Canonical Allele Identifier: CA1346227912

Gene: RAF1 MKRN2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12585761C= , CM000665.2:g.12585761C=	GRCh38
NC_000003.11:g.12627260C= , CM000665.1:g.12627260C=	GRCh37
NC_000003.10:g.12602260C=	NCBI36
NG_007467.1:g.83419G= , LRG_413:g.83419G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1121G= (RAF1)	ENSP00000401088.1:n.*1121G=
ENST00000432427.3:c.773G= (RAF1)
ENST00000460610.2:n.5201G= (RAF1)
ENST00000471449.2:n.266G= (RAF1)
ENST00000475353.2:n.3169G= (RAF1)
ENST00000684903.1:c.*1133G= (RAF1)	ENSP00000508612.1:n.*1133G=
ENST00000685348.1:c.*1095-355G= (RAF1)	ENSP00000510285.1:n.*1095-355G=
ENST00000685437.1:c.1357G= (RAF1)	ENSP00000508794.1:p.Asp453=
ENST00000685653.1:c.1456G= (RAF1)	ENSP00000509968.1:p.Asp486=
ENST00000685697.1:n.2191G= (RAF1)
ENST00000685738.1:c.*420G= (RAF1)	ENSP00000510156.1:n.*420G=
ENST00000686409.1:n.4298G= (RAF1)
ENST00000686455.1:n.3610G= (RAF1)
ENST00000686762.1:c.*15G= (RAF1)	ENSP00000509767.1:n.*15G=
ENST00000687257.1:n.3483G= (RAF1)
ENST00000687326.1:c.*2181G= (RAF1)	ENSP00000509665.1:n.*2181G=
ENST00000687505.1:n.1574G= (RAF1)
ENST00000687923.1:c.1345G= (RAF1)	ENSP00000510255.1:p.Asp449=
ENST00000688269.1:n.2052G= (RAF1)
ENST00000688444.1:n.3573G= (RAF1)
ENST00000688543.1:c.1357G= (RAF1)	ENSP00000509612.1:p.Asp453=
ENST00000688625.1:c.*2825G= (RAF1)	ENSP00000509522.1:n.*2825G=
ENST00000688803.1:n.2965-508G= (RAF1)
ENST00000688914.1:n.442G= (RAF1)
ENST00000689097.1:c.*1133G= (RAF1)	ENSP00000509756.1:n.*1133G=
ENST00000689389.1:c.1279G= (RAF1)	ENSP00000510213.1:p.Asp427=
ENST00000689418.1:c.*2924G= (RAF1)	ENSP00000509467.1:n.*2924G=
ENST00000689540.1:n.3397G= (RAF1)
ENST00000689876.1:c.1418-355G= (RAF1)	ENSP00000508535.1:n.1418-355G=
ENST00000689914.1:c.*390G= (RAF1)	ENSP00000509847.1:n.*390G=
ENST00000690397.1:c.1345G= (RAF1)	ENSP00000508730.1:p.Asp449=
ENST00000690460.1:c.1444G= (RAF1)	ENSP00000509106.1:p.Asp482=
ENST00000690585.1:c.263-508G= (RAF1)
ENST00000690625.1:n.2492G= (RAF1)
ENST00000691396.1:c.*1328G= (RAF1)	ENSP00000510712.1:n.*1328G=
ENST00000691643.1:n.2082G= (RAF1)
ENST00000691724.1:c.*413G= (RAF1)	ENSP00000509255.1:n.*413G=
ENST00000691779.1:c.*1034G= (RAF1)	ENSP00000508592.1:n.*1034G=
ENST00000691888.1:c.330G= (RAF1)
ENST00000691899.1:c.1456G= (RAF1)	ENSP00000508763.1:p.Asp486=
ENST00000692069.1:n.3813G= (RAF1)
ENST00000692093.1:c.1357G= (RAF1)	ENSP00000509669.1:p.Asp453=
ENST00000692311.1:n.2280G= (RAF1)
ENST00000692558.1:n.3612G= (RAF1)
ENST00000692773.1:c.*1193G= (RAF1)	ENSP00000509055.1:n.*1193G=
ENST00000692830.1:c.*1201G= (RAF1)	ENSP00000509461.1:n.*1201G=
ENST00000693312.1:c.1231G= (RAF1)	ENSP00000508686.1:p.Asp411=
ENST00000693664.1:c.1488-508G= (RAF1)	ENSP00000509614.1:n.1488-508G=
