Canonical Allele Identifier: CA351496904

Gene: RAF1 MKRN2

Linked Data

• MyVariant Identifiers: chr3:g.12626449G>T (hg19) ; chr3:g.12584950G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584950G>T , CM000665.2:g.12584950G>T	GRCh38
NC_000003.11:g.12626449G>T , CM000665.1:g.12626449G>T	GRCh37
NC_000003.10:g.12601449G>T	NCBI36
NG_007467.1:g.84230C>A , LRG_413:g.84230C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1365C>A (RAF1)	ENSP00000401088.1:n.*1365C>A
ENST00000432427.3:c.1017C>A (RAF1)
ENST00000460610.2:n.6012C>A (RAF1)
ENST00000471449.2:n.510C>A (RAF1)
ENST00000475353.2:n.3980C>A (RAF1)
ENST00000684903.1:c.*1377C>A (RAF1)	ENSP00000508612.1:n.*1377C>A
ENST00000685348.1:c.*1411C>A (RAF1)	ENSP00000510285.1:n.*1411C>A
ENST00000685437.1:c.1601C>A (RAF1)	ENSP00000508794.1:p.Ser534Tyr
ENST00000685653.1:c.1700C>A (RAF1)	ENSP00000509968.1:p.Ser567Tyr
ENST00000685697.1:n.2435C>A (RAF1)
ENST00000685738.1:c.*664C>A (RAF1)	ENSP00000510156.1:n.*664C>A
ENST00000686409.1:n.5109C>A (RAF1)
ENST00000686455.1:n.4421C>A (RAF1)
ENST00000686762.1:c.*259C>A (RAF1)	ENSP00000509767.1:n.*259C>A
ENST00000687257.1:n.4154C>A (RAF1)
ENST00000687326.1:c.*2992C>A (RAF1)	ENSP00000509665.1:n.*2992C>A
ENST00000687505.1:n.1818C>A (RAF1)
ENST00000687923.1:c.1589C>A (RAF1)	ENSP00000510255.1:p.Ser530Tyr
ENST00000688269.1:n.2296C>A (RAF1)
ENST00000688444.1:n.3817C>A (RAF1)
ENST00000688543.1:c.1601C>A (RAF1)	ENSP00000509612.1:p.Ser534Tyr
ENST00000688625.1:c.*3069C>A (RAF1)	ENSP00000509522.1:n.*3069C>A
ENST00000688803.1:n.3128C>A (RAF1)
ENST00000688914.1:n.1113C>A (RAF1)
ENST00000689097.1:c.*1377C>A (RAF1)	ENSP00000509756.1:n.*1377C>A
ENST00000689389.1:c.1523C>A (RAF1)	ENSP00000510213.1:p.Ser508Tyr
ENST00000689418.1:c.*3595C>A (RAF1)	ENSP00000509467.1:n.*3595C>A
ENST00000689540.1:n.4068C>A (RAF1)
ENST00000689876.1:c.*249C>A (RAF1)	ENSP00000508535.1:n.*249C>A
ENST00000689914.1:c.*634C>A (RAF1)	ENSP00000509847.1:n.*634C>A
ENST00000690397.1:c.1589C>A (RAF1)	ENSP00000508730.1:p.Ser530Tyr
ENST00000690460.1:c.1688C>A (RAF1)	ENSP00000509106.1:p.Ser563Tyr
ENST00000690585.1:c.426C>A (RAF1)
ENST00000690625.1:n.2736C>A (RAF1)
ENST00000691396.1:c.*1572C>A (RAF1)	ENSP00000510712.1:n.*1572C>A
ENST00000691643.1:n.2753C>A (RAF1)
ENST00000691724.1:c.*657C>A (RAF1)	ENSP00000509255.1:n.*657C>A
ENST00000691779.1:c.*1278C>A (RAF1)	ENSP00000508592.1:n.*1278C>A
ENST00000691888.1:c.574C>A (RAF1)
ENST00000691899.1:c.1700C>A (RAF1)	ENSP00000508763.1:p.Ser567Tyr
ENST00000692069.1:n.4624C>A (RAF1)
ENST00000692093.1:c.1601C>A (RAF1)	ENSP00000509669.1:p.Ser534Tyr
ENST00000692311.1:n.2524C>A (RAF1)
ENST00000692558.1:n.4283C>A (RAF1)
ENST00000692773.1:c.*1437C>A (RAF1)	ENSP00000509055.1:n.*1437C>A
ENST00000692830.1:c.*1445C>A (RAF1)	ENSP00000509461.1:n.*1445C>A
ENST00000693312.1:c.1475C>A (RAF1)	ENSP00000508686.1:p.Ser492Tyr
