Canonical Allele Identifier: CA2989122062

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12584536del , CM000665.2:g.12584536del GRCh38
NC_000003.11:g.12626035del , CM000665.1:g.12626035del GRCh37
NC_000003.10:g.12601035del NCBI36
NG_007467.1:g.84647del , LRG_413:g.84647del

Transcript Alleles

HGVS Amino-acid Change
ENST00000423275.6:c.*1593del (RAF1) ENSP00000401088.1:n.*1593del
ENST00000432427.3:c.1245del (RAF1)
ENST00000460610.2:n.6240del (RAF1)
ENST00000471449.2:n.738del (RAF1)
ENST00000475353.2:n.4208del (RAF1)
ENST00000684903.1:c.*1605del (RAF1) ENSP00000508612.1:n.*1605del
ENST00000685348.1:c.*1639del (RAF1) ENSP00000510285.1:n.*1639del
ENST00000685437.1:c.1829del (RAF1) ENSP00000508794.1:p.Pro610ArgfsTer8
ENST00000685653.1:c.1928del (RAF1) ENSP00000509968.1:p.Pro643ArgfsTer8
ENST00000685697.1:n.2663del (RAF1)
ENST00000685738.1:c.*892del (RAF1) ENSP00000510156.1:n.*892del
ENST00000686409.1:n.5337del (RAF1)
ENST00000686455.1:n.4649del (RAF1)
ENST00000686762.1:c.*487del (RAF1) ENSP00000509767.1:n.*487del
ENST00000687257.1:n.4382del (RAF1)
ENST00000687326.1:c.*3220del (RAF1) ENSP00000509665.1:n.*3220del
ENST00000687505.1:n.2046del (RAF1)
ENST00000687923.1:c.1817del (RAF1) ENSP00000510255.1:p.Pro606ArgfsTer8
ENST00000688269.1:n.2524del (RAF1)
ENST00000688444.1:n.4045del (RAF1)
ENST00000688543.1:c.1829del (RAF1) ENSP00000509612.1:p.Pro610ArgfsTer8
ENST00000688625.1:c.*3297del (RAF1) ENSP00000509522.1:n.*3297del
ENST00000688803.1:n.3356del (RAF1)
ENST00000689097.1:c.*1605del (RAF1) ENSP00000509756.1:n.*1605del
ENST00000689389.1:c.1751del (RAF1) ENSP00000510213.1:p.Pro584ArgfsTer8
ENST00000689418.1:c.*3823del (RAF1) ENSP00000509467.1:n.*3823del
ENST00000689540.1:n.4296del (RAF1)
ENST00000689876.1:c.*477del (RAF1) ENSP00000508535.1:n.*477del
ENST00000689914.1:c.*862del (RAF1) ENSP00000509847.1:n.*862del
ENST00000690397.1:c.1817del (RAF1) ENSP00000508730.1:p.Pro606ArgfsTer8
ENST00000690460.1:c.1916del (RAF1) ENSP00000509106.1:p.Pro639ArgfsTer8
ENST00000690585.1:c.654del (RAF1)
ENST00000690625.1:n.2964del (RAF1)
ENST00000691396.1:c.*1800del (RAF1) ENSP00000510712.1:n.*1800del
ENST00000691643.1:n.2981del (RAF1)
ENST00000691724.1:c.*885del (RAF1) ENSP00000509255.1:n.*885del
ENST00000691779.1:c.*1506del (RAF1) ENSP00000508592.1:n.*1506del
ENST00000691888.1:c.802del (RAF1)
ENST00000691899.1:c.1928del (RAF1) ENSP00000508763.1:p.Pro643ArgfsTer8
ENST00000692069.1:n.4852del (RAF1)
ENST00000692093.1:c.1829del (RAF1) ENSP00000509669.1:p.Pro610ArgfsTer8
ENST00000692311.1:n.2752del (RAF1)
ENST00000692558.1:n.4511del (RAF1)
ENST00000692773.1:c.*1665del (RAF1) ENSP00000509055.1:n.*1665del
ENST00000692830.1:c.*1673del (RAF1) ENSP00000509461.1:n.*1673del
ENST00000693312.1:c.1703del (RAF1) ENSP00000508686.1:p.Pro568ArgfsTer8
ENST00000693664.1:c.*379del (RAF1) ENSP00000509614.1:n.*379del
ENST00000693705.1:c.*1307del (RAF1) ENSP00000510697.1:n.*1307del
