Canonical Allele Identifier: CA351497111

Gene: RAF1 MKRN2

Linked Data

• MyVariant Identifiers: chr3:g.12626480T>C (hg19) ; chr3:g.12584981T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584981T>C , CM000665.2:g.12584981T>C	GRCh38
NC_000003.11:g.12626480T>C , CM000665.1:g.12626480T>C	GRCh37
NC_000003.10:g.12601480T>C	NCBI36
NG_007467.1:g.84199A>G , LRG_413:g.84199A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1334A>G (RAF1)	ENSP00000401088.1:n.*1334A>G
ENST00000432427.3:c.986A>G (RAF1)
ENST00000460610.2:n.5981A>G (RAF1)
ENST00000471449.2:n.479A>G (RAF1)
ENST00000475353.2:n.3949A>G (RAF1)
ENST00000684903.1:c.*1346A>G (RAF1)	ENSP00000508612.1:n.*1346A>G
ENST00000685348.1:c.*1380A>G (RAF1)	ENSP00000510285.1:n.*1380A>G
ENST00000685437.1:c.1570A>G (RAF1)	ENSP00000508794.1:p.Ile524Val
ENST00000685653.1:c.1669A>G (RAF1)	ENSP00000509968.1:p.Ile557Val
ENST00000685697.1:n.2404A>G (RAF1)
ENST00000685738.1:c.*633A>G (RAF1)	ENSP00000510156.1:n.*633A>G
ENST00000686409.1:n.5078A>G (RAF1)
ENST00000686455.1:n.4390A>G (RAF1)
ENST00000686762.1:c.*228A>G (RAF1)	ENSP00000509767.1:n.*228A>G
ENST00000687257.1:n.4123A>G (RAF1)
ENST00000687326.1:c.*2961A>G (RAF1)	ENSP00000509665.1:n.*2961A>G
ENST00000687505.1:n.1787A>G (RAF1)
ENST00000687923.1:c.1558A>G (RAF1)	ENSP00000510255.1:p.Ile520Val
ENST00000688269.1:n.2265A>G (RAF1)
ENST00000688444.1:n.3786A>G (RAF1)
ENST00000688543.1:c.1570A>G (RAF1)	ENSP00000509612.1:p.Ile524Val
ENST00000688625.1:c.*3038A>G (RAF1)	ENSP00000509522.1:n.*3038A>G
ENST00000688803.1:n.3097A>G (RAF1)
ENST00000688914.1:n.1082A>G (RAF1)
ENST00000689097.1:c.*1346A>G (RAF1)	ENSP00000509756.1:n.*1346A>G
ENST00000689389.1:c.1492A>G (RAF1)	ENSP00000510213.1:p.Ile498Val
ENST00000689418.1:c.*3564A>G (RAF1)	ENSP00000509467.1:n.*3564A>G
ENST00000689540.1:n.4037A>G (RAF1)
ENST00000689876.1:c.*218A>G (RAF1)	ENSP00000508535.1:n.*218A>G
ENST00000689914.1:c.*603A>G (RAF1)	ENSP00000509847.1:n.*603A>G
ENST00000690397.1:c.1558A>G (RAF1)	ENSP00000508730.1:p.Ile520Val
ENST00000690460.1:c.1657A>G (RAF1)	ENSP00000509106.1:p.Ile553Val
ENST00000690585.1:c.395A>G (RAF1)
ENST00000690625.1:n.2705A>G (RAF1)
ENST00000691396.1:c.*1541A>G (RAF1)	ENSP00000510712.1:n.*1541A>G
ENST00000691643.1:n.2722A>G (RAF1)
ENST00000691724.1:c.*626A>G (RAF1)	ENSP00000509255.1:n.*626A>G
ENST00000691779.1:c.*1247A>G (RAF1)	ENSP00000508592.1:n.*1247A>G
ENST00000691888.1:c.543A>G (RAF1)
ENST00000691899.1:c.1669A>G (RAF1)	ENSP00000508763.1:p.Ile557Val
ENST00000692069.1:n.4593A>G (RAF1)
ENST00000692093.1:c.1570A>G (RAF1)	ENSP00000509669.1:p.Ile524Val
ENST00000692311.1:n.2493A>G (RAF1)
ENST00000692558.1:n.4252A>G (RAF1)
ENST00000692773.1:c.*1406A>G (RAF1)	ENSP00000509055.1:n.*1406A>G
ENST00000692830.1:c.*1414A>G (RAF1)	ENSP00000509461.1:n.*1414A>G
ENST00000693312.1:c.1444A>G (RAF1)	ENSP00000508686.1:p.Ile482Val
