Canonical Allele Identifier: CA351495438

Gene: RAF1 MKRN2

Linked Data

• dbSNP Id: rs1382398408
• MyVariant Identifiers: chr3:g.12626032G>C (hg19) ; chr3:g.12584533G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584533G>C , CM000665.2:g.12584533G>C	GRCh38
NC_000003.11:g.12626032G>C , CM000665.1:g.12626032G>C	GRCh37
NC_000003.10:g.12601032G>C	NCBI36
NG_007467.1:g.84647C>G , LRG_413:g.84647C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000423275.6:c.*1593C>G (RAF1)	ENSP00000401088.1:n.*1593C>G
ENST00000432427.3:c.1245C>G (RAF1)
ENST00000460610.2:n.6240C>G (RAF1)
ENST00000471449.2:n.738C>G (RAF1)
ENST00000475353.2:n.4208C>G (RAF1)
ENST00000684903.1:c.*1605C>G (RAF1)	ENSP00000508612.1:n.*1605C>G
ENST00000685348.1:c.*1639C>G (RAF1)	ENSP00000510285.1:n.*1639C>G
ENST00000685437.1:c.1829C>G (RAF1)	ENSP00000508794.1:p.Pro610Arg
ENST00000685653.1:c.1928C>G (RAF1)	ENSP00000509968.1:p.Pro643Arg
ENST00000685697.1:n.2663C>G (RAF1)
ENST00000685738.1:c.*892C>G (RAF1)	ENSP00000510156.1:n.*892C>G
ENST00000686409.1:n.5337C>G (RAF1)
ENST00000686455.1:n.4649C>G (RAF1)
ENST00000686762.1:c.*487C>G (RAF1)	ENSP00000509767.1:n.*487C>G
ENST00000687257.1:n.4382C>G (RAF1)
ENST00000687326.1:c.*3220C>G (RAF1)	ENSP00000509665.1:n.*3220C>G
ENST00000687505.1:n.2046C>G (RAF1)
ENST00000687923.1:c.1817C>G (RAF1)	ENSP00000510255.1:p.Pro606Arg
ENST00000688269.1:n.2524C>G (RAF1)
ENST00000688444.1:n.4045C>G (RAF1)
ENST00000688543.1:c.1829C>G (RAF1)	ENSP00000509612.1:p.Pro610Arg
ENST00000688625.1:c.*3297C>G (RAF1)	ENSP00000509522.1:n.*3297C>G
ENST00000688803.1:n.3356C>G (RAF1)
ENST00000689097.1:c.*1605C>G (RAF1)	ENSP00000509756.1:n.*1605C>G
ENST00000689389.1:c.1751C>G (RAF1)	ENSP00000510213.1:p.Pro584Arg
ENST00000689418.1:c.*3823C>G (RAF1)	ENSP00000509467.1:n.*3823C>G
ENST00000689540.1:n.4296C>G (RAF1)
ENST00000689876.1:c.*477C>G (RAF1)	ENSP00000508535.1:n.*477C>G
ENST00000689914.1:c.*862C>G (RAF1)	ENSP00000509847.1:n.*862C>G
ENST00000690397.1:c.1817C>G (RAF1)	ENSP00000508730.1:p.Pro606Arg
ENST00000690460.1:c.1916C>G (RAF1)	ENSP00000509106.1:p.Pro639Arg
ENST00000690585.1:c.654C>G (RAF1)
ENST00000690625.1:n.2964C>G (RAF1)
ENST00000691396.1:c.*1800C>G (RAF1)	ENSP00000510712.1:n.*1800C>G
ENST00000691643.1:n.2981C>G (RAF1)
ENST00000691724.1:c.*885C>G (RAF1)	ENSP00000509255.1:n.*885C>G
ENST00000691779.1:c.*1506C>G (RAF1)	ENSP00000508592.1:n.*1506C>G
ENST00000691888.1:c.802C>G (RAF1)
ENST00000691899.1:c.1928C>G (RAF1)	ENSP00000508763.1:p.Pro643Arg
ENST00000692069.1:n.4852C>G (RAF1)
ENST00000692093.1:c.1829C>G (RAF1)	ENSP00000509669.1:p.Pro610Arg
ENST00000692311.1:n.2752C>G (RAF1)
ENST00000692558.1:n.4511C>G (RAF1)
ENST00000692773.1:c.*1665C>G (RAF1)	ENSP00000509055.1:n.*1665C>G
ENST00000692830.1:c.*1673C>G (RAF1)	ENSP00000509461.1:n.*1673C>G
ENST00000693312.1:c.1703C>G (RAF1)	ENSP00000508686.1:p.Pro568Arg
