Canonical Allele Identifier: CA2702196599

Gene: RAF1 MKRN2

Linked Data

• dbSNP Id: rs2125319864

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584950del , CM000665.2:g.12584950del	GRCh38
NC_000003.11:g.12626449del , CM000665.1:g.12626449del	GRCh37
NC_000003.10:g.12601449del	NCBI36
NG_007467.1:g.84233del , LRG_413:g.84233del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1368del (RAF1)	ENSP00000401088.1:n.*1368del
ENST00000432427.3:c.1020del (RAF1)
ENST00000460610.2:n.6015del (RAF1)
ENST00000471449.2:n.513del (RAF1)
ENST00000475353.2:n.3983del (RAF1)
ENST00000684903.1:c.*1380del (RAF1)	ENSP00000508612.1:n.*1380del
ENST00000685348.1:c.*1414del (RAF1)	ENSP00000510285.1:n.*1414del
ENST00000685437.1:c.1604del (RAF1)	ENSP00000508794.1:p.Pro535GlnfsTer14
ENST00000685653.1:c.1703del (RAF1)	ENSP00000509968.1:p.Pro568GlnfsTer14
ENST00000685697.1:n.2438del (RAF1)
ENST00000685738.1:c.*667del (RAF1)	ENSP00000510156.1:n.*667del
ENST00000686409.1:n.5112del (RAF1)
ENST00000686455.1:n.4424del (RAF1)
ENST00000686762.1:c.*262del (RAF1)	ENSP00000509767.1:n.*262del
ENST00000687257.1:n.4157del (RAF1)
ENST00000687326.1:c.*2995del (RAF1)	ENSP00000509665.1:n.*2995del
ENST00000687505.1:n.1821del (RAF1)
ENST00000687923.1:c.1592del (RAF1)	ENSP00000510255.1:p.Pro531GlnfsTer14
ENST00000688269.1:n.2299del (RAF1)
ENST00000688444.1:n.3820del (RAF1)
ENST00000688543.1:c.1604del (RAF1)	ENSP00000509612.1:p.Pro535GlnfsTer14
ENST00000688625.1:c.*3072del (RAF1)	ENSP00000509522.1:n.*3072del
ENST00000688803.1:n.3131del (RAF1)
ENST00000688914.1:n.1116del (RAF1)
ENST00000689097.1:c.*1380del (RAF1)	ENSP00000509756.1:n.*1380del
ENST00000689389.1:c.1526del (RAF1)	ENSP00000510213.1:p.Pro509GlnfsTer14
ENST00000689418.1:c.*3598del (RAF1)	ENSP00000509467.1:n.*3598del
ENST00000689540.1:n.4071del (RAF1)
ENST00000689876.1:c.*252del (RAF1)	ENSP00000508535.1:n.*252del
ENST00000689914.1:c.*637del (RAF1)	ENSP00000509847.1:n.*637del
ENST00000690397.1:c.1592del (RAF1)	ENSP00000508730.1:p.Pro531GlnfsTer14
ENST00000690460.1:c.1691del (RAF1)	ENSP00000509106.1:p.Pro564GlnfsTer14
ENST00000690585.1:c.429del (RAF1)
ENST00000690625.1:n.2739del (RAF1)
ENST00000691396.1:c.*1575del (RAF1)	ENSP00000510712.1:n.*1575del
ENST00000691643.1:n.2756del (RAF1)
ENST00000691724.1:c.*660del (RAF1)	ENSP00000509255.1:n.*660del
ENST00000691779.1:c.*1281del (RAF1)	ENSP00000508592.1:n.*1281del
ENST00000691888.1:c.577del (RAF1)
ENST00000691899.1:c.1703del (RAF1)	ENSP00000508763.1:p.Pro568GlnfsTer14
ENST00000692069.1:n.4627del (RAF1)
ENST00000692093.1:c.1604del (RAF1)	ENSP00000509669.1:p.Pro535GlnfsTer14
ENST00000692311.1:n.2527del (RAF1)
ENST00000692558.1:n.4286del (RAF1)
ENST00000692773.1:c.*1440del (RAF1)	ENSP00000509055.1:n.*1440del
ENST00000692830.1:c.*1448del (RAF1)	ENSP00000509461.1:n.*1448del
ENST00000693312.1:c.1478del (RAF1)	ENSP00000508686.1:p.Pro493GlnfsTer14
ENST00000693664.1:c.*154del (RAF1)	ENSP00000509614.1:n.*154del
ENST00000693705.1:c.*1082del (RAF1)	ENSP00000510697.1:n.*1082del
