Canonical Allele Identifier: CA1346227770

Gene: RAF1 MKRN2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12585682A= , CM000665.2:g.12585682A=	GRCh38
NC_000003.11:g.12627181A= , CM000665.1:g.12627181A=	GRCh37
NC_000003.10:g.12602181A=	NCBI36
NG_007467.1:g.83498T= , LRG_413:g.83498T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1200T= (RAF1)	ENSP00000401088.1:n.*1200T=
ENST00000432427.3:c.852T= (RAF1)
ENST00000460610.2:n.5280T= (RAF1)
ENST00000471449.2:n.345T= (RAF1)
ENST00000475353.2:n.3248T= (RAF1)
ENST00000684903.1:c.*1212T= (RAF1)	ENSP00000508612.1:n.*1212T=
ENST00000685348.1:c.*1095-276T= (RAF1)	ENSP00000510285.1:n.*1095-276T=
ENST00000685437.1:c.1436T= (RAF1)	ENSP00000508794.1:p.Met479=
ENST00000685653.1:c.1535T= (RAF1)	ENSP00000509968.1:p.Met512=
ENST00000685697.1:n.2270T= (RAF1)
ENST00000685738.1:c.*499T= (RAF1)	ENSP00000510156.1:n.*499T=
ENST00000686409.1:n.4377T= (RAF1)
ENST00000686455.1:n.3689T= (RAF1)
ENST00000686762.1:c.*94T= (RAF1)	ENSP00000509767.1:n.*94T=
ENST00000687257.1:n.3562T= (RAF1)
ENST00000687326.1:c.*2260T= (RAF1)	ENSP00000509665.1:n.*2260T=
ENST00000687505.1:n.1653T= (RAF1)
ENST00000687923.1:c.1424T= (RAF1)	ENSP00000510255.1:p.Met475=
ENST00000688269.1:n.2131T= (RAF1)
ENST00000688444.1:n.3652T= (RAF1)
ENST00000688543.1:c.1436T= (RAF1)	ENSP00000509612.1:p.Met479=
ENST00000688625.1:c.*2904T= (RAF1)	ENSP00000509522.1:n.*2904T=
ENST00000688803.1:n.2965-429T= (RAF1)
ENST00000688914.1:n.521T= (RAF1)
ENST00000689097.1:c.*1212T= (RAF1)	ENSP00000509756.1:n.*1212T=
ENST00000689389.1:c.1358T= (RAF1)	ENSP00000510213.1:p.Met453=
ENST00000689418.1:c.*3003T= (RAF1)	ENSP00000509467.1:n.*3003T=
ENST00000689540.1:n.3476T= (RAF1)
ENST00000689876.1:c.1418-276T= (RAF1)	ENSP00000508535.1:n.1418-276T=
ENST00000689914.1:c.*469T= (RAF1)	ENSP00000509847.1:n.*469T=
ENST00000690397.1:c.1424T= (RAF1)	ENSP00000508730.1:p.Met475=
ENST00000690460.1:c.1523T= (RAF1)	ENSP00000509106.1:p.Met508=
ENST00000690585.1:c.263-429T= (RAF1)
ENST00000690625.1:n.2571T= (RAF1)
ENST00000691396.1:c.*1407T= (RAF1)	ENSP00000510712.1:n.*1407T=
ENST00000691643.1:n.2161T= (RAF1)
ENST00000691724.1:c.*492T= (RAF1)	ENSP00000509255.1:n.*492T=
ENST00000691779.1:c.*1113T= (RAF1)	ENSP00000508592.1:n.*1113T=
ENST00000691888.1:c.409T= (RAF1)
ENST00000691899.1:c.1535T= (RAF1)	ENSP00000508763.1:p.Met512=
ENST00000692069.1:n.3892T= (RAF1)
ENST00000692093.1:c.1436T= (RAF1)	ENSP00000509669.1:p.Met479=
ENST00000692311.1:n.2359T= (RAF1)
ENST00000692558.1:n.3691T= (RAF1)
ENST00000692773.1:c.*1272T= (RAF1)	ENSP00000509055.1:n.*1272T=
ENST00000692830.1:c.*1280T= (RAF1)	ENSP00000509461.1:n.*1280T=
ENST00000693312.1:c.1310T= (RAF1)	ENSP00000508686.1:p.Met437=
ENST00000693664.1:c.1488-429T= (RAF1)	ENSP00000509614.1:n.1488-429T=
