Canonical Allele Identifier: CA351495676

Gene: RAF1 MKRN2

Linked Data

• dbSNP Id: rs2125316155
• MyVariant Identifiers: chr3:g.12626062T>A (hg19) ; chr3:g.12584563T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584563T>A , CM000665.2:g.12584563T>A	GRCh38
NC_000003.11:g.12626062T>A , CM000665.1:g.12626062T>A	GRCh37
NC_000003.10:g.12601062T>A	NCBI36
NG_007467.1:g.84617A>T , LRG_413:g.84617A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1563A>T (RAF1)	ENSP00000401088.1:n.*1563A>T
ENST00000432427.3:c.1215A>T (RAF1)
ENST00000460610.2:n.6210A>T (RAF1)
ENST00000471449.2:n.708A>T (RAF1)
ENST00000475353.2:n.4178A>T (RAF1)
ENST00000684903.1:c.*1575A>T (RAF1)	ENSP00000508612.1:n.*1575A>T
ENST00000685348.1:c.*1609A>T (RAF1)	ENSP00000510285.1:n.*1609A>T
ENST00000685437.1:c.1799A>T (RAF1)	ENSP00000508794.1:p.Asp600Val
ENST00000685653.1:c.1898A>T (RAF1)	ENSP00000509968.1:p.Asp633Val
ENST00000685697.1:n.2633A>T (RAF1)
ENST00000685738.1:c.*862A>T (RAF1)	ENSP00000510156.1:n.*862A>T
ENST00000686409.1:n.5307A>T (RAF1)
ENST00000686455.1:n.4619A>T (RAF1)
ENST00000686762.1:c.*457A>T (RAF1)	ENSP00000509767.1:n.*457A>T
ENST00000687257.1:n.4352A>T (RAF1)
ENST00000687326.1:c.*3190A>T (RAF1)	ENSP00000509665.1:n.*3190A>T
ENST00000687505.1:n.2016A>T (RAF1)
ENST00000687923.1:c.1787A>T (RAF1)	ENSP00000510255.1:p.Asp596Val
ENST00000688269.1:n.2494A>T (RAF1)
ENST00000688444.1:n.4015A>T (RAF1)
ENST00000688543.1:c.1799A>T (RAF1)	ENSP00000509612.1:p.Asp600Val
ENST00000688625.1:c.*3267A>T (RAF1)	ENSP00000509522.1:n.*3267A>T
ENST00000688803.1:n.3326A>T (RAF1)
ENST00000689097.1:c.*1575A>T (RAF1)	ENSP00000509756.1:n.*1575A>T
ENST00000689389.1:c.1721A>T (RAF1)	ENSP00000510213.1:p.Asp574Val
ENST00000689418.1:c.*3793A>T (RAF1)	ENSP00000509467.1:n.*3793A>T
ENST00000689540.1:n.4266A>T (RAF1)
ENST00000689876.1:c.*447A>T (RAF1)	ENSP00000508535.1:n.*447A>T
ENST00000689914.1:c.*832A>T (RAF1)	ENSP00000509847.1:n.*832A>T
ENST00000690397.1:c.1787A>T (RAF1)	ENSP00000508730.1:p.Asp596Val
ENST00000690460.1:c.1886A>T (RAF1)	ENSP00000509106.1:p.Asp629Val
ENST00000690585.1:c.624A>T (RAF1)
ENST00000690625.1:n.2934A>T (RAF1)
ENST00000691396.1:c.*1770A>T (RAF1)	ENSP00000510712.1:n.*1770A>T
ENST00000691643.1:n.2951A>T (RAF1)
ENST00000691724.1:c.*855A>T (RAF1)	ENSP00000509255.1:n.*855A>T
ENST00000691779.1:c.*1476A>T (RAF1)	ENSP00000508592.1:n.*1476A>T
ENST00000691888.1:c.772A>T (RAF1)
ENST00000691899.1:c.1898A>T (RAF1)	ENSP00000508763.1:p.Asp633Val
ENST00000692069.1:n.4822A>T (RAF1)
ENST00000692093.1:c.1799A>T (RAF1)	ENSP00000509669.1:p.Asp600Val
ENST00000692311.1:n.2722A>T (RAF1)
ENST00000692558.1:n.4481A>T (RAF1)
ENST00000692773.1:c.*1635A>T (RAF1)	ENSP00000509055.1:n.*1635A>T
ENST00000692830.1:c.*1643A>T (RAF1)	ENSP00000509461.1:n.*1643A>T
ENST00000693312.1:c.1673A>T (RAF1)	ENSP00000508686.1:p.Asp558Val
