Canonical Allele Identifier: CA1346226123

Gene: RAF1 MKRN2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584547C= , CM000665.2:g.12584547C=	GRCh38
NC_000003.11:g.12626046C= , CM000665.1:g.12626046C=	GRCh37
NC_000003.10:g.12601046C=	NCBI36
NG_007467.1:g.84633G= , LRG_413:g.84633G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000423275.6:c.*1579G= (RAF1)	ENSP00000401088.1:n.*1579G=
ENST00000432427.3:c.1231G= (RAF1)
ENST00000460610.2:n.6226G= (RAF1)
ENST00000471449.2:n.724G= (RAF1)
ENST00000475353.2:n.4194G= (RAF1)
ENST00000684903.1:c.*1591G= (RAF1)	ENSP00000508612.1:n.*1591G=
ENST00000685348.1:c.*1625G= (RAF1)	ENSP00000510285.1:n.*1625G=
ENST00000685437.1:c.1815G= (RAF1)	ENSP00000508794.1:p.Thr605=
ENST00000685653.1:c.1914G= (RAF1)	ENSP00000509968.1:p.Thr638=
ENST00000685697.1:n.2649G= (RAF1)
ENST00000685738.1:c.*878G= (RAF1)	ENSP00000510156.1:n.*878G=
ENST00000686409.1:n.5323G= (RAF1)
ENST00000686455.1:n.4635G= (RAF1)
ENST00000686762.1:c.*473G= (RAF1)	ENSP00000509767.1:n.*473G=
ENST00000687257.1:n.4368G= (RAF1)
ENST00000687326.1:c.*3206G= (RAF1)	ENSP00000509665.1:n.*3206G=
ENST00000687505.1:n.2032G= (RAF1)
ENST00000687923.1:c.1803G= (RAF1)	ENSP00000510255.1:p.Thr601=
ENST00000688269.1:n.2510G= (RAF1)
ENST00000688444.1:n.4031G= (RAF1)
ENST00000688543.1:c.1815G= (RAF1)	ENSP00000509612.1:p.Thr605=
ENST00000688625.1:c.*3283G= (RAF1)	ENSP00000509522.1:n.*3283G=
ENST00000688803.1:n.3342G= (RAF1)
ENST00000689097.1:c.*1591G= (RAF1)	ENSP00000509756.1:n.*1591G=
ENST00000689389.1:c.1737G= (RAF1)	ENSP00000510213.1:p.Thr579=
ENST00000689418.1:c.*3809G= (RAF1)	ENSP00000509467.1:n.*3809G=
ENST00000689540.1:n.4282G= (RAF1)
ENST00000689876.1:c.*463G= (RAF1)	ENSP00000508535.1:n.*463G=
ENST00000689914.1:c.*848G= (RAF1)	ENSP00000509847.1:n.*848G=
ENST00000690397.1:c.1803G= (RAF1)	ENSP00000508730.1:p.Thr601=
ENST00000690460.1:c.1902G= (RAF1)	ENSP00000509106.1:p.Thr634=
ENST00000690585.1:c.640G= (RAF1)
ENST00000690625.1:n.2950G= (RAF1)
ENST00000691396.1:c.*1786G= (RAF1)	ENSP00000510712.1:n.*1786G=
ENST00000691643.1:n.2967G= (RAF1)
ENST00000691724.1:c.*871G= (RAF1)	ENSP00000509255.1:n.*871G=
ENST00000691779.1:c.*1492G= (RAF1)	ENSP00000508592.1:n.*1492G=
ENST00000691888.1:c.788G= (RAF1)
ENST00000691899.1:c.1914G= (RAF1)	ENSP00000508763.1:p.Thr638=
ENST00000692069.1:n.4838G= (RAF1)
ENST00000692093.1:c.1815G= (RAF1)	ENSP00000509669.1:p.Thr605=
ENST00000692311.1:n.2738G= (RAF1)
ENST00000692558.1:n.4497G= (RAF1)
ENST00000692773.1:c.*1651G= (RAF1)	ENSP00000509055.1:n.*1651G=
ENST00000692830.1:c.*1659G= (RAF1)	ENSP00000509461.1:n.*1659G=
ENST00000693312.1:c.1689G= (RAF1)	ENSP00000508686.1:p.Thr563=
ENST00000693664.1:c.*365G= (RAF1)	ENSP00000509614.1:n.*365G=