ENST00000251849.9:c.1703del (RAF1) MANE Select	ENSP00000251849.4:p.Pro568GlnfsTer14
ENST00000442415.7:c.1763del (RAF1)	ENSP00000401888.2:p.Pro588GlnfsTer14
ENST00000676541.1:c.*2697del (MKRN2)	ENSP00000503730.1:n.*2697del
ENST00000677142.1:c.*2697del (MKRN2)	ENSP00000504455.1:n.*2697del
ENST00000677816.1:c.*1252del (MKRN2)	ENSP00000502893.1:n.*1252del
ENST00000677941.1:n.2760del (MKRN2)
ENST00000251849.8:c.1703del (RAF1)	ENSP00000251849.4:p.Pro568GlnfsTer14
ENST00000423275.5:c.*1380del (RAF1)	ENSP00000401088.1:n.*1380del
ENST00000432427.2:c.1340del (RAF1)	ENSP00000398591.2:p.Pro447GlnfsTer14
ENST00000442415.6:c.1763del (RAF1)	ENSP00000401888.2:p.Pro588GlnfsTer14
ENST00000471449.1:n.392del (RAF1)
NM_002880.3:c.1703del , LRG_413t1:c.1703del (RAF1)	NP_002871.1:p.Pro568GlnfsTer14
XM_005265355.1:c.1703del (RAF1)	XP_005265412.1:p.Pro568GlnfsTer14
XM_005265357.1:c.1604del (RAF1)	XP_005265414.1:p.Pro535GlnfsTer14
XM_005265358.3:c.1460del (RAF1)	XP_005265415.1:p.Pro487GlnfsTer14
XM_005265359.3:c.1361del (RAF1)	XP_005265416.1:p.Pro454GlnfsTer14
XM_011533974.1:c.1703del (RAF1)	XP_011532276.1:p.Pro568GlnfsTer14
XM_011533975.1:c.1460del (RAF1)	XP_011532277.1:p.Pro487GlnfsTer14
NM_001354689.1:c.1763del (RAF1)	NP_001341618.1:p.Pro588GlnfsTer14
NM_001354690.1:c.1703del (RAF1)	NP_001341619.1:p.Pro568GlnfsTer14
NM_001354691.1:c.1460del (RAF1)	NP_001341620.1:p.Pro487GlnfsTer14
NM_001354692.1:c.1460del (RAF1)	NP_001341621.1:p.Pro487GlnfsTer14
NM_001354693.1:c.1604del (RAF1)	NP_001341622.1:p.Pro535GlnfsTer14
NM_001354694.1:c.1520del (RAF1)	NP_001341623.1:p.Pro507GlnfsTer14
NM_001354695.1:c.1361del (RAF1)	NP_001341624.1:p.Pro454GlnfsTer14
NR_148940.1:n.2231del (RAF1)
NR_148941.1:n.2177del (RAF1)
NR_148942.1:n.2116del (RAF1)
XM_011533974.3:c.1703del (RAF1)	XP_011532276.1:p.Pro568GlnfsTer14
XM_017006966.1:c.1604del (RAF1)	XP_016862455.1:p.Pro535GlnfsTer14
NM_001354689.3:c.1763del (RAF1)	NP_001341618.1:p.Pro588GlnfsTer14
NM_001354690.2:c.1703del (RAF1)	NP_001341619.1:p.Pro568GlnfsTer14
NM_001354691.2:c.1460del (RAF1)	NP_001341620.1:p.Pro487GlnfsTer14
NM_001354692.2:c.1460del (RAF1)	NP_001341621.1:p.Pro487GlnfsTer14
NM_001354693.2:c.1604del (RAF1)	NP_001341622.1:p.Pro535GlnfsTer14
NM_001354694.2:c.1520del (RAF1)	NP_001341623.1:p.Pro507GlnfsTer14
NM_001354695.2:c.1361del (RAF1)	NP_001341624.1:p.Pro454GlnfsTer14
NR_148940.2:n.2147del (RAF1)
NR_148941.2:n.2093del (RAF1)
NR_148942.2:n.2032del (RAF1)
NM_001354690.3:c.1703del (RAF1)	NP_001341619.1:p.Pro568GlnfsTer14
NM_001354691.3:c.1460del (RAF1)	NP_001341620.1:p.Pro487GlnfsTer14
NM_001354692.3:c.1460del (RAF1)	NP_001341621.1:p.Pro487GlnfsTer14
NM_001354693.3:c.1604del (RAF1)	NP_001341622.1:p.Pro535GlnfsTer14
NM_001354694.3:c.1520del (RAF1)	NP_001341623.1:p.Pro507GlnfsTer14
NM_001354695.3:c.1361del (RAF1)	NP_001341624.1:p.Pro454GlnfsTer14
NM_002880.4:c.1703del (RAF1) MANE Select	NP_002871.1:p.Pro568GlnfsTer14
NR_148940.3:n.2147del (RAF1)
NR_148941.3:n.2093del (RAF1)
NR_148942.3:n.2032del (RAF1)