Canonical Allele Identifier: CA351496707

Gene: RAF1 MKRN2

Linked Data

• MyVariant Identifiers: chr3:g.12626405T>A (hg19) ; chr3:g.12584906T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584906T>A , CM000665.2:g.12584906T>A	GRCh38
NC_000003.11:g.12626405T>A , CM000665.1:g.12626405T>A	GRCh37
NC_000003.10:g.12601405T>A	NCBI36
NG_007467.1:g.84274A>T , LRG_413:g.84274A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1409A>T (RAF1)	ENSP00000401088.1:n.*1409A>T
ENST00000432427.3:c.1061A>T (RAF1)
ENST00000460610.2:n.6056A>T (RAF1)
ENST00000471449.2:n.554A>T (RAF1)
ENST00000475353.2:n.4024A>T (RAF1)
ENST00000684903.1:c.*1421A>T (RAF1)	ENSP00000508612.1:n.*1421A>T
ENST00000685348.1:c.*1455A>T (RAF1)	ENSP00000510285.1:n.*1455A>T
ENST00000685437.1:c.1645A>T (RAF1)	ENSP00000508794.1:p.Lys549Ter
ENST00000685653.1:c.1744A>T (RAF1)	ENSP00000509968.1:p.Lys582Ter
ENST00000685697.1:n.2479A>T (RAF1)
ENST00000685738.1:c.*708A>T (RAF1)	ENSP00000510156.1:n.*708A>T
ENST00000686409.1:n.5153A>T (RAF1)
ENST00000686455.1:n.4465A>T (RAF1)
ENST00000686762.1:c.*303A>T (RAF1)	ENSP00000509767.1:n.*303A>T
ENST00000687257.1:n.4198A>T (RAF1)
ENST00000687326.1:c.*3036A>T (RAF1)	ENSP00000509665.1:n.*3036A>T
ENST00000687505.1:n.1862A>T (RAF1)
ENST00000687923.1:c.1633A>T (RAF1)	ENSP00000510255.1:p.Lys545Ter
ENST00000688269.1:n.2340A>T (RAF1)
ENST00000688444.1:n.3861A>T (RAF1)
ENST00000688543.1:c.1645A>T (RAF1)	ENSP00000509612.1:p.Lys549Ter
ENST00000688625.1:c.*3113A>T (RAF1)	ENSP00000509522.1:n.*3113A>T
ENST00000688803.1:n.3172A>T (RAF1)
ENST00000688914.1:n.1157A>T (RAF1)
ENST00000689097.1:c.*1421A>T (RAF1)	ENSP00000509756.1:n.*1421A>T
ENST00000689389.1:c.1567A>T (RAF1)	ENSP00000510213.1:p.Lys523Ter
ENST00000689418.1:c.*3639A>T (RAF1)	ENSP00000509467.1:n.*3639A>T
ENST00000689540.1:n.4112A>T (RAF1)
ENST00000689876.1:c.*293A>T (RAF1)	ENSP00000508535.1:n.*293A>T
ENST00000689914.1:c.*678A>T (RAF1)	ENSP00000509847.1:n.*678A>T
ENST00000690397.1:c.1633A>T (RAF1)	ENSP00000508730.1:p.Lys545Ter
ENST00000690460.1:c.1732A>T (RAF1)	ENSP00000509106.1:p.Lys578Ter
ENST00000690585.1:c.470A>T (RAF1)
ENST00000690625.1:n.2780A>T (RAF1)
ENST00000691396.1:c.*1616A>T (RAF1)	ENSP00000510712.1:n.*1616A>T
ENST00000691643.1:n.2797A>T (RAF1)
ENST00000691724.1:c.*701A>T (RAF1)	ENSP00000509255.1:n.*701A>T
ENST00000691779.1:c.*1322A>T (RAF1)	ENSP00000508592.1:n.*1322A>T
ENST00000691888.1:c.618A>T (RAF1)
ENST00000691899.1:c.1744A>T (RAF1)	ENSP00000508763.1:p.Lys582Ter
ENST00000692069.1:n.4668A>T (RAF1)
ENST00000692093.1:c.1645A>T (RAF1)	ENSP00000509669.1:p.Lys549Ter
ENST00000692311.1:n.2568A>T (RAF1)
ENST00000692558.1:n.4327A>T (RAF1)
ENST00000692773.1:c.*1481A>T (RAF1)	ENSP00000509055.1:n.*1481A>T
ENST00000692830.1:c.*1489A>T (RAF1)	ENSP00000509461.1:n.*1489A>T
ENST00000693312.1:c.1519A>T (RAF1)	ENSP00000508686.1:p.Lys507Ter