ENST00000693664.1:c.*349A>T (RAF1)	ENSP00000509614.1:n.*349A>T
ENST00000693705.1:c.*1277A>T (RAF1)	ENSP00000510697.1:n.*1277A>T
ENST00000251849.9:c.1898A>T (RAF1) MANE Select	ENSP00000251849.4:p.Asp633Val
ENST00000442415.7:c.1958A>T (RAF1)	ENSP00000401888.2:p.Asp653Val
ENST00000676541.1:c.*2310T>A (MKRN2)	ENSP00000503730.1:n.*2310T>A
ENST00000677142.1:c.*2310T>A (MKRN2)	ENSP00000504455.1:n.*2310T>A
ENST00000677816.1:c.*865T>A (MKRN2)	ENSP00000502893.1:n.*865T>A
ENST00000677941.1:n.2373T>A (MKRN2)
ENST00000251849.8:c.1898A>T (RAF1)	ENSP00000251849.4:p.Asp633Val
ENST00000423275.5:c.*1575A>T (RAF1)	ENSP00000401088.1:n.*1575A>T
ENST00000432427.2:c.1535A>T (RAF1)	ENSP00000398591.2:p.Asp512Val
ENST00000442415.6:c.1958A>T (RAF1)	ENSP00000401888.2:p.Asp653Val
ENST00000471449.1:n.587A>T (RAF1)
NM_002880.3:c.1898A>T , LRG_413t1:c.1898A>T (RAF1)	NP_002871.1:p.Asp633Val
XM_005265355.1:c.1898A>T (RAF1)	XP_005265412.1:p.Asp633Val
XM_005265357.1:c.1799A>T (RAF1)	XP_005265414.1:p.Asp600Val
XM_005265358.3:c.1655A>T (RAF1)	XP_005265415.1:p.Asp552Val
XM_005265359.3:c.1556A>T (RAF1)	XP_005265416.1:p.Asp519Val
XM_011533974.1:c.1898A>T (RAF1)	XP_011532276.1:p.Asp633Val
XM_011533975.1:c.1655A>T (RAF1)	XP_011532277.1:p.Asp552Val
NM_001354689.1:c.1958A>T (RAF1)	NP_001341618.1:p.Asp653Val
NM_001354690.1:c.1898A>T (RAF1)	NP_001341619.1:p.Asp633Val
NM_001354691.1:c.1655A>T (RAF1)	NP_001341620.1:p.Asp552Val
NM_001354692.1:c.1655A>T (RAF1)	NP_001341621.1:p.Asp552Val
NM_001354693.1:c.1799A>T (RAF1)	NP_001341622.1:p.Asp600Val
NM_001354694.1:c.1715A>T (RAF1)	NP_001341623.1:p.Asp572Val
NM_001354695.1:c.1556A>T (RAF1)	NP_001341624.1:p.Asp519Val
NR_148940.1:n.2426A>T (RAF1)
NR_148941.1:n.2372A>T (RAF1)
NR_148942.1:n.2311A>T (RAF1)
XM_011533974.3:c.1898A>T (RAF1)	XP_011532276.1:p.Asp633Val
XM_017006966.1:c.1799A>T (RAF1)	XP_016862455.1:p.Asp600Val
NM_001354689.3:c.1958A>T (RAF1)	NP_001341618.1:p.Asp653Val
NM_001354690.2:c.1898A>T (RAF1)	NP_001341619.1:p.Asp633Val
NM_001354691.2:c.1655A>T (RAF1)	NP_001341620.1:p.Asp552Val
NM_001354692.2:c.1655A>T (RAF1)	NP_001341621.1:p.Asp552Val
NM_001354693.2:c.1799A>T (RAF1)	NP_001341622.1:p.Asp600Val
NM_001354694.2:c.1715A>T (RAF1)	NP_001341623.1:p.Asp572Val
NM_001354695.2:c.1556A>T (RAF1)	NP_001341624.1:p.Asp519Val
NR_148940.2:n.2342A>T (RAF1)
NR_148941.2:n.2288A>T (RAF1)
NR_148942.2:n.2227A>T (RAF1)
NM_001354690.3:c.1898A>T (RAF1)	NP_001341619.1:p.Asp633Val
NM_001354691.3:c.1655A>T (RAF1)	NP_001341620.1:p.Asp552Val
NM_001354692.3:c.1655A>T (RAF1)	NP_001341621.1:p.Asp552Val
NM_001354693.3:c.1799A>T (RAF1)	NP_001341622.1:p.Asp600Val
NM_001354694.3:c.1715A>T (RAF1)	NP_001341623.1:p.Asp572Val
NM_001354695.3:c.1556A>T (RAF1)	NP_001341624.1:p.Asp519Val
NM_002880.4:c.1898A>T (RAF1) MANE Select	NP_002871.1:p.Asp633Val
NR_148940.3:n.2342A>T (RAF1)
NR_148941.3:n.2288A>T (RAF1)
NR_148942.3:n.2227A>T (RAF1)