Canonical Allele Identifier: CA351496455

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12584860G>T , CM000665.2:g.12584860G>T GRCh38
NC_000003.11:g.12626359G>T , CM000665.1:g.12626359G>T GRCh37
NC_000003.10:g.12601359G>T NCBI36
NG_007467.1:g.84320C>A , LRG_413:g.84320C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000423275.6:c.*1455C>A (RAF1) ENSP00000401088.1:n.*1455C>A
ENST00000432427.3:c.1107C>A (RAF1)
ENST00000460610.2:n.6102C>A (RAF1)
ENST00000471449.2:n.600C>A (RAF1)
ENST00000475353.2:n.4070C>A (RAF1)
ENST00000684903.1:c.*1467C>A (RAF1) ENSP00000508612.1:n.*1467C>A
ENST00000685348.1:c.*1501C>A (RAF1) ENSP00000510285.1:n.*1501C>A
ENST00000685437.1:c.1691C>A (RAF1) ENSP00000508794.1:p.Pro564His
ENST00000685653.1:c.1790C>A (RAF1) ENSP00000509968.1:p.Pro597His
ENST00000685697.1:n.2525C>A (RAF1)
ENST00000685738.1:c.*754C>A (RAF1) ENSP00000510156.1:n.*754C>A
ENST00000686409.1:n.5199C>A (RAF1)
ENST00000686455.1:n.4511C>A (RAF1)
ENST00000686762.1:c.*349C>A (RAF1) ENSP00000509767.1:n.*349C>A
ENST00000687257.1:n.4244C>A (RAF1)
ENST00000687326.1:c.*3082C>A (RAF1) ENSP00000509665.1:n.*3082C>A
ENST00000687505.1:n.1908C>A (RAF1)
ENST00000687923.1:c.1679C>A (RAF1) ENSP00000510255.1:p.Pro560His
ENST00000688269.1:n.2386C>A (RAF1)
ENST00000688444.1:n.3907C>A (RAF1)
ENST00000688543.1:c.1691C>A (RAF1) ENSP00000509612.1:p.Pro564His
ENST00000688625.1:c.*3159C>A (RAF1) ENSP00000509522.1:n.*3159C>A
ENST00000688803.1:n.3218C>A (RAF1)
ENST00000689097.1:c.*1467C>A (RAF1) ENSP00000509756.1:n.*1467C>A
ENST00000689389.1:c.1613C>A (RAF1) ENSP00000510213.1:p.Pro538His
ENST00000689418.1:c.*3685C>A (RAF1) ENSP00000509467.1:n.*3685C>A
ENST00000689540.1:n.4158C>A (RAF1)
ENST00000689876.1:c.*339C>A (RAF1) ENSP00000508535.1:n.*339C>A
ENST00000689914.1:c.*724C>A (RAF1) ENSP00000509847.1:n.*724C>A
ENST00000690397.1:c.1679C>A (RAF1) ENSP00000508730.1:p.Pro560His
ENST00000690460.1:c.1778C>A (RAF1) ENSP00000509106.1:p.Pro593His
ENST00000690585.1:c.516C>A (RAF1)
ENST00000690625.1:n.2826C>A (RAF1)
ENST00000691396.1:c.*1662C>A (RAF1) ENSP00000510712.1:n.*1662C>A
ENST00000691643.1:n.2843C>A (RAF1)
ENST00000691724.1:c.*747C>A (RAF1) ENSP00000509255.1:n.*747C>A
ENST00000691779.1:c.*1368C>A (RAF1) ENSP00000508592.1:n.*1368C>A
ENST00000691888.1:c.664C>A (RAF1)
ENST00000691899.1:c.1790C>A (RAF1) ENSP00000508763.1:p.Pro597His
ENST00000692069.1:n.4714C>A (RAF1)
ENST00000692093.1:c.1691C>A (RAF1) ENSP00000509669.1:p.Pro564His
ENST00000692311.1:n.2614C>A (RAF1)
ENST00000692558.1:n.4373C>A (RAF1)
ENST00000692773.1:c.*1527C>A (RAF1) ENSP00000509055.1:n.*1527C>A
ENST00000692830.1:c.*1535C>A (RAF1) ENSP00000509461.1:n.*1535C>A
ENST00000693312.1:c.1565C>A (RAF1) ENSP00000508686.1:p.Pro522His
ENST00000693664.1:c.*241C>A (RAF1) ENSP00000509614.1:n.*241C>A
