Canonical Allele Identifier: CA351497056

Gene: RAF1 MKRN2

Linked Data

• MyVariant Identifiers: chr3:g.12626472G>T (hg19) ; chr3:g.12584973G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584973G>T , CM000665.2:g.12584973G>T	GRCh38
NC_000003.11:g.12626472G>T , CM000665.1:g.12626472G>T	GRCh37
NC_000003.10:g.12601472G>T	NCBI36
NG_007467.1:g.84207C>A , LRG_413:g.84207C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1342C>A (RAF1)	ENSP00000401088.1:n.*1342C>A
ENST00000432427.3:c.994C>A (RAF1)
ENST00000460610.2:n.5989C>A (RAF1)
ENST00000471449.2:n.487C>A (RAF1)
ENST00000475353.2:n.3957C>A (RAF1)
ENST00000684903.1:c.*1354C>A (RAF1)	ENSP00000508612.1:n.*1354C>A
ENST00000685348.1:c.*1388C>A (RAF1)	ENSP00000510285.1:n.*1388C>A
ENST00000685437.1:c.1578C>A (RAF1)	ENSP00000508794.1:p.Phe526Leu
ENST00000685653.1:c.1677C>A (RAF1)	ENSP00000509968.1:p.Phe559Leu
ENST00000685697.1:n.2412C>A (RAF1)
ENST00000685738.1:c.*641C>A (RAF1)	ENSP00000510156.1:n.*641C>A
ENST00000686409.1:n.5086C>A (RAF1)
ENST00000686455.1:n.4398C>A (RAF1)
ENST00000686762.1:c.*236C>A (RAF1)	ENSP00000509767.1:n.*236C>A
ENST00000687257.1:n.4131C>A (RAF1)
ENST00000687326.1:c.*2969C>A (RAF1)	ENSP00000509665.1:n.*2969C>A
ENST00000687505.1:n.1795C>A (RAF1)
ENST00000687923.1:c.1566C>A (RAF1)	ENSP00000510255.1:p.Phe522Leu
ENST00000688269.1:n.2273C>A (RAF1)
ENST00000688444.1:n.3794C>A (RAF1)
ENST00000688543.1:c.1578C>A (RAF1)	ENSP00000509612.1:p.Phe526Leu
ENST00000688625.1:c.*3046C>A (RAF1)	ENSP00000509522.1:n.*3046C>A
ENST00000688803.1:n.3105C>A (RAF1)
ENST00000688914.1:n.1090C>A (RAF1)
ENST00000689097.1:c.*1354C>A (RAF1)	ENSP00000509756.1:n.*1354C>A
ENST00000689389.1:c.1500C>A (RAF1)	ENSP00000510213.1:p.Phe500Leu
ENST00000689418.1:c.*3572C>A (RAF1)	ENSP00000509467.1:n.*3572C>A
ENST00000689540.1:n.4045C>A (RAF1)
ENST00000689876.1:c.*226C>A (RAF1)	ENSP00000508535.1:n.*226C>A
ENST00000689914.1:c.*611C>A (RAF1)	ENSP00000509847.1:n.*611C>A
ENST00000690397.1:c.1566C>A (RAF1)	ENSP00000508730.1:p.Phe522Leu
ENST00000690460.1:c.1665C>A (RAF1)	ENSP00000509106.1:p.Phe555Leu
ENST00000690585.1:c.403C>A (RAF1)
ENST00000690625.1:n.2713C>A (RAF1)
ENST00000691396.1:c.*1549C>A (RAF1)	ENSP00000510712.1:n.*1549C>A
ENST00000691643.1:n.2730C>A (RAF1)
ENST00000691724.1:c.*634C>A (RAF1)	ENSP00000509255.1:n.*634C>A
ENST00000691779.1:c.*1255C>A (RAF1)	ENSP00000508592.1:n.*1255C>A
ENST00000691888.1:c.551C>A (RAF1)
ENST00000691899.1:c.1677C>A (RAF1)	ENSP00000508763.1:p.Phe559Leu
