Canonical Allele Identifier: CA351495665

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12584561T>C , CM000665.2:g.12584561T>C GRCh38
NC_000003.11:g.12626060T>C , CM000665.1:g.12626060T>C GRCh37
NC_000003.10:g.12601060T>C NCBI36
NG_007467.1:g.84619A>G , LRG_413:g.84619A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000423275.6:c.*1565A>G (RAF1) ENSP00000401088.1:n.*1565A>G
ENST00000432427.3:c.1217A>G (RAF1)
ENST00000460610.2:n.6212A>G (RAF1)
ENST00000471449.2:n.710A>G (RAF1)
ENST00000475353.2:n.4180A>G (RAF1)
ENST00000684903.1:c.*1577A>G (RAF1) ENSP00000508612.1:n.*1577A>G
ENST00000685348.1:c.*1611A>G (RAF1) ENSP00000510285.1:n.*1611A>G
ENST00000685437.1:c.1801A>G (RAF1) ENSP00000508794.1:p.Ile601Val
ENST00000685653.1:c.1900A>G (RAF1) ENSP00000509968.1:p.Ile634Val
ENST00000685697.1:n.2635A>G (RAF1)
ENST00000685738.1:c.*864A>G (RAF1) ENSP00000510156.1:n.*864A>G
ENST00000686409.1:n.5309A>G (RAF1)
ENST00000686455.1:n.4621A>G (RAF1)
ENST00000686762.1:c.*459A>G (RAF1) ENSP00000509767.1:n.*459A>G
ENST00000687257.1:n.4354A>G (RAF1)
ENST00000687326.1:c.*3192A>G (RAF1) ENSP00000509665.1:n.*3192A>G
ENST00000687505.1:n.2018A>G (RAF1)
ENST00000687923.1:c.1789A>G (RAF1) ENSP00000510255.1:p.Ile597Val
ENST00000688269.1:n.2496A>G (RAF1)
ENST00000688444.1:n.4017A>G (RAF1)
ENST00000688543.1:c.1801A>G (RAF1) ENSP00000509612.1:p.Ile601Val
ENST00000688625.1:c.*3269A>G (RAF1) ENSP00000509522.1:n.*3269A>G
ENST00000688803.1:n.3328A>G (RAF1)
ENST00000689097.1:c.*1577A>G (RAF1) ENSP00000509756.1:n.*1577A>G
ENST00000689389.1:c.1723A>G (RAF1) ENSP00000510213.1:p.Ile575Val
ENST00000689418.1:c.*3795A>G (RAF1) ENSP00000509467.1:n.*3795A>G
ENST00000689540.1:n.4268A>G (RAF1)
ENST00000689876.1:c.*449A>G (RAF1) ENSP00000508535.1:n.*449A>G
ENST00000689914.1:c.*834A>G (RAF1) ENSP00000509847.1:n.*834A>G
ENST00000690397.1:c.1789A>G (RAF1) ENSP00000508730.1:p.Ile597Val
ENST00000690460.1:c.1888A>G (RAF1) ENSP00000509106.1:p.Ile630Val
ENST00000690585.1:c.626A>G (RAF1)
ENST00000690625.1:n.2936A>G (RAF1)
ENST00000691396.1:c.*1772A>G (RAF1) ENSP00000510712.1:n.*1772A>G
ENST00000691643.1:n.2953A>G (RAF1)
ENST00000691724.1:c.*857A>G (RAF1) ENSP00000509255.1:n.*857A>G
ENST00000691779.1:c.*1478A>G (RAF1) ENSP00000508592.1:n.*1478A>G
ENST00000691888.1:c.774A>G (RAF1)
ENST00000691899.1:c.1900A>G (RAF1) ENSP00000508763.1:p.Ile634Val
ENST00000692069.1:n.4824A>G (RAF1)
ENST00000692093.1:c.1801A>G (RAF1) ENSP00000509669.1:p.Ile601Val
ENST00000692311.1:n.2724A>G (RAF1)
ENST00000692558.1:n.4483A>G (RAF1)
ENST00000692773.1:c.*1637A>G (RAF1) ENSP00000509055.1:n.*1637A>G
ENST00000692830.1:c.*1645A>G (RAF1) ENSP00000509461.1:n.*1645A>G
ENST00000693312.1:c.1675A>G (RAF1) ENSP00000508686.1:p.Ile559Val
ENST00000693664.1:c.*351A>G (RAF1) ENSP00000509614.1:n.*351A>G
