Canonical Allele Identifier: CA432522003

Linked Data

dbSNP Id: rs2125319365
MyVariant Identifiers: chr3:g.12626370C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12584871C>T , CM000665.2:g.12584871C>T GRCh38
NC_000003.11:g.12626370C>T , CM000665.1:g.12626370C>T GRCh37
NC_000003.10:g.12601370C>T NCBI36
NG_007467.1:g.84309G>A , LRG_413:g.84309G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000423275.6:c.*1444G>A (RAF1) ENSP00000401088.1:n.*1444G>A
ENST00000432427.3:c.1096G>A (RAF1)
ENST00000460610.2:n.6091G>A (RAF1)
ENST00000471449.2:n.589G>A (RAF1)
ENST00000475353.2:n.4059G>A (RAF1)
ENST00000684903.1:c.*1456G>A (RAF1) ENSP00000508612.1:n.*1456G>A
ENST00000685348.1:c.*1490G>A (RAF1) ENSP00000510285.1:n.*1490G>A
ENST00000685437.1:c.1680G>A (RAF1) ENSP00000508794.1:p.Lys560=
ENST00000685653.1:c.1779G>A (RAF1) ENSP00000509968.1:p.Lys593=
ENST00000685697.1:n.2514G>A (RAF1)
ENST00000685738.1:c.*743G>A (RAF1) ENSP00000510156.1:n.*743G>A
ENST00000686409.1:n.5188G>A (RAF1)
ENST00000686455.1:n.4500G>A (RAF1)
ENST00000686762.1:c.*338G>A (RAF1) ENSP00000509767.1:n.*338G>A
ENST00000687257.1:n.4233G>A (RAF1)
ENST00000687326.1:c.*3071G>A (RAF1) ENSP00000509665.1:n.*3071G>A
ENST00000687505.1:n.1897G>A (RAF1)
ENST00000687923.1:c.1668G>A (RAF1) ENSP00000510255.1:p.Lys556=
ENST00000688269.1:n.2375G>A (RAF1)
ENST00000688444.1:n.3896G>A (RAF1)
ENST00000688543.1:c.1680G>A (RAF1) ENSP00000509612.1:p.Lys560=
ENST00000688625.1:c.*3148G>A (RAF1) ENSP00000509522.1:n.*3148G>A
ENST00000688803.1:n.3207G>A (RAF1)
ENST00000689097.1:c.*1456G>A (RAF1) ENSP00000509756.1:n.*1456G>A
ENST00000689389.1:c.1602G>A (RAF1) ENSP00000510213.1:p.Lys534=
ENST00000689418.1:c.*3674G>A (RAF1) ENSP00000509467.1:n.*3674G>A
ENST00000689540.1:n.4147G>A (RAF1)
ENST00000689876.1:c.*328G>A (RAF1) ENSP00000508535.1:n.*328G>A
ENST00000689914.1:c.*713G>A (RAF1) ENSP00000509847.1:n.*713G>A
ENST00000690397.1:c.1668G>A (RAF1) ENSP00000508730.1:p.Lys556=
ENST00000690460.1:c.1767G>A (RAF1) ENSP00000509106.1:p.Lys589=
ENST00000690585.1:c.505G>A (RAF1)
ENST00000690625.1:n.2815G>A (RAF1)
ENST00000691396.1:c.*1651G>A (RAF1) ENSP00000510712.1:n.*1651G>A
ENST00000691643.1:n.2832G>A (RAF1)
ENST00000691724.1:c.*736G>A (RAF1) ENSP00000509255.1:n.*736G>A
ENST00000691779.1:c.*1357G>A (RAF1) ENSP00000508592.1:n.*1357G>A
ENST00000691888.1:c.653G>A (RAF1)
ENST00000691899.1:c.1779G>A (RAF1) ENSP00000508763.1:p.Lys593=
ENST00000692069.1:n.4703G>A (RAF1)
ENST00000692093.1:c.1680G>A (RAF1) ENSP00000509669.1:p.Lys560=
ENST00000692311.1:n.2603G>A (RAF1)
ENST00000692558.1:n.4362G>A (RAF1)
ENST00000692773.1:c.*1516G>A (RAF1) ENSP00000509055.1:n.*1516G>A
ENST00000692830.1:c.*1524G>A (RAF1) ENSP00000509461.1:n.*1524G>A
ENST00000693312.1:c.1554G>A (RAF1) ENSP00000508686.1:p.Lys518=
