Canonical Allele Identifier: CA351497067

Gene: RAF1 MKRN2

Linked Data

• MyVariant Identifiers: chr3:g.12626474A>G (hg19) ; chr3:g.12584975A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584975A>G , CM000665.2:g.12584975A>G	GRCh38
NC_000003.11:g.12626474A>G , CM000665.1:g.12626474A>G	GRCh37
NC_000003.10:g.12601474A>G	NCBI36
NG_007467.1:g.84205T>C , LRG_413:g.84205T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1340T>C (RAF1)	ENSP00000401088.1:n.*1340T>C
ENST00000432427.3:c.992T>C (RAF1)
ENST00000460610.2:n.5987T>C (RAF1)
ENST00000471449.2:n.485T>C (RAF1)
ENST00000475353.2:n.3955T>C (RAF1)
ENST00000684903.1:c.*1352T>C (RAF1)	ENSP00000508612.1:n.*1352T>C
ENST00000685348.1:c.*1386T>C (RAF1)	ENSP00000510285.1:n.*1386T>C
ENST00000685437.1:c.1576T>C (RAF1)	ENSP00000508794.1:p.Phe526Leu
ENST00000685653.1:c.1675T>C (RAF1)	ENSP00000509968.1:p.Phe559Leu
ENST00000685697.1:n.2410T>C (RAF1)
ENST00000685738.1:c.*639T>C (RAF1)	ENSP00000510156.1:n.*639T>C
ENST00000686409.1:n.5084T>C (RAF1)
ENST00000686455.1:n.4396T>C (RAF1)
ENST00000686762.1:c.*234T>C (RAF1)	ENSP00000509767.1:n.*234T>C
ENST00000687257.1:n.4129T>C (RAF1)
ENST00000687326.1:c.*2967T>C (RAF1)	ENSP00000509665.1:n.*2967T>C
ENST00000687505.1:n.1793T>C (RAF1)
ENST00000687923.1:c.1564T>C (RAF1)	ENSP00000510255.1:p.Phe522Leu
ENST00000688269.1:n.2271T>C (RAF1)
ENST00000688444.1:n.3792T>C (RAF1)
ENST00000688543.1:c.1576T>C (RAF1)	ENSP00000509612.1:p.Phe526Leu
ENST00000688625.1:c.*3044T>C (RAF1)	ENSP00000509522.1:n.*3044T>C
ENST00000688803.1:n.3103T>C (RAF1)
ENST00000688914.1:n.1088T>C (RAF1)
ENST00000689097.1:c.*1352T>C (RAF1)	ENSP00000509756.1:n.*1352T>C
ENST00000689389.1:c.1498T>C (RAF1)	ENSP00000510213.1:p.Phe500Leu
ENST00000689418.1:c.*3570T>C (RAF1)	ENSP00000509467.1:n.*3570T>C
ENST00000689540.1:n.4043T>C (RAF1)
ENST00000689876.1:c.*224T>C (RAF1)	ENSP00000508535.1:n.*224T>C
ENST00000689914.1:c.*609T>C (RAF1)	ENSP00000509847.1:n.*609T>C
ENST00000690397.1:c.1564T>C (RAF1)	ENSP00000508730.1:p.Phe522Leu
ENST00000690460.1:c.1663T>C (RAF1)	ENSP00000509106.1:p.Phe555Leu
ENST00000690585.1:c.401T>C (RAF1)
ENST00000690625.1:n.2711T>C (RAF1)
ENST00000691396.1:c.*1547T>C (RAF1)	ENSP00000510712.1:n.*1547T>C
ENST00000691643.1:n.2728T>C (RAF1)
ENST00000691724.1:c.*632T>C (RAF1)	ENSP00000509255.1:n.*632T>C
ENST00000691779.1:c.*1253T>C (RAF1)	ENSP00000508592.1:n.*1253T>C
ENST00000691888.1:c.549T>C (RAF1)
ENST00000691899.1:c.1675T>C (RAF1)	ENSP00000508763.1:p.Phe559Leu
ENST00000692069.1:n.4599T>C (RAF1)
ENST00000692093.1:c.1576T>C (RAF1)	ENSP00000509669.1:p.Phe526Leu
ENST00000692311.1:n.2499T>C (RAF1)
ENST00000692558.1:n.4258T>C (RAF1)
ENST00000692773.1:c.*1412T>C (RAF1)	ENSP00000509055.1:n.*1412T>C
ENST00000692830.1:c.*1420T>C (RAF1)	ENSP00000509461.1:n.*1420T>C
ENST00000693312.1:c.1450T>C (RAF1)	ENSP00000508686.1:p.Phe484Leu
