Canonical Allele Identifier: CA351496745

Gene: RAF1 MKRN2

Linked Data

• MyVariant Identifiers: chr3:g.12626414T>C (hg19) ; chr3:g.12584915T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584915T>C , CM000665.2:g.12584915T>C	GRCh38
NC_000003.11:g.12626414T>C , CM000665.1:g.12626414T>C	GRCh37
NC_000003.10:g.12601414T>C	NCBI36
NG_007467.1:g.84265A>G , LRG_413:g.84265A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1400A>G (RAF1)	ENSP00000401088.1:n.*1400A>G
ENST00000432427.3:c.1052A>G (RAF1)
ENST00000460610.2:n.6047A>G (RAF1)
ENST00000471449.2:n.545A>G (RAF1)
ENST00000475353.2:n.4015A>G (RAF1)
ENST00000684903.1:c.*1412A>G (RAF1)	ENSP00000508612.1:n.*1412A>G
ENST00000685348.1:c.*1446A>G (RAF1)	ENSP00000510285.1:n.*1446A>G
ENST00000685437.1:c.1636A>G (RAF1)	ENSP00000508794.1:p.Lys546Glu
ENST00000685653.1:c.1735A>G (RAF1)	ENSP00000509968.1:p.Lys579Glu
ENST00000685697.1:n.2470A>G (RAF1)
ENST00000685738.1:c.*699A>G (RAF1)	ENSP00000510156.1:n.*699A>G
ENST00000686409.1:n.5144A>G (RAF1)
ENST00000686455.1:n.4456A>G (RAF1)
ENST00000686762.1:c.*294A>G (RAF1)	ENSP00000509767.1:n.*294A>G
ENST00000687257.1:n.4189A>G (RAF1)
ENST00000687326.1:c.*3027A>G (RAF1)	ENSP00000509665.1:n.*3027A>G
ENST00000687505.1:n.1853A>G (RAF1)
ENST00000687923.1:c.1624A>G (RAF1)	ENSP00000510255.1:p.Lys542Glu
ENST00000688269.1:n.2331A>G (RAF1)
ENST00000688444.1:n.3852A>G (RAF1)
ENST00000688543.1:c.1636A>G (RAF1)	ENSP00000509612.1:p.Lys546Glu
ENST00000688625.1:c.*3104A>G (RAF1)	ENSP00000509522.1:n.*3104A>G
ENST00000688803.1:n.3163A>G (RAF1)
ENST00000688914.1:n.1148A>G (RAF1)
ENST00000689097.1:c.*1412A>G (RAF1)	ENSP00000509756.1:n.*1412A>G
ENST00000689389.1:c.1558A>G (RAF1)	ENSP00000510213.1:p.Lys520Glu
ENST00000689418.1:c.*3630A>G (RAF1)	ENSP00000509467.1:n.*3630A>G
ENST00000689540.1:n.4103A>G (RAF1)
ENST00000689876.1:c.*284A>G (RAF1)	ENSP00000508535.1:n.*284A>G
ENST00000689914.1:c.*669A>G (RAF1)	ENSP00000509847.1:n.*669A>G
ENST00000690397.1:c.1624A>G (RAF1)	ENSP00000508730.1:p.Lys542Glu
ENST00000690460.1:c.1723A>G (RAF1)	ENSP00000509106.1:p.Lys575Glu
ENST00000690585.1:c.461A>G (RAF1)
ENST00000690625.1:n.2771A>G (RAF1)
ENST00000691396.1:c.*1607A>G (RAF1)	ENSP00000510712.1:n.*1607A>G
ENST00000691643.1:n.2788A>G (RAF1)
ENST00000691724.1:c.*692A>G (RAF1)	ENSP00000509255.1:n.*692A>G
ENST00000691779.1:c.*1313A>G (RAF1)	ENSP00000508592.1:n.*1313A>G
ENST00000691888.1:c.609A>G (RAF1)
ENST00000691899.1:c.1735A>G (RAF1)	ENSP00000508763.1:p.Lys579Glu
ENST00000692069.1:n.4659A>G (RAF1)
ENST00000692093.1:c.1636A>G (RAF1)	ENSP00000509669.1:p.Lys546Glu
ENST00000692311.1:n.2559A>G (RAF1)
ENST00000692558.1:n.4318A>G (RAF1)
ENST00000692773.1:c.*1472A>G (RAF1)	ENSP00000509055.1:n.*1472A>G
ENST00000692830.1:c.*1480A>G (RAF1)	ENSP00000509461.1:n.*1480A>G
ENST00000693312.1:c.1510A>G (RAF1)	ENSP00000508686.1:p.Lys504Glu
