Canonical Allele Identifier: CA351496781

Gene: RAF1 MKRN2

Linked Data

• MyVariant Identifiers: chr3:g.12626422T>G (hg19) ; chr3:g.12584923T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584923T>G , CM000665.2:g.12584923T>G	GRCh38
NC_000003.11:g.12626422T>G , CM000665.1:g.12626422T>G	GRCh37
NC_000003.10:g.12601422T>G	NCBI36
NG_007467.1:g.84257A>C , LRG_413:g.84257A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1392A>C (RAF1)	ENSP00000401088.1:n.*1392A>C
ENST00000432427.3:c.1044A>C (RAF1)
ENST00000460610.2:n.6039A>C (RAF1)
ENST00000471449.2:n.537A>C (RAF1)
ENST00000475353.2:n.4007A>C (RAF1)
ENST00000684903.1:c.*1404A>C (RAF1)	ENSP00000508612.1:n.*1404A>C
ENST00000685348.1:c.*1438A>C (RAF1)	ENSP00000510285.1:n.*1438A>C
ENST00000685437.1:c.1628A>C (RAF1)	ENSP00000508794.1:p.Asn543Thr
ENST00000685653.1:c.1727A>C (RAF1)	ENSP00000509968.1:p.Asn576Thr
ENST00000685697.1:n.2462A>C (RAF1)
ENST00000685738.1:c.*691A>C (RAF1)	ENSP00000510156.1:n.*691A>C
ENST00000686409.1:n.5136A>C (RAF1)
ENST00000686455.1:n.4448A>C (RAF1)
ENST00000686762.1:c.*286A>C (RAF1)	ENSP00000509767.1:n.*286A>C
ENST00000687257.1:n.4181A>C (RAF1)
ENST00000687326.1:c.*3019A>C (RAF1)	ENSP00000509665.1:n.*3019A>C
ENST00000687505.1:n.1845A>C (RAF1)
ENST00000687923.1:c.1616A>C (RAF1)	ENSP00000510255.1:p.Asn539Thr
ENST00000688269.1:n.2323A>C (RAF1)
ENST00000688444.1:n.3844A>C (RAF1)
ENST00000688543.1:c.1628A>C (RAF1)	ENSP00000509612.1:p.Asn543Thr
ENST00000688625.1:c.*3096A>C (RAF1)	ENSP00000509522.1:n.*3096A>C
ENST00000688803.1:n.3155A>C (RAF1)
ENST00000688914.1:n.1140A>C (RAF1)
ENST00000689097.1:c.*1404A>C (RAF1)	ENSP00000509756.1:n.*1404A>C
ENST00000689389.1:c.1550A>C (RAF1)	ENSP00000510213.1:p.Asn517Thr
ENST00000689418.1:c.*3622A>C (RAF1)	ENSP00000509467.1:n.*3622A>C
ENST00000689540.1:n.4095A>C (RAF1)
ENST00000689876.1:c.*276A>C (RAF1)	ENSP00000508535.1:n.*276A>C
ENST00000689914.1:c.*661A>C (RAF1)	ENSP00000509847.1:n.*661A>C
ENST00000690397.1:c.1616A>C (RAF1)	ENSP00000508730.1:p.Asn539Thr
ENST00000690460.1:c.1715A>C (RAF1)	ENSP00000509106.1:p.Asn572Thr
ENST00000690585.1:c.453A>C (RAF1)
ENST00000690625.1:n.2763A>C (RAF1)
ENST00000691396.1:c.*1599A>C (RAF1)	ENSP00000510712.1:n.*1599A>C
ENST00000691643.1:n.2780A>C (RAF1)
ENST00000691724.1:c.*684A>C (RAF1)	ENSP00000509255.1:n.*684A>C
ENST00000691779.1:c.*1305A>C (RAF1)	ENSP00000508592.1:n.*1305A>C
ENST00000691888.1:c.601A>C (RAF1)
ENST00000691899.1:c.1727A>C (RAF1)	ENSP00000508763.1:p.Asn576Thr
ENST00000692069.1:n.4651A>C (RAF1)
ENST00000692093.1:c.1628A>C (RAF1)	ENSP00000509669.1:p.Asn543Thr
ENST00000692311.1:n.2551A>C (RAF1)
ENST00000692558.1:n.4310A>C (RAF1)
ENST00000692773.1:c.*1464A>C (RAF1)	ENSP00000509055.1:n.*1464A>C
ENST00000692830.1:c.*1472A>C (RAF1)	ENSP00000509461.1:n.*1472A>C
ENST00000693312.1:c.1502A>C (RAF1)	ENSP00000508686.1:p.Asn501Thr
