Canonical Allele Identifier: CA351495367

Linked Data

dbSNP Id: rs2125315719

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12584527A>T , CM000665.2:g.12584527A>T GRCh38
NC_000003.11:g.12626026A>T , CM000665.1:g.12626026A>T GRCh37
NC_000003.10:g.12601026A>T NCBI36
NG_007467.1:g.84653T>A , LRG_413:g.84653T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000423275.6:c.*1599T>A (RAF1) ENSP00000401088.1:n.*1599T>A
ENST00000432427.3:c.1251T>A (RAF1)
ENST00000460610.2:n.6246T>A (RAF1)
ENST00000471449.2:n.744T>A (RAF1)
ENST00000475353.2:n.4214T>A (RAF1)
ENST00000684903.1:c.*1611T>A (RAF1) ENSP00000508612.1:n.*1611T>A
ENST00000685348.1:c.*1645T>A (RAF1) ENSP00000510285.1:n.*1645T>A
ENST00000685437.1:c.1835T>A (RAF1) ENSP00000508794.1:p.Leu612Gln
ENST00000685653.1:c.1934T>A (RAF1) ENSP00000509968.1:p.Leu645Gln
ENST00000685697.1:n.2669T>A (RAF1)
ENST00000685738.1:c.*898T>A (RAF1) ENSP00000510156.1:n.*898T>A
ENST00000686409.1:n.5343T>A (RAF1)
ENST00000686455.1:n.4655T>A (RAF1)
ENST00000686762.1:c.*493T>A (RAF1) ENSP00000509767.1:n.*493T>A
ENST00000687257.1:n.4388T>A (RAF1)
ENST00000687326.1:c.*3226T>A (RAF1) ENSP00000509665.1:n.*3226T>A
ENST00000687505.1:n.2052T>A (RAF1)
ENST00000687923.1:c.1823T>A (RAF1) ENSP00000510255.1:p.Leu608Gln
ENST00000688269.1:n.2530T>A (RAF1)
ENST00000688444.1:n.4051T>A (RAF1)
ENST00000688543.1:c.1835T>A (RAF1) ENSP00000509612.1:p.Leu612Gln
ENST00000688625.1:c.*3303T>A (RAF1) ENSP00000509522.1:n.*3303T>A
ENST00000688803.1:n.3362T>A (RAF1)
ENST00000689097.1:c.*1611T>A (RAF1) ENSP00000509756.1:n.*1611T>A
ENST00000689389.1:c.1757T>A (RAF1) ENSP00000510213.1:p.Leu586Gln
ENST00000689418.1:c.*3829T>A (RAF1) ENSP00000509467.1:n.*3829T>A
ENST00000689540.1:n.4302T>A (RAF1)
ENST00000689876.1:c.*483T>A (RAF1) ENSP00000508535.1:n.*483T>A
ENST00000689914.1:c.*868T>A (RAF1) ENSP00000509847.1:n.*868T>A
ENST00000690397.1:c.1823T>A (RAF1) ENSP00000508730.1:p.Leu608Gln
ENST00000690460.1:c.1922T>A (RAF1) ENSP00000509106.1:p.Leu641Gln
ENST00000690585.1:c.660T>A (RAF1)
ENST00000690625.1:n.2970T>A (RAF1)
ENST00000691396.1:c.*1806T>A (RAF1) ENSP00000510712.1:n.*1806T>A
ENST00000691643.1:n.2987T>A (RAF1)
ENST00000691724.1:c.*891T>A (RAF1) ENSP00000509255.1:n.*891T>A
ENST00000691779.1:c.*1512T>A (RAF1) ENSP00000508592.1:n.*1512T>A
ENST00000691888.1:c.808T>A (RAF1)
ENST00000691899.1:c.1934T>A (RAF1) ENSP00000508763.1:p.Leu645Gln
ENST00000692069.1:n.4858T>A (RAF1)
ENST00000692093.1:c.1835T>A (RAF1) ENSP00000509669.1:p.Leu612Gln
ENST00000692311.1:n.2758T>A (RAF1)
ENST00000692558.1:n.4517T>A (RAF1)
ENST00000692773.1:c.*1671T>A (RAF1) ENSP00000509055.1:n.*1671T>A
ENST00000692830.1:c.*1679T>A (RAF1) ENSP00000509461.1:n.*1679T>A
ENST00000693312.1:c.1709T>A (RAF1) ENSP00000508686.1:p.Leu570Gln
ENST00000693664.1:c.*385T>A (RAF1) ENSP00000509614.1:n.*385T>A
