Canonical Allele Identifier: CA351496172

Linked Data

dbSNP Id: rs2125317167

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12584638A>T , CM000665.2:g.12584638A>T GRCh38
NC_000003.11:g.12626137A>T , CM000665.1:g.12626137A>T GRCh37
NC_000003.10:g.12601137A>T NCBI36
NG_007467.1:g.84542T>A , LRG_413:g.84542T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000423275.6:c.*1488T>A (RAF1) ENSP00000401088.1:n.*1488T>A
ENST00000432427.3:c.1140T>A (RAF1)
ENST00000460610.2:n.6135T>A (RAF1)
ENST00000471449.2:n.633T>A (RAF1)
ENST00000475353.2:n.4103T>A (RAF1)
ENST00000684903.1:c.*1500T>A (RAF1) ENSP00000508612.1:n.*1500T>A
ENST00000685348.1:c.*1534T>A (RAF1) ENSP00000510285.1:n.*1534T>A
ENST00000685437.1:c.1724T>A (RAF1) ENSP00000508794.1:p.Leu575Gln
ENST00000685653.1:c.1823T>A (RAF1) ENSP00000509968.1:p.Leu608Gln
ENST00000685697.1:n.2558T>A (RAF1)
ENST00000685738.1:c.*787T>A (RAF1) ENSP00000510156.1:n.*787T>A
ENST00000686409.1:n.5232T>A (RAF1)
ENST00000686455.1:n.4544T>A (RAF1)
ENST00000686762.1:c.*382T>A (RAF1) ENSP00000509767.1:n.*382T>A
ENST00000687257.1:n.4277T>A (RAF1)
ENST00000687326.1:c.*3115T>A (RAF1) ENSP00000509665.1:n.*3115T>A
ENST00000687505.1:n.1941T>A (RAF1)
ENST00000687923.1:c.1712T>A (RAF1) ENSP00000510255.1:p.Leu571Gln
ENST00000688269.1:n.2419T>A (RAF1)
ENST00000688444.1:n.3940T>A (RAF1)
ENST00000688543.1:c.1724T>A (RAF1) ENSP00000509612.1:p.Leu575Gln
ENST00000688625.1:c.*3192T>A (RAF1) ENSP00000509522.1:n.*3192T>A
ENST00000688803.1:n.3251T>A (RAF1)
ENST00000689097.1:c.*1500T>A (RAF1) ENSP00000509756.1:n.*1500T>A
ENST00000689389.1:c.1646T>A (RAF1) ENSP00000510213.1:p.Leu549Gln
ENST00000689418.1:c.*3718T>A (RAF1) ENSP00000509467.1:n.*3718T>A
ENST00000689540.1:n.4191T>A (RAF1)
ENST00000689876.1:c.*372T>A (RAF1) ENSP00000508535.1:n.*372T>A
ENST00000689914.1:c.*757T>A (RAF1) ENSP00000509847.1:n.*757T>A
ENST00000690397.1:c.1712T>A (RAF1) ENSP00000508730.1:p.Leu571Gln
ENST00000690460.1:c.1811T>A (RAF1) ENSP00000509106.1:p.Leu604Gln
ENST00000690585.1:c.549T>A (RAF1)
ENST00000690625.1:n.2859T>A (RAF1)
ENST00000691396.1:c.*1695T>A (RAF1) ENSP00000510712.1:n.*1695T>A
ENST00000691643.1:n.2876T>A (RAF1)
ENST00000691724.1:c.*780T>A (RAF1) ENSP00000509255.1:n.*780T>A
ENST00000691779.1:c.*1401T>A (RAF1) ENSP00000508592.1:n.*1401T>A
ENST00000691888.1:c.697T>A (RAF1)
ENST00000691899.1:c.1823T>A (RAF1) ENSP00000508763.1:p.Leu608Gln
ENST00000692069.1:n.4747T>A (RAF1)
ENST00000692093.1:c.1724T>A (RAF1) ENSP00000509669.1:p.Leu575Gln
ENST00000692311.1:n.2647T>A (RAF1)
ENST00000692558.1:n.4406T>A (RAF1)
ENST00000692773.1:c.*1560T>A (RAF1) ENSP00000509055.1:n.*1560T>A
ENST00000692830.1:c.*1568T>A (RAF1) ENSP00000509461.1:n.*1568T>A
ENST00000693312.1:c.1598T>A (RAF1) ENSP00000508686.1:p.Leu533Gln
ENST00000693664.1:c.*274T>A (RAF1) ENSP00000509614.1:n.*274T>A