ENST00000693664.1:c.*230G>A (RAF1) ENSP00000509614.1:n.*230G>A
ENST00000693705.1:c.*1158G>A (RAF1) ENSP00000510697.1:n.*1158G>A
ENST00000251849.9:c.1779G>A (RAF1) MANE Select ENSP00000251849.4:p.Lys593=
ENST00000442415.7:c.1839G>A (RAF1) ENSP00000401888.2:p.Lys613=
ENST00000676541.1:c.*2618C>T (MKRN2) ENSP00000503730.1:n.*2618C>T
ENST00000677142.1:c.*2618C>T (MKRN2) ENSP00000504455.1:n.*2618C>T
ENST00000677816.1:c.*1173C>T (MKRN2) ENSP00000502893.1:n.*1173C>T
ENST00000677941.1:n.2681C>T (MKRN2)
ENST00000251849.8:c.1779G>A (RAF1) ENSP00000251849.4:p.Lys593=
ENST00000423275.5:c.*1456G>A (RAF1) ENSP00000401088.1:n.*1456G>A
ENST00000432427.2:c.1416G>A (RAF1) ENSP00000398591.2:p.Lys472=
ENST00000442415.6:c.1839G>A (RAF1) ENSP00000401888.2:p.Lys613=
ENST00000471449.1:n.468G>A (RAF1)
NM_002880.3:c.1779G>A , LRG_413t1:c.1779G>A (RAF1) NP_002871.1:p.Lys593=
XM_005265355.1:c.1779G>A (RAF1) XP_005265412.1:p.Lys593=
XM_005265357.1:c.1680G>A (RAF1) XP_005265414.1:p.Lys560=
XM_005265358.3:c.1536G>A (RAF1) XP_005265415.1:p.Lys512=
XM_005265359.3:c.1437G>A (RAF1) XP_005265416.1:p.Lys479=
XM_011533974.1:c.1779G>A (RAF1) XP_011532276.1:p.Lys593=
XM_011533975.1:c.1536G>A (RAF1) XP_011532277.1:p.Lys512=
NM_001354689.1:c.1839G>A (RAF1) NP_001341618.1:p.Lys613=
NM_001354690.1:c.1779G>A (RAF1) NP_001341619.1:p.Lys593=
NM_001354691.1:c.1536G>A (RAF1) NP_001341620.1:p.Lys512=
NM_001354692.1:c.1536G>A (RAF1) NP_001341621.1:p.Lys512=
NM_001354693.1:c.1680G>A (RAF1) NP_001341622.1:p.Lys560=
NM_001354694.1:c.1596G>A (RAF1) NP_001341623.1:p.Lys532=
NM_001354695.1:c.1437G>A (RAF1) NP_001341624.1:p.Lys479=
NR_148940.1:n.2307G>A (RAF1)
NR_148941.1:n.2253G>A (RAF1)
NR_148942.1:n.2192G>A (RAF1)
XM_011533974.3:c.1779G>A (RAF1) XP_011532276.1:p.Lys593=
XM_017006966.1:c.1680G>A (RAF1) XP_016862455.1:p.Lys560=
NM_001354689.3:c.1839G>A (RAF1) NP_001341618.1:p.Lys613=
NM_001354690.2:c.1779G>A (RAF1) NP_001341619.1:p.Lys593=
NM_001354691.2:c.1536G>A (RAF1) NP_001341620.1:p.Lys512=
NM_001354692.2:c.1536G>A (RAF1) NP_001341621.1:p.Lys512=
NM_001354693.2:c.1680G>A (RAF1) NP_001341622.1:p.Lys560=
NM_001354694.2:c.1596G>A (RAF1) NP_001341623.1:p.Lys532=
NM_001354695.2:c.1437G>A (RAF1) NP_001341624.1:p.Lys479=
NR_148940.2:n.2223G>A (RAF1)
NR_148941.2:n.2169G>A (RAF1)
NR_148942.2:n.2108G>A (RAF1)
NM_001354690.3:c.1779G>A (RAF1) NP_001341619.1:p.Lys593=
NM_001354691.3:c.1536G>A (RAF1) NP_001341620.1:p.Lys512=
NM_001354692.3:c.1536G>A (RAF1) NP_001341621.1:p.Lys512=
NM_001354693.3:c.1680G>A (RAF1) NP_001341622.1:p.Lys560=
NM_001354694.3:c.1596G>A (RAF1) NP_001341623.1:p.Lys532=
NM_001354695.3:c.1437G>A (RAF1) NP_001341624.1:p.Lys479=
NM_002880.4:c.1779G>A (RAF1) MANE Select NP_002871.1:p.Lys593=
NR_148940.3:n.2223G>A (RAF1)
NR_148941.3:n.2169G>A (RAF1)
NR_148942.3:n.2108G>A (RAF1)