Canonical Allele Identifier: CA351496417

Gene: RAF1 MKRN2

Linked Data

• MyVariant Identifiers: chr3:g.12626353A>T (hg19) ; chr3:g.12584854A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584854A>T , CM000665.2:g.12584854A>T	GRCh38
NC_000003.11:g.12626353A>T , CM000665.1:g.12626353A>T	GRCh37
NC_000003.10:g.12601353A>T	NCBI36
NG_007467.1:g.84326T>A , LRG_413:g.84326T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1461T>A (RAF1)	ENSP00000401088.1:n.*1461T>A
ENST00000432427.3:c.1113T>A (RAF1)
ENST00000460610.2:n.6108T>A (RAF1)
ENST00000471449.2:n.606T>A (RAF1)
ENST00000475353.2:n.4076T>A (RAF1)
ENST00000684903.1:c.*1473T>A (RAF1)	ENSP00000508612.1:n.*1473T>A
ENST00000685348.1:c.*1507T>A (RAF1)	ENSP00000510285.1:n.*1507T>A
ENST00000685437.1:c.1697T>A (RAF1)	ENSP00000508794.1:p.Phe566Tyr
ENST00000685653.1:c.1796T>A (RAF1)	ENSP00000509968.1:p.Phe599Tyr
ENST00000685697.1:n.2531T>A (RAF1)
ENST00000685738.1:c.*760T>A (RAF1)	ENSP00000510156.1:n.*760T>A
ENST00000686409.1:n.5205T>A (RAF1)
ENST00000686455.1:n.4517T>A (RAF1)
ENST00000686762.1:c.*355T>A (RAF1)	ENSP00000509767.1:n.*355T>A
ENST00000687257.1:n.4250T>A (RAF1)
ENST00000687326.1:c.*3088T>A (RAF1)	ENSP00000509665.1:n.*3088T>A
ENST00000687505.1:n.1914T>A (RAF1)
ENST00000687923.1:c.1685T>A (RAF1)	ENSP00000510255.1:p.Phe562Tyr
ENST00000688269.1:n.2392T>A (RAF1)
ENST00000688444.1:n.3913T>A (RAF1)
ENST00000688543.1:c.1697T>A (RAF1)	ENSP00000509612.1:p.Phe566Tyr
ENST00000688625.1:c.*3165T>A (RAF1)	ENSP00000509522.1:n.*3165T>A
ENST00000688803.1:n.3224T>A (RAF1)
ENST00000689097.1:c.*1473T>A (RAF1)	ENSP00000509756.1:n.*1473T>A
ENST00000689389.1:c.1619T>A (RAF1)	ENSP00000510213.1:p.Phe540Tyr
ENST00000689418.1:c.*3691T>A (RAF1)	ENSP00000509467.1:n.*3691T>A
ENST00000689540.1:n.4164T>A (RAF1)
ENST00000689876.1:c.*345T>A (RAF1)	ENSP00000508535.1:n.*345T>A
ENST00000689914.1:c.*730T>A (RAF1)	ENSP00000509847.1:n.*730T>A
ENST00000690397.1:c.1685T>A (RAF1)	ENSP00000508730.1:p.Phe562Tyr
ENST00000690460.1:c.1784T>A (RAF1)	ENSP00000509106.1:p.Phe595Tyr
ENST00000690585.1:c.522T>A (RAF1)
ENST00000690625.1:n.2832T>A (RAF1)
ENST00000691396.1:c.*1668T>A (RAF1)	ENSP00000510712.1:n.*1668T>A
ENST00000691643.1:n.2849T>A (RAF1)
ENST00000691724.1:c.*753T>A (RAF1)	ENSP00000509255.1:n.*753T>A
ENST00000691779.1:c.*1374T>A (RAF1)	ENSP00000508592.1:n.*1374T>A
ENST00000691888.1:c.670T>A (RAF1)
ENST00000691899.1:c.1796T>A (RAF1)	ENSP00000508763.1:p.Phe599Tyr
ENST00000692069.1:n.4720T>A (RAF1)
ENST00000692093.1:c.1697T>A (RAF1)	ENSP00000509669.1:p.Phe566Tyr
ENST00000692311.1:n.2620T>A (RAF1)
ENST00000692558.1:n.4379T>A (RAF1)
ENST00000692773.1:c.*1533T>A (RAF1)	ENSP00000509055.1:n.*1533T>A
ENST00000692830.1:c.*1541T>A (RAF1)	ENSP00000509461.1:n.*1541T>A
ENST00000693312.1:c.1571T>A (RAF1)	ENSP00000508686.1:p.Phe524Tyr
ENST00000693664.1:c.*247T>A (RAF1)	ENSP00000509614.1:n.*247T>A
