Canonical Allele Identifier: CA432522032

Gene: RAF1 MKRN2

Linked Data

• MyVariant Identifiers: chr3:g.12626415G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584916G>T , CM000665.2:g.12584916G>T	GRCh38
NC_000003.11:g.12626415G>T , CM000665.1:g.12626415G>T	GRCh37
NC_000003.10:g.12601415G>T	NCBI36
NG_007467.1:g.84264C>A , LRG_413:g.84264C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1399C>A (RAF1)	ENSP00000401088.1:n.*1399C>A
ENST00000432427.3:c.1051C>A (RAF1)
ENST00000460610.2:n.6046C>A (RAF1)
ENST00000471449.2:n.544C>A (RAF1)
ENST00000475353.2:n.4014C>A (RAF1)
ENST00000684903.1:c.*1411C>A (RAF1)	ENSP00000508612.1:n.*1411C>A
ENST00000685348.1:c.*1445C>A (RAF1)	ENSP00000510285.1:n.*1445C>A
ENST00000685437.1:c.1635C>A (RAF1)	ENSP00000508794.1:p.Pro545=
ENST00000685653.1:c.1734C>A (RAF1)	ENSP00000509968.1:p.Pro578=
ENST00000685697.1:n.2469C>A (RAF1)
ENST00000685738.1:c.*698C>A (RAF1)	ENSP00000510156.1:n.*698C>A
ENST00000686409.1:n.5143C>A (RAF1)
ENST00000686455.1:n.4455C>A (RAF1)
ENST00000686762.1:c.*293C>A (RAF1)	ENSP00000509767.1:n.*293C>A
ENST00000687257.1:n.4188C>A (RAF1)
ENST00000687326.1:c.*3026C>A (RAF1)	ENSP00000509665.1:n.*3026C>A
ENST00000687505.1:n.1852C>A (RAF1)
ENST00000687923.1:c.1623C>A (RAF1)	ENSP00000510255.1:p.Pro541=
ENST00000688269.1:n.2330C>A (RAF1)
ENST00000688444.1:n.3851C>A (RAF1)
ENST00000688543.1:c.1635C>A (RAF1)	ENSP00000509612.1:p.Pro545=
ENST00000688625.1:c.*3103C>A (RAF1)	ENSP00000509522.1:n.*3103C>A
ENST00000688803.1:n.3162C>A (RAF1)
ENST00000688914.1:n.1147C>A (RAF1)
ENST00000689097.1:c.*1411C>A (RAF1)	ENSP00000509756.1:n.*1411C>A
ENST00000689389.1:c.1557C>A (RAF1)	ENSP00000510213.1:p.Pro519=
ENST00000689418.1:c.*3629C>A (RAF1)	ENSP00000509467.1:n.*3629C>A
ENST00000689540.1:n.4102C>A (RAF1)
ENST00000689876.1:c.*283C>A (RAF1)	ENSP00000508535.1:n.*283C>A
ENST00000689914.1:c.*668C>A (RAF1)	ENSP00000509847.1:n.*668C>A
ENST00000690397.1:c.1623C>A (RAF1)	ENSP00000508730.1:p.Pro541=
ENST00000690460.1:c.1722C>A (RAF1)	ENSP00000509106.1:p.Pro574=
ENST00000690585.1:c.460C>A (RAF1)
ENST00000690625.1:n.2770C>A (RAF1)
ENST00000691396.1:c.*1606C>A (RAF1)	ENSP00000510712.1:n.*1606C>A
ENST00000691643.1:n.2787C>A (RAF1)
ENST00000691724.1:c.*691C>A (RAF1)	ENSP00000509255.1:n.*691C>A
ENST00000691779.1:c.*1312C>A (RAF1)	ENSP00000508592.1:n.*1312C>A
ENST00000691888.1:c.608C>A (RAF1)
ENST00000691899.1:c.1734C>A (RAF1)	ENSP00000508763.1:p.Pro578=
ENST00000692069.1:n.4658C>A (RAF1)
ENST00000692093.1:c.1635C>A (RAF1)	ENSP00000509669.1:p.Pro545=
ENST00000692311.1:n.2558C>A (RAF1)
ENST00000692558.1:n.4317C>A (RAF1)
ENST00000692773.1:c.*1471C>A (RAF1)	ENSP00000509055.1:n.*1471C>A
ENST00000692830.1:c.*1479C>A (RAF1)	ENSP00000509461.1:n.*1479C>A
ENST00000693312.1:c.1509C>A (RAF1)	ENSP00000508686.1:p.Pro503=
