Canonical Allele Identifier: CA351495524

Gene: RAF1 MKRN2

Linked Data

• MyVariant Identifiers: chr3:g.12626044A>G (hg19) ; chr3:g.12584545A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584545A>G , CM000665.2:g.12584545A>G	GRCh38
NC_000003.11:g.12626044A>G , CM000665.1:g.12626044A>G	GRCh37
NC_000003.10:g.12601044A>G	NCBI36
NG_007467.1:g.84635T>C , LRG_413:g.84635T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000423275.6:c.*1581T>C (RAF1)	ENSP00000401088.1:n.*1581T>C
ENST00000432427.3:c.1233T>C (RAF1)
ENST00000460610.2:n.6228T>C (RAF1)
ENST00000471449.2:n.726T>C (RAF1)
ENST00000475353.2:n.4196T>C (RAF1)
ENST00000684903.1:c.*1593T>C (RAF1)	ENSP00000508612.1:n.*1593T>C
ENST00000685348.1:c.*1627T>C (RAF1)	ENSP00000510285.1:n.*1627T>C
ENST00000685437.1:c.1817T>C (RAF1)	ENSP00000508794.1:p.Leu606Pro
ENST00000685653.1:c.1916T>C (RAF1)	ENSP00000509968.1:p.Leu639Pro
ENST00000685697.1:n.2651T>C (RAF1)
ENST00000685738.1:c.*880T>C (RAF1)	ENSP00000510156.1:n.*880T>C
ENST00000686409.1:n.5325T>C (RAF1)
ENST00000686455.1:n.4637T>C (RAF1)
ENST00000686762.1:c.*475T>C (RAF1)	ENSP00000509767.1:n.*475T>C
ENST00000687257.1:n.4370T>C (RAF1)
ENST00000687326.1:c.*3208T>C (RAF1)	ENSP00000509665.1:n.*3208T>C
ENST00000687505.1:n.2034T>C (RAF1)
ENST00000687923.1:c.1805T>C (RAF1)	ENSP00000510255.1:p.Leu602Pro
ENST00000688269.1:n.2512T>C (RAF1)
ENST00000688444.1:n.4033T>C (RAF1)
ENST00000688543.1:c.1817T>C (RAF1)	ENSP00000509612.1:p.Leu606Pro
ENST00000688625.1:c.*3285T>C (RAF1)	ENSP00000509522.1:n.*3285T>C
ENST00000688803.1:n.3344T>C (RAF1)
ENST00000689097.1:c.*1593T>C (RAF1)	ENSP00000509756.1:n.*1593T>C
ENST00000689389.1:c.1739T>C (RAF1)	ENSP00000510213.1:p.Leu580Pro
ENST00000689418.1:c.*3811T>C (RAF1)	ENSP00000509467.1:n.*3811T>C
ENST00000689540.1:n.4284T>C (RAF1)
ENST00000689876.1:c.*465T>C (RAF1)	ENSP00000508535.1:n.*465T>C
ENST00000689914.1:c.*850T>C (RAF1)	ENSP00000509847.1:n.*850T>C
ENST00000690397.1:c.1805T>C (RAF1)	ENSP00000508730.1:p.Leu602Pro
ENST00000690460.1:c.1904T>C (RAF1)	ENSP00000509106.1:p.Leu635Pro
ENST00000690585.1:c.642T>C (RAF1)
ENST00000690625.1:n.2952T>C (RAF1)
ENST00000691396.1:c.*1788T>C (RAF1)	ENSP00000510712.1:n.*1788T>C
ENST00000691643.1:n.2969T>C (RAF1)
ENST00000691724.1:c.*873T>C (RAF1)	ENSP00000509255.1:n.*873T>C
ENST00000691779.1:c.*1494T>C (RAF1)	ENSP00000508592.1:n.*1494T>C
ENST00000691888.1:c.790T>C (RAF1)
ENST00000691899.1:c.1916T>C (RAF1)	ENSP00000508763.1:p.Leu639Pro
ENST00000692069.1:n.4840T>C (RAF1)
ENST00000692093.1:c.1817T>C (RAF1)	ENSP00000509669.1:p.Leu606Pro
ENST00000692311.1:n.2740T>C (RAF1)
ENST00000692558.1:n.4499T>C (RAF1)
ENST00000692773.1:c.*1653T>C (RAF1)	ENSP00000509055.1:n.*1653T>C
ENST00000692830.1:c.*1661T>C (RAF1)	ENSP00000509461.1:n.*1661T>C
ENST00000693312.1:c.1691T>C (RAF1)	ENSP00000508686.1:p.Leu564Pro
