Canonical Allele Identifier: CA351495681

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12584564C>T , CM000665.2:g.12584564C>T GRCh38
NC_000003.11:g.12626063C>T , CM000665.1:g.12626063C>T GRCh37
NC_000003.10:g.12601063C>T NCBI36
NG_007467.1:g.84616G>A , LRG_413:g.84616G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000423275.6:c.*1562G>A (RAF1) ENSP00000401088.1:n.*1562G>A
ENST00000432427.3:c.1214G>A (RAF1)
ENST00000460610.2:n.6209G>A (RAF1)
ENST00000471449.2:n.707G>A (RAF1)
ENST00000475353.2:n.4177G>A (RAF1)
ENST00000684903.1:c.*1574G>A (RAF1) ENSP00000508612.1:n.*1574G>A
ENST00000685348.1:c.*1608G>A (RAF1) ENSP00000510285.1:n.*1608G>A
ENST00000685437.1:c.1798G>A (RAF1) ENSP00000508794.1:p.Asp600Asn
ENST00000685653.1:c.1897G>A (RAF1) ENSP00000509968.1:p.Asp633Asn
ENST00000685697.1:n.2632G>A (RAF1)
ENST00000685738.1:c.*861G>A (RAF1) ENSP00000510156.1:n.*861G>A
ENST00000686409.1:n.5306G>A (RAF1)
ENST00000686455.1:n.4618G>A (RAF1)
ENST00000686762.1:c.*456G>A (RAF1) ENSP00000509767.1:n.*456G>A
ENST00000687257.1:n.4351G>A (RAF1)
ENST00000687326.1:c.*3189G>A (RAF1) ENSP00000509665.1:n.*3189G>A
ENST00000687505.1:n.2015G>A (RAF1)
ENST00000687923.1:c.1786G>A (RAF1) ENSP00000510255.1:p.Asp596Asn
ENST00000688269.1:n.2493G>A (RAF1)
ENST00000688444.1:n.4014G>A (RAF1)
ENST00000688543.1:c.1798G>A (RAF1) ENSP00000509612.1:p.Asp600Asn
ENST00000688625.1:c.*3266G>A (RAF1) ENSP00000509522.1:n.*3266G>A
ENST00000688803.1:n.3325G>A (RAF1)
ENST00000689097.1:c.*1574G>A (RAF1) ENSP00000509756.1:n.*1574G>A
ENST00000689389.1:c.1720G>A (RAF1) ENSP00000510213.1:p.Asp574Asn
ENST00000689418.1:c.*3792G>A (RAF1) ENSP00000509467.1:n.*3792G>A
ENST00000689540.1:n.4265G>A (RAF1)
ENST00000689876.1:c.*446G>A (RAF1) ENSP00000508535.1:n.*446G>A
ENST00000689914.1:c.*831G>A (RAF1) ENSP00000509847.1:n.*831G>A
ENST00000690397.1:c.1786G>A (RAF1) ENSP00000508730.1:p.Asp596Asn
ENST00000690460.1:c.1885G>A (RAF1) ENSP00000509106.1:p.Asp629Asn
ENST00000690585.1:c.623G>A (RAF1)
ENST00000690625.1:n.2933G>A (RAF1)
ENST00000691396.1:c.*1769G>A (RAF1) ENSP00000510712.1:n.*1769G>A
ENST00000691643.1:n.2950G>A (RAF1)
ENST00000691724.1:c.*854G>A (RAF1) ENSP00000509255.1:n.*854G>A
ENST00000691779.1:c.*1475G>A (RAF1) ENSP00000508592.1:n.*1475G>A
ENST00000691888.1:c.771G>A (RAF1)
ENST00000691899.1:c.1897G>A (RAF1) ENSP00000508763.1:p.Asp633Asn
ENST00000692069.1:n.4821G>A (RAF1)
ENST00000692093.1:c.1798G>A (RAF1) ENSP00000509669.1:p.Asp600Asn
ENST00000692311.1:n.2721G>A (RAF1)
ENST00000692558.1:n.4480G>A (RAF1)
ENST00000692773.1:c.*1634G>A (RAF1) ENSP00000509055.1:n.*1634G>A
ENST00000692830.1:c.*1642G>A (RAF1) ENSP00000509461.1:n.*1642G>A
ENST00000693312.1:c.1672G>A (RAF1) ENSP00000508686.1:p.Asp558Asn
ENST00000693664.1:c.*348G>A (RAF1) ENSP00000509614.1:n.*348G>A
