Canonical Allele Identifier: CA351499151

Gene: RAF1 MKRN2

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12585759A>C , CM000665.2:g.12585759A>C	GRCh38
NC_000003.11:g.12627258A>C , CM000665.1:g.12627258A>C	GRCh37
NC_000003.10:g.12602258A>C	NCBI36
NG_007467.1:g.83421T>G , LRG_413:g.83421T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1123T>G (RAF1)	ENSP00000401088.1:n.*1123T>G
ENST00000432427.3:c.775T>G (RAF1)
ENST00000460610.2:n.5203T>G (RAF1)
ENST00000471449.2:n.268T>G (RAF1)
ENST00000475353.2:n.3171T>G (RAF1)
ENST00000684903.1:c.*1135T>G (RAF1)	ENSP00000508612.1:n.*1135T>G
ENST00000685348.1:c.*1095-353T>G (RAF1)	ENSP00000510285.1:n.*1095-353T>G
ENST00000685437.1:c.1359T>G (RAF1)	ENSP00000508794.1:p.Asp453Glu
ENST00000685653.1:c.1458T>G (RAF1)	ENSP00000509968.1:p.Asp486Glu
ENST00000685697.1:n.2193T>G (RAF1)
ENST00000685738.1:c.*422T>G (RAF1)	ENSP00000510156.1:n.*422T>G
ENST00000686409.1:n.4300T>G (RAF1)
ENST00000686455.1:n.3612T>G (RAF1)
ENST00000686762.1:c.*17T>G (RAF1)	ENSP00000509767.1:n.*17T>G
ENST00000687257.1:n.3485T>G (RAF1)
ENST00000687326.1:c.*2183T>G (RAF1)	ENSP00000509665.1:n.*2183T>G
ENST00000687505.1:n.1576T>G (RAF1)
ENST00000687923.1:c.1347T>G (RAF1)	ENSP00000510255.1:p.Asp449Glu
ENST00000688269.1:n.2054T>G (RAF1)
ENST00000688444.1:n.3575T>G (RAF1)
ENST00000688543.1:c.1359T>G (RAF1)	ENSP00000509612.1:p.Asp453Glu
ENST00000688625.1:c.*2827T>G (RAF1)	ENSP00000509522.1:n.*2827T>G
ENST00000688803.1:n.2965-506T>G (RAF1)
ENST00000688914.1:n.444T>G (RAF1)
ENST00000689097.1:c.*1135T>G (RAF1)	ENSP00000509756.1:n.*1135T>G
ENST00000689389.1:c.1281T>G (RAF1)	ENSP00000510213.1:p.Asp427Glu
ENST00000689418.1:c.*2926T>G (RAF1)	ENSP00000509467.1:n.*2926T>G
ENST00000689540.1:n.3399T>G (RAF1)
ENST00000689876.1:c.1418-353T>G (RAF1)	ENSP00000508535.1:n.1418-353T>G
ENST00000689914.1:c.*392T>G (RAF1)	ENSP00000509847.1:n.*392T>G
ENST00000690397.1:c.1347T>G (RAF1)	ENSP00000508730.1:p.Asp449Glu
ENST00000690460.1:c.1446T>G (RAF1)	ENSP00000509106.1:p.Asp482Glu
ENST00000690585.1:c.263-506T>G (RAF1)
ENST00000690625.1:n.2494T>G (RAF1)
ENST00000691396.1:c.*1330T>G (RAF1)	ENSP00000510712.1:n.*1330T>G
ENST00000691643.1:n.2084T>G (RAF1)
ENST00000691724.1:c.*415T>G (RAF1)	ENSP00000509255.1:n.*415T>G
ENST00000691779.1:c.*1036T>G (RAF1)	ENSP00000508592.1:n.*1036T>G
ENST00000691888.1:c.332T>G (RAF1)
ENST00000691899.1:c.1458T>G (RAF1)	ENSP00000508763.1:p.Asp486Glu
ENST00000692069.1:n.3815T>G (RAF1)
ENST00000692093.1:c.1359T>G (RAF1)	ENSP00000509669.1:p.Asp453Glu
ENST00000692311.1:n.2282T>G (RAF1)
ENST00000692558.1:n.3614T>G (RAF1)
ENST00000692773.1:c.*1195T>G (RAF1)	ENSP00000509055.1:n.*1195T>G
ENST00000692830.1:c.*1203T>G (RAF1)	ENSP00000509461.1:n.*1203T>G
ENST00000693312.1:c.1233T>G (RAF1)	ENSP00000508686.1:p.Asp411Glu
ENST00000693664.1:c.1488-506T>G (RAF1)	ENSP00000509614.1:n.1488-506T>G