ENST00000693705.1:c.*1313T>A (RAF1) ENSP00000510697.1:n.*1313T>A
ENST00000251849.9:c.1934T>A (RAF1) MANE Select ENSP00000251849.4:p.Leu645Gln
ENST00000442415.7:c.1994T>A (RAF1) ENSP00000401888.2:p.Leu665Gln
ENST00000676541.1:c.*2274A>T (MKRN2) ENSP00000503730.1:n.*2274A>T
ENST00000677142.1:c.*2274A>T (MKRN2) ENSP00000504455.1:n.*2274A>T
ENST00000677816.1:c.*829A>T (MKRN2) ENSP00000502893.1:n.*829A>T
ENST00000677941.1:n.2337A>T (MKRN2)
ENST00000251849.8:c.1934T>A (RAF1) ENSP00000251849.4:p.Leu645Gln
ENST00000423275.5:c.*1611T>A (RAF1) ENSP00000401088.1:n.*1611T>A
ENST00000432427.2:c.1571T>A (RAF1) ENSP00000398591.2:p.Leu524Gln
ENST00000442415.6:c.1994T>A (RAF1) ENSP00000401888.2:p.Leu665Gln
ENST00000471449.1:n.623T>A (RAF1)
NM_002880.3:c.1934T>A , LRG_413t1:c.1934T>A (RAF1) NP_002871.1:p.Leu645Gln
XM_005265355.1:c.1934T>A (RAF1) XP_005265412.1:p.Leu645Gln
XM_005265357.1:c.1835T>A (RAF1) XP_005265414.1:p.Leu612Gln
XM_005265358.3:c.1691T>A (RAF1) XP_005265415.1:p.Leu564Gln
XM_005265359.3:c.1592T>A (RAF1) XP_005265416.1:p.Leu531Gln
XM_011533974.1:c.1934T>A (RAF1) XP_011532276.1:p.Leu645Gln
XM_011533975.1:c.1691T>A (RAF1) XP_011532277.1:p.Leu564Gln
NM_001354689.1:c.1994T>A (RAF1) NP_001341618.1:p.Leu665Gln
NM_001354690.1:c.1934T>A (RAF1) NP_001341619.1:p.Leu645Gln
NM_001354691.1:c.1691T>A (RAF1) NP_001341620.1:p.Leu564Gln
NM_001354692.1:c.1691T>A (RAF1) NP_001341621.1:p.Leu564Gln
NM_001354693.1:c.1835T>A (RAF1) NP_001341622.1:p.Leu612Gln
NM_001354694.1:c.1751T>A (RAF1) NP_001341623.1:p.Leu584Gln
NM_001354695.1:c.1592T>A (RAF1) NP_001341624.1:p.Leu531Gln
NR_148940.1:n.2462T>A (RAF1)
NR_148941.1:n.2408T>A (RAF1)
NR_148942.1:n.2347T>A (RAF1)
XM_011533974.3:c.1934T>A (RAF1) XP_011532276.1:p.Leu645Gln
XM_017006966.1:c.1835T>A (RAF1) XP_016862455.1:p.Leu612Gln
NM_001354689.3:c.1994T>A (RAF1) NP_001341618.1:p.Leu665Gln
NM_001354690.2:c.1934T>A (RAF1) NP_001341619.1:p.Leu645Gln
NM_001354691.2:c.1691T>A (RAF1) NP_001341620.1:p.Leu564Gln
NM_001354692.2:c.1691T>A (RAF1) NP_001341621.1:p.Leu564Gln
NM_001354693.2:c.1835T>A (RAF1) NP_001341622.1:p.Leu612Gln
NM_001354694.2:c.1751T>A (RAF1) NP_001341623.1:p.Leu584Gln
NM_001354695.2:c.1592T>A (RAF1) NP_001341624.1:p.Leu531Gln
NR_148940.2:n.2378T>A (RAF1)
NR_148941.2:n.2324T>A (RAF1)
NR_148942.2:n.2263T>A (RAF1)
NM_001354690.3:c.1934T>A (RAF1) NP_001341619.1:p.Leu645Gln
NM_001354691.3:c.1691T>A (RAF1) NP_001341620.1:p.Leu564Gln
NM_001354692.3:c.1691T>A (RAF1) NP_001341621.1:p.Leu564Gln
NM_001354693.3:c.1835T>A (RAF1) NP_001341622.1:p.Leu612Gln
NM_001354694.3:c.1751T>A (RAF1) NP_001341623.1:p.Leu584Gln
NM_001354695.3:c.1592T>A (RAF1) NP_001341624.1:p.Leu531Gln
NM_002880.4:c.1934T>A (RAF1) MANE Select NP_002871.1:p.Leu645Gln
NR_148940.3:n.2378T>A (RAF1)
NR_148941.3:n.2324T>A (RAF1)
NR_148942.3:n.2263T>A (RAF1)