ENST00000693705.1:c.*1048-780G= (RAF1)	ENSP00000510697.1:n.*1048-780G=
ENST00000251849.9:c.1456G= (RAF1) MANE Select	ENSP00000251849.4:p.Asp486=
ENST00000442415.7:c.1516G= (RAF1)	ENSP00000401888.2:p.Asp506=
ENST00000676541.1:c.*3508C= (MKRN2)	ENSP00000503730.1:n.*3508C=
ENST00000677142.1:c.*3508C= (MKRN2)	ENSP00000504455.1:n.*3508C=
ENST00000677816.1:c.*2063C= (MKRN2)	ENSP00000502893.1:n.*2063C=
ENST00000677941.1:n.3571C= (MKRN2)
ENST00000251849.8:c.1456G= (RAF1)	ENSP00000251849.4:p.Asp486=
ENST00000423275.5:c.*1133G= (RAF1)	ENSP00000401088.1:n.*1133G=
ENST00000432427.2:c.1093G= (RAF1)	ENSP00000398591.2:p.Asp365=
ENST00000442415.6:c.1516G= (RAF1)	ENSP00000401888.2:p.Asp506=
ENST00000471449.1:n.145G= (RAF1)
NM_002880.3:c.1456G= , LRG_413t1:c.1456G= (RAF1)	NP_002871.1:p.Asp486=
XM_005265355.1:c.1456G= (RAF1)	XP_005265412.1:p.Asp486=
XM_005265357.1:c.1357G= (RAF1)	XP_005265414.1:p.Asp453=
XM_005265358.3:c.1213G= (RAF1)	XP_005265415.1:p.Asp405=
XM_005265359.3:c.1114G= (RAF1)	XP_005265416.1:p.Asp372=
XM_005265360.1:c.1418-355G= (RAF1)	XP_005265417.1:n.1418-355G=
XM_011533974.1:c.1456G= (RAF1)	XP_011532276.1:p.Asp486=
XM_011533975.1:c.1213G= (RAF1)	XP_011532277.1:p.Asp405=
NM_001354689.1:c.1516G= (RAF1)	NP_001341618.1:p.Asp506=
NM_001354690.1:c.1456G= (RAF1)	NP_001341619.1:p.Asp486=
NM_001354691.1:c.1213G= (RAF1)	NP_001341620.1:p.Asp405=
NM_001354692.1:c.1213G= (RAF1)	NP_001341621.1:p.Asp405=
NM_001354693.1:c.1357G= (RAF1)	NP_001341622.1:p.Asp453=
NM_001354694.1:c.1273G= (RAF1)	NP_001341623.1:p.Asp425=
NM_001354695.1:c.1114G= (RAF1)	NP_001341624.1:p.Asp372=
NR_148940.1:n.1984G= (RAF1)
NR_148941.1:n.1930G= (RAF1)
NR_148942.1:n.1869G= (RAF1)
XM_011533974.3:c.1456G= (RAF1)	XP_011532276.1:p.Asp486=
XM_017006966.1:c.1357G= (RAF1)	XP_016862455.1:p.Asp453=
NM_001354689.3:c.1516G= (RAF1)	NP_001341618.1:p.Asp506=
NM_001354690.2:c.1456G= (RAF1)	NP_001341619.1:p.Asp486=
NM_001354691.2:c.1213G= (RAF1)	NP_001341620.1:p.Asp405=
NM_001354692.2:c.1213G= (RAF1)	NP_001341621.1:p.Asp405=
NM_001354693.2:c.1357G= (RAF1)	NP_001341622.1:p.Asp453=
NM_001354694.2:c.1273G= (RAF1)	NP_001341623.1:p.Asp425=
NM_001354695.2:c.1114G= (RAF1)	NP_001341624.1:p.Asp372=
NR_148940.2:n.1900G= (RAF1)
NR_148941.2:n.1846G= (RAF1)
NR_148942.2:n.1785G= (RAF1)
NM_001354690.3:c.1456G= (RAF1)	NP_001341619.1:p.Asp486=
NM_001354691.3:c.1213G= (RAF1)	NP_001341620.1:p.Asp405=
NM_001354692.3:c.1213G= (RAF1)	NP_001341621.1:p.Asp405=
NM_001354693.3:c.1357G= (RAF1)	NP_001341622.1:p.Asp453=
NM_001354694.3:c.1273G= (RAF1)	NP_001341623.1:p.Asp425=
NM_001354695.3:c.1114G= (RAF1)	NP_001341624.1:p.Asp372=
NM_002880.4:c.1456G= (RAF1) MANE Select	NP_002871.1:p.Asp486=
NR_148940.3:n.1900G= (RAF1)
NR_148941.3:n.1846G= (RAF1)
NR_148942.3:n.1785G= (RAF1)