ENST00000693664.1:c.*186A>G (RAF1)	ENSP00000509614.1:n.*186A>G
ENST00000693705.1:c.*1114A>G (RAF1)	ENSP00000510697.1:n.*1114A>G
ENST00000251849.9:c.1735A>G (RAF1) MANE Select	ENSP00000251849.4:p.Lys579Glu
ENST00000442415.7:c.1795A>G (RAF1)	ENSP00000401888.2:p.Lys599Glu
ENST00000676541.1:c.*2662T>C (MKRN2)	ENSP00000503730.1:n.*2662T>C
ENST00000677142.1:c.*2662T>C (MKRN2)	ENSP00000504455.1:n.*2662T>C
ENST00000677816.1:c.*1217T>C (MKRN2)	ENSP00000502893.1:n.*1217T>C
ENST00000677941.1:n.2725T>C (MKRN2)
ENST00000251849.8:c.1735A>G (RAF1)	ENSP00000251849.4:p.Lys579Glu
ENST00000423275.5:c.*1412A>G (RAF1)	ENSP00000401088.1:n.*1412A>G
ENST00000432427.2:c.1372A>G (RAF1)	ENSP00000398591.2:p.Lys458Glu
ENST00000442415.6:c.1795A>G (RAF1)	ENSP00000401888.2:p.Lys599Glu
ENST00000471449.1:n.424A>G (RAF1)
NM_002880.3:c.1735A>G , LRG_413t1:c.1735A>G (RAF1)	NP_002871.1:p.Lys579Glu
XM_005265355.1:c.1735A>G (RAF1)	XP_005265412.1:p.Lys579Glu
XM_005265357.1:c.1636A>G (RAF1)	XP_005265414.1:p.Lys546Glu
XM_005265358.3:c.1492A>G (RAF1)	XP_005265415.1:p.Lys498Glu
XM_005265359.3:c.1393A>G (RAF1)	XP_005265416.1:p.Lys465Glu
XM_011533974.1:c.1735A>G (RAF1)	XP_011532276.1:p.Lys579Glu
XM_011533975.1:c.1492A>G (RAF1)	XP_011532277.1:p.Lys498Glu
NM_001354689.1:c.1795A>G (RAF1)	NP_001341618.1:p.Lys599Glu
NM_001354690.1:c.1735A>G (RAF1)	NP_001341619.1:p.Lys579Glu
NM_001354691.1:c.1492A>G (RAF1)	NP_001341620.1:p.Lys498Glu
NM_001354692.1:c.1492A>G (RAF1)	NP_001341621.1:p.Lys498Glu
NM_001354693.1:c.1636A>G (RAF1)	NP_001341622.1:p.Lys546Glu
NM_001354694.1:c.1552A>G (RAF1)	NP_001341623.1:p.Lys518Glu
NM_001354695.1:c.1393A>G (RAF1)	NP_001341624.1:p.Lys465Glu
NR_148940.1:n.2263A>G (RAF1)
NR_148941.1:n.2209A>G (RAF1)
NR_148942.1:n.2148A>G (RAF1)
XM_011533974.3:c.1735A>G (RAF1)	XP_011532276.1:p.Lys579Glu
XM_017006966.1:c.1636A>G (RAF1)	XP_016862455.1:p.Lys546Glu
NM_001354689.3:c.1795A>G (RAF1)	NP_001341618.1:p.Lys599Glu
NM_001354690.2:c.1735A>G (RAF1)	NP_001341619.1:p.Lys579Glu
NM_001354691.2:c.1492A>G (RAF1)	NP_001341620.1:p.Lys498Glu
NM_001354692.2:c.1492A>G (RAF1)	NP_001341621.1:p.Lys498Glu
NM_001354693.2:c.1636A>G (RAF1)	NP_001341622.1:p.Lys546Glu
NM_001354694.2:c.1552A>G (RAF1)	NP_001341623.1:p.Lys518Glu
NM_001354695.2:c.1393A>G (RAF1)	NP_001341624.1:p.Lys465Glu
NR_148940.2:n.2179A>G (RAF1)
NR_148941.2:n.2125A>G (RAF1)
NR_148942.2:n.2064A>G (RAF1)
NM_001354690.3:c.1735A>G (RAF1)	NP_001341619.1:p.Lys579Glu
NM_001354691.3:c.1492A>G (RAF1)	NP_001341620.1:p.Lys498Glu
NM_001354692.3:c.1492A>G (RAF1)	NP_001341621.1:p.Lys498Glu
NM_001354693.3:c.1636A>G (RAF1)	NP_001341622.1:p.Lys546Glu
NM_001354694.3:c.1552A>G (RAF1)	NP_001341623.1:p.Lys518Glu
NM_001354695.3:c.1393A>G (RAF1)	NP_001341624.1:p.Lys465Glu
NM_002880.4:c.1735A>G (RAF1) MANE Select	NP_002871.1:p.Lys579Glu
NR_148940.3:n.2179A>G (RAF1)
NR_148941.3:n.2125A>G (RAF1)
NR_148942.3:n.2064A>G (RAF1)