ENST00000693705.1:c.*1279A>G (RAF1) ENSP00000510697.1:n.*1279A>G
ENST00000251849.9:c.1900A>G (RAF1) MANE Select ENSP00000251849.4:p.Ile634Val
ENST00000442415.7:c.1960A>G (RAF1) ENSP00000401888.2:p.Ile654Val
ENST00000676541.1:c.*2308T>C (MKRN2) ENSP00000503730.1:n.*2308T>C
ENST00000677142.1:c.*2308T>C (MKRN2) ENSP00000504455.1:n.*2308T>C
ENST00000677816.1:c.*863T>C (MKRN2) ENSP00000502893.1:n.*863T>C
ENST00000677941.1:n.2371T>C (MKRN2)
ENST00000251849.8:c.1900A>G (RAF1) ENSP00000251849.4:p.Ile634Val
ENST00000423275.5:c.*1577A>G (RAF1) ENSP00000401088.1:n.*1577A>G
ENST00000432427.2:c.1537A>G (RAF1) ENSP00000398591.2:p.Ile513Val
ENST00000442415.6:c.1960A>G (RAF1) ENSP00000401888.2:p.Ile654Val
ENST00000471449.1:n.589A>G (RAF1)
NM_002880.3:c.1900A>G , LRG_413t1:c.1900A>G (RAF1) NP_002871.1:p.Ile634Val
XM_005265355.1:c.1900A>G (RAF1) XP_005265412.1:p.Ile634Val
XM_005265357.1:c.1801A>G (RAF1) XP_005265414.1:p.Ile601Val
XM_005265358.3:c.1657A>G (RAF1) XP_005265415.1:p.Ile553Val
XM_005265359.3:c.1558A>G (RAF1) XP_005265416.1:p.Ile520Val
XM_011533974.1:c.1900A>G (RAF1) XP_011532276.1:p.Ile634Val
XM_011533975.1:c.1657A>G (RAF1) XP_011532277.1:p.Ile553Val
NM_001354689.1:c.1960A>G (RAF1) NP_001341618.1:p.Ile654Val
NM_001354690.1:c.1900A>G (RAF1) NP_001341619.1:p.Ile634Val
NM_001354691.1:c.1657A>G (RAF1) NP_001341620.1:p.Ile553Val
NM_001354692.1:c.1657A>G (RAF1) NP_001341621.1:p.Ile553Val
NM_001354693.1:c.1801A>G (RAF1) NP_001341622.1:p.Ile601Val
NM_001354694.1:c.1717A>G (RAF1) NP_001341623.1:p.Ile573Val
NM_001354695.1:c.1558A>G (RAF1) NP_001341624.1:p.Ile520Val
NR_148940.1:n.2428A>G (RAF1)
NR_148941.1:n.2374A>G (RAF1)
NR_148942.1:n.2313A>G (RAF1)
XM_011533974.3:c.1900A>G (RAF1) XP_011532276.1:p.Ile634Val
XM_017006966.1:c.1801A>G (RAF1) XP_016862455.1:p.Ile601Val
NM_001354689.3:c.1960A>G (RAF1) NP_001341618.1:p.Ile654Val
NM_001354690.2:c.1900A>G (RAF1) NP_001341619.1:p.Ile634Val
NM_001354691.2:c.1657A>G (RAF1) NP_001341620.1:p.Ile553Val
NM_001354692.2:c.1657A>G (RAF1) NP_001341621.1:p.Ile553Val
NM_001354693.2:c.1801A>G (RAF1) NP_001341622.1:p.Ile601Val
NM_001354694.2:c.1717A>G (RAF1) NP_001341623.1:p.Ile573Val
NM_001354695.2:c.1558A>G (RAF1) NP_001341624.1:p.Ile520Val
NR_148940.2:n.2344A>G (RAF1)
NR_148941.2:n.2290A>G (RAF1)
NR_148942.2:n.2229A>G (RAF1)
NM_001354690.3:c.1900A>G (RAF1) NP_001341619.1:p.Ile634Val
NM_001354691.3:c.1657A>G (RAF1) NP_001341620.1:p.Ile553Val
NM_001354692.3:c.1657A>G (RAF1) NP_001341621.1:p.Ile553Val
NM_001354693.3:c.1801A>G (RAF1) NP_001341622.1:p.Ile601Val
NM_001354694.3:c.1717A>G (RAF1) NP_001341623.1:p.Ile573Val
NM_001354695.3:c.1558A>G (RAF1) NP_001341624.1:p.Ile520Val
NM_002880.4:c.1900A>G (RAF1) MANE Select NP_002871.1:p.Ile634Val
NR_148940.3:n.2344A>G (RAF1)
NR_148941.3:n.2290A>G (RAF1)
NR_148942.3:n.2229A>G (RAF1)