ENST00000693705.1:c.*1276G>A (RAF1) ENSP00000510697.1:n.*1276G>A
ENST00000251849.9:c.1897G>A (RAF1) MANE Select ENSP00000251849.4:p.Asp633Asn
ENST00000442415.7:c.1957G>A (RAF1) ENSP00000401888.2:p.Asp653Asn
ENST00000676541.1:c.*2311C>T (MKRN2) ENSP00000503730.1:n.*2311C>T
ENST00000677142.1:c.*2311C>T (MKRN2) ENSP00000504455.1:n.*2311C>T
ENST00000677816.1:c.*866C>T (MKRN2) ENSP00000502893.1:n.*866C>T
ENST00000677941.1:n.2374C>T (MKRN2)
ENST00000251849.8:c.1897G>A (RAF1) ENSP00000251849.4:p.Asp633Asn
ENST00000423275.5:c.*1574G>A (RAF1) ENSP00000401088.1:n.*1574G>A
ENST00000432427.2:c.1534G>A (RAF1) ENSP00000398591.2:p.Asp512Asn
ENST00000442415.6:c.1957G>A (RAF1) ENSP00000401888.2:p.Asp653Asn
ENST00000471449.1:n.586G>A (RAF1)
NM_002880.3:c.1897G>A , LRG_413t1:c.1897G>A (RAF1) NP_002871.1:p.Asp633Asn
XM_005265355.1:c.1897G>A (RAF1) XP_005265412.1:p.Asp633Asn
XM_005265357.1:c.1798G>A (RAF1) XP_005265414.1:p.Asp600Asn
XM_005265358.3:c.1654G>A (RAF1) XP_005265415.1:p.Asp552Asn
XM_005265359.3:c.1555G>A (RAF1) XP_005265416.1:p.Asp519Asn
XM_011533974.1:c.1897G>A (RAF1) XP_011532276.1:p.Asp633Asn
XM_011533975.1:c.1654G>A (RAF1) XP_011532277.1:p.Asp552Asn
NM_001354689.1:c.1957G>A (RAF1) NP_001341618.1:p.Asp653Asn
NM_001354690.1:c.1897G>A (RAF1) NP_001341619.1:p.Asp633Asn
NM_001354691.1:c.1654G>A (RAF1) NP_001341620.1:p.Asp552Asn
NM_001354692.1:c.1654G>A (RAF1) NP_001341621.1:p.Asp552Asn
NM_001354693.1:c.1798G>A (RAF1) NP_001341622.1:p.Asp600Asn
NM_001354694.1:c.1714G>A (RAF1) NP_001341623.1:p.Asp572Asn
NM_001354695.1:c.1555G>A (RAF1) NP_001341624.1:p.Asp519Asn
NR_148940.1:n.2425G>A (RAF1)
NR_148941.1:n.2371G>A (RAF1)
NR_148942.1:n.2310G>A (RAF1)
XM_011533974.3:c.1897G>A (RAF1) XP_011532276.1:p.Asp633Asn
XM_017006966.1:c.1798G>A (RAF1) XP_016862455.1:p.Asp600Asn
NM_001354689.3:c.1957G>A (RAF1) NP_001341618.1:p.Asp653Asn
NM_001354690.2:c.1897G>A (RAF1) NP_001341619.1:p.Asp633Asn
NM_001354691.2:c.1654G>A (RAF1) NP_001341620.1:p.Asp552Asn
NM_001354692.2:c.1654G>A (RAF1) NP_001341621.1:p.Asp552Asn
NM_001354693.2:c.1798G>A (RAF1) NP_001341622.1:p.Asp600Asn
NM_001354694.2:c.1714G>A (RAF1) NP_001341623.1:p.Asp572Asn
NM_001354695.2:c.1555G>A (RAF1) NP_001341624.1:p.Asp519Asn
NR_148940.2:n.2341G>A (RAF1)
NR_148941.2:n.2287G>A (RAF1)
NR_148942.2:n.2226G>A (RAF1)
NM_001354690.3:c.1897G>A (RAF1) NP_001341619.1:p.Asp633Asn
NM_001354691.3:c.1654G>A (RAF1) NP_001341620.1:p.Asp552Asn
NM_001354692.3:c.1654G>A (RAF1) NP_001341621.1:p.Asp552Asn
NM_001354693.3:c.1798G>A (RAF1) NP_001341622.1:p.Asp600Asn
NM_001354694.3:c.1714G>A (RAF1) NP_001341623.1:p.Asp572Asn
NM_001354695.3:c.1555G>A (RAF1) NP_001341624.1:p.Asp519Asn
NM_002880.4:c.1897G>A (RAF1) MANE Select NP_002871.1:p.Asp633Asn
NR_148940.3:n.2341G>A (RAF1)
NR_148941.3:n.2287G>A (RAF1)
NR_148942.3:n.2226G>A (RAF1)