Canonical Allele Identifier: CA351496226

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12584645T>A , CM000665.2:g.12584645T>A GRCh38
NC_000003.11:g.12626144T>A , CM000665.1:g.12626144T>A GRCh37
NC_000003.10:g.12601144T>A NCBI36
NG_007467.1:g.84535A>T , LRG_413:g.84535A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000423275.6:c.*1481A>T (RAF1) ENSP00000401088.1:n.*1481A>T
ENST00000432427.3:c.1133A>T (RAF1)
ENST00000460610.2:n.6128A>T (RAF1)
ENST00000471449.2:n.626A>T (RAF1)
ENST00000475353.2:n.4096A>T (RAF1)
ENST00000684903.1:c.*1493A>T (RAF1) ENSP00000508612.1:n.*1493A>T
ENST00000685348.1:c.*1527A>T (RAF1) ENSP00000510285.1:n.*1527A>T
ENST00000685437.1:c.1717A>T (RAF1) ENSP00000508794.1:p.Ile573Phe
ENST00000685653.1:c.1816A>T (RAF1) ENSP00000509968.1:p.Ile606Phe
ENST00000685697.1:n.2551A>T (RAF1)
ENST00000685738.1:c.*780A>T (RAF1) ENSP00000510156.1:n.*780A>T
ENST00000686409.1:n.5225A>T (RAF1)
ENST00000686455.1:n.4537A>T (RAF1)
ENST00000686762.1:c.*375A>T (RAF1) ENSP00000509767.1:n.*375A>T
ENST00000687257.1:n.4270A>T (RAF1)
ENST00000687326.1:c.*3108A>T (RAF1) ENSP00000509665.1:n.*3108A>T
ENST00000687505.1:n.1934A>T (RAF1)
ENST00000687923.1:c.1705A>T (RAF1) ENSP00000510255.1:p.Ile569Phe
ENST00000688269.1:n.2412A>T (RAF1)
ENST00000688444.1:n.3933A>T (RAF1)
ENST00000688543.1:c.1717A>T (RAF1) ENSP00000509612.1:p.Ile573Phe
ENST00000688625.1:c.*3185A>T (RAF1) ENSP00000509522.1:n.*3185A>T
ENST00000688803.1:n.3244A>T (RAF1)
ENST00000689097.1:c.*1493A>T (RAF1) ENSP00000509756.1:n.*1493A>T
ENST00000689389.1:c.1639A>T (RAF1) ENSP00000510213.1:p.Ile547Phe
ENST00000689418.1:c.*3711A>T (RAF1) ENSP00000509467.1:n.*3711A>T
ENST00000689540.1:n.4184A>T (RAF1)
ENST00000689876.1:c.*365A>T (RAF1) ENSP00000508535.1:n.*365A>T
ENST00000689914.1:c.*750A>T (RAF1) ENSP00000509847.1:n.*750A>T
ENST00000690397.1:c.1705A>T (RAF1) ENSP00000508730.1:p.Ile569Phe
ENST00000690460.1:c.1804A>T (RAF1) ENSP00000509106.1:p.Ile602Phe
ENST00000690585.1:c.542A>T (RAF1)
ENST00000690625.1:n.2852A>T (RAF1)
ENST00000691396.1:c.*1688A>T (RAF1) ENSP00000510712.1:n.*1688A>T
ENST00000691643.1:n.2869A>T (RAF1)
ENST00000691724.1:c.*773A>T (RAF1) ENSP00000509255.1:n.*773A>T
ENST00000691779.1:c.*1394A>T (RAF1) ENSP00000508592.1:n.*1394A>T
ENST00000691888.1:c.690A>T (RAF1)
ENST00000691899.1:c.1816A>T (RAF1) ENSP00000508763.1:p.Ile606Phe
ENST00000692069.1:n.4740A>T (RAF1)
ENST00000692093.1:c.1717A>T (RAF1) ENSP00000509669.1:p.Ile573Phe
ENST00000692311.1:n.2640A>T (RAF1)
ENST00000692558.1:n.4399A>T (RAF1)
ENST00000692773.1:c.*1553A>T (RAF1) ENSP00000509055.1:n.*1553A>T
ENST00000692830.1:c.*1561A>T (RAF1) ENSP00000509461.1:n.*1561A>T
ENST00000693312.1:c.1591A>T (RAF1) ENSP00000508686.1:p.Ile531Phe
ENST00000693664.1:c.*267A>T (RAF1) ENSP00000509614.1:n.*267A>T
