Canonical Allele Identifier: CA351496940

Gene: RAF1 MKRN2

Linked Data

• MyVariant Identifiers: chr3:g.12626454A>T (hg19) ; chr3:g.12584955A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584955A>T , CM000665.2:g.12584955A>T	GRCh38
NC_000003.11:g.12626454A>T , CM000665.1:g.12626454A>T	GRCh37
NC_000003.10:g.12601454A>T	NCBI36
NG_007467.1:g.84225T>A , LRG_413:g.84225T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1360T>A (RAF1)	ENSP00000401088.1:n.*1360T>A
ENST00000432427.3:c.1012T>A (RAF1)
ENST00000460610.2:n.6007T>A (RAF1)
ENST00000471449.2:n.505T>A (RAF1)
ENST00000475353.2:n.3975T>A (RAF1)
ENST00000684903.1:c.*1372T>A (RAF1)	ENSP00000508612.1:n.*1372T>A
ENST00000685348.1:c.*1406T>A (RAF1)	ENSP00000510285.1:n.*1406T>A
ENST00000685437.1:c.1596T>A (RAF1)	ENSP00000508794.1:p.Tyr532Ter
ENST00000685653.1:c.1695T>A (RAF1)	ENSP00000509968.1:p.Tyr565Ter
ENST00000685697.1:n.2430T>A (RAF1)
ENST00000685738.1:c.*659T>A (RAF1)	ENSP00000510156.1:n.*659T>A
ENST00000686409.1:n.5104T>A (RAF1)
ENST00000686455.1:n.4416T>A (RAF1)
ENST00000686762.1:c.*254T>A (RAF1)	ENSP00000509767.1:n.*254T>A
ENST00000687257.1:n.4149T>A (RAF1)
ENST00000687326.1:c.*2987T>A (RAF1)	ENSP00000509665.1:n.*2987T>A
ENST00000687505.1:n.1813T>A (RAF1)
ENST00000687923.1:c.1584T>A (RAF1)	ENSP00000510255.1:p.Tyr528Ter
ENST00000688269.1:n.2291T>A (RAF1)
ENST00000688444.1:n.3812T>A (RAF1)
ENST00000688543.1:c.1596T>A (RAF1)	ENSP00000509612.1:p.Tyr532Ter
ENST00000688625.1:c.*3064T>A (RAF1)	ENSP00000509522.1:n.*3064T>A
ENST00000688803.1:n.3123T>A (RAF1)
ENST00000688914.1:n.1108T>A (RAF1)
ENST00000689097.1:c.*1372T>A (RAF1)	ENSP00000509756.1:n.*1372T>A
ENST00000689389.1:c.1518T>A (RAF1)	ENSP00000510213.1:p.Tyr506Ter
ENST00000689418.1:c.*3590T>A (RAF1)	ENSP00000509467.1:n.*3590T>A
ENST00000689540.1:n.4063T>A (RAF1)
ENST00000689876.1:c.*244T>A (RAF1)	ENSP00000508535.1:n.*244T>A
ENST00000689914.1:c.*629T>A (RAF1)	ENSP00000509847.1:n.*629T>A
ENST00000690397.1:c.1584T>A (RAF1)	ENSP00000508730.1:p.Tyr528Ter
ENST00000690460.1:c.1683T>A (RAF1)	ENSP00000509106.1:p.Tyr561Ter
ENST00000690585.1:c.421T>A (RAF1)
ENST00000690625.1:n.2731T>A (RAF1)
ENST00000691396.1:c.*1567T>A (RAF1)	ENSP00000510712.1:n.*1567T>A
ENST00000691643.1:n.2748T>A (RAF1)
ENST00000691724.1:c.*652T>A (RAF1)	ENSP00000509255.1:n.*652T>A
ENST00000691779.1:c.*1273T>A (RAF1)	ENSP00000508592.1:n.*1273T>A
ENST00000691888.1:c.569T>A (RAF1)
ENST00000691899.1:c.1695T>A (RAF1)	ENSP00000508763.1:p.Tyr565Ter
ENST00000692069.1:n.4619T>A (RAF1)
ENST00000692093.1:c.1596T>A (RAF1)	ENSP00000509669.1:p.Tyr532Ter
ENST00000692311.1:n.2519T>A (RAF1)
ENST00000692558.1:n.4278T>A (RAF1)
ENST00000692773.1:c.*1432T>A (RAF1)	ENSP00000509055.1:n.*1432T>A
ENST00000692830.1:c.*1440T>A (RAF1)	ENSP00000509461.1:n.*1440T>A
ENST00000693312.1:c.1470T>A (RAF1)	ENSP00000508686.1:p.Tyr490Ter