ENST00000251849.9:c.1928del (RAF1) MANE Select ENSP00000251849.4:p.Pro643ArgfsTer8
ENST00000442415.7:c.1988del (RAF1) ENSP00000401888.2:p.Pro663ArgfsTer8
ENST00000676541.1:c.*2283del (MKRN2) ENSP00000503730.1:n.*2283del
ENST00000677142.1:c.*2283del (MKRN2) ENSP00000504455.1:n.*2283del
ENST00000677816.1:c.*838del (MKRN2) ENSP00000502893.1:n.*838del
ENST00000677941.1:n.2346del (MKRN2)
ENST00000251849.8:c.1928del (RAF1) ENSP00000251849.4:p.Pro643ArgfsTer8
ENST00000423275.5:c.*1605del (RAF1) ENSP00000401088.1:n.*1605del
ENST00000432427.2:c.1565del (RAF1) ENSP00000398591.2:p.Pro522ArgfsTer8
ENST00000442415.6:c.1988del (RAF1) ENSP00000401888.2:p.Pro663ArgfsTer8
ENST00000471449.1:n.617del (RAF1)
NM_002880.3:c.1928del , LRG_413t1:c.1928del (RAF1) NP_002871.1:p.Pro643ArgfsTer8
XM_005265355.1:c.1928del (RAF1) XP_005265412.1:p.Pro643ArgfsTer8
XM_005265357.1:c.1829del (RAF1) XP_005265414.1:p.Pro610ArgfsTer8
XM_005265358.3:c.1685del (RAF1) XP_005265415.1:p.Pro562ArgfsTer8
XM_005265359.3:c.1586del (RAF1) XP_005265416.1:p.Pro529ArgfsTer8
XM_011533974.1:c.1928del (RAF1) XP_011532276.1:p.Pro643ArgfsTer8
XM_011533975.1:c.1685del (RAF1) XP_011532277.1:p.Pro562ArgfsTer8
NM_001354689.1:c.1988del (RAF1) NP_001341618.1:p.Pro663ArgfsTer8
NM_001354690.1:c.1928del (RAF1) NP_001341619.1:p.Pro643ArgfsTer8
NM_001354691.1:c.1685del (RAF1) NP_001341620.1:p.Pro562ArgfsTer8
NM_001354692.1:c.1685del (RAF1) NP_001341621.1:p.Pro562ArgfsTer8
NM_001354693.1:c.1829del (RAF1) NP_001341622.1:p.Pro610ArgfsTer8
NM_001354694.1:c.1745del (RAF1) NP_001341623.1:p.Pro582ArgfsTer8
NM_001354695.1:c.1586del (RAF1) NP_001341624.1:p.Pro529ArgfsTer8
NR_148940.1:n.2456del (RAF1)
NR_148941.1:n.2402del (RAF1)
NR_148942.1:n.2341del (RAF1)
XM_011533974.3:c.1928del (RAF1) XP_011532276.1:p.Pro643ArgfsTer8
XM_017006966.1:c.1829del (RAF1) XP_016862455.1:p.Pro610ArgfsTer8
NM_001354689.3:c.1988del (RAF1) NP_001341618.1:p.Pro663ArgfsTer8
NM_001354690.2:c.1928del (RAF1) NP_001341619.1:p.Pro643ArgfsTer8
NM_001354691.2:c.1685del (RAF1) NP_001341620.1:p.Pro562ArgfsTer8
NM_001354692.2:c.1685del (RAF1) NP_001341621.1:p.Pro562ArgfsTer8
NM_001354693.2:c.1829del (RAF1) NP_001341622.1:p.Pro610ArgfsTer8
NM_001354694.2:c.1745del (RAF1) NP_001341623.1:p.Pro582ArgfsTer8
NM_001354695.2:c.1586del (RAF1) NP_001341624.1:p.Pro529ArgfsTer8
NR_148940.2:n.2372del (RAF1)
NR_148941.2:n.2318del (RAF1)
NR_148942.2:n.2257del (RAF1)
NM_001354690.3:c.1928del (RAF1) NP_001341619.1:p.Pro643ArgfsTer8
NM_001354691.3:c.1685del (RAF1) NP_001341620.1:p.Pro562ArgfsTer8
NM_001354692.3:c.1685del (RAF1) NP_001341621.1:p.Pro562ArgfsTer8
NM_001354693.3:c.1829del (RAF1) NP_001341622.1:p.Pro610ArgfsTer8
NM_001354694.3:c.1745del (RAF1) NP_001341623.1:p.Pro582ArgfsTer8
NM_001354695.3:c.1586del (RAF1) NP_001341624.1:p.Pro529ArgfsTer8
NM_002880.4:c.1928del (RAF1) MANE Select NP_002871.1:p.Pro643ArgfsTer8
NR_148940.3:n.2372del (RAF1)
NR_148941.3:n.2318del (RAF1)
NR_148942.3:n.2257del (RAF1)