Canonical Allele Identifier: CA2664506797

Linked Data

dbSNP Id: rs2125315013
gnomAD v4: 3-12584448-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12584448G>A , CM000665.2:g.12584448G>A GRCh38
NC_000003.11:g.12625947G>A , CM000665.1:g.12625947G>A GRCh37
NC_000003.10:g.12600947G>A NCBI36
NG_007467.1:g.84732C>T , LRG_413:g.84732C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000423275.6:c.*1678C>T (RAF1) ENSP00000401088.1:n.*1678C>T
ENST00000432427.3:c.1330C>T (RAF1)
ENST00000460610.2:n.6325C>T (RAF1)
ENST00000471449.2:n.823C>T (RAF1)
ENST00000475353.2:n.4293C>T (RAF1)
ENST00000684903.1:c.*1690C>T (RAF1) ENSP00000508612.1:n.*1690C>T
ENST00000685348.1:c.*1724C>T (RAF1) ENSP00000510285.1:n.*1724C>T
ENST00000685437.1:c.*66C>T (RAF1) ENSP00000508794.1:n.*66C>T
ENST00000685653.1:c.*66C>T (RAF1) ENSP00000509968.1:n.*66C>T
ENST00000685697.1:n.2748C>T (RAF1)
ENST00000685738.1:c.*977C>T (RAF1) ENSP00000510156.1:n.*977C>T
ENST00000686409.1:n.5422C>T (RAF1)
ENST00000686455.1:n.4734C>T (RAF1)
ENST00000686762.1:c.*572C>T (RAF1) ENSP00000509767.1:n.*572C>T
ENST00000687257.1:n.4467C>T (RAF1)
ENST00000687326.1:c.*3305C>T (RAF1) ENSP00000509665.1:n.*3305C>T
ENST00000687505.1:n.2131C>T (RAF1)
ENST00000687923.1:c.*66C>T (RAF1) ENSP00000510255.1:n.*66C>T
ENST00000688269.1:n.2609C>T (RAF1)
ENST00000688444.1:n.4130C>T (RAF1)
ENST00000688543.1:c.*66C>T (RAF1) ENSP00000509612.1:n.*66C>T
ENST00000688625.1:c.*3382C>T (RAF1) ENSP00000509522.1:n.*3382C>T
ENST00000688803.1:n.3441C>T (RAF1)
ENST00000689097.1:c.*1690C>T (RAF1) ENSP00000509756.1:n.*1690C>T
ENST00000689389.1:c.*66C>T (RAF1) ENSP00000510213.1:n.*66C>T
ENST00000689418.1:c.*3908C>T (RAF1) ENSP00000509467.1:n.*3908C>T
ENST00000689540.1:n.4381C>T (RAF1)
ENST00000689876.1:c.*562C>T (RAF1) ENSP00000508535.1:n.*562C>T
ENST00000689914.1:c.*947C>T (RAF1) ENSP00000509847.1:n.*947C>T
ENST00000690397.1:c.*66C>T (RAF1) ENSP00000508730.1:n.*66C>T
ENST00000690460.1:c.*66C>T (RAF1) ENSP00000509106.1:n.*66C>T
ENST00000690585.1:c.739C>T (RAF1)
ENST00000690625.1:n.3049C>T (RAF1)
ENST00000691396.1:c.*1885C>T (RAF1) ENSP00000510712.1:n.*1885C>T
ENST00000691643.1:n.3066C>T (RAF1)
ENST00000691724.1:c.*970C>T (RAF1) ENSP00000509255.1:n.*970C>T
ENST00000691779.1:c.*1591C>T (RAF1) ENSP00000508592.1:n.*1591C>T
ENST00000691888.1:c.887C>T (RAF1)
ENST00000691899.1:c.*66C>T (RAF1) ENSP00000508763.1:n.*66C>T
ENST00000692069.1:n.4937C>T (RAF1)
ENST00000692093.1:c.*66C>T (RAF1) ENSP00000509669.1:n.*66C>T
ENST00000692311.1:n.2837C>T (RAF1)
ENST00000692558.1:n.4596C>T (RAF1)
ENST00000692773.1:c.*1750C>T (RAF1) ENSP00000509055.1:n.*1750C>T
ENST00000692830.1:c.*1758C>T (RAF1) ENSP00000509461.1:n.*1758C>T
ENST00000693312.1:c.*66C>T (RAF1) ENSP00000508686.1:n.*66C>T
