Canonical Allele Identifier: CA432522024

Gene: RAF1 MKRN2

Linked Data

• MyVariant Identifiers: chr3:g.12626402T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584903T>G , CM000665.2:g.12584903T>G	GRCh38
NC_000003.11:g.12626402T>G , CM000665.1:g.12626402T>G	GRCh37
NC_000003.10:g.12601402T>G	NCBI36
NG_007467.1:g.84277A>C , LRG_413:g.84277A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1412A>C (RAF1)	ENSP00000401088.1:n.*1412A>C
ENST00000432427.3:c.1064A>C (RAF1)
ENST00000460610.2:n.6059A>C (RAF1)
ENST00000471449.2:n.557A>C (RAF1)
ENST00000475353.2:n.4027A>C (RAF1)
ENST00000684903.1:c.*1424A>C (RAF1)	ENSP00000508612.1:n.*1424A>C
ENST00000685348.1:c.*1458A>C (RAF1)	ENSP00000510285.1:n.*1458A>C
ENST00000685437.1:c.1648A>C (RAF1)	ENSP00000508794.1:p.Arg550=
ENST00000685653.1:c.1747A>C (RAF1)	ENSP00000509968.1:p.Arg583=
ENST00000685697.1:n.2482A>C (RAF1)
ENST00000685738.1:c.*711A>C (RAF1)	ENSP00000510156.1:n.*711A>C
ENST00000686409.1:n.5156A>C (RAF1)
ENST00000686455.1:n.4468A>C (RAF1)
ENST00000686762.1:c.*306A>C (RAF1)	ENSP00000509767.1:n.*306A>C
ENST00000687257.1:n.4201A>C (RAF1)
ENST00000687326.1:c.*3039A>C (RAF1)	ENSP00000509665.1:n.*3039A>C
ENST00000687505.1:n.1865A>C (RAF1)
ENST00000687923.1:c.1636A>C (RAF1)	ENSP00000510255.1:p.Arg546=
ENST00000688269.1:n.2343A>C (RAF1)
ENST00000688444.1:n.3864A>C (RAF1)
ENST00000688543.1:c.1648A>C (RAF1)	ENSP00000509612.1:p.Arg550=
ENST00000688625.1:c.*3116A>C (RAF1)	ENSP00000509522.1:n.*3116A>C
ENST00000688803.1:n.3175A>C (RAF1)
ENST00000688914.1:n.1160A>C (RAF1)
ENST00000689097.1:c.*1424A>C (RAF1)	ENSP00000509756.1:n.*1424A>C
ENST00000689389.1:c.1570A>C (RAF1)	ENSP00000510213.1:p.Arg524=
ENST00000689418.1:c.*3642A>C (RAF1)	ENSP00000509467.1:n.*3642A>C
ENST00000689540.1:n.4115A>C (RAF1)
ENST00000689876.1:c.*296A>C (RAF1)	ENSP00000508535.1:n.*296A>C
ENST00000689914.1:c.*681A>C (RAF1)	ENSP00000509847.1:n.*681A>C
ENST00000690397.1:c.1636A>C (RAF1)	ENSP00000508730.1:p.Arg546=
ENST00000690460.1:c.1735A>C (RAF1)	ENSP00000509106.1:p.Arg579=
ENST00000690585.1:c.473A>C (RAF1)
ENST00000690625.1:n.2783A>C (RAF1)
ENST00000691396.1:c.*1619A>C (RAF1)	ENSP00000510712.1:n.*1619A>C
ENST00000691643.1:n.2800A>C (RAF1)
ENST00000691724.1:c.*704A>C (RAF1)	ENSP00000509255.1:n.*704A>C
ENST00000691779.1:c.*1325A>C (RAF1)	ENSP00000508592.1:n.*1325A>C
ENST00000691888.1:c.621A>C (RAF1)
ENST00000691899.1:c.1747A>C (RAF1)	ENSP00000508763.1:p.Arg583=
ENST00000692069.1:n.4671A>C (RAF1)
ENST00000692093.1:c.1648A>C (RAF1)	ENSP00000509669.1:p.Arg550=
ENST00000692311.1:n.2571A>C (RAF1)
ENST00000692558.1:n.4330A>C (RAF1)
ENST00000692773.1:c.*1484A>C (RAF1)	ENSP00000509055.1:n.*1484A>C
ENST00000692830.1:c.*1492A>C (RAF1)	ENSP00000509461.1:n.*1492A>C
ENST00000693312.1:c.1522A>C (RAF1)	ENSP00000508686.1:p.Arg508=
