Canonical Allele Identifier: CA351496661

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12584896A>T , CM000665.2:g.12584896A>T GRCh38
NC_000003.11:g.12626395A>T , CM000665.1:g.12626395A>T GRCh37
NC_000003.10:g.12601395A>T NCBI36
NG_007467.1:g.84284T>A , LRG_413:g.84284T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000423275.6:c.*1419T>A (RAF1) ENSP00000401088.1:n.*1419T>A
ENST00000432427.3:c.1071T>A (RAF1)
ENST00000460610.2:n.6066T>A (RAF1)
ENST00000471449.2:n.564T>A (RAF1)
ENST00000475353.2:n.4034T>A (RAF1)
ENST00000684903.1:c.*1431T>A (RAF1) ENSP00000508612.1:n.*1431T>A
ENST00000685348.1:c.*1465T>A (RAF1) ENSP00000510285.1:n.*1465T>A
ENST00000685437.1:c.1655T>A (RAF1) ENSP00000508794.1:p.Val552Glu
ENST00000685653.1:c.1754T>A (RAF1) ENSP00000509968.1:p.Val585Glu
ENST00000685697.1:n.2489T>A (RAF1)
ENST00000685738.1:c.*718T>A (RAF1) ENSP00000510156.1:n.*718T>A
ENST00000686409.1:n.5163T>A (RAF1)
ENST00000686455.1:n.4475T>A (RAF1)
ENST00000686762.1:c.*313T>A (RAF1) ENSP00000509767.1:n.*313T>A
ENST00000687257.1:n.4208T>A (RAF1)
ENST00000687326.1:c.*3046T>A (RAF1) ENSP00000509665.1:n.*3046T>A
ENST00000687505.1:n.1872T>A (RAF1)
ENST00000687923.1:c.1643T>A (RAF1) ENSP00000510255.1:p.Val548Glu
ENST00000688269.1:n.2350T>A (RAF1)
ENST00000688444.1:n.3871T>A (RAF1)
ENST00000688543.1:c.1655T>A (RAF1) ENSP00000509612.1:p.Val552Glu
ENST00000688625.1:c.*3123T>A (RAF1) ENSP00000509522.1:n.*3123T>A
ENST00000688803.1:n.3182T>A (RAF1)
ENST00000688914.1:n.1167T>A (RAF1)
ENST00000689097.1:c.*1431T>A (RAF1) ENSP00000509756.1:n.*1431T>A
ENST00000689389.1:c.1577T>A (RAF1) ENSP00000510213.1:p.Val526Glu
ENST00000689418.1:c.*3649T>A (RAF1) ENSP00000509467.1:n.*3649T>A
ENST00000689540.1:n.4122T>A (RAF1)
ENST00000689876.1:c.*303T>A (RAF1) ENSP00000508535.1:n.*303T>A
ENST00000689914.1:c.*688T>A (RAF1) ENSP00000509847.1:n.*688T>A
ENST00000690397.1:c.1643T>A (RAF1) ENSP00000508730.1:p.Val548Glu
ENST00000690460.1:c.1742T>A (RAF1) ENSP00000509106.1:p.Val581Glu
ENST00000690585.1:c.480T>A (RAF1)
ENST00000690625.1:n.2790T>A (RAF1)
ENST00000691396.1:c.*1626T>A (RAF1) ENSP00000510712.1:n.*1626T>A
ENST00000691643.1:n.2807T>A (RAF1)
ENST00000691724.1:c.*711T>A (RAF1) ENSP00000509255.1:n.*711T>A
ENST00000691779.1:c.*1332T>A (RAF1) ENSP00000508592.1:n.*1332T>A
ENST00000691888.1:c.628T>A (RAF1)
ENST00000691899.1:c.1754T>A (RAF1) ENSP00000508763.1:p.Val585Glu
ENST00000692069.1:n.4678T>A (RAF1)
ENST00000692093.1:c.1655T>A (RAF1) ENSP00000509669.1:p.Val552Glu
ENST00000692311.1:n.2578T>A (RAF1)
ENST00000692558.1:n.4337T>A (RAF1)
ENST00000692773.1:c.*1491T>A (RAF1) ENSP00000509055.1:n.*1491T>A
ENST00000692830.1:c.*1499T>A (RAF1) ENSP00000509461.1:n.*1499T>A
ENST00000693312.1:c.1529T>A (RAF1) ENSP00000508686.1:p.Val510Glu
ENST00000693664.1:c.*205T>A (RAF1) ENSP00000509614.1:n.*205T>A