ENST00000693664.1:c.*195A>T (RAF1)	ENSP00000509614.1:n.*195A>T
ENST00000693705.1:c.*1123A>T (RAF1)	ENSP00000510697.1:n.*1123A>T
ENST00000251849.9:c.1744A>T (RAF1) MANE Select	ENSP00000251849.4:p.Lys582Ter
ENST00000442415.7:c.1804A>T (RAF1)	ENSP00000401888.2:p.Lys602Ter
ENST00000676541.1:c.*2653T>A (MKRN2)	ENSP00000503730.1:n.*2653T>A
ENST00000677142.1:c.*2653T>A (MKRN2)	ENSP00000504455.1:n.*2653T>A
ENST00000677816.1:c.*1208T>A (MKRN2)	ENSP00000502893.1:n.*1208T>A
ENST00000677941.1:n.2716T>A (MKRN2)
ENST00000251849.8:c.1744A>T (RAF1)	ENSP00000251849.4:p.Lys582Ter
ENST00000423275.5:c.*1421A>T (RAF1)	ENSP00000401088.1:n.*1421A>T
ENST00000432427.2:c.1381A>T (RAF1)	ENSP00000398591.2:p.Lys461Ter
ENST00000442415.6:c.1804A>T (RAF1)	ENSP00000401888.2:p.Lys602Ter
ENST00000471449.1:n.433A>T (RAF1)
NM_002880.3:c.1744A>T , LRG_413t1:c.1744A>T (RAF1)	NP_002871.1:p.Lys582Ter
XM_005265355.1:c.1744A>T (RAF1)	XP_005265412.1:p.Lys582Ter
XM_005265357.1:c.1645A>T (RAF1)	XP_005265414.1:p.Lys549Ter
XM_005265358.3:c.1501A>T (RAF1)	XP_005265415.1:p.Lys501Ter
XM_005265359.3:c.1402A>T (RAF1)	XP_005265416.1:p.Lys468Ter
XM_011533974.1:c.1744A>T (RAF1)	XP_011532276.1:p.Lys582Ter
XM_011533975.1:c.1501A>T (RAF1)	XP_011532277.1:p.Lys501Ter
NM_001354689.1:c.1804A>T (RAF1)	NP_001341618.1:p.Lys602Ter
NM_001354690.1:c.1744A>T (RAF1)	NP_001341619.1:p.Lys582Ter
NM_001354691.1:c.1501A>T (RAF1)	NP_001341620.1:p.Lys501Ter
NM_001354692.1:c.1501A>T (RAF1)	NP_001341621.1:p.Lys501Ter
NM_001354693.1:c.1645A>T (RAF1)	NP_001341622.1:p.Lys549Ter
NM_001354694.1:c.1561A>T (RAF1)	NP_001341623.1:p.Lys521Ter
NM_001354695.1:c.1402A>T (RAF1)	NP_001341624.1:p.Lys468Ter
NR_148940.1:n.2272A>T (RAF1)
NR_148941.1:n.2218A>T (RAF1)
NR_148942.1:n.2157A>T (RAF1)
XM_011533974.3:c.1744A>T (RAF1)	XP_011532276.1:p.Lys582Ter
XM_017006966.1:c.1645A>T (RAF1)	XP_016862455.1:p.Lys549Ter
NM_001354689.3:c.1804A>T (RAF1)	NP_001341618.1:p.Lys602Ter
NM_001354690.2:c.1744A>T (RAF1)	NP_001341619.1:p.Lys582Ter
NM_001354691.2:c.1501A>T (RAF1)	NP_001341620.1:p.Lys501Ter
NM_001354692.2:c.1501A>T (RAF1)	NP_001341621.1:p.Lys501Ter
NM_001354693.2:c.1645A>T (RAF1)	NP_001341622.1:p.Lys549Ter
NM_001354694.2:c.1561A>T (RAF1)	NP_001341623.1:p.Lys521Ter
NM_001354695.2:c.1402A>T (RAF1)	NP_001341624.1:p.Lys468Ter
NR_148940.2:n.2188A>T (RAF1)
NR_148941.2:n.2134A>T (RAF1)
NR_148942.2:n.2073A>T (RAF1)
NM_001354690.3:c.1744A>T (RAF1)	NP_001341619.1:p.Lys582Ter
NM_001354691.3:c.1501A>T (RAF1)	NP_001341620.1:p.Lys501Ter
NM_001354692.3:c.1501A>T (RAF1)	NP_001341621.1:p.Lys501Ter
NM_001354693.3:c.1645A>T (RAF1)	NP_001341622.1:p.Lys549Ter
NM_001354694.3:c.1561A>T (RAF1)	NP_001341623.1:p.Lys521Ter
NM_001354695.3:c.1402A>T (RAF1)	NP_001341624.1:p.Lys468Ter
NM_002880.4:c.1744A>T (RAF1) MANE Select	NP_002871.1:p.Lys582Ter
NR_148940.3:n.2188A>T (RAF1)
NR_148941.3:n.2134A>T (RAF1)
NR_148942.3:n.2073A>T (RAF1)