000510156.1:n.*573G>A
ENST00000686409.1:n.4878G>A (RAF1)
ENST00000686455.1:n.4190G>A (RAF1)
ENST00000686762.1:c.*168G>A (RAF1) ENSP00000509767.1:n.*168G>A
ENST00000687257.1:n.4063G>A (RAF1)
ENST00000687326.1:c.*2761G>A (RAF1) ENSP00000509665.1:n.*2761G>A
ENST00000687505.1:n.1727G>A (RAF1)
ENST00000687923.1:c.1498G>A (RAF1) ENSP00000510255.1:p.Val500Ile
ENST00000688269.1:n.2205G>A (RAF1)
ENST00000688444.1:n.3726G>A (RAF1)
ENST00000688543.1:c.1510G>A (RAF1) ENSP00000509612.1:p.Val504Ile
ENST00000688625.1:c.*2978G>A (RAF1) ENSP00000509522.1:n.*2978G>A
ENST00000688803.1:n.3037G>A (RAF1)
ENST00000688914.1:n.1022G>A (RAF1)
ENST00000689097.1:c.*1286G>A (RAF1) ENSP00000509756.1:n.*1286G>A
ENST00000689389.1:c.1432G>A (RAF1) ENSP00000510213.1:p.Val478Ile
ENST00000689418.1:c.*3504G>A (RAF1) ENSP00000509467.1:n.*3504G>A
ENST00000689540.1:n.3977G>A (RAF1)
ENST00000689876.1:c.*158G>A (RAF1) ENSP00000508535.1:n.*158G>A
ENST00000689914.1:c.*543G>A (RAF1) ENSP00000509847.1:n.*543G>A
ENST00000690397.1:c.1498G>A (RAF1) ENSP00000508730.1:p.Val500Ile
ENST00000690460.1:c.1597G>A (RAF1) ENSP00000509106.1:p.Val533Ile
ENST00000690585.1:c.335G>A (RAF1)
ENST00000690625.1:n.2645G>A (RAF1)
ENST00000691396.1:c.*1481G>A (RAF1) ENSP00000510712.1:n.*1481G>A
ENST00000691643.1:n.2662G>A (RAF1)
ENST00000691724.1:c.*566G>A (RAF1) ENSP00000509255.1:n.*566G>A
ENST00000691779.1:c.*1187G>A (RAF1) ENSP00000508592.1:n.*1187G>A
ENST00000691888.1:c.483G>A (RAF1)
ENST00000691899.1:c.1609G>A (RAF1) ENSP00000508763.1:p.Val537Ile
ENST00000692069.1:n.4393G>A (RAF1)
ENST00000692093.1:c.1510G>A (RAF1) ENSP00000509669.1:p.Val504Ile
ENST00000692311.1:n.2433G>A (RAF1)
ENST00000692558.1:n.4192G>A (RAF1)
ENST00000692773.1:c.*1346G>A (RAF1) ENSP00000509055.1:n.*1346G>A
ENST00000692830.1:c.*1354G>A (RAF1) ENSP00000509461.1:n.*1354G>A
ENST00000693312.1:c.1384G>A (RAF1) ENSP00000508686.1:p.Val462Ile
ENST00000693664.1:c.*60G>A (RAF1) ENSP00000509614.1:n.*60G>A
ENST00000693705.1:c.*1048-200G>A (RAF1) ENSP00000510697.1:n.*1048-200G>A
ENST00000251849.9:c.1609G>A (RAF1) MANE Select ENSP00000251849.4:p.Val537Ile
ENST00000442415.7:c.1669G>A (RAF1) ENSP00000401888.2:p.Val557Ile
ENST00000676541.1:c.*2928C>T (MKRN2) ENSP00000503730.1:n.*2928C>T
ENST00000677142.1:c.*2928C>T (MKRN2) ENSP00000504455.1:n.*2928C>T
ENST00000677816.1:c.*1483C>T (MKRN2) ENSP00000502893.1:n.*1483C>T