ENST00000693664.1:c.*379C>G (RAF1)	ENSP00000509614.1:n.*379C>G
ENST00000693705.1:c.*1307C>G (RAF1)	ENSP00000510697.1:n.*1307C>G
ENST00000251849.9:c.1928C>G (RAF1) MANE Select	ENSP00000251849.4:p.Pro643Arg
ENST00000442415.7:c.1988C>G (RAF1)	ENSP00000401888.2:p.Pro663Arg
ENST00000676541.1:c.*2280G>C (MKRN2)	ENSP00000503730.1:n.*2280G>C
ENST00000677142.1:c.*2280G>C (MKRN2)	ENSP00000504455.1:n.*2280G>C
ENST00000677816.1:c.*835G>C (MKRN2)	ENSP00000502893.1:n.*835G>C
ENST00000677941.1:n.2343G>C (MKRN2)
ENST00000251849.8:c.1928C>G (RAF1)	ENSP00000251849.4:p.Pro643Arg
ENST00000423275.5:c.*1605C>G (RAF1)	ENSP00000401088.1:n.*1605C>G
ENST00000432427.2:c.1565C>G (RAF1)	ENSP00000398591.2:p.Pro522Arg
ENST00000442415.6:c.1988C>G (RAF1)	ENSP00000401888.2:p.Pro663Arg
ENST00000471449.1:n.617C>G (RAF1)
NM_002880.3:c.1928C>G , LRG_413t1:c.1928C>G (RAF1)	NP_002871.1:p.Pro643Arg
XM_005265355.1:c.1928C>G (RAF1)	XP_005265412.1:p.Pro643Arg
XM_005265357.1:c.1829C>G (RAF1)	XP_005265414.1:p.Pro610Arg
XM_005265358.3:c.1685C>G (RAF1)	XP_005265415.1:p.Pro562Arg
XM_005265359.3:c.1586C>G (RAF1)	XP_005265416.1:p.Pro529Arg
XM_011533974.1:c.1928C>G (RAF1)	XP_011532276.1:p.Pro643Arg
XM_011533975.1:c.1685C>G (RAF1)	XP_011532277.1:p.Pro562Arg
NM_001354689.1:c.1988C>G (RAF1)	NP_001341618.1:p.Pro663Arg
NM_001354690.1:c.1928C>G (RAF1)	NP_001341619.1:p.Pro643Arg
NM_001354691.1:c.1685C>G (RAF1)	NP_001341620.1:p.Pro562Arg
NM_001354692.1:c.1685C>G (RAF1)	NP_001341621.1:p.Pro562Arg
NM_001354693.1:c.1829C>G (RAF1)	NP_001341622.1:p.Pro610Arg
NM_001354694.1:c.1745C>G (RAF1)	NP_001341623.1:p.Pro582Arg
NM_001354695.1:c.1586C>G (RAF1)	NP_001341624.1:p.Pro529Arg
NR_148940.1:n.2456C>G (RAF1)
NR_148941.1:n.2402C>G (RAF1)
NR_148942.1:n.2341C>G (RAF1)
XM_011533974.3:c.1928C>G (RAF1)	XP_011532276.1:p.Pro643Arg
XM_017006966.1:c.1829C>G (RAF1)	XP_016862455.1:p.Pro610Arg
NM_001354689.3:c.1988C>G (RAF1)	NP_001341618.1:p.Pro663Arg
NM_001354690.2:c.1928C>G (RAF1)	NP_001341619.1:p.Pro643Arg
NM_001354691.2:c.1685C>G (RAF1)	NP_001341620.1:p.Pro562Arg
NM_001354692.2:c.1685C>G (RAF1)	NP_001341621.1:p.Pro562Arg
NM_001354693.2:c.1829C>G (RAF1)	NP_001341622.1:p.Pro610Arg
NM_001354694.2:c.1745C>G (RAF1)	NP_001341623.1:p.Pro582Arg
NM_001354695.2:c.1586C>G (RAF1)	NP_001341624.1:p.Pro529Arg
NR_148940.2:n.2372C>G (RAF1)
NR_148941.2:n.2318C>G (RAF1)
NR_148942.2:n.2257C>G (RAF1)
NM_001354690.3:c.1928C>G (RAF1)	NP_001341619.1:p.Pro643Arg
NM_001354691.3:c.1685C>G (RAF1)	NP_001341620.1:p.Pro562Arg
NM_001354692.3:c.1685C>G (RAF1)	NP_001341621.1:p.Pro562Arg
NM_001354693.3:c.1829C>G (RAF1)	NP_001341622.1:p.Pro610Arg
NM_001354694.3:c.1745C>G (RAF1)	NP_001341623.1:p.Pro582Arg
NM_001354695.3:c.1586C>G (RAF1)	NP_001341624.1:p.Pro529Arg
NM_002880.4:c.1928C>G (RAF1) MANE Select	NP_002871.1:p.Pro643Arg
NR_148940.3:n.2372C>G (RAF1)
NR_148941.3:n.2318C>G (RAF1)
NR_148942.3:n.2257C>G (RAF1)