Canonical Allele Identifier: CA351495832

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12584593G>A , CM000665.2:g.12584593G>A GRCh38
NC_000003.11:g.12626092G>A , CM000665.1:g.12626092G>A GRCh37
NC_000003.10:g.12601092G>A NCBI36
NG_007467.1:g.84587C>T , LRG_413:g.84587C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000423275.6:c.*1533C>T (RAF1) ENSP00000401088.1:n.*1533C>T
ENST00000432427.3:c.1185C>T (RAF1)
ENST00000460610.2:n.6180C>T (RAF1)
ENST00000471449.2:n.678C>T (RAF1)
ENST00000475353.2:n.4148C>T (RAF1)
ENST00000684903.1:c.*1545C>T (RAF1) ENSP00000508612.1:n.*1545C>T
ENST00000685348.1:c.*1579C>T (RAF1) ENSP00000510285.1:n.*1579C>T
ENST00000685437.1:c.1769C>T (RAF1) ENSP00000508794.1:p.Pro590Leu
ENST00000685653.1:c.1868C>T (RAF1) ENSP00000509968.1:p.Pro623Leu
ENST00000685697.1:n.2603C>T (RAF1)
ENST00000685738.1:c.*832C>T (RAF1) ENSP00000510156.1:n.*832C>T
ENST00000686409.1:n.5277C>T (RAF1)
ENST00000686455.1:n.4589C>T (RAF1)
ENST00000686762.1:c.*427C>T (RAF1) ENSP00000509767.1:n.*427C>T
ENST00000687257.1:n.4322C>T (RAF1)
ENST00000687326.1:c.*3160C>T (RAF1) ENSP00000509665.1:n.*3160C>T
ENST00000687505.1:n.1986C>T (RAF1)
ENST00000687923.1:c.1757C>T (RAF1) ENSP00000510255.1:p.Pro586Leu
ENST00000688269.1:n.2464C>T (RAF1)
ENST00000688444.1:n.3985C>T (RAF1)
ENST00000688543.1:c.1769C>T (RAF1) ENSP00000509612.1:p.Pro590Leu
ENST00000688625.1:c.*3237C>T (RAF1) ENSP00000509522.1:n.*3237C>T
ENST00000688803.1:n.3296C>T (RAF1)
ENST00000689097.1:c.*1545C>T (RAF1) ENSP00000509756.1:n.*1545C>T
ENST00000689389.1:c.1691C>T (RAF1) ENSP00000510213.1:p.Pro564Leu
ENST00000689418.1:c.*3763C>T (RAF1) ENSP00000509467.1:n.*3763C>T
ENST00000689540.1:n.4236C>T (RAF1)
ENST00000689876.1:c.*417C>T (RAF1) ENSP00000508535.1:n.*417C>T
ENST00000689914.1:c.*802C>T (RAF1) ENSP00000509847.1:n.*802C>T
ENST00000690397.1:c.1757C>T (RAF1) ENSP00000508730.1:p.Pro586Leu
ENST00000690460.1:c.1856C>T (RAF1) ENSP00000509106.1:p.Pro619Leu
ENST00000690585.1:c.594C>T (RAF1)
ENST00000690625.1:n.2904C>T (RAF1)
ENST00000691396.1:c.*1740C>T (RAF1) ENSP00000510712.1:n.*1740C>T
ENST00000691643.1:n.2921C>T (RAF1)
ENST00000691724.1:c.*825C>T (RAF1) ENSP00000509255.1:n.*825C>T
ENST00000691779.1:c.*1446C>T (RAF1) ENSP00000508592.1:n.*1446C>T
ENST00000691888.1:c.742C>T (RAF1)
ENST00000691899.1:c.1868C>T (RAF1) ENSP00000508763.1:p.Pro623Leu
ENST00000692069.1:n.4792C>T (RAF1)
ENST00000692093.1:c.1769C>T (RAF1) ENSP00000509669.1:p.Pro590Leu
ENST00000692311.1:n.2692C>T (RAF1)
ENST00000692558.1:n.4451C>T (RAF1)
ENST00000692773.1:c.*1605C>T (RAF1) ENSP00000509055.1:n.*1605C>T
ENST00000692830.1:c.*1613C>T (RAF1) ENSP00000509461.1:n.*1613C>T
ENST00000693312.1:c.1643C>T (RAF1) ENSP00000508686.1:p.Pro548Leu
ENST00000693664.1:c.*319C>T (RAF1) ENSP00000509614.1:n.*319C>T