ENST00000693664.1:c.*120A>G (RAF1)	ENSP00000509614.1:n.*120A>G
ENST00000693705.1:c.*1048A>G (RAF1)	ENSP00000510697.1:n.*1048A>G
ENST00000251849.9:c.1669A>G (RAF1) MANE Select	ENSP00000251849.4:p.Ile557Val
ENST00000442415.7:c.1729A>G (RAF1)	ENSP00000401888.2:p.Ile577Val
ENST00000676541.1:c.*2728T>C (MKRN2)	ENSP00000503730.1:n.*2728T>C
ENST00000677142.1:c.*2728T>C (MKRN2)	ENSP00000504455.1:n.*2728T>C
ENST00000677816.1:c.*1283T>C (MKRN2)	ENSP00000502893.1:n.*1283T>C
ENST00000677941.1:n.2791T>C (MKRN2)
ENST00000251849.8:c.1669A>G (RAF1)	ENSP00000251849.4:p.Ile557Val
ENST00000423275.5:c.*1346A>G (RAF1)	ENSP00000401088.1:n.*1346A>G
ENST00000432427.2:c.1306A>G (RAF1)	ENSP00000398591.2:p.Ile436Val
ENST00000442415.6:c.1729A>G (RAF1)	ENSP00000401888.2:p.Ile577Val
ENST00000471449.1:n.358A>G (RAF1)
NM_002880.3:c.1669A>G , LRG_413t1:c.1669A>G (RAF1)	NP_002871.1:p.Ile557Val
XM_005265355.1:c.1669A>G (RAF1)	XP_005265412.1:p.Ile557Val
XM_005265357.1:c.1570A>G (RAF1)	XP_005265414.1:p.Ile524Val
XM_005265358.3:c.1426A>G (RAF1)	XP_005265415.1:p.Ile476Val
XM_005265359.3:c.1327A>G (RAF1)	XP_005265416.1:p.Ile443Val
XM_011533974.1:c.1669A>G (RAF1)	XP_011532276.1:p.Ile557Val
XM_011533975.1:c.1426A>G (RAF1)	XP_011532277.1:p.Ile476Val
NM_001354689.1:c.1729A>G (RAF1)	NP_001341618.1:p.Ile577Val
NM_001354690.1:c.1669A>G (RAF1)	NP_001341619.1:p.Ile557Val
NM_001354691.1:c.1426A>G (RAF1)	NP_001341620.1:p.Ile476Val
NM_001354692.1:c.1426A>G (RAF1)	NP_001341621.1:p.Ile476Val
NM_001354693.1:c.1570A>G (RAF1)	NP_001341622.1:p.Ile524Val
NM_001354694.1:c.1486A>G (RAF1)	NP_001341623.1:p.Ile496Val
NM_001354695.1:c.1327A>G (RAF1)	NP_001341624.1:p.Ile443Val
NR_148940.1:n.2197A>G (RAF1)
NR_148941.1:n.2143A>G (RAF1)
NR_148942.1:n.2082A>G (RAF1)
XM_011533974.3:c.1669A>G (RAF1)	XP_011532276.1:p.Ile557Val
XM_017006966.1:c.1570A>G (RAF1)	XP_016862455.1:p.Ile524Val
NM_001354689.3:c.1729A>G (RAF1)	NP_001341618.1:p.Ile577Val
NM_001354690.2:c.1669A>G (RAF1)	NP_001341619.1:p.Ile557Val
NM_001354691.2:c.1426A>G (RAF1)	NP_001341620.1:p.Ile476Val
NM_001354692.2:c.1426A>G (RAF1)	NP_001341621.1:p.Ile476Val
NM_001354693.2:c.1570A>G (RAF1)	NP_001341622.1:p.Ile524Val
NM_001354694.2:c.1486A>G (RAF1)	NP_001341623.1:p.Ile496Val
NM_001354695.2:c.1327A>G (RAF1)	NP_001341624.1:p.Ile443Val
NR_148940.2:n.2113A>G (RAF1)
NR_148941.2:n.2059A>G (RAF1)
NR_148942.2:n.1998A>G (RAF1)
NM_001354690.3:c.1669A>G (RAF1)	NP_001341619.1:p.Ile557Val
NM_001354691.3:c.1426A>G (RAF1)	NP_001341620.1:p.Ile476Val
NM_001354692.3:c.1426A>G (RAF1)	NP_001341621.1:p.Ile476Val
NM_001354693.3:c.1570A>G (RAF1)	NP_001341622.1:p.Ile524Val
NM_001354694.3:c.1486A>G (RAF1)	NP_001341623.1:p.Ile496Val
NM_001354695.3:c.1327A>G (RAF1)	NP_001341624.1:p.Ile443Val
NM_002880.4:c.1669A>G (RAF1) MANE Select	NP_002871.1:p.Ile557Val
NR_148940.3:n.2113A>G (RAF1)
NR_148941.3:n.2059A>G (RAF1)
NR_148942.3:n.1998A>G (RAF1)