Canonical Allele Identifier: CA69602160

Gene: RAF1 MKRN2

Linked Data

• dbSNP Id: rs1033351642
• MyVariant Identifiers: chr3:g.12626040G>C (hg19) ; chr3:g.12584541G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584541G>C , CM000665.2:g.12584541G>C	GRCh38
NC_000003.11:g.12626040G>C , CM000665.1:g.12626040G>C	GRCh37
NC_000003.10:g.12601040G>C	NCBI36
NG_007467.1:g.84639C>G , LRG_413:g.84639C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000423275.6:c.*1585C>G (RAF1)	ENSP00000401088.1:n.*1585C>G
ENST00000432427.3:c.1237C>G (RAF1)
ENST00000460610.2:n.6232C>G (RAF1)
ENST00000471449.2:n.730C>G (RAF1)
ENST00000475353.2:n.4200C>G (RAF1)
ENST00000684903.1:c.*1597C>G (RAF1)	ENSP00000508612.1:n.*1597C>G
ENST00000685348.1:c.*1631C>G (RAF1)	ENSP00000510285.1:n.*1631C>G
ENST00000685437.1:c.1821C>G (RAF1)	ENSP00000508794.1:p.Thr607=
ENST00000685653.1:c.1920C>G (RAF1)	ENSP00000509968.1:p.Thr640=
ENST00000685697.1:n.2655C>G (RAF1)
ENST00000685738.1:c.*884C>G (RAF1)	ENSP00000510156.1:n.*884C>G
ENST00000686409.1:n.5329C>G (RAF1)
ENST00000686455.1:n.4641C>G (RAF1)
ENST00000686762.1:c.*479C>G (RAF1)	ENSP00000509767.1:n.*479C>G
ENST00000687257.1:n.4374C>G (RAF1)
ENST00000687326.1:c.*3212C>G (RAF1)	ENSP00000509665.1:n.*3212C>G
ENST00000687505.1:n.2038C>G (RAF1)
ENST00000687923.1:c.1809C>G (RAF1)	ENSP00000510255.1:p.Thr603=
ENST00000688269.1:n.2516C>G (RAF1)
ENST00000688444.1:n.4037C>G (RAF1)
ENST00000688543.1:c.1821C>G (RAF1)	ENSP00000509612.1:p.Thr607=
ENST00000688625.1:c.*3289C>G (RAF1)	ENSP00000509522.1:n.*3289C>G
ENST00000688803.1:n.3348C>G (RAF1)
ENST00000689097.1:c.*1597C>G (RAF1)	ENSP00000509756.1:n.*1597C>G
ENST00000689389.1:c.1743C>G (RAF1)	ENSP00000510213.1:p.Thr581=
ENST00000689418.1:c.*3815C>G (RAF1)	ENSP00000509467.1:n.*3815C>G
ENST00000689540.1:n.4288C>G (RAF1)
ENST00000689876.1:c.*469C>G (RAF1)	ENSP00000508535.1:n.*469C>G
ENST00000689914.1:c.*854C>G (RAF1)	ENSP00000509847.1:n.*854C>G
ENST00000690397.1:c.1809C>G (RAF1)	ENSP00000508730.1:p.Thr603=
ENST00000690460.1:c.1908C>G (RAF1)	ENSP00000509106.1:p.Thr636=
ENST00000690585.1:c.646C>G (RAF1)
ENST00000690625.1:n.2956C>G (RAF1)
ENST00000691396.1:c.*1792C>G (RAF1)	ENSP00000510712.1:n.*1792C>G
ENST00000691643.1:n.2973C>G (RAF1)
ENST00000691724.1:c.*877C>G (RAF1)	ENSP00000509255.1:n.*877C>G
ENST00000691779.1:c.*1498C>G (RAF1)	ENSP00000508592.1:n.*1498C>G
ENST00000691888.1:c.794C>G (RAF1)
ENST00000691899.1:c.1920C>G (RAF1)	ENSP00000508763.1:p.Thr640=
ENST00000692069.1:n.4844C>G (RAF1)
ENST00000692093.1:c.1821C>G (RAF1)	ENSP00000509669.1:p.Thr607=
ENST00000692311.1:n.2744C>G (RAF1)
ENST00000692558.1:n.4503C>G (RAF1)
ENST00000692773.1:c.*1657C>G (RAF1)	ENSP00000509055.1:n.*1657C>G
ENST00000692830.1:c.*1665C>G (RAF1)	ENSP00000509461.1:n.*1665C>G
ENST00000693312.1:c.1695C>G (RAF1)	ENSP00000508686.1:p.Thr565=