ENST00000693664.1:c.*126T>C (RAF1)	ENSP00000509614.1:n.*126T>C
ENST00000693705.1:c.*1054T>C (RAF1)	ENSP00000510697.1:n.*1054T>C
ENST00000251849.9:c.1675T>C (RAF1) MANE Select	ENSP00000251849.4:p.Phe559Leu
ENST00000442415.7:c.1735T>C (RAF1)	ENSP00000401888.2:p.Phe579Leu
ENST00000676541.1:c.*2722A>G (MKRN2)	ENSP00000503730.1:n.*2722A>G
ENST00000677142.1:c.*2722A>G (MKRN2)	ENSP00000504455.1:n.*2722A>G
ENST00000677816.1:c.*1277A>G (MKRN2)	ENSP00000502893.1:n.*1277A>G
ENST00000677941.1:n.2785A>G (MKRN2)
ENST00000251849.8:c.1675T>C (RAF1)	ENSP00000251849.4:p.Phe559Leu
ENST00000423275.5:c.*1352T>C (RAF1)	ENSP00000401088.1:n.*1352T>C
ENST00000432427.2:c.1312T>C (RAF1)	ENSP00000398591.2:p.Phe438Leu
ENST00000442415.6:c.1735T>C (RAF1)	ENSP00000401888.2:p.Phe579Leu
ENST00000471449.1:n.364T>C (RAF1)
NM_002880.3:c.1675T>C , LRG_413t1:c.1675T>C (RAF1)	NP_002871.1:p.Phe559Leu
XM_005265355.1:c.1675T>C (RAF1)	XP_005265412.1:p.Phe559Leu
XM_005265357.1:c.1576T>C (RAF1)	XP_005265414.1:p.Phe526Leu
XM_005265358.3:c.1432T>C (RAF1)	XP_005265415.1:p.Phe478Leu
XM_005265359.3:c.1333T>C (RAF1)	XP_005265416.1:p.Phe445Leu
XM_011533974.1:c.1675T>C (RAF1)	XP_011532276.1:p.Phe559Leu
XM_011533975.1:c.1432T>C (RAF1)	XP_011532277.1:p.Phe478Leu
NM_001354689.1:c.1735T>C (RAF1)	NP_001341618.1:p.Phe579Leu
NM_001354690.1:c.1675T>C (RAF1)	NP_001341619.1:p.Phe559Leu
NM_001354691.1:c.1432T>C (RAF1)	NP_001341620.1:p.Phe478Leu
NM_001354692.1:c.1432T>C (RAF1)	NP_001341621.1:p.Phe478Leu
NM_001354693.1:c.1576T>C (RAF1)	NP_001341622.1:p.Phe526Leu
NM_001354694.1:c.1492T>C (RAF1)	NP_001341623.1:p.Phe498Leu
NM_001354695.1:c.1333T>C (RAF1)	NP_001341624.1:p.Phe445Leu
NR_148940.1:n.2203T>C (RAF1)
NR_148941.1:n.2149T>C (RAF1)
NR_148942.1:n.2088T>C (RAF1)
XM_011533974.3:c.1675T>C (RAF1)	XP_011532276.1:p.Phe559Leu
XM_017006966.1:c.1576T>C (RAF1)	XP_016862455.1:p.Phe526Leu
NM_001354689.3:c.1735T>C (RAF1)	NP_001341618.1:p.Phe579Leu
NM_001354690.2:c.1675T>C (RAF1)	NP_001341619.1:p.Phe559Leu
NM_001354691.2:c.1432T>C (RAF1)	NP_001341620.1:p.Phe478Leu
NM_001354692.2:c.1432T>C (RAF1)	NP_001341621.1:p.Phe478Leu
NM_001354693.2:c.1576T>C (RAF1)	NP_001341622.1:p.Phe526Leu
NM_001354694.2:c.1492T>C (RAF1)	NP_001341623.1:p.Phe498Leu
NM_001354695.2:c.1333T>C (RAF1)	NP_001341624.1:p.Phe445Leu
NR_148940.2:n.2119T>C (RAF1)
NR_148941.2:n.2065T>C (RAF1)
NR_148942.2:n.2004T>C (RAF1)
NM_001354690.3:c.1675T>C (RAF1)	NP_001341619.1:p.Phe559Leu
NM_001354691.3:c.1432T>C (RAF1)	NP_001341620.1:p.Phe478Leu
NM_001354692.3:c.1432T>C (RAF1)	NP_001341621.1:p.Phe478Leu
NM_001354693.3:c.1576T>C (RAF1)	NP_001341622.1:p.Phe526Leu
NM_001354694.3:c.1492T>C (RAF1)	NP_001341623.1:p.Phe498Leu
NM_001354695.3:c.1333T>C (RAF1)	NP_001341624.1:p.Phe445Leu
NM_002880.4:c.1675T>C (RAF1) MANE Select	NP_002871.1:p.Phe559Leu
NR_148940.3:n.2119T>C (RAF1)
NR_148941.3:n.2065T>C (RAF1)
NR_148942.3:n.2004T>C (RAF1)