ENST00000693664.1:c.*151C>A (RAF1)	ENSP00000509614.1:n.*151C>A
ENST00000693705.1:c.*1079C>A (RAF1)	ENSP00000510697.1:n.*1079C>A
ENST00000251849.9:c.1700C>A (RAF1) MANE Select	ENSP00000251849.4:p.Ser567Tyr
ENST00000442415.7:c.1760C>A (RAF1)	ENSP00000401888.2:p.Ser587Tyr
ENST00000676541.1:c.*2697G>T (MKRN2)	ENSP00000503730.1:n.*2697G>T
ENST00000677142.1:c.*2697G>T (MKRN2)	ENSP00000504455.1:n.*2697G>T
ENST00000677816.1:c.*1252G>T (MKRN2)	ENSP00000502893.1:n.*1252G>T
ENST00000677941.1:n.2760G>T (MKRN2)
ENST00000251849.8:c.1700C>A (RAF1)	ENSP00000251849.4:p.Ser567Tyr
ENST00000423275.5:c.*1377C>A (RAF1)	ENSP00000401088.1:n.*1377C>A
ENST00000432427.2:c.1337C>A (RAF1)	ENSP00000398591.2:p.Ser446Tyr
ENST00000442415.6:c.1760C>A (RAF1)	ENSP00000401888.2:p.Ser587Tyr
ENST00000471449.1:n.389C>A (RAF1)
NM_002880.3:c.1700C>A , LRG_413t1:c.1700C>A (RAF1)	NP_002871.1:p.Ser567Tyr
XM_005265355.1:c.1700C>A (RAF1)	XP_005265412.1:p.Ser567Tyr
XM_005265357.1:c.1601C>A (RAF1)	XP_005265414.1:p.Ser534Tyr
XM_005265358.3:c.1457C>A (RAF1)	XP_005265415.1:p.Ser486Tyr
XM_005265359.3:c.1358C>A (RAF1)	XP_005265416.1:p.Ser453Tyr
XM_011533974.1:c.1700C>A (RAF1)	XP_011532276.1:p.Ser567Tyr
XM_011533975.1:c.1457C>A (RAF1)	XP_011532277.1:p.Ser486Tyr
NM_001354689.1:c.1760C>A (RAF1)	NP_001341618.1:p.Ser587Tyr
NM_001354690.1:c.1700C>A (RAF1)	NP_001341619.1:p.Ser567Tyr
NM_001354691.1:c.1457C>A (RAF1)	NP_001341620.1:p.Ser486Tyr
NM_001354692.1:c.1457C>A (RAF1)	NP_001341621.1:p.Ser486Tyr
NM_001354693.1:c.1601C>A (RAF1)	NP_001341622.1:p.Ser534Tyr
NM_001354694.1:c.1517C>A (RAF1)	NP_001341623.1:p.Ser506Tyr
NM_001354695.1:c.1358C>A (RAF1)	NP_001341624.1:p.Ser453Tyr
NR_148940.1:n.2228C>A (RAF1)
NR_148941.1:n.2174C>A (RAF1)
NR_148942.1:n.2113C>A (RAF1)
XM_011533974.3:c.1700C>A (RAF1)	XP_011532276.1:p.Ser567Tyr
XM_017006966.1:c.1601C>A (RAF1)	XP_016862455.1:p.Ser534Tyr
NM_001354689.3:c.1760C>A (RAF1)	NP_001341618.1:p.Ser587Tyr
NM_001354690.2:c.1700C>A (RAF1)	NP_001341619.1:p.Ser567Tyr
NM_001354691.2:c.1457C>A (RAF1)	NP_001341620.1:p.Ser486Tyr
NM_001354692.2:c.1457C>A (RAF1)	NP_001341621.1:p.Ser486Tyr
NM_001354693.2:c.1601C>A (RAF1)	NP_001341622.1:p.Ser534Tyr
NM_001354694.2:c.1517C>A (RAF1)	NP_001341623.1:p.Ser506Tyr
NM_001354695.2:c.1358C>A (RAF1)	NP_001341624.1:p.Ser453Tyr
NR_148940.2:n.2144C>A (RAF1)
NR_148941.2:n.2090C>A (RAF1)
NR_148942.2:n.2029C>A (RAF1)
NM_001354690.3:c.1700C>A (RAF1)	NP_001341619.1:p.Ser567Tyr
NM_001354691.3:c.1457C>A (RAF1)	NP_001341620.1:p.Ser486Tyr
NM_001354692.3:c.1457C>A (RAF1)	NP_001341621.1:p.Ser486Tyr
NM_001354693.3:c.1601C>A (RAF1)	NP_001341622.1:p.Ser534Tyr
NM_001354694.3:c.1517C>A (RAF1)	NP_001341623.1:p.Ser506Tyr
NM_001354695.3:c.1358C>A (RAF1)	NP_001341624.1:p.Ser453Tyr
NM_002880.4:c.1700C>A (RAF1) MANE Select	NP_002871.1:p.Ser567Tyr
NR_148940.3:n.2144C>A (RAF1)
NR_148941.3:n.2090C>A (RAF1)
NR_148942.3:n.2029C>A (RAF1)