ENST00000693664.1:c.*367T>C (RAF1)	ENSP00000509614.1:n.*367T>C
ENST00000693705.1:c.*1295T>C (RAF1)	ENSP00000510697.1:n.*1295T>C
ENST00000251849.9:c.1916T>C (RAF1) MANE Select	ENSP00000251849.4:p.Leu639Pro
ENST00000442415.7:c.1976T>C (RAF1)	ENSP00000401888.2:p.Leu659Pro
ENST00000676541.1:c.*2292A>G (MKRN2)	ENSP00000503730.1:n.*2292A>G
ENST00000677142.1:c.*2292A>G (MKRN2)	ENSP00000504455.1:n.*2292A>G
ENST00000677816.1:c.*847A>G (MKRN2)	ENSP00000502893.1:n.*847A>G
ENST00000677941.1:n.2355A>G (MKRN2)
ENST00000251849.8:c.1916T>C (RAF1)	ENSP00000251849.4:p.Leu639Pro
ENST00000423275.5:c.*1593T>C (RAF1)	ENSP00000401088.1:n.*1593T>C
ENST00000432427.2:c.1553T>C (RAF1)	ENSP00000398591.2:p.Leu518Pro
ENST00000442415.6:c.1976T>C (RAF1)	ENSP00000401888.2:p.Leu659Pro
ENST00000471449.1:n.605T>C (RAF1)
NM_002880.3:c.1916T>C , LRG_413t1:c.1916T>C (RAF1)	NP_002871.1:p.Leu639Pro
XM_005265355.1:c.1916T>C (RAF1)	XP_005265412.1:p.Leu639Pro
XM_005265357.1:c.1817T>C (RAF1)	XP_005265414.1:p.Leu606Pro
XM_005265358.3:c.1673T>C (RAF1)	XP_005265415.1:p.Leu558Pro
XM_005265359.3:c.1574T>C (RAF1)	XP_005265416.1:p.Leu525Pro
XM_011533974.1:c.1916T>C (RAF1)	XP_011532276.1:p.Leu639Pro
XM_011533975.1:c.1673T>C (RAF1)	XP_011532277.1:p.Leu558Pro
NM_001354689.1:c.1976T>C (RAF1)	NP_001341618.1:p.Leu659Pro
NM_001354690.1:c.1916T>C (RAF1)	NP_001341619.1:p.Leu639Pro
NM_001354691.1:c.1673T>C (RAF1)	NP_001341620.1:p.Leu558Pro
NM_001354692.1:c.1673T>C (RAF1)	NP_001341621.1:p.Leu558Pro
NM_001354693.1:c.1817T>C (RAF1)	NP_001341622.1:p.Leu606Pro
NM_001354694.1:c.1733T>C (RAF1)	NP_001341623.1:p.Leu578Pro
NM_001354695.1:c.1574T>C (RAF1)	NP_001341624.1:p.Leu525Pro
NR_148940.1:n.2444T>C (RAF1)
NR_148941.1:n.2390T>C (RAF1)
NR_148942.1:n.2329T>C (RAF1)
XM_011533974.3:c.1916T>C (RAF1)	XP_011532276.1:p.Leu639Pro
XM_017006966.1:c.1817T>C (RAF1)	XP_016862455.1:p.Leu606Pro
NM_001354689.3:c.1976T>C (RAF1)	NP_001341618.1:p.Leu659Pro
NM_001354690.2:c.1916T>C (RAF1)	NP_001341619.1:p.Leu639Pro
NM_001354691.2:c.1673T>C (RAF1)	NP_001341620.1:p.Leu558Pro
NM_001354692.2:c.1673T>C (RAF1)	NP_001341621.1:p.Leu558Pro
NM_001354693.2:c.1817T>C (RAF1)	NP_001341622.1:p.Leu606Pro
NM_001354694.2:c.1733T>C (RAF1)	NP_001341623.1:p.Leu578Pro
NM_001354695.2:c.1574T>C (RAF1)	NP_001341624.1:p.Leu525Pro
NR_148940.2:n.2360T>C (RAF1)
NR_148941.2:n.2306T>C (RAF1)
NR_148942.2:n.2245T>C (RAF1)
NM_001354690.3:c.1916T>C (RAF1)	NP_001341619.1:p.Leu639Pro
NM_001354691.3:c.1673T>C (RAF1)	NP_001341620.1:p.Leu558Pro
NM_001354692.3:c.1673T>C (RAF1)	NP_001341621.1:p.Leu558Pro
NM_001354693.3:c.1817T>C (RAF1)	NP_001341622.1:p.Leu606Pro
NM_001354694.3:c.1733T>C (RAF1)	NP_001341623.1:p.Leu578Pro
NM_001354695.3:c.1574T>C (RAF1)	NP_001341624.1:p.Leu525Pro
NM_002880.4:c.1916T>C (RAF1) MANE Select	NP_002871.1:p.Leu639Pro
NR_148940.3:n.2360T>C (RAF1)
NR_148941.3:n.2306T>C (RAF1)
NR_148942.3:n.2245T>C (RAF1)