ENST00000693705.1:c.*1247C>T (RAF1) ENSP00000510697.1:n.*1247C>T
ENST00000251849.9:c.1868C>T (RAF1) MANE Select ENSP00000251849.4:p.Pro623Leu
ENST00000442415.7:c.1928C>T (RAF1) ENSP00000401888.2:p.Pro643Leu
ENST00000676541.1:c.*2340G>A (MKRN2) ENSP00000503730.1:n.*2340G>A
ENST00000677142.1:c.*2340G>A (MKRN2) ENSP00000504455.1:n.*2340G>A
ENST00000677816.1:c.*895G>A (MKRN2) ENSP00000502893.1:n.*895G>A
ENST00000677941.1:n.2403G>A (MKRN2)
ENST00000251849.8:c.1868C>T (RAF1) ENSP00000251849.4:p.Pro623Leu
ENST00000423275.5:c.*1545C>T (RAF1) ENSP00000401088.1:n.*1545C>T
ENST00000432427.2:c.1505C>T (RAF1) ENSP00000398591.2:p.Pro502Leu
ENST00000442415.6:c.1928C>T (RAF1) ENSP00000401888.2:p.Pro643Leu
ENST00000471449.1:n.557C>T (RAF1)
NM_002880.3:c.1868C>T , LRG_413t1:c.1868C>T (RAF1) NP_002871.1:p.Pro623Leu
XM_005265355.1:c.1868C>T (RAF1) XP_005265412.1:p.Pro623Leu
XM_005265357.1:c.1769C>T (RAF1) XP_005265414.1:p.Pro590Leu
XM_005265358.3:c.1625C>T (RAF1) XP_005265415.1:p.Pro542Leu
XM_005265359.3:c.1526C>T (RAF1) XP_005265416.1:p.Pro509Leu
XM_011533974.1:c.1868C>T (RAF1) XP_011532276.1:p.Pro623Leu
XM_011533975.1:c.1625C>T (RAF1) XP_011532277.1:p.Pro542Leu
NM_001354689.1:c.1928C>T (RAF1) NP_001341618.1:p.Pro643Leu
NM_001354690.1:c.1868C>T (RAF1) NP_001341619.1:p.Pro623Leu
NM_001354691.1:c.1625C>T (RAF1) NP_001341620.1:p.Pro542Leu
NM_001354692.1:c.1625C>T (RAF1) NP_001341621.1:p.Pro542Leu
NM_001354693.1:c.1769C>T (RAF1) NP_001341622.1:p.Pro590Leu
NM_001354694.1:c.1685C>T (RAF1) NP_001341623.1:p.Pro562Leu
NM_001354695.1:c.1526C>T (RAF1) NP_001341624.1:p.Pro509Leu
NR_148940.1:n.2396C>T (RAF1)
NR_148941.1:n.2342C>T (RAF1)
NR_148942.1:n.2281C>T (RAF1)
XM_011533974.3:c.1868C>T (RAF1) XP_011532276.1:p.Pro623Leu
XM_017006966.1:c.1769C>T (RAF1) XP_016862455.1:p.Pro590Leu
NM_001354689.3:c.1928C>T (RAF1) NP_001341618.1:p.Pro643Leu
NM_001354690.2:c.1868C>T (RAF1) NP_001341619.1:p.Pro623Leu
NM_001354691.2:c.1625C>T (RAF1) NP_001341620.1:p.Pro542Leu
NM_001354692.2:c.1625C>T (RAF1) NP_001341621.1:p.Pro542Leu
NM_001354693.2:c.1769C>T (RAF1) NP_001341622.1:p.Pro590Leu
NM_001354694.2:c.1685C>T (RAF1) NP_001341623.1:p.Pro562Leu
NM_001354695.2:c.1526C>T (RAF1) NP_001341624.1:p.Pro509Leu
NR_148940.2:n.2312C>T (RAF1)
NR_148941.2:n.2258C>T (RAF1)
NR_148942.2:n.2197C>T (RAF1)
NM_001354690.3:c.1868C>T (RAF1) NP_001341619.1:p.Pro623Leu
NM_001354691.3:c.1625C>T (RAF1) NP_001341620.1:p.Pro542Leu
NM_001354692.3:c.1625C>T (RAF1) NP_001341621.1:p.Pro542Leu
NM_001354693.3:c.1769C>T (RAF1) NP_001341622.1:p.Pro590Leu
NM_001354694.3:c.1685C>T (RAF1) NP_001341623.1:p.Pro562Leu
NM_001354695.3:c.1526C>T (RAF1) NP_001341624.1:p.Pro509Leu
NM_002880.4:c.1868C>T (RAF1) MANE Select NP_002871.1:p.Pro623Leu
NR_148940.3:n.2312C>T (RAF1)
NR_148941.3:n.2258C>T (RAF1)
NR_148942.3:n.2197C>T (RAF1)