Canonical Allele Identifier: CA351495709

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12584569G>T , CM000665.2:g.12584569G>T GRCh38
NC_000003.11:g.12626068G>T , CM000665.1:g.12626068G>T GRCh37
NC_000003.10:g.12601068G>T NCBI36
NG_007467.1:g.84611C>A , LRG_413:g.84611C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000423275.6:c.*1557C>A (RAF1) ENSP00000401088.1:n.*1557C>A
ENST00000432427.3:c.1209C>A (RAF1)
ENST00000460610.2:n.6204C>A (RAF1)
ENST00000471449.2:n.702C>A (RAF1)
ENST00000475353.2:n.4172C>A (RAF1)
ENST00000684903.1:c.*1569C>A (RAF1) ENSP00000508612.1:n.*1569C>A
ENST00000685348.1:c.*1603C>A (RAF1) ENSP00000510285.1:n.*1603C>A
ENST00000685437.1:c.1793C>A (RAF1) ENSP00000508794.1:p.Thr598Asn
ENST00000685653.1:c.1892C>A (RAF1) ENSP00000509968.1:p.Thr631Asn
ENST00000685697.1:n.2627C>A (RAF1)
ENST00000685738.1:c.*856C>A (RAF1) ENSP00000510156.1:n.*856C>A
ENST00000686409.1:n.5301C>A (RAF1)
ENST00000686455.1:n.4613C>A (RAF1)
ENST00000686762.1:c.*451C>A (RAF1) ENSP00000509767.1:n.*451C>A
ENST00000687257.1:n.4346C>A (RAF1)
ENST00000687326.1:c.*3184C>A (RAF1) ENSP00000509665.1:n.*3184C>A
ENST00000687505.1:n.2010C>A (RAF1)
ENST00000687923.1:c.1781C>A (RAF1) ENSP00000510255.1:p.Thr594Asn
ENST00000688269.1:n.2488C>A (RAF1)
ENST00000688444.1:n.4009C>A (RAF1)
ENST00000688543.1:c.1793C>A (RAF1) ENSP00000509612.1:p.Thr598Asn
ENST00000688625.1:c.*3261C>A (RAF1) ENSP00000509522.1:n.*3261C>A
ENST00000688803.1:n.3320C>A (RAF1)
ENST00000689097.1:c.*1569C>A (RAF1) ENSP00000509756.1:n.*1569C>A
ENST00000689389.1:c.1715C>A (RAF1) ENSP00000510213.1:p.Thr572Asn
ENST00000689418.1:c.*3787C>A (RAF1) ENSP00000509467.1:n.*3787C>A
ENST00000689540.1:n.4260C>A (RAF1)
ENST00000689876.1:c.*441C>A (RAF1) ENSP00000508535.1:n.*441C>A
ENST00000689914.1:c.*826C>A (RAF1) ENSP00000509847.1:n.*826C>A
ENST00000690397.1:c.1781C>A (RAF1) ENSP00000508730.1:p.Thr594Asn
ENST00000690460.1:c.1880C>A (RAF1) ENSP00000509106.1:p.Thr627Asn
ENST00000690585.1:c.618C>A (RAF1)
ENST00000690625.1:n.2928C>A (RAF1)
ENST00000691396.1:c.*1764C>A (RAF1) ENSP00000510712.1:n.*1764C>A
ENST00000691643.1:n.2945C>A (RAF1)
ENST00000691724.1:c.*849C>A (RAF1) ENSP00000509255.1:n.*849C>A
ENST00000691779.1:c.*1470C>A (RAF1) ENSP00000508592.1:n.*1470C>A
ENST00000691888.1:c.766C>A (RAF1)
ENST00000691899.1:c.1892C>A (RAF1) ENSP00000508763.1:p.Thr631Asn
ENST00000692069.1:n.4816C>A (RAF1)
ENST00000692093.1:c.1793C>A (RAF1) ENSP00000509669.1:p.Thr598Asn
ENST00000692311.1:n.2716C>A (RAF1)
ENST00000692558.1:n.4475C>A (RAF1)
ENST00000692773.1:c.*1629C>A (RAF1) ENSP00000509055.1:n.*1629C>A
ENST00000692830.1:c.*1637C>A (RAF1) ENSP00000509461.1:n.*1637C>A
ENST00000693312.1:c.1667C>A (RAF1) ENSP00000508686.1:p.Thr556Asn
ENST00000693664.1:c.*343C>A (RAF1) ENSP00000509614.1:n.*343C>A