ENST00000693705.1:c.*1169C>A (RAF1) ENSP00000510697.1:n.*1169C>A
ENST00000251849.9:c.1790C>A (RAF1) MANE Select ENSP00000251849.4:p.Pro597His
ENST00000442415.7:c.1850C>A (RAF1) ENSP00000401888.2:p.Pro617His
ENST00000676541.1:c.*2607G>T (MKRN2) ENSP00000503730.1:n.*2607G>T
ENST00000677142.1:c.*2607G>T (MKRN2) ENSP00000504455.1:n.*2607G>T
ENST00000677816.1:c.*1162G>T (MKRN2) ENSP00000502893.1:n.*1162G>T
ENST00000677941.1:n.2670G>T (MKRN2)
ENST00000251849.8:c.1790C>A (RAF1) ENSP00000251849.4:p.Pro597His
ENST00000423275.5:c.*1467C>A (RAF1) ENSP00000401088.1:n.*1467C>A
ENST00000432427.2:c.1427C>A (RAF1) ENSP00000398591.2:p.Pro476His
ENST00000442415.6:c.1850C>A (RAF1) ENSP00000401888.2:p.Pro617His
ENST00000471449.1:n.479C>A (RAF1)
NM_002880.3:c.1790C>A , LRG_413t1:c.1790C>A (RAF1) NP_002871.1:p.Pro597His
XM_005265355.1:c.1790C>A (RAF1) XP_005265412.1:p.Pro597His
XM_005265357.1:c.1691C>A (RAF1) XP_005265414.1:p.Pro564His
XM_005265358.3:c.1547C>A (RAF1) XP_005265415.1:p.Pro516His
XM_005265359.3:c.1448C>A (RAF1) XP_005265416.1:p.Pro483His
XM_011533974.1:c.1790C>A (RAF1) XP_011532276.1:p.Pro597His
XM_011533975.1:c.1547C>A (RAF1) XP_011532277.1:p.Pro516His
NM_001354689.1:c.1850C>A (RAF1) NP_001341618.1:p.Pro617His
NM_001354690.1:c.1790C>A (RAF1) NP_001341619.1:p.Pro597His
NM_001354691.1:c.1547C>A (RAF1) NP_001341620.1:p.Pro516His
NM_001354692.1:c.1547C>A (RAF1) NP_001341621.1:p.Pro516His
NM_001354693.1:c.1691C>A (RAF1) NP_001341622.1:p.Pro564His
NM_001354694.1:c.1607C>A (RAF1) NP_001341623.1:p.Pro536His
NM_001354695.1:c.1448C>A (RAF1) NP_001341624.1:p.Pro483His
NR_148940.1:n.2318C>A (RAF1)
NR_148941.1:n.2264C>A (RAF1)
NR_148942.1:n.2203C>A (RAF1)
XM_011533974.3:c.1790C>A (RAF1) XP_011532276.1:p.Pro597His
XM_017006966.1:c.1691C>A (RAF1) XP_016862455.1:p.Pro564His
NM_001354689.3:c.1850C>A (RAF1) NP_001341618.1:p.Pro617His
NM_001354690.2:c.1790C>A (RAF1) NP_001341619.1:p.Pro597His
NM_001354691.2:c.1547C>A (RAF1) NP_001341620.1:p.Pro516His
NM_001354692.2:c.1547C>A (RAF1) NP_001341621.1:p.Pro516His
NM_001354693.2:c.1691C>A (RAF1) NP_001341622.1:p.Pro564His
NM_001354694.2:c.1607C>A (RAF1) NP_001341623.1:p.Pro536His
NM_001354695.2:c.1448C>A (RAF1) NP_001341624.1:p.Pro483His
NR_148940.2:n.2234C>A (RAF1)
NR_148941.2:n.2180C>A (RAF1)
NR_148942.2:n.2119C>A (RAF1)
NM_001354690.3:c.1790C>A (RAF1) NP_001341619.1:p.Pro597His
NM_001354691.3:c.1547C>A (RAF1) NP_001341620.1:p.Pro516His
NM_001354692.3:c.1547C>A (RAF1) NP_001341621.1:p.Pro516His
NM_001354693.3:c.1691C>A (RAF1) NP_001341622.1:p.Pro564His
NM_001354694.3:c.1607C>A (RAF1) NP_001341623.1:p.Pro536His
NM_001354695.3:c.1448C>A (RAF1) NP_001341624.1:p.Pro483His
NM_002880.4:c.1790C>A (RAF1) MANE Select NP_002871.1:p.Pro597His
NR_148940.3:n.2234C>A (RAF1)
NR_148941.3:n.2180C>A (RAF1)
NR_148942.3:n.2119C>A (RAF1)