ENST00000693664.1:c.*371C>G (RAF1)	ENSP00000509614.1:n.*371C>G
ENST00000693705.1:c.*1299C>G (RAF1)	ENSP00000510697.1:n.*1299C>G
ENST00000251849.9:c.1920C>G (RAF1) MANE Select	ENSP00000251849.4:p.Thr640=
ENST00000442415.7:c.1980C>G (RAF1)	ENSP00000401888.2:p.Thr660=
ENST00000676541.1:c.*2288G>C (MKRN2)	ENSP00000503730.1:n.*2288G>C
ENST00000677142.1:c.*2288G>C (MKRN2)	ENSP00000504455.1:n.*2288G>C
ENST00000677816.1:c.*843G>C (MKRN2)	ENSP00000502893.1:n.*843G>C
ENST00000677941.1:n.2351G>C (MKRN2)
ENST00000251849.8:c.1920C>G (RAF1)	ENSP00000251849.4:p.Thr640=
ENST00000423275.5:c.*1597C>G (RAF1)	ENSP00000401088.1:n.*1597C>G
ENST00000432427.2:c.1557C>G (RAF1)	ENSP00000398591.2:p.Thr519=
ENST00000442415.6:c.1980C>G (RAF1)	ENSP00000401888.2:p.Thr660=
ENST00000471449.1:n.609C>G (RAF1)
NM_002880.3:c.1920C>G , LRG_413t1:c.1920C>G (RAF1)	NP_002871.1:p.Thr640=
XM_005265355.1:c.1920C>G (RAF1)	XP_005265412.1:p.Thr640=
XM_005265357.1:c.1821C>G (RAF1)	XP_005265414.1:p.Thr607=
XM_005265358.3:c.1677C>G (RAF1)	XP_005265415.1:p.Thr559=
XM_005265359.3:c.1578C>G (RAF1)	XP_005265416.1:p.Thr526=
XM_011533974.1:c.1920C>G (RAF1)	XP_011532276.1:p.Thr640=
XM_011533975.1:c.1677C>G (RAF1)	XP_011532277.1:p.Thr559=
NM_001354689.1:c.1980C>G (RAF1)	NP_001341618.1:p.Thr660=
NM_001354690.1:c.1920C>G (RAF1)	NP_001341619.1:p.Thr640=
NM_001354691.1:c.1677C>G (RAF1)	NP_001341620.1:p.Thr559=
NM_001354692.1:c.1677C>G (RAF1)	NP_001341621.1:p.Thr559=
NM_001354693.1:c.1821C>G (RAF1)	NP_001341622.1:p.Thr607=
NM_001354694.1:c.1737C>G (RAF1)	NP_001341623.1:p.Thr579=
NM_001354695.1:c.1578C>G (RAF1)	NP_001341624.1:p.Thr526=
NR_148940.1:n.2448C>G (RAF1)
NR_148941.1:n.2394C>G (RAF1)
NR_148942.1:n.2333C>G (RAF1)
XM_011533974.3:c.1920C>G (RAF1)	XP_011532276.1:p.Thr640=
XM_017006966.1:c.1821C>G (RAF1)	XP_016862455.1:p.Thr607=
NM_001354689.3:c.1980C>G (RAF1)	NP_001341618.1:p.Thr660=
NM_001354690.2:c.1920C>G (RAF1)	NP_001341619.1:p.Thr640=
NM_001354691.2:c.1677C>G (RAF1)	NP_001341620.1:p.Thr559=
NM_001354692.2:c.1677C>G (RAF1)	NP_001341621.1:p.Thr559=
NM_001354693.2:c.1821C>G (RAF1)	NP_001341622.1:p.Thr607=
NM_001354694.2:c.1737C>G (RAF1)	NP_001341623.1:p.Thr579=
NM_001354695.2:c.1578C>G (RAF1)	NP_001341624.1:p.Thr526=
NR_148940.2:n.2364C>G (RAF1)
NR_148941.2:n.2310C>G (RAF1)
NR_148942.2:n.2249C>G (RAF1)
NM_001354690.3:c.1920C>G (RAF1)	NP_001341619.1:p.Thr640=
NM_001354691.3:c.1677C>G (RAF1)	NP_001341620.1:p.Thr559=
NM_001354692.3:c.1677C>G (RAF1)	NP_001341621.1:p.Thr559=
NM_001354693.3:c.1821C>G (RAF1)	NP_001341622.1:p.Thr607=
NM_001354694.3:c.1737C>G (RAF1)	NP_001341623.1:p.Thr579=
NM_001354695.3:c.1578C>G (RAF1)	NP_001341624.1:p.Thr526=
NM_002880.4:c.1920C>G (RAF1) MANE Select	NP_002871.1:p.Thr640=
NR_148940.3:n.2364C>G (RAF1)
NR_148941.3:n.2310C>G (RAF1)
NR_148942.3:n.2249C>G (RAF1)