ENST00000693705.1:c.*1133T>A (RAF1) ENSP00000510697.1:n.*1133T>A
ENST00000251849.9:c.1754T>A (RAF1) MANE Select ENSP00000251849.4:p.Val585Glu
ENST00000442415.7:c.1814T>A (RAF1) ENSP00000401888.2:p.Val605Glu
ENST00000676541.1:c.*2643A>T (MKRN2) ENSP00000503730.1:n.*2643A>T
ENST00000677142.1:c.*2643A>T (MKRN2) ENSP00000504455.1:n.*2643A>T
ENST00000677816.1:c.*1198A>T (MKRN2) ENSP00000502893.1:n.*1198A>T
ENST00000677941.1:n.2706A>T (MKRN2)
ENST00000251849.8:c.1754T>A (RAF1) ENSP00000251849.4:p.Val585Glu
ENST00000423275.5:c.*1431T>A (RAF1) ENSP00000401088.1:n.*1431T>A
ENST00000432427.2:c.1391T>A (RAF1) ENSP00000398591.2:p.Val464Glu
ENST00000442415.6:c.1814T>A (RAF1) ENSP00000401888.2:p.Val605Glu
ENST00000471449.1:n.443T>A (RAF1)
NM_002880.3:c.1754T>A , LRG_413t1:c.1754T>A (RAF1) NP_002871.1:p.Val585Glu
XM_005265355.1:c.1754T>A (RAF1) XP_005265412.1:p.Val585Glu
XM_005265357.1:c.1655T>A (RAF1) XP_005265414.1:p.Val552Glu
XM_005265358.3:c.1511T>A (RAF1) XP_005265415.1:p.Val504Glu
XM_005265359.3:c.1412T>A (RAF1) XP_005265416.1:p.Val471Glu
XM_011533974.1:c.1754T>A (RAF1) XP_011532276.1:p.Val585Glu
XM_011533975.1:c.1511T>A (RAF1) XP_011532277.1:p.Val504Glu
NM_001354689.1:c.1814T>A (RAF1) NP_001341618.1:p.Val605Glu
NM_001354690.1:c.1754T>A (RAF1) NP_001341619.1:p.Val585Glu
NM_001354691.1:c.1511T>A (RAF1) NP_001341620.1:p.Val504Glu
NM_001354692.1:c.1511T>A (RAF1) NP_001341621.1:p.Val504Glu
NM_001354693.1:c.1655T>A (RAF1) NP_001341622.1:p.Val552Glu
NM_001354694.1:c.1571T>A (RAF1) NP_001341623.1:p.Val524Glu
NM_001354695.1:c.1412T>A (RAF1) NP_001341624.1:p.Val471Glu
NR_148940.1:n.2282T>A (RAF1)
NR_148941.1:n.2228T>A (RAF1)
NR_148942.1:n.2167T>A (RAF1)
XM_011533974.3:c.1754T>A (RAF1) XP_011532276.1:p.Val585Glu
XM_017006966.1:c.1655T>A (RAF1) XP_016862455.1:p.Val552Glu
NM_001354689.3:c.1814T>A (RAF1) NP_001341618.1:p.Val605Glu
NM_001354690.2:c.1754T>A (RAF1) NP_001341619.1:p.Val585Glu
NM_001354691.2:c.1511T>A (RAF1) NP_001341620.1:p.Val504Glu
NM_001354692.2:c.1511T>A (RAF1) NP_001341621.1:p.Val504Glu
NM_001354693.2:c.1655T>A (RAF1) NP_001341622.1:p.Val552Glu
NM_001354694.2:c.1571T>A (RAF1) NP_001341623.1:p.Val524Glu
NM_001354695.2:c.1412T>A (RAF1) NP_001341624.1:p.Val471Glu
NR_148940.2:n.2198T>A (RAF1)
NR_148941.2:n.2144T>A (RAF1)
NR_148942.2:n.2083T>A (RAF1)
NM_001354690.3:c.1754T>A (RAF1) NP_001341619.1:p.Val585Glu
NM_001354691.3:c.1511T>A (RAF1) NP_001341620.1:p.Val504Glu
NM_001354692.3:c.1511T>A (RAF1) NP_001341621.1:p.Val504Glu
NM_001354693.3:c.1655T>A (RAF1) NP_001341622.1:p.Val552Glu
NM_001354694.3:c.1571T>A (RAF1) NP_001341623.1:p.Val524Glu
NM_001354695.3:c.1412T>A (RAF1) NP_001341624.1:p.Val471Glu
NM_002880.4:c.1754T>A (RAF1) MANE Select NP_002871.1:p.Val585Glu
NR_148940.3:n.2198T>A (RAF1)
NR_148941.3:n.2144T>A (RAF1)
NR_148942.3:n.2083T>A (RAF1)