ENST00000693705.1:c.*1048-701T= (RAF1)	ENSP00000510697.1:n.*1048-701T=
ENST00000251849.9:c.1535T= (RAF1) MANE Select	ENSP00000251849.4:p.Met512=
ENST00000442415.7:c.1595T= (RAF1)	ENSP00000401888.2:p.Met532=
ENST00000676541.1:c.*3429A= (MKRN2)	ENSP00000503730.1:n.*3429A=
ENST00000677142.1:c.*3429A= (MKRN2)	ENSP00000504455.1:n.*3429A=
ENST00000677816.1:c.*1984A= (MKRN2)	ENSP00000502893.1:n.*1984A=
ENST00000677941.1:n.3492A= (MKRN2)
ENST00000251849.8:c.1535T= (RAF1)	ENSP00000251849.4:p.Met512=
ENST00000423275.5:c.*1212T= (RAF1)	ENSP00000401088.1:n.*1212T=
ENST00000432427.2:c.1172T= (RAF1)	ENSP00000398591.2:p.Met391=
ENST00000442415.6:c.1595T= (RAF1)	ENSP00000401888.2:p.Met532=
ENST00000471449.1:n.224T= (RAF1)
NM_002880.3:c.1535T= , LRG_413t1:c.1535T= (RAF1)	NP_002871.1:p.Met512=
XM_005265355.1:c.1535T= (RAF1)	XP_005265412.1:p.Met512=
XM_005265357.1:c.1436T= (RAF1)	XP_005265414.1:p.Met479=
XM_005265358.3:c.1292T= (RAF1)	XP_005265415.1:p.Met431=
XM_005265359.3:c.1193T= (RAF1)	XP_005265416.1:p.Met398=
XM_005265360.1:c.1418-276T= (RAF1)	XP_005265417.1:n.1418-276T=
XM_011533974.1:c.1535T= (RAF1)	XP_011532276.1:p.Met512=
XM_011533975.1:c.1292T= (RAF1)	XP_011532277.1:p.Met431=
NM_001354689.1:c.1595T= (RAF1)	NP_001341618.1:p.Met532=
NM_001354690.1:c.1535T= (RAF1)	NP_001341619.1:p.Met512=
NM_001354691.1:c.1292T= (RAF1)	NP_001341620.1:p.Met431=
NM_001354692.1:c.1292T= (RAF1)	NP_001341621.1:p.Met431=
NM_001354693.1:c.1436T= (RAF1)	NP_001341622.1:p.Met479=
NM_001354694.1:c.1352T= (RAF1)	NP_001341623.1:p.Met451=
NM_001354695.1:c.1193T= (RAF1)	NP_001341624.1:p.Met398=
NR_148940.1:n.2063T= (RAF1)
NR_148941.1:n.2009T= (RAF1)
NR_148942.1:n.1948T= (RAF1)
XM_011533974.3:c.1535T= (RAF1)	XP_011532276.1:p.Met512=
XM_017006966.1:c.1436T= (RAF1)	XP_016862455.1:p.Met479=
NM_001354689.3:c.1595T= (RAF1)	NP_001341618.1:p.Met532=
NM_001354690.2:c.1535T= (RAF1)	NP_001341619.1:p.Met512=
NM_001354691.2:c.1292T= (RAF1)	NP_001341620.1:p.Met431=
NM_001354692.2:c.1292T= (RAF1)	NP_001341621.1:p.Met431=
NM_001354693.2:c.1436T= (RAF1)	NP_001341622.1:p.Met479=
NM_001354694.2:c.1352T= (RAF1)	NP_001341623.1:p.Met451=
NM_001354695.2:c.1193T= (RAF1)	NP_001341624.1:p.Met398=
NR_148940.2:n.1979T= (RAF1)
NR_148941.2:n.1925T= (RAF1)
NR_148942.2:n.1864T= (RAF1)
NM_001354690.3:c.1535T= (RAF1)	NP_001341619.1:p.Met512=
NM_001354691.3:c.1292T= (RAF1)	NP_001341620.1:p.Met431=
NM_001354692.3:c.1292T= (RAF1)	NP_001341621.1:p.Met431=
NM_001354693.3:c.1436T= (RAF1)	NP_001341622.1:p.Met479=
NM_001354694.3:c.1352T= (RAF1)	NP_001341623.1:p.Met451=
NM_001354695.3:c.1193T= (RAF1)	NP_001341624.1:p.Met398=
NM_002880.4:c.1535T= (RAF1) MANE Select	NP_002871.1:p.Met512=
NR_148940.3:n.1979T= (RAF1)
NR_148941.3:n.1925T= (RAF1)
NR_148942.3:n.1864T= (RAF1)