ENST00000693705.1:c.*1202T>A (RAF1) ENSP00000510697.1:n.*1202T>A
ENST00000251849.9:c.1823T>A (RAF1) MANE Select ENSP00000251849.4:p.Leu608Gln
ENST00000442415.7:c.1883T>A (RAF1) ENSP00000401888.2:p.Leu628Gln
ENST00000676541.1:c.*2385A>T (MKRN2) ENSP00000503730.1:n.*2385A>T
ENST00000677142.1:c.*2385A>T (MKRN2) ENSP00000504455.1:n.*2385A>T
ENST00000677816.1:c.*940A>T (MKRN2) ENSP00000502893.1:n.*940A>T
ENST00000677941.1:n.2448A>T (MKRN2)
ENST00000251849.8:c.1823T>A (RAF1) ENSP00000251849.4:p.Leu608Gln
ENST00000423275.5:c.*1500T>A (RAF1) ENSP00000401088.1:n.*1500T>A
ENST00000432427.2:c.1460T>A (RAF1) ENSP00000398591.2:p.Leu487Gln
ENST00000442415.6:c.1883T>A (RAF1) ENSP00000401888.2:p.Leu628Gln
ENST00000471449.1:n.512T>A (RAF1)
NM_002880.3:c.1823T>A , LRG_413t1:c.1823T>A (RAF1) NP_002871.1:p.Leu608Gln
XM_005265355.1:c.1823T>A (RAF1) XP_005265412.1:p.Leu608Gln
XM_005265357.1:c.1724T>A (RAF1) XP_005265414.1:p.Leu575Gln
XM_005265358.3:c.1580T>A (RAF1) XP_005265415.1:p.Leu527Gln
XM_005265359.3:c.1481T>A (RAF1) XP_005265416.1:p.Leu494Gln
XM_011533974.1:c.1823T>A (RAF1) XP_011532276.1:p.Leu608Gln
XM_011533975.1:c.1580T>A (RAF1) XP_011532277.1:p.Leu527Gln
NM_001354689.1:c.1883T>A (RAF1) NP_001341618.1:p.Leu628Gln
NM_001354690.1:c.1823T>A (RAF1) NP_001341619.1:p.Leu608Gln
NM_001354691.1:c.1580T>A (RAF1) NP_001341620.1:p.Leu527Gln
NM_001354692.1:c.1580T>A (RAF1) NP_001341621.1:p.Leu527Gln
NM_001354693.1:c.1724T>A (RAF1) NP_001341622.1:p.Leu575Gln
NM_001354694.1:c.1640T>A (RAF1) NP_001341623.1:p.Leu547Gln
NM_001354695.1:c.1481T>A (RAF1) NP_001341624.1:p.Leu494Gln
NR_148940.1:n.2351T>A (RAF1)
NR_148941.1:n.2297T>A (RAF1)
NR_148942.1:n.2236T>A (RAF1)
XM_011533974.3:c.1823T>A (RAF1) XP_011532276.1:p.Leu608Gln
XM_017006966.1:c.1724T>A (RAF1) XP_016862455.1:p.Leu575Gln
NM_001354689.3:c.1883T>A (RAF1) NP_001341618.1:p.Leu628Gln
NM_001354690.2:c.1823T>A (RAF1) NP_001341619.1:p.Leu608Gln
NM_001354691.2:c.1580T>A (RAF1) NP_001341620.1:p.Leu527Gln
NM_001354692.2:c.1580T>A (RAF1) NP_001341621.1:p.Leu527Gln
NM_001354693.2:c.1724T>A (RAF1) NP_001341622.1:p.Leu575Gln
NM_001354694.2:c.1640T>A (RAF1) NP_001341623.1:p.Leu547Gln
NM_001354695.2:c.1481T>A (RAF1) NP_001341624.1:p.Leu494Gln
NR_148940.2:n.2267T>A (RAF1)
NR_148941.2:n.2213T>A (RAF1)
NR_148942.2:n.2152T>A (RAF1)
NM_001354690.3:c.1823T>A (RAF1) NP_001341619.1:p.Leu608Gln
NM_001354691.3:c.1580T>A (RAF1) NP_001341620.1:p.Leu527Gln
NM_001354692.3:c.1580T>A (RAF1) NP_001341621.1:p.Leu527Gln
NM_001354693.3:c.1724T>A (RAF1) NP_001341622.1:p.Leu575Gln
NM_001354694.3:c.1640T>A (RAF1) NP_001341623.1:p.Leu547Gln
NM_001354695.3:c.1481T>A (RAF1) NP_001341624.1:p.Leu494Gln
NM_002880.4:c.1823T>A (RAF1) MANE Select NP_002871.1:p.Leu608Gln
NR_148940.3:n.2267T>A (RAF1)
NR_148941.3:n.2213T>A (RAF1)
NR_148942.3:n.2152T>A (RAF1)