ENST00000693664.1:c.*146T>A (RAF1)	ENSP00000509614.1:n.*146T>A
ENST00000693705.1:c.*1074T>A (RAF1)	ENSP00000510697.1:n.*1074T>A
ENST00000251849.9:c.1695T>A (RAF1) MANE Select	ENSP00000251849.4:p.Tyr565Ter
ENST00000442415.7:c.1755T>A (RAF1)	ENSP00000401888.2:p.Tyr585Ter
ENST00000676541.1:c.*2702A>T (MKRN2)	ENSP00000503730.1:n.*2702A>T
ENST00000677142.1:c.*2702A>T (MKRN2)	ENSP00000504455.1:n.*2702A>T
ENST00000677816.1:c.*1257A>T (MKRN2)	ENSP00000502893.1:n.*1257A>T
ENST00000677941.1:n.2765A>T (MKRN2)
ENST00000251849.8:c.1695T>A (RAF1)	ENSP00000251849.4:p.Tyr565Ter
ENST00000423275.5:c.*1372T>A (RAF1)	ENSP00000401088.1:n.*1372T>A
ENST00000432427.2:c.1332T>A (RAF1)	ENSP00000398591.2:p.Tyr444Ter
ENST00000442415.6:c.1755T>A (RAF1)	ENSP00000401888.2:p.Tyr585Ter
ENST00000471449.1:n.384T>A (RAF1)
NM_002880.3:c.1695T>A , LRG_413t1:c.1695T>A (RAF1)	NP_002871.1:p.Tyr565Ter
XM_005265355.1:c.1695T>A (RAF1)	XP_005265412.1:p.Tyr565Ter
XM_005265357.1:c.1596T>A (RAF1)	XP_005265414.1:p.Tyr532Ter
XM_005265358.3:c.1452T>A (RAF1)	XP_005265415.1:p.Tyr484Ter
XM_005265359.3:c.1353T>A (RAF1)	XP_005265416.1:p.Tyr451Ter
XM_011533974.1:c.1695T>A (RAF1)	XP_011532276.1:p.Tyr565Ter
XM_011533975.1:c.1452T>A (RAF1)	XP_011532277.1:p.Tyr484Ter
NM_001354689.1:c.1755T>A (RAF1)	NP_001341618.1:p.Tyr585Ter
NM_001354690.1:c.1695T>A (RAF1)	NP_001341619.1:p.Tyr565Ter
NM_001354691.1:c.1452T>A (RAF1)	NP_001341620.1:p.Tyr484Ter
NM_001354692.1:c.1452T>A (RAF1)	NP_001341621.1:p.Tyr484Ter
NM_001354693.1:c.1596T>A (RAF1)	NP_001341622.1:p.Tyr532Ter
NM_001354694.1:c.1512T>A (RAF1)	NP_001341623.1:p.Tyr504Ter
NM_001354695.1:c.1353T>A (RAF1)	NP_001341624.1:p.Tyr451Ter
NR_148940.1:n.2223T>A (RAF1)
NR_148941.1:n.2169T>A (RAF1)
NR_148942.1:n.2108T>A (RAF1)
XM_011533974.3:c.1695T>A (RAF1)	XP_011532276.1:p.Tyr565Ter
XM_017006966.1:c.1596T>A (RAF1)	XP_016862455.1:p.Tyr532Ter
NM_001354689.3:c.1755T>A (RAF1)	NP_001341618.1:p.Tyr585Ter
NM_001354690.2:c.1695T>A (RAF1)	NP_001341619.1:p.Tyr565Ter
NM_001354691.2:c.1452T>A (RAF1)	NP_001341620.1:p.Tyr484Ter
NM_001354692.2:c.1452T>A (RAF1)	NP_001341621.1:p.Tyr484Ter
NM_001354693.2:c.1596T>A (RAF1)	NP_001341622.1:p.Tyr532Ter
NM_001354694.2:c.1512T>A (RAF1)	NP_001341623.1:p.Tyr504Ter
NM_001354695.2:c.1353T>A (RAF1)	NP_001341624.1:p.Tyr451Ter
NR_148940.2:n.2139T>A (RAF1)
NR_148941.2:n.2085T>A (RAF1)
NR_148942.2:n.2024T>A (RAF1)
NM_001354690.3:c.1695T>A (RAF1)	NP_001341619.1:p.Tyr565Ter
NM_001354691.3:c.1452T>A (RAF1)	NP_001341620.1:p.Tyr484Ter
NM_001354692.3:c.1452T>A (RAF1)	NP_001341621.1:p.Tyr484Ter
NM_001354693.3:c.1596T>A (RAF1)	NP_001341622.1:p.Tyr532Ter
NM_001354694.3:c.1512T>A (RAF1)	NP_001341623.1:p.Tyr504Ter
NM_001354695.3:c.1353T>A (RAF1)	NP_001341624.1:p.Tyr451Ter
NM_002880.4:c.1695T>A (RAF1) MANE Select	NP_002871.1:p.Tyr565Ter
NR_148940.3:n.2139T>A (RAF1)
NR_148941.3:n.2085T>A (RAF1)
NR_148942.3:n.2024T>A (RAF1)