ENST00000677941.1:n.2991C>T (MKRN2)
ENST00000251849.8:c.1609G>A (RAF1) ENSP00000251849.4:p.Val537Ile
ENST00000423275.5:c.*1286G>A (RAF1) ENSP00000401088.1:n.*1286G>A
ENST00000432427.2:c.1246G>A (RAF1) ENSP00000398591.2:p.Val416Ile
ENST00000442415.6:c.1669G>A (RAF1) ENSP00000401888.2:p.Val557Ile
ENST00000471449.1:n.298G>A (RAF1)
NM_002880.3:c.1609G>A , LRG_413t1:c.1609G>A (RAF1) NP_002871.1:p.Val537Ile
XM_005265355.1:c.1609G>A (RAF1) XP_005265412.1:p.Val537Ile
XM_005265357.1:c.1510G>A (RAF1) XP_005265414.1:p.Val504Ile
XM_005265358.3:c.1366G>A (RAF1) XP_005265415.1:p.Val456Ile
XM_005265359.3:c.1267G>A (RAF1) XP_005265416.1:p.Val423Ile
XM_011533974.1:c.1609G>A (RAF1) XP_011532276.1:p.Val537Ile
XM_011533975.1:c.1366G>A (RAF1) XP_011532277.1:p.Val456Ile
NM_001354689.1:c.1669G>A (RAF1) NP_001341618.1:p.Val557Ile
NM_001354690.1:c.1609G>A (RAF1) NP_001341619.1:p.Val537Ile
NM_001354691.1:c.1366G>A (RAF1) NP_001341620.1:p.Val456Ile
NM_001354692.1:c.1366G>A (RAF1) NP_001341621.1:p.Val456Ile
NM_001354693.1:c.1510G>A (RAF1) NP_001341622.1:p.Val504Ile
NM_001354694.1:c.1426G>A (RAF1) NP_001341623.1:p.Val476Ile
NM_001354695.1:c.1267G>A (RAF1) NP_001341624.1:p.Val423Ile
NR_148940.1:n.2137G>A (RAF1)
NR_148941.1:n.2083G>A (RAF1)
NR_148942.1:n.2022G>A (RAF1)
XM_011533974.3:c.1609G>A (RAF1) XP_011532276.1:p.Val537Ile
XM_017006966.1:c.1510G>A (RAF1) XP_016862455.1:p.Val504Ile
NM_001354689.3:c.1669G>A (RAF1) NP_001341618.1:p.Val557Ile
NM_001354690.2:c.1609G>A (RAF1) NP_001341619.1:p.Val537Ile
NM_001354691.2:c.1366G>A (RAF1) NP_001341620.1:p.Val456Ile
NM_001354692.2:c.1366G>A (RAF1) NP_001341621.1:p.Val456Ile
NM_001354693.2:c.1510G>A (RAF1) NP_001341622.1:p.Val504Ile
NM_001354694.2:c.1426G>A (RAF1) NP_001341623.1:p.Val476Ile
NM_001354695.2:c.1267G>A (RAF1) NP_001341624.1:p.Val423Ile
NR_148940.2:n.2053G>A (RAF1)
NR_148941.2:n.1999G>A (RAF1)
NR_148942.2:n.1938G>A (RAF1)
NM_001354690.3:c.1609G>A (RAF1) NP_001341619.1:p.Val537Ile
NM_001354691.3:c.1366G>A (RAF1) NP_001341620.1:p.Val456Ile
NM_001354692.3:c.1366G>A (RAF1) NP_001341621.1:p.Val456Ile
NM_001354693.3:c.1510G>A (RAF1) NP_001341622.1:p.Val504Ile
NM_001354694.3:c.1426G>A (RAF1) NP_001341623.1:p.Val476Ile
NM_001354695.3:c.1267G>A (RAF1) NP_001341624.1:p.Val423Ile
NM_002880.4:c.1609G>A (RAF1) MANE Select NP_002871.1:p.Val537Ile
NR_148940.3:n.2053G>A (RAF1)
NR_148941.3:n.1999G>A (RAF1)
NR_148942.3:n.1938G>A (RAF1)