ENST00000693705.1:c.*1293G= (RAF1)	ENSP00000510697.1:n.*1293G=
ENST00000251849.9:c.1914G= (RAF1) MANE Select	ENSP00000251849.4:p.Thr638=
ENST00000442415.7:c.1974G= (RAF1)	ENSP00000401888.2:p.Thr658=
ENST00000676541.1:c.*2294C= (MKRN2)	ENSP00000503730.1:n.*2294C=
ENST00000677142.1:c.*2294C= (MKRN2)	ENSP00000504455.1:n.*2294C=
ENST00000677816.1:c.*849C= (MKRN2)	ENSP00000502893.1:n.*849C=
ENST00000677941.1:n.2357C= (MKRN2)
ENST00000251849.8:c.1914G= (RAF1)	ENSP00000251849.4:p.Thr638=
ENST00000423275.5:c.*1591G= (RAF1)	ENSP00000401088.1:n.*1591G=
ENST00000432427.2:c.1551G= (RAF1)	ENSP00000398591.2:p.Thr517=
ENST00000442415.6:c.1974G= (RAF1)	ENSP00000401888.2:p.Thr658=
ENST00000471449.1:n.603G= (RAF1)
NM_002880.3:c.1914G= , LRG_413t1:c.1914G= (RAF1)	NP_002871.1:p.Thr638=
XM_005265355.1:c.1914G= (RAF1)	XP_005265412.1:p.Thr638=
XM_005265357.1:c.1815G= (RAF1)	XP_005265414.1:p.Thr605=
XM_005265358.3:c.1671G= (RAF1)	XP_005265415.1:p.Thr557=
XM_005265359.3:c.1572G= (RAF1)	XP_005265416.1:p.Thr524=
XM_011533974.1:c.1914G= (RAF1)	XP_011532276.1:p.Thr638=
XM_011533975.1:c.1671G= (RAF1)	XP_011532277.1:p.Thr557=
NM_001354689.1:c.1974G= (RAF1)	NP_001341618.1:p.Thr658=
NM_001354690.1:c.1914G= (RAF1)	NP_001341619.1:p.Thr638=
NM_001354691.1:c.1671G= (RAF1)	NP_001341620.1:p.Thr557=
NM_001354692.1:c.1671G= (RAF1)	NP_001341621.1:p.Thr557=
NM_001354693.1:c.1815G= (RAF1)	NP_001341622.1:p.Thr605=
NM_001354694.1:c.1731G= (RAF1)	NP_001341623.1:p.Thr577=
NM_001354695.1:c.1572G= (RAF1)	NP_001341624.1:p.Thr524=
NR_148940.1:n.2442G= (RAF1)
NR_148941.1:n.2388G= (RAF1)
NR_148942.1:n.2327G= (RAF1)
XM_011533974.3:c.1914G= (RAF1)	XP_011532276.1:p.Thr638=
XM_017006966.1:c.1815G= (RAF1)	XP_016862455.1:p.Thr605=
NM_001354689.3:c.1974G= (RAF1)	NP_001341618.1:p.Thr658=
NM_001354690.2:c.1914G= (RAF1)	NP_001341619.1:p.Thr638=
NM_001354691.2:c.1671G= (RAF1)	NP_001341620.1:p.Thr557=
NM_001354692.2:c.1671G= (RAF1)	NP_001341621.1:p.Thr557=
NM_001354693.2:c.1815G= (RAF1)	NP_001341622.1:p.Thr605=
NM_001354694.2:c.1731G= (RAF1)	NP_001341623.1:p.Thr577=
NM_001354695.2:c.1572G= (RAF1)	NP_001341624.1:p.Thr524=
NR_148940.2:n.2358G= (RAF1)
NR_148941.2:n.2304G= (RAF1)
NR_148942.2:n.2243G= (RAF1)
NM_001354690.3:c.1914G= (RAF1)	NP_001341619.1:p.Thr638=
NM_001354691.3:c.1671G= (RAF1)	NP_001341620.1:p.Thr557=
NM_001354692.3:c.1671G= (RAF1)	NP_001341621.1:p.Thr557=
NM_001354693.3:c.1815G= (RAF1)	NP_001341622.1:p.Thr605=
NM_001354694.3:c.1731G= (RAF1)	NP_001341623.1:p.Thr577=
NM_001354695.3:c.1572G= (RAF1)	NP_001341624.1:p.Thr524=
NM_002880.4:c.1914G= (RAF1) MANE Select	NP_002871.1:p.Thr638=
NR_148940.3:n.2358G= (RAF1)
NR_148941.3:n.2304G= (RAF1)
NR_148942.3:n.2243G= (RAF1)