ENST00000693705.1:c.*1175T>A (RAF1)	ENSP00000510697.1:n.*1175T>A
ENST00000251849.9:c.1796T>A (RAF1) MANE Select	ENSP00000251849.4:p.Phe599Tyr
ENST00000442415.7:c.1856T>A (RAF1)	ENSP00000401888.2:p.Phe619Tyr
ENST00000676541.1:c.*2601A>T (MKRN2)	ENSP00000503730.1:n.*2601A>T
ENST00000677142.1:c.*2601A>T (MKRN2)	ENSP00000504455.1:n.*2601A>T
ENST00000677816.1:c.*1156A>T (MKRN2)	ENSP00000502893.1:n.*1156A>T
ENST00000677941.1:n.2664A>T (MKRN2)
ENST00000251849.8:c.1796T>A (RAF1)	ENSP00000251849.4:p.Phe599Tyr
ENST00000423275.5:c.*1473T>A (RAF1)	ENSP00000401088.1:n.*1473T>A
ENST00000432427.2:c.1433T>A (RAF1)	ENSP00000398591.2:p.Phe478Tyr
ENST00000442415.6:c.1856T>A (RAF1)	ENSP00000401888.2:p.Phe619Tyr
ENST00000471449.1:n.485T>A (RAF1)
NM_002880.3:c.1796T>A , LRG_413t1:c.1796T>A (RAF1)	NP_002871.1:p.Phe599Tyr
XM_005265355.1:c.1796T>A (RAF1)	XP_005265412.1:p.Phe599Tyr
XM_005265357.1:c.1697T>A (RAF1)	XP_005265414.1:p.Phe566Tyr
XM_005265358.3:c.1553T>A (RAF1)	XP_005265415.1:p.Phe518Tyr
XM_005265359.3:c.1454T>A (RAF1)	XP_005265416.1:p.Phe485Tyr
XM_011533974.1:c.1796T>A (RAF1)	XP_011532276.1:p.Phe599Tyr
XM_011533975.1:c.1553T>A (RAF1)	XP_011532277.1:p.Phe518Tyr
NM_001354689.1:c.1856T>A (RAF1)	NP_001341618.1:p.Phe619Tyr
NM_001354690.1:c.1796T>A (RAF1)	NP_001341619.1:p.Phe599Tyr
NM_001354691.1:c.1553T>A (RAF1)	NP_001341620.1:p.Phe518Tyr
NM_001354692.1:c.1553T>A (RAF1)	NP_001341621.1:p.Phe518Tyr
NM_001354693.1:c.1697T>A (RAF1)	NP_001341622.1:p.Phe566Tyr
NM_001354694.1:c.1613T>A (RAF1)	NP_001341623.1:p.Phe538Tyr
NM_001354695.1:c.1454T>A (RAF1)	NP_001341624.1:p.Phe485Tyr
NR_148940.1:n.2324T>A (RAF1)
NR_148941.1:n.2270T>A (RAF1)
NR_148942.1:n.2209T>A (RAF1)
XM_011533974.3:c.1796T>A (RAF1)	XP_011532276.1:p.Phe599Tyr
XM_017006966.1:c.1697T>A (RAF1)	XP_016862455.1:p.Phe566Tyr
NM_001354689.3:c.1856T>A (RAF1)	NP_001341618.1:p.Phe619Tyr
NM_001354690.2:c.1796T>A (RAF1)	NP_001341619.1:p.Phe599Tyr
NM_001354691.2:c.1553T>A (RAF1)	NP_001341620.1:p.Phe518Tyr
NM_001354692.2:c.1553T>A (RAF1)	NP_001341621.1:p.Phe518Tyr
NM_001354693.2:c.1697T>A (RAF1)	NP_001341622.1:p.Phe566Tyr
NM_001354694.2:c.1613T>A (RAF1)	NP_001341623.1:p.Phe538Tyr
NM_001354695.2:c.1454T>A (RAF1)	NP_001341624.1:p.Phe485Tyr
NR_148940.2:n.2240T>A (RAF1)
NR_148941.2:n.2186T>A (RAF1)
NR_148942.2:n.2125T>A (RAF1)
NM_001354690.3:c.1796T>A (RAF1)	NP_001341619.1:p.Phe599Tyr
NM_001354691.3:c.1553T>A (RAF1)	NP_001341620.1:p.Phe518Tyr
NM_001354692.3:c.1553T>A (RAF1)	NP_001341621.1:p.Phe518Tyr
NM_001354693.3:c.1697T>A (RAF1)	NP_001341622.1:p.Phe566Tyr
NM_001354694.3:c.1613T>A (RAF1)	NP_001341623.1:p.Phe538Tyr
NM_001354695.3:c.1454T>A (RAF1)	NP_001341624.1:p.Phe485Tyr
NM_002880.4:c.1796T>A (RAF1) MANE Select	NP_002871.1:p.Phe599Tyr
NR_148940.3:n.2240T>A (RAF1)
NR_148941.3:n.2186T>A (RAF1)
NR_148942.3:n.2125T>A (RAF1)