ENST00000693705.1:c.*1195A>T (RAF1) ENSP00000510697.1:n.*1195A>T
ENST00000251849.9:c.1816A>T (RAF1) MANE Select ENSP00000251849.4:p.Ile606Phe
ENST00000442415.7:c.1876A>T (RAF1) ENSP00000401888.2:p.Ile626Phe
ENST00000676541.1:c.*2392T>A (MKRN2) ENSP00000503730.1:n.*2392T>A
ENST00000677142.1:c.*2392T>A (MKRN2) ENSP00000504455.1:n.*2392T>A
ENST00000677816.1:c.*947T>A (MKRN2) ENSP00000502893.1:n.*947T>A
ENST00000677941.1:n.2455T>A (MKRN2)
ENST00000251849.8:c.1816A>T (RAF1) ENSP00000251849.4:p.Ile606Phe
ENST00000423275.5:c.*1493A>T (RAF1) ENSP00000401088.1:n.*1493A>T
ENST00000432427.2:c.1453A>T (RAF1) ENSP00000398591.2:p.Ile485Phe
ENST00000442415.6:c.1876A>T (RAF1) ENSP00000401888.2:p.Ile626Phe
ENST00000471449.1:n.505A>T (RAF1)
NM_002880.3:c.1816A>T , LRG_413t1:c.1816A>T (RAF1) NP_002871.1:p.Ile606Phe
XM_005265355.1:c.1816A>T (RAF1) XP_005265412.1:p.Ile606Phe
XM_005265357.1:c.1717A>T (RAF1) XP_005265414.1:p.Ile573Phe
XM_005265358.3:c.1573A>T (RAF1) XP_005265415.1:p.Ile525Phe
XM_005265359.3:c.1474A>T (RAF1) XP_005265416.1:p.Ile492Phe
XM_011533974.1:c.1816A>T (RAF1) XP_011532276.1:p.Ile606Phe
XM_011533975.1:c.1573A>T (RAF1) XP_011532277.1:p.Ile525Phe
NM_001354689.1:c.1876A>T (RAF1) NP_001341618.1:p.Ile626Phe
NM_001354690.1:c.1816A>T (RAF1) NP_001341619.1:p.Ile606Phe
NM_001354691.1:c.1573A>T (RAF1) NP_001341620.1:p.Ile525Phe
NM_001354692.1:c.1573A>T (RAF1) NP_001341621.1:p.Ile525Phe
NM_001354693.1:c.1717A>T (RAF1) NP_001341622.1:p.Ile573Phe
NM_001354694.1:c.1633A>T (RAF1) NP_001341623.1:p.Ile545Phe
NM_001354695.1:c.1474A>T (RAF1) NP_001341624.1:p.Ile492Phe
NR_148940.1:n.2344A>T (RAF1)
NR_148941.1:n.2290A>T (RAF1)
NR_148942.1:n.2229A>T (RAF1)
XM_011533974.3:c.1816A>T (RAF1) XP_011532276.1:p.Ile606Phe
XM_017006966.1:c.1717A>T (RAF1) XP_016862455.1:p.Ile573Phe
NM_001354689.3:c.1876A>T (RAF1) NP_001341618.1:p.Ile626Phe
NM_001354690.2:c.1816A>T (RAF1) NP_001341619.1:p.Ile606Phe
NM_001354691.2:c.1573A>T (RAF1) NP_001341620.1:p.Ile525Phe
NM_001354692.2:c.1573A>T (RAF1) NP_001341621.1:p.Ile525Phe
NM_001354693.2:c.1717A>T (RAF1) NP_001341622.1:p.Ile573Phe
NM_001354694.2:c.1633A>T (RAF1) NP_001341623.1:p.Ile545Phe
NM_001354695.2:c.1474A>T (RAF1) NP_001341624.1:p.Ile492Phe
NR_148940.2:n.2260A>T (RAF1)
NR_148941.2:n.2206A>T (RAF1)
NR_148942.2:n.2145A>T (RAF1)
NM_001354690.3:c.1816A>T (RAF1) NP_001341619.1:p.Ile606Phe
NM_001354691.3:c.1573A>T (RAF1) NP_001341620.1:p.Ile525Phe
NM_001354692.3:c.1573A>T (RAF1) NP_001341621.1:p.Ile525Phe
NM_001354693.3:c.1717A>T (RAF1) NP_001341622.1:p.Ile573Phe
NM_001354694.3:c.1633A>T (RAF1) NP_001341623.1:p.Ile545Phe
NM_001354695.3:c.1474A>T (RAF1) NP_001341624.1:p.Ile492Phe
NM_002880.4:c.1816A>T (RAF1) MANE Select NP_002871.1:p.Ile606Phe
NR_148940.3:n.2260A>T (RAF1)
NR_148941.3:n.2206A>T (RAF1)
NR_148942.3:n.2145A>T (RAF1)