ENST00000693664.1:c.*464C>T (RAF1) ENSP00000509614.1:n.*464C>T
ENST00000693705.1:c.*1392C>T (RAF1) ENSP00000510697.1:n.*1392C>T
ENST00000251849.9:c.*66C>T (RAF1) MANE Select ENSP00000251849.4:n.*66C>T
ENST00000442415.7:c.*66C>T (RAF1) ENSP00000401888.2:n.*66C>T
ENST00000676541.1:c.*2195G>A (MKRN2) ENSP00000503730.1:n.*2195G>A
ENST00000677142.1:c.*2195G>A (MKRN2) ENSP00000504455.1:n.*2195G>A
ENST00000677816.1:c.*750G>A (MKRN2) ENSP00000502893.1:n.*750G>A
ENST00000677941.1:n.2258G>A (MKRN2)
ENST00000251849.8:c.*66C>T (RAF1) ENSP00000251849.4:n.*66C>T
ENST00000423275.5:c.*1690C>T (RAF1) ENSP00000401088.1:n.*1690C>T
ENST00000432427.2:c.1650C>T (RAF1) ENSP00000398591.2:n.1650C>T
ENST00000442415.6:c.*66C>T (RAF1) ENSP00000401888.2:n.*66C>T
ENST00000471449.1:n.702C>T (RAF1)
NM_002880.3:c.*66C>T , LRG_413t1:c.*66C>T (RAF1) NP_002871.1:n.*66C>T
XM_005265355.1:c.*66C>T (RAF1) XP_005265412.1:n.*66C>T
XM_005265357.1:c.*66C>T (RAF1) XP_005265414.1:n.*66C>T
XM_005265358.3:c.*66C>T (RAF1) XP_005265415.1:n.*66C>T
XM_005265359.3:c.*66C>T (RAF1) XP_005265416.1:n.*66C>T
XM_011533974.1:c.*66C>T (RAF1) XP_011532276.1:n.*66C>T
XM_011533975.1:c.*66C>T (RAF1) XP_011532277.1:n.*66C>T
NM_001354689.1:c.*66C>T (RAF1) NP_001341618.1:n.*66C>T
NM_001354690.1:c.*66C>T (RAF1) NP_001341619.1:n.*66C>T
NM_001354691.1:c.*66C>T (RAF1) NP_001341620.1:n.*66C>T
NM_001354692.1:c.*66C>T (RAF1) NP_001341621.1:n.*66C>T
NM_001354693.1:c.*66C>T (RAF1) NP_001341622.1:n.*66C>T
NM_001354694.1:c.*66C>T (RAF1) NP_001341623.1:n.*66C>T
NM_001354695.1:c.*66C>T (RAF1) NP_001341624.1:n.*66C>T
NR_148940.1:n.2541C>T (RAF1)
NR_148941.1:n.2487C>T (RAF1)
NR_148942.1:n.2426C>T (RAF1)
XM_011533974.3:c.*66C>T (RAF1) XP_011532276.1:n.*66C>T
XM_017006966.1:c.*66C>T (RAF1) XP_016862455.1:n.*66C>T
NM_001354689.3:c.*66C>T (RAF1) NP_001341618.1:n.*66C>T
NM_001354690.2:c.*66C>T (RAF1) NP_001341619.1:n.*66C>T
NM_001354691.2:c.*66C>T (RAF1) NP_001341620.1:n.*66C>T
NM_001354692.2:c.*66C>T (RAF1) NP_001341621.1:n.*66C>T
NM_001354693.2:c.*66C>T (RAF1) NP_001341622.1:n.*66C>T
NM_001354694.2:c.*66C>T (RAF1) NP_001341623.1:n.*66C>T
NM_001354695.2:c.*66C>T (RAF1) NP_001341624.1:n.*66C>T
NR_148940.2:n.2457C>T (RAF1)
NR_148941.2:n.2403C>T (RAF1)
NR_148942.2:n.2342C>T (RAF1)
NM_001354690.3:c.*66C>T (RAF1) NP_001341619.1:n.*66C>T
NM_001354691.3:c.*66C>T (RAF1) NP_001341620.1:n.*66C>T
NM_001354692.3:c.*66C>T (RAF1) NP_001341621.1:n.*66C>T
NM_001354693.3:c.*66C>T (RAF1) NP_001341622.1:n.*66C>T
NM_001354694.3:c.*66C>T (RAF1) NP_001341623.1:n.*66C>T
NM_001354695.3:c.*66C>T (RAF1) NP_001341624.1:n.*66C>T
NM_002880.4:c.*66C>T (RAF1) MANE Select NP_002871.1:n.*66C>T
NR_148940.3:n.2457C>T (RAF1)
NR_148941.3:n.2403C>T (RAF1)
NR_148942.3:n.2342C>T (RAF1)