Canonical Allele Identifier: CA351495506

Gene: RAF1 MKRN2

Linked Data

• dbSNP Id: rs2125315911
• MyVariant Identifiers: chr3:g.12626041G>C (hg19) ; chr3:g.12584542G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584542G>C , CM000665.2:g.12584542G>C	GRCh38
NC_000003.11:g.12626041G>C , CM000665.1:g.12626041G>C	GRCh37
NC_000003.10:g.12601041G>C	NCBI36
NG_007467.1:g.84638C>G , LRG_413:g.84638C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000423275.6:c.*1584C>G (RAF1)	ENSP00000401088.1:n.*1584C>G
ENST00000432427.3:c.1236C>G (RAF1)
ENST00000460610.2:n.6231C>G (RAF1)
ENST00000471449.2:n.729C>G (RAF1)
ENST00000475353.2:n.4199C>G (RAF1)
ENST00000684903.1:c.*1596C>G (RAF1)	ENSP00000508612.1:n.*1596C>G
ENST00000685348.1:c.*1630C>G (RAF1)	ENSP00000510285.1:n.*1630C>G
ENST00000685437.1:c.1820C>G (RAF1)	ENSP00000508794.1:p.Thr607Ser
ENST00000685653.1:c.1919C>G (RAF1)	ENSP00000509968.1:p.Thr640Ser
ENST00000685697.1:n.2654C>G (RAF1)
ENST00000685738.1:c.*883C>G (RAF1)	ENSP00000510156.1:n.*883C>G
ENST00000686409.1:n.5328C>G (RAF1)
ENST00000686455.1:n.4640C>G (RAF1)
ENST00000686762.1:c.*478C>G (RAF1)	ENSP00000509767.1:n.*478C>G
ENST00000687257.1:n.4373C>G (RAF1)
ENST00000687326.1:c.*3211C>G (RAF1)	ENSP00000509665.1:n.*3211C>G
ENST00000687505.1:n.2037C>G (RAF1)
ENST00000687923.1:c.1808C>G (RAF1)	ENSP00000510255.1:p.Thr603Ser
ENST00000688269.1:n.2515C>G (RAF1)
ENST00000688444.1:n.4036C>G (RAF1)
ENST00000688543.1:c.1820C>G (RAF1)	ENSP00000509612.1:p.Thr607Ser
ENST00000688625.1:c.*3288C>G (RAF1)	ENSP00000509522.1:n.*3288C>G
ENST00000688803.1:n.3347C>G (RAF1)
ENST00000689097.1:c.*1596C>G (RAF1)	ENSP00000509756.1:n.*1596C>G
ENST00000689389.1:c.1742C>G (RAF1)	ENSP00000510213.1:p.Thr581Ser
ENST00000689418.1:c.*3814C>G (RAF1)	ENSP00000509467.1:n.*3814C>G
ENST00000689540.1:n.4287C>G (RAF1)
ENST00000689876.1:c.*468C>G (RAF1)	ENSP00000508535.1:n.*468C>G
ENST00000689914.1:c.*853C>G (RAF1)	ENSP00000509847.1:n.*853C>G
ENST00000690397.1:c.1808C>G (RAF1)	ENSP00000508730.1:p.Thr603Ser
ENST00000690460.1:c.1907C>G (RAF1)	ENSP00000509106.1:p.Thr636Ser
ENST00000690585.1:c.645C>G (RAF1)
ENST00000690625.1:n.2955C>G (RAF1)
ENST00000691396.1:c.*1791C>G (RAF1)	ENSP00000510712.1:n.*1791C>G
ENST00000691643.1:n.2972C>G (RAF1)
ENST00000691724.1:c.*876C>G (RAF1)	ENSP00000509255.1:n.*876C>G
ENST00000691779.1:c.*1497C>G (RAF1)	ENSP00000508592.1:n.*1497C>G
ENST00000691888.1:c.793C>G (RAF1)
ENST00000691899.1:c.1919C>G (RAF1)	ENSP00000508763.1:p.Thr640Ser
ENST00000692069.1:n.4843C>G (RAF1)
ENST00000692093.1:c.1820C>G (RAF1)	ENSP00000509669.1:p.Thr607Ser
ENST00000692311.1:n.2743C>G (RAF1)
ENST00000692558.1:n.4502C>G (RAF1)
ENST00000692773.1:c.*1656C>G (RAF1)	ENSP00000509055.1:n.*1656C>G
ENST00000692830.1:c.*1664C>G (RAF1)	ENSP00000509461.1:n.*1664C>G
ENST00000693312.1:c.1694C>G (RAF1)	ENSP00000508686.1:p.Thr565Ser