ENST00000693664.1:c.*178A>C (RAF1)	ENSP00000509614.1:n.*178A>C
ENST00000693705.1:c.*1106A>C (RAF1)	ENSP00000510697.1:n.*1106A>C
ENST00000251849.9:c.1727A>C (RAF1) MANE Select	ENSP00000251849.4:p.Asn576Thr
ENST00000442415.7:c.1787A>C (RAF1)	ENSP00000401888.2:p.Asn596Thr
ENST00000676541.1:c.*2670T>G (MKRN2)	ENSP00000503730.1:n.*2670T>G
ENST00000677142.1:c.*2670T>G (MKRN2)	ENSP00000504455.1:n.*2670T>G
ENST00000677816.1:c.*1225T>G (MKRN2)	ENSP00000502893.1:n.*1225T>G
ENST00000677941.1:n.2733T>G (MKRN2)
ENST00000251849.8:c.1727A>C (RAF1)	ENSP00000251849.4:p.Asn576Thr
ENST00000423275.5:c.*1404A>C (RAF1)	ENSP00000401088.1:n.*1404A>C
ENST00000432427.2:c.1364A>C (RAF1)	ENSP00000398591.2:p.Asn455Thr
ENST00000442415.6:c.1787A>C (RAF1)	ENSP00000401888.2:p.Asn596Thr
ENST00000471449.1:n.416A>C (RAF1)
NM_002880.3:c.1727A>C , LRG_413t1:c.1727A>C (RAF1)	NP_002871.1:p.Asn576Thr
XM_005265355.1:c.1727A>C (RAF1)	XP_005265412.1:p.Asn576Thr
XM_005265357.1:c.1628A>C (RAF1)	XP_005265414.1:p.Asn543Thr
XM_005265358.3:c.1484A>C (RAF1)	XP_005265415.1:p.Asn495Thr
XM_005265359.3:c.1385A>C (RAF1)	XP_005265416.1:p.Asn462Thr
XM_011533974.1:c.1727A>C (RAF1)	XP_011532276.1:p.Asn576Thr
XM_011533975.1:c.1484A>C (RAF1)	XP_011532277.1:p.Asn495Thr
NM_001354689.1:c.1787A>C (RAF1)	NP_001341618.1:p.Asn596Thr
NM_001354690.1:c.1727A>C (RAF1)	NP_001341619.1:p.Asn576Thr
NM_001354691.1:c.1484A>C (RAF1)	NP_001341620.1:p.Asn495Thr
NM_001354692.1:c.1484A>C (RAF1)	NP_001341621.1:p.Asn495Thr
NM_001354693.1:c.1628A>C (RAF1)	NP_001341622.1:p.Asn543Thr
NM_001354694.1:c.1544A>C (RAF1)	NP_001341623.1:p.Asn515Thr
NM_001354695.1:c.1385A>C (RAF1)	NP_001341624.1:p.Asn462Thr
NR_148940.1:n.2255A>C (RAF1)
NR_148941.1:n.2201A>C (RAF1)
NR_148942.1:n.2140A>C (RAF1)
XM_011533974.3:c.1727A>C (RAF1)	XP_011532276.1:p.Asn576Thr
XM_017006966.1:c.1628A>C (RAF1)	XP_016862455.1:p.Asn543Thr
NM_001354689.3:c.1787A>C (RAF1)	NP_001341618.1:p.Asn596Thr
NM_001354690.2:c.1727A>C (RAF1)	NP_001341619.1:p.Asn576Thr
NM_001354691.2:c.1484A>C (RAF1)	NP_001341620.1:p.Asn495Thr
NM_001354692.2:c.1484A>C (RAF1)	NP_001341621.1:p.Asn495Thr
NM_001354693.2:c.1628A>C (RAF1)	NP_001341622.1:p.Asn543Thr
NM_001354694.2:c.1544A>C (RAF1)	NP_001341623.1:p.Asn515Thr
NM_001354695.2:c.1385A>C (RAF1)	NP_001341624.1:p.Asn462Thr
NR_148940.2:n.2171A>C (RAF1)
NR_148941.2:n.2117A>C (RAF1)
NR_148942.2:n.2056A>C (RAF1)
NM_001354690.3:c.1727A>C (RAF1)	NP_001341619.1:p.Asn576Thr
NM_001354691.3:c.1484A>C (RAF1)	NP_001341620.1:p.Asn495Thr
NM_001354692.3:c.1484A>C (RAF1)	NP_001341621.1:p.Asn495Thr
NM_001354693.3:c.1628A>C (RAF1)	NP_001341622.1:p.Asn543Thr
NM_001354694.3:c.1544A>C (RAF1)	NP_001341623.1:p.Asn515Thr
NM_001354695.3:c.1385A>C (RAF1)	NP_001341624.1:p.Asn462Thr
NM_002880.4:c.1727A>C (RAF1) MANE Select	NP_002871.1:p.Asn576Thr
NR_148940.3:n.2171A>C (RAF1)
NR_148941.3:n.2117A>C (RAF1)
NR_148942.3:n.2056A>C (RAF1)