ENST00000693664.1:c.*198A>C (RAF1)	ENSP00000509614.1:n.*198A>C
ENST00000693705.1:c.*1126A>C (RAF1)	ENSP00000510697.1:n.*1126A>C
ENST00000251849.9:c.1747A>C (RAF1) MANE Select	ENSP00000251849.4:p.Arg583=
ENST00000442415.7:c.1807A>C (RAF1)	ENSP00000401888.2:p.Arg603=
ENST00000676541.1:c.*2650T>G (MKRN2)	ENSP00000503730.1:n.*2650T>G
ENST00000677142.1:c.*2650T>G (MKRN2)	ENSP00000504455.1:n.*2650T>G
ENST00000677816.1:c.*1205T>G (MKRN2)	ENSP00000502893.1:n.*1205T>G
ENST00000677941.1:n.2713T>G (MKRN2)
ENST00000251849.8:c.1747A>C (RAF1)	ENSP00000251849.4:p.Arg583=
ENST00000423275.5:c.*1424A>C (RAF1)	ENSP00000401088.1:n.*1424A>C
ENST00000432427.2:c.1384A>C (RAF1)	ENSP00000398591.2:p.Arg462=
ENST00000442415.6:c.1807A>C (RAF1)	ENSP00000401888.2:p.Arg603=
ENST00000471449.1:n.436A>C (RAF1)
NM_002880.3:c.1747A>C , LRG_413t1:c.1747A>C (RAF1)	NP_002871.1:p.Arg583=
XM_005265355.1:c.1747A>C (RAF1)	XP_005265412.1:p.Arg583=
XM_005265357.1:c.1648A>C (RAF1)	XP_005265414.1:p.Arg550=
XM_005265358.3:c.1504A>C (RAF1)	XP_005265415.1:p.Arg502=
XM_005265359.3:c.1405A>C (RAF1)	XP_005265416.1:p.Arg469=
XM_011533974.1:c.1747A>C (RAF1)	XP_011532276.1:p.Arg583=
XM_011533975.1:c.1504A>C (RAF1)	XP_011532277.1:p.Arg502=
NM_001354689.1:c.1807A>C (RAF1)	NP_001341618.1:p.Arg603=
NM_001354690.1:c.1747A>C (RAF1)	NP_001341619.1:p.Arg583=
NM_001354691.1:c.1504A>C (RAF1)	NP_001341620.1:p.Arg502=
NM_001354692.1:c.1504A>C (RAF1)	NP_001341621.1:p.Arg502=
NM_001354693.1:c.1648A>C (RAF1)	NP_001341622.1:p.Arg550=
NM_001354694.1:c.1564A>C (RAF1)	NP_001341623.1:p.Arg522=
NM_001354695.1:c.1405A>C (RAF1)	NP_001341624.1:p.Arg469=
NR_148940.1:n.2275A>C (RAF1)
NR_148941.1:n.2221A>C (RAF1)
NR_148942.1:n.2160A>C (RAF1)
XM_011533974.3:c.1747A>C (RAF1)	XP_011532276.1:p.Arg583=
XM_017006966.1:c.1648A>C (RAF1)	XP_016862455.1:p.Arg550=
NM_001354689.3:c.1807A>C (RAF1)	NP_001341618.1:p.Arg603=
NM_001354690.2:c.1747A>C (RAF1)	NP_001341619.1:p.Arg583=
NM_001354691.2:c.1504A>C (RAF1)	NP_001341620.1:p.Arg502=
NM_001354692.2:c.1504A>C (RAF1)	NP_001341621.1:p.Arg502=
NM_001354693.2:c.1648A>C (RAF1)	NP_001341622.1:p.Arg550=
NM_001354694.2:c.1564A>C (RAF1)	NP_001341623.1:p.Arg522=
NM_001354695.2:c.1405A>C (RAF1)	NP_001341624.1:p.Arg469=
NR_148940.2:n.2191A>C (RAF1)
NR_148941.2:n.2137A>C (RAF1)
NR_148942.2:n.2076A>C (RAF1)
NM_001354690.3:c.1747A>C (RAF1)	NP_001341619.1:p.Arg583=
NM_001354691.3:c.1504A>C (RAF1)	NP_001341620.1:p.Arg502=
NM_001354692.3:c.1504A>C (RAF1)	NP_001341621.1:p.Arg502=
NM_001354693.3:c.1648A>C (RAF1)	NP_001341622.1:p.Arg550=
NM_001354694.3:c.1564A>C (RAF1)	NP_001341623.1:p.Arg522=
NM_001354695.3:c.1405A>C (RAF1)	NP_001341624.1:p.Arg469=
NM_002880.4:c.1747A>C (RAF1) MANE Select	NP_002871.1:p.Arg583=
NR_148940.3:n.2191A>C (RAF1)
NR_148941.3:n.2137A>C (RAF1)
NR_148942.3:n.2076A>C (RAF1)