ENST00000693705.1:c.*1048-778T>G (RAF1)	ENSP00000510697.1:n.*1048-778T>G
ENST00000251849.9:c.1458T>G (RAF1) MANE Select	ENSP00000251849.4:p.Asp486Glu
ENST00000442415.7:c.1518T>G (RAF1)	ENSP00000401888.2:p.Asp506Glu
ENST00000676541.1:c.*3506A>C (MKRN2)	ENSP00000503730.1:n.*3506A>C
ENST00000677142.1:c.*3506A>C (MKRN2)	ENSP00000504455.1:n.*3506A>C
ENST00000677816.1:c.*2061A>C (MKRN2)	ENSP00000502893.1:n.*2061A>C
ENST00000677941.1:n.3569A>C (MKRN2)
ENST00000251849.8:c.1458T>G (RAF1)	ENSP00000251849.4:p.Asp486Glu
ENST00000423275.5:c.*1135T>G (RAF1)	ENSP00000401088.1:n.*1135T>G
ENST00000432427.2:c.1095T>G (RAF1)	ENSP00000398591.2:p.Asp365Glu
ENST00000442415.6:c.1518T>G (RAF1)	ENSP00000401888.2:p.Asp506Glu
ENST00000471449.1:n.147T>G (RAF1)
NM_002880.3:c.1458T>G , LRG_413t1:c.1458T>G (RAF1)	NP_002871.1:p.Asp486Glu
XM_005265355.1:c.1458T>G (RAF1)	XP_005265412.1:p.Asp486Glu
XM_005265357.1:c.1359T>G (RAF1)	XP_005265414.1:p.Asp453Glu
XM_005265358.3:c.1215T>G (RAF1)	XP_005265415.1:p.Asp405Glu
XM_005265359.3:c.1116T>G (RAF1)	XP_005265416.1:p.Asp372Glu
XM_005265360.1:c.1418-353T>G (RAF1)	XP_005265417.1:n.1418-353T>G
XM_011533974.1:c.1458T>G (RAF1)	XP_011532276.1:p.Asp486Glu
XM_011533975.1:c.1215T>G (RAF1)	XP_011532277.1:p.Asp405Glu
NM_001354689.1:c.1518T>G (RAF1)	NP_001341618.1:p.Asp506Glu
NM_001354690.1:c.1458T>G (RAF1)	NP_001341619.1:p.Asp486Glu
NM_001354691.1:c.1215T>G (RAF1)	NP_001341620.1:p.Asp405Glu
NM_001354692.1:c.1215T>G (RAF1)	NP_001341621.1:p.Asp405Glu
NM_001354693.1:c.1359T>G (RAF1)	NP_001341622.1:p.Asp453Glu
NM_001354694.1:c.1275T>G (RAF1)	NP_001341623.1:p.Asp425Glu
NM_001354695.1:c.1116T>G (RAF1)	NP_001341624.1:p.Asp372Glu
NR_148940.1:n.1986T>G (RAF1)
NR_148941.1:n.1932T>G (RAF1)
NR_148942.1:n.1871T>G (RAF1)
XM_011533974.3:c.1458T>G (RAF1)	XP_011532276.1:p.Asp486Glu
XM_017006966.1:c.1359T>G (RAF1)	XP_016862455.1:p.Asp453Glu
NM_001354689.3:c.1518T>G (RAF1)	NP_001341618.1:p.Asp506Glu
NM_001354690.2:c.1458T>G (RAF1)	NP_001341619.1:p.Asp486Glu
NM_001354691.2:c.1215T>G (RAF1)	NP_001341620.1:p.Asp405Glu
NM_001354692.2:c.1215T>G (RAF1)	NP_001341621.1:p.Asp405Glu
NM_001354693.2:c.1359T>G (RAF1)	NP_001341622.1:p.Asp453Glu
NM_001354694.2:c.1275T>G (RAF1)	NP_001341623.1:p.Asp425Glu
NM_001354695.2:c.1116T>G (RAF1)	NP_001341624.1:p.Asp372Glu
NR_148940.2:n.1902T>G (RAF1)
NR_148941.2:n.1848T>G (RAF1)
NR_148942.2:n.1787T>G (RAF1)
NM_001354690.3:c.1458T>G (RAF1)	NP_001341619.1:p.Asp486Glu
NM_001354691.3:c.1215T>G (RAF1)	NP_001341620.1:p.Asp405Glu
NM_001354692.3:c.1215T>G (RAF1)	NP_001341621.1:p.Asp405Glu
NM_001354693.3:c.1359T>G (RAF1)	NP_001341622.1:p.Asp453Glu
NM_001354694.3:c.1275T>G (RAF1)	NP_001341623.1:p.Asp425Glu
NM_001354695.3:c.1116T>G (RAF1)	NP_001341624.1:p.Asp372Glu
NM_002880.4:c.1458T>G (RAF1) MANE Select	NP_002871.1:p.Asp486Glu
NR_148940.3:n.1902T>G (RAF1)
NR_148941.3:n.1848T>G (RAF1)
NR_148942.3:n.1787T>G (RAF1)