Canonical Allele Identifier: CA432522002

Gene: RAF1 MKRN2

Linked Data

• MyVariant Identifiers: chr3:g.12626367T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584868T>C , CM000665.2:g.12584868T>C	GRCh38
NC_000003.11:g.12626367T>C , CM000665.1:g.12626367T>C	GRCh37
NC_000003.10:g.12601367T>C	NCBI36
NG_007467.1:g.84312A>G , LRG_413:g.84312A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1447A>G (RAF1)	ENSP00000401088.1:n.*1447A>G
ENST00000432427.3:c.1099A>G (RAF1)
ENST00000460610.2:n.6094A>G (RAF1)
ENST00000471449.2:n.592A>G (RAF1)
ENST00000475353.2:n.4062A>G (RAF1)
ENST00000684903.1:c.*1459A>G (RAF1)	ENSP00000508612.1:n.*1459A>G
ENST00000685348.1:c.*1493A>G (RAF1)	ENSP00000510285.1:n.*1493A>G
ENST00000685437.1:c.1683A>G (RAF1)	ENSP00000508794.1:p.Glu561=
ENST00000685653.1:c.1782A>G (RAF1)	ENSP00000509968.1:p.Glu594=
ENST00000685697.1:n.2517A>G (RAF1)
ENST00000685738.1:c.*746A>G (RAF1)	ENSP00000510156.1:n.*746A>G
ENST00000686409.1:n.5191A>G (RAF1)
ENST00000686455.1:n.4503A>G (RAF1)
ENST00000686762.1:c.*341A>G (RAF1)	ENSP00000509767.1:n.*341A>G
ENST00000687257.1:n.4236A>G (RAF1)
ENST00000687326.1:c.*3074A>G (RAF1)	ENSP00000509665.1:n.*3074A>G
ENST00000687505.1:n.1900A>G (RAF1)
ENST00000687923.1:c.1671A>G (RAF1)	ENSP00000510255.1:p.Glu557=
ENST00000688269.1:n.2378A>G (RAF1)
ENST00000688444.1:n.3899A>G (RAF1)
ENST00000688543.1:c.1683A>G (RAF1)	ENSP00000509612.1:p.Glu561=
ENST00000688625.1:c.*3151A>G (RAF1)	ENSP00000509522.1:n.*3151A>G
ENST00000688803.1:n.3210A>G (RAF1)
ENST00000689097.1:c.*1459A>G (RAF1)	ENSP00000509756.1:n.*1459A>G
ENST00000689389.1:c.1605A>G (RAF1)	ENSP00000510213.1:p.Glu535=
ENST00000689418.1:c.*3677A>G (RAF1)	ENSP00000509467.1:n.*3677A>G
ENST00000689540.1:n.4150A>G (RAF1)
ENST00000689876.1:c.*331A>G (RAF1)	ENSP00000508535.1:n.*331A>G
ENST00000689914.1:c.*716A>G (RAF1)	ENSP00000509847.1:n.*716A>G
ENST00000690397.1:c.1671A>G (RAF1)	ENSP00000508730.1:p.Glu557=
ENST00000690460.1:c.1770A>G (RAF1)	ENSP00000509106.1:p.Glu590=
ENST00000690585.1:c.508A>G (RAF1)
ENST00000690625.1:n.2818A>G (RAF1)
ENST00000691396.1:c.*1654A>G (RAF1)	ENSP00000510712.1:n.*1654A>G
ENST00000691643.1:n.2835A>G (RAF1)
ENST00000691724.1:c.*739A>G (RAF1)	ENSP00000509255.1:n.*739A>G
ENST00000691779.1:c.*1360A>G (RAF1)	ENSP00000508592.1:n.*1360A>G
ENST00000691888.1:c.656A>G (RAF1)
ENST00000691899.1:c.1782A>G (RAF1)	ENSP00000508763.1:p.Glu594=
ENST00000692069.1:n.4706A>G (RAF1)
ENST00000692093.1:c.1683A>G (RAF1)	ENSP00000509669.1:p.Glu561=
ENST00000692311.1:n.2606A>G (RAF1)
ENST00000692558.1:n.4365A>G (RAF1)
ENST00000692773.1:c.*1519A>G (RAF1)	ENSP00000509055.1:n.*1519A>G
ENST00000692830.1:c.*1527A>G (RAF1)	ENSP00000509461.1:n.*1527A>G
ENST00000693312.1:c.1557A>G (RAF1)	ENSP00000508686.1:p.Glu519=