ENST00000693664.1:c.*370C>G (RAF1)	ENSP00000509614.1:n.*370C>G
ENST00000693705.1:c.*1298C>G (RAF1)	ENSP00000510697.1:n.*1298C>G
ENST00000251849.9:c.1919C>G (RAF1) MANE Select	ENSP00000251849.4:p.Thr640Ser
ENST00000442415.7:c.1979C>G (RAF1)	ENSP00000401888.2:p.Thr660Ser
ENST00000676541.1:c.*2289G>C (MKRN2)	ENSP00000503730.1:n.*2289G>C
ENST00000677142.1:c.*2289G>C (MKRN2)	ENSP00000504455.1:n.*2289G>C
ENST00000677816.1:c.*844G>C (MKRN2)	ENSP00000502893.1:n.*844G>C
ENST00000677941.1:n.2352G>C (MKRN2)
ENST00000251849.8:c.1919C>G (RAF1)	ENSP00000251849.4:p.Thr640Ser
ENST00000423275.5:c.*1596C>G (RAF1)	ENSP00000401088.1:n.*1596C>G
ENST00000432427.2:c.1556C>G (RAF1)	ENSP00000398591.2:p.Thr519Ser
ENST00000442415.6:c.1979C>G (RAF1)	ENSP00000401888.2:p.Thr660Ser
ENST00000471449.1:n.608C>G (RAF1)
NM_002880.3:c.1919C>G , LRG_413t1:c.1919C>G (RAF1)	NP_002871.1:p.Thr640Ser
XM_005265355.1:c.1919C>G (RAF1)	XP_005265412.1:p.Thr640Ser
XM_005265357.1:c.1820C>G (RAF1)	XP_005265414.1:p.Thr607Ser
XM_005265358.3:c.1676C>G (RAF1)	XP_005265415.1:p.Thr559Ser
XM_005265359.3:c.1577C>G (RAF1)	XP_005265416.1:p.Thr526Ser
XM_011533974.1:c.1919C>G (RAF1)	XP_011532276.1:p.Thr640Ser
XM_011533975.1:c.1676C>G (RAF1)	XP_011532277.1:p.Thr559Ser
NM_001354689.1:c.1979C>G (RAF1)	NP_001341618.1:p.Thr660Ser
NM_001354690.1:c.1919C>G (RAF1)	NP_001341619.1:p.Thr640Ser
NM_001354691.1:c.1676C>G (RAF1)	NP_001341620.1:p.Thr559Ser
NM_001354692.1:c.1676C>G (RAF1)	NP_001341621.1:p.Thr559Ser
NM_001354693.1:c.1820C>G (RAF1)	NP_001341622.1:p.Thr607Ser
NM_001354694.1:c.1736C>G (RAF1)	NP_001341623.1:p.Thr579Ser
NM_001354695.1:c.1577C>G (RAF1)	NP_001341624.1:p.Thr526Ser
NR_148940.1:n.2447C>G (RAF1)
NR_148941.1:n.2393C>G (RAF1)
NR_148942.1:n.2332C>G (RAF1)
XM_011533974.3:c.1919C>G (RAF1)	XP_011532276.1:p.Thr640Ser
XM_017006966.1:c.1820C>G (RAF1)	XP_016862455.1:p.Thr607Ser
NM_001354689.3:c.1979C>G (RAF1)	NP_001341618.1:p.Thr660Ser
NM_001354690.2:c.1919C>G (RAF1)	NP_001341619.1:p.Thr640Ser
NM_001354691.2:c.1676C>G (RAF1)	NP_001341620.1:p.Thr559Ser
NM_001354692.2:c.1676C>G (RAF1)	NP_001341621.1:p.Thr559Ser
NM_001354693.2:c.1820C>G (RAF1)	NP_001341622.1:p.Thr607Ser
NM_001354694.2:c.1736C>G (RAF1)	NP_001341623.1:p.Thr579Ser
NM_001354695.2:c.1577C>G (RAF1)	NP_001341624.1:p.Thr526Ser
NR_148940.2:n.2363C>G (RAF1)
NR_148941.2:n.2309C>G (RAF1)
NR_148942.2:n.2248C>G (RAF1)
NM_001354690.3:c.1919C>G (RAF1)	NP_001341619.1:p.Thr640Ser
NM_001354691.3:c.1676C>G (RAF1)	NP_001341620.1:p.Thr559Ser
NM_001354692.3:c.1676C>G (RAF1)	NP_001341621.1:p.Thr559Ser
NM_001354693.3:c.1820C>G (RAF1)	NP_001341622.1:p.Thr607Ser
NM_001354694.3:c.1736C>G (RAF1)	NP_001341623.1:p.Thr579Ser
NM_001354695.3:c.1577C>G (RAF1)	NP_001341624.1:p.Thr526Ser
NM_002880.4:c.1919C>G (RAF1) MANE Select	NP_002871.1:p.Thr640Ser
NR_148940.3:n.2363C>G (RAF1)
NR_148941.3:n.2309C>G (RAF1)
NR_148942.3:n.2248C>G (RAF1)