ENST00000693705.1:c.*1271C>A (RAF1) ENSP00000510697.1:n.*1271C>A
ENST00000251849.9:c.1892C>A (RAF1) MANE Select ENSP00000251849.4:p.Thr631Asn
ENST00000442415.7:c.1952C>A (RAF1) ENSP00000401888.2:p.Thr651Asn
ENST00000676541.1:c.*2316G>T (MKRN2) ENSP00000503730.1:n.*2316G>T
ENST00000677142.1:c.*2316G>T (MKRN2) ENSP00000504455.1:n.*2316G>T
ENST00000677816.1:c.*871G>T (MKRN2) ENSP00000502893.1:n.*871G>T
ENST00000677941.1:n.2379G>T (MKRN2)
ENST00000251849.8:c.1892C>A (RAF1) ENSP00000251849.4:p.Thr631Asn
ENST00000423275.5:c.*1569C>A (RAF1) ENSP00000401088.1:n.*1569C>A
ENST00000432427.2:c.1529C>A (RAF1) ENSP00000398591.2:p.Thr510Asn
ENST00000442415.6:c.1952C>A (RAF1) ENSP00000401888.2:p.Thr651Asn
ENST00000471449.1:n.581C>A (RAF1)
NM_002880.3:c.1892C>A , LRG_413t1:c.1892C>A (RAF1) NP_002871.1:p.Thr631Asn
XM_005265355.1:c.1892C>A (RAF1) XP_005265412.1:p.Thr631Asn
XM_005265357.1:c.1793C>A (RAF1) XP_005265414.1:p.Thr598Asn
XM_005265358.3:c.1649C>A (RAF1) XP_005265415.1:p.Thr550Asn
XM_005265359.3:c.1550C>A (RAF1) XP_005265416.1:p.Thr517Asn
XM_011533974.1:c.1892C>A (RAF1) XP_011532276.1:p.Thr631Asn
XM_011533975.1:c.1649C>A (RAF1) XP_011532277.1:p.Thr550Asn
NM_001354689.1:c.1952C>A (RAF1) NP_001341618.1:p.Thr651Asn
NM_001354690.1:c.1892C>A (RAF1) NP_001341619.1:p.Thr631Asn
NM_001354691.1:c.1649C>A (RAF1) NP_001341620.1:p.Thr550Asn
NM_001354692.1:c.1649C>A (RAF1) NP_001341621.1:p.Thr550Asn
NM_001354693.1:c.1793C>A (RAF1) NP_001341622.1:p.Thr598Asn
NM_001354694.1:c.1709C>A (RAF1) NP_001341623.1:p.Thr570Asn
NM_001354695.1:c.1550C>A (RAF1) NP_001341624.1:p.Thr517Asn
NR_148940.1:n.2420C>A (RAF1)
NR_148941.1:n.2366C>A (RAF1)
NR_148942.1:n.2305C>A (RAF1)
XM_011533974.3:c.1892C>A (RAF1) XP_011532276.1:p.Thr631Asn
XM_017006966.1:c.1793C>A (RAF1) XP_016862455.1:p.Thr598Asn
NM_001354689.3:c.1952C>A (RAF1) NP_001341618.1:p.Thr651Asn
NM_001354690.2:c.1892C>A (RAF1) NP_001341619.1:p.Thr631Asn
NM_001354691.2:c.1649C>A (RAF1) NP_001341620.1:p.Thr550Asn
NM_001354692.2:c.1649C>A (RAF1) NP_001341621.1:p.Thr550Asn
NM_001354693.2:c.1793C>A (RAF1) NP_001341622.1:p.Thr598Asn
NM_001354694.2:c.1709C>A (RAF1) NP_001341623.1:p.Thr570Asn
NM_001354695.2:c.1550C>A (RAF1) NP_001341624.1:p.Thr517Asn
NR_148940.2:n.2336C>A (RAF1)
NR_148941.2:n.2282C>A (RAF1)
NR_148942.2:n.2221C>A (RAF1)
NM_001354690.3:c.1892C>A (RAF1) NP_001341619.1:p.Thr631Asn
NM_001354691.3:c.1649C>A (RAF1) NP_001341620.1:p.Thr550Asn
NM_001354692.3:c.1649C>A (RAF1) NP_001341621.1:p.Thr550Asn
NM_001354693.3:c.1793C>A (RAF1) NP_001341622.1:p.Thr598Asn
NM_001354694.3:c.1709C>A (RAF1) NP_001341623.1:p.Thr570Asn
NM_001354695.3:c.1550C>A (RAF1) NP_001341624.1:p.Thr517Asn
NM_002880.4:c.1892C>A (RAF1) MANE Select NP_002871.1:p.Thr631Asn
NR_148940.3:n.2336C>A (RAF1)
NR_148941.3:n.2282C>A (RAF1)
NR_148942.3:n.2221C>A (RAF1)