ENST00000693664.1:c.*233A>G (RAF1)	ENSP00000509614.1:n.*233A>G
ENST00000693705.1:c.*1161A>G (RAF1)	ENSP00000510697.1:n.*1161A>G
ENST00000251849.9:c.1782A>G (RAF1) MANE Select	ENSP00000251849.4:p.Glu594=
ENST00000442415.7:c.1842A>G (RAF1)	ENSP00000401888.2:p.Glu614=
ENST00000676541.1:c.*2615T>C (MKRN2)	ENSP00000503730.1:n.*2615T>C
ENST00000677142.1:c.*2615T>C (MKRN2)	ENSP00000504455.1:n.*2615T>C
ENST00000677816.1:c.*1170T>C (MKRN2)	ENSP00000502893.1:n.*1170T>C
ENST00000677941.1:n.2678T>C (MKRN2)
ENST00000251849.8:c.1782A>G (RAF1)	ENSP00000251849.4:p.Glu594=
ENST00000423275.5:c.*1459A>G (RAF1)	ENSP00000401088.1:n.*1459A>G
ENST00000432427.2:c.1419A>G (RAF1)	ENSP00000398591.2:p.Glu473=
ENST00000442415.6:c.1842A>G (RAF1)	ENSP00000401888.2:p.Glu614=
ENST00000471449.1:n.471A>G (RAF1)
NM_002880.3:c.1782A>G , LRG_413t1:c.1782A>G (RAF1)	NP_002871.1:p.Glu594=
XM_005265355.1:c.1782A>G (RAF1)	XP_005265412.1:p.Glu594=
XM_005265357.1:c.1683A>G (RAF1)	XP_005265414.1:p.Glu561=
XM_005265358.3:c.1539A>G (RAF1)	XP_005265415.1:p.Glu513=
XM_005265359.3:c.1440A>G (RAF1)	XP_005265416.1:p.Glu480=
XM_011533974.1:c.1782A>G (RAF1)	XP_011532276.1:p.Glu594=
XM_011533975.1:c.1539A>G (RAF1)	XP_011532277.1:p.Glu513=
NM_001354689.1:c.1842A>G (RAF1)	NP_001341618.1:p.Glu614=
NM_001354690.1:c.1782A>G (RAF1)	NP_001341619.1:p.Glu594=
NM_001354691.1:c.1539A>G (RAF1)	NP_001341620.1:p.Glu513=
NM_001354692.1:c.1539A>G (RAF1)	NP_001341621.1:p.Glu513=
NM_001354693.1:c.1683A>G (RAF1)	NP_001341622.1:p.Glu561=
NM_001354694.1:c.1599A>G (RAF1)	NP_001341623.1:p.Glu533=
NM_001354695.1:c.1440A>G (RAF1)	NP_001341624.1:p.Glu480=
NR_148940.1:n.2310A>G (RAF1)
NR_148941.1:n.2256A>G (RAF1)
NR_148942.1:n.2195A>G (RAF1)
XM_011533974.3:c.1782A>G (RAF1)	XP_011532276.1:p.Glu594=
XM_017006966.1:c.1683A>G (RAF1)	XP_016862455.1:p.Glu561=
NM_001354689.3:c.1842A>G (RAF1)	NP_001341618.1:p.Glu614=
NM_001354690.2:c.1782A>G (RAF1)	NP_001341619.1:p.Glu594=
NM_001354691.2:c.1539A>G (RAF1)	NP_001341620.1:p.Glu513=
NM_001354692.2:c.1539A>G (RAF1)	NP_001341621.1:p.Glu513=
NM_001354693.2:c.1683A>G (RAF1)	NP_001341622.1:p.Glu561=
NM_001354694.2:c.1599A>G (RAF1)	NP_001341623.1:p.Glu533=
NM_001354695.2:c.1440A>G (RAF1)	NP_001341624.1:p.Glu480=
NR_148940.2:n.2226A>G (RAF1)
NR_148941.2:n.2172A>G (RAF1)
NR_148942.2:n.2111A>G (RAF1)
NM_001354690.3:c.1782A>G (RAF1)	NP_001341619.1:p.Glu594=
NM_001354691.3:c.1539A>G (RAF1)	NP_001341620.1:p.Glu513=
NM_001354692.3:c.1539A>G (RAF1)	NP_001341621.1:p.Glu513=
NM_001354693.3:c.1683A>G (RAF1)	NP_001341622.1:p.Glu561=
NM_001354694.3:c.1599A>G (RAF1)	NP_001341623.1:p.Glu533=
NM_001354695.3:c.1440A>G (RAF1)	NP_001341624.1:p.Glu480=
NM_002880.4:c.1782A>G (RAF1) MANE Select	NP_002871.1:p.Glu594=
NR_148940.3:n.2226A>G (RAF1)
NR_148941.3:n.2172A>G (RAF1)
NR_148942.3:n.2111A>G (RAF1)