ENST00000693664.1:c.*185C>A (RAF1)	ENSP00000509614.1:n.*185C>A
ENST00000693705.1:c.*1113C>A (RAF1)	ENSP00000510697.1:n.*1113C>A
ENST00000251849.9:c.1734C>A (RAF1) MANE Select	ENSP00000251849.4:p.Pro578=
ENST00000442415.7:c.1794C>A (RAF1)	ENSP00000401888.2:p.Pro598=
ENST00000676541.1:c.*2663G>T (MKRN2)	ENSP00000503730.1:n.*2663G>T
ENST00000677142.1:c.*2663G>T (MKRN2)	ENSP00000504455.1:n.*2663G>T
ENST00000677816.1:c.*1218G>T (MKRN2)	ENSP00000502893.1:n.*1218G>T
ENST00000677941.1:n.2726G>T (MKRN2)
ENST00000251849.8:c.1734C>A (RAF1)	ENSP00000251849.4:p.Pro578=
ENST00000423275.5:c.*1411C>A (RAF1)	ENSP00000401088.1:n.*1411C>A
ENST00000432427.2:c.1371C>A (RAF1)	ENSP00000398591.2:p.Pro457=
ENST00000442415.6:c.1794C>A (RAF1)	ENSP00000401888.2:p.Pro598=
ENST00000471449.1:n.423C>A (RAF1)
NM_002880.3:c.1734C>A , LRG_413t1:c.1734C>A (RAF1)	NP_002871.1:p.Pro578=
XM_005265355.1:c.1734C>A (RAF1)	XP_005265412.1:p.Pro578=
XM_005265357.1:c.1635C>A (RAF1)	XP_005265414.1:p.Pro545=
XM_005265358.3:c.1491C>A (RAF1)	XP_005265415.1:p.Pro497=
XM_005265359.3:c.1392C>A (RAF1)	XP_005265416.1:p.Pro464=
XM_011533974.1:c.1734C>A (RAF1)	XP_011532276.1:p.Pro578=
XM_011533975.1:c.1491C>A (RAF1)	XP_011532277.1:p.Pro497=
NM_001354689.1:c.1794C>A (RAF1)	NP_001341618.1:p.Pro598=
NM_001354690.1:c.1734C>A (RAF1)	NP_001341619.1:p.Pro578=
NM_001354691.1:c.1491C>A (RAF1)	NP_001341620.1:p.Pro497=
NM_001354692.1:c.1491C>A (RAF1)	NP_001341621.1:p.Pro497=
NM_001354693.1:c.1635C>A (RAF1)	NP_001341622.1:p.Pro545=
NM_001354694.1:c.1551C>A (RAF1)	NP_001341623.1:p.Pro517=
NM_001354695.1:c.1392C>A (RAF1)	NP_001341624.1:p.Pro464=
NR_148940.1:n.2262C>A (RAF1)
NR_148941.1:n.2208C>A (RAF1)
NR_148942.1:n.2147C>A (RAF1)
XM_011533974.3:c.1734C>A (RAF1)	XP_011532276.1:p.Pro578=
XM_017006966.1:c.1635C>A (RAF1)	XP_016862455.1:p.Pro545=
NM_001354689.3:c.1794C>A (RAF1)	NP_001341618.1:p.Pro598=
NM_001354690.2:c.1734C>A (RAF1)	NP_001341619.1:p.Pro578=
NM_001354691.2:c.1491C>A (RAF1)	NP_001341620.1:p.Pro497=
NM_001354692.2:c.1491C>A (RAF1)	NP_001341621.1:p.Pro497=
NM_001354693.2:c.1635C>A (RAF1)	NP_001341622.1:p.Pro545=
NM_001354694.2:c.1551C>A (RAF1)	NP_001341623.1:p.Pro517=
NM_001354695.2:c.1392C>A (RAF1)	NP_001341624.1:p.Pro464=
NR_148940.2:n.2178C>A (RAF1)
NR_148941.2:n.2124C>A (RAF1)
NR_148942.2:n.2063C>A (RAF1)
NM_001354690.3:c.1734C>A (RAF1)	NP_001341619.1:p.Pro578=
NM_001354691.3:c.1491C>A (RAF1)	NP_001341620.1:p.Pro497=
NM_001354692.3:c.1491C>A (RAF1)	NP_001341621.1:p.Pro497=
NM_001354693.3:c.1635C>A (RAF1)	NP_001341622.1:p.Pro545=
NM_001354694.3:c.1551C>A (RAF1)	NP_001341623.1:p.Pro517=
NM_001354695.3:c.1392C>A (RAF1)	NP_001341624.1:p.Pro464=
NM_002880.4:c.1734C>A (RAF1) MANE Select	NP_002871.1:p.Pro578=
NR_148940.3:n.2178C>A (RAF1)
NR_148941.3:n.2124C>A (RAF1)
NR_148942.3:n.2063C>A (RAF1)