ENST00000692069.1:n.4601C>A (RAF1)
ENST00000692093.1:c.1578C>A (RAF1)	ENSP00000509669.1:p.Phe526Leu
ENST00000692311.1:n.2501C>A (RAF1)
ENST00000692558.1:n.4260C>A (RAF1)
ENST00000692773.1:c.*1414C>A (RAF1)	ENSP00000509055.1:n.*1414C>A
ENST00000692830.1:c.*1422C>A (RAF1)	ENSP00000509461.1:n.*1422C>A
ENST00000693312.1:c.1452C>A (RAF1)	ENSP00000508686.1:p.Phe484Leu
ENST00000693664.1:c.*128C>A (RAF1)	ENSP00000509614.1:n.*128C>A
ENST00000693705.1:c.*1056C>A (RAF1)	ENSP00000510697.1:n.*1056C>A
ENST00000251849.9:c.1677C>A (RAF1) MANE Select	ENSP00000251849.4:p.Phe559Leu
ENST00000442415.7:c.1737C>A (RAF1)	ENSP00000401888.2:p.Phe579Leu
ENST00000676541.1:c.*2720G>T (MKRN2)	ENSP00000503730.1:n.*2720G>T
ENST00000677142.1:c.*2720G>T (MKRN2)	ENSP00000504455.1:n.*2720G>T
ENST00000677816.1:c.*1275G>T (MKRN2)	ENSP00000502893.1:n.*1275G>T
ENST00000677941.1:n.2783G>T (MKRN2)
ENST00000251849.8:c.1677C>A (RAF1)	ENSP00000251849.4:p.Phe559Leu
ENST00000423275.5:c.*1354C>A (RAF1)	ENSP00000401088.1:n.*1354C>A
ENST00000432427.2:c.1314C>A (RAF1)	ENSP00000398591.2:p.Phe438Leu
ENST00000442415.6:c.1737C>A (RAF1)	ENSP00000401888.2:p.Phe579Leu
ENST00000471449.1:n.366C>A (RAF1)
NM_002880.3:c.1677C>A , LRG_413t1:c.1677C>A (RAF1)	NP_002871.1:p.Phe559Leu
XM_005265355.1:c.1677C>A (RAF1)	XP_005265412.1:p.Phe559Leu
XM_005265357.1:c.1578C>A (RAF1)	XP_005265414.1:p.Phe526Leu
XM_005265358.3:c.1434C>A (RAF1)	XP_005265415.1:p.Phe478Leu
XM_005265359.3:c.1335C>A (RAF1)	XP_005265416.1:p.Phe445Leu
XM_011533974.1:c.1677C>A (RAF1)	XP_011532276.1:p.Phe559Leu
XM_011533975.1:c.1434C>A (RAF1)	XP_011532277.1:p.Phe478Leu
NM_001354689.1:c.1737C>A (RAF1)	NP_001341618.1:p.Phe579Leu
NM_001354690.1:c.1677C>A (RAF1)	NP_001341619.1:p.Phe559Leu
NM_001354691.1:c.1434C>A (RAF1)	NP_001341620.1:p.Phe478Leu
NM_001354692.1:c.1434C>A (RAF1)	NP_001341621.1:p.Phe478Leu
NM_001354693.1:c.1578C>A (RAF1)	NP_001341622.1:p.Phe526Leu
NM_001354694.1:c.1494C>A (RAF1)	NP_001341623.1:p.Phe498Leu
NM_001354695.1:c.1335C>A (RAF1)	NP_001341624.1:p.Phe445Leu
NR_148940.1:n.2205C>A (RAF1)
NR_148941.1:n.2151C>A (RAF1)
NR_148942.1:n.2090C>A (RAF1)
XM_011533974.3:c.1677C>A (RAF1)	XP_011532276.1:p.Phe559Leu
XM_017006966.1:c.1578C>A (RAF1)	XP_016862455.1:p.Phe526Leu
NM_001354689.3:c.1737C>A (RAF1)	NP_001341618.1:p.Phe579Leu
NM_001354690.2:c.1677C>A (RAF1)	NP_001341619.1:p.Phe559Leu
NM_001354691.2:c.1434C>A (RAF1)	NP_001341620.1:p.Phe478Leu
NM_001354692.2:c.1434C>A (RAF1)	NP_001341621.1:p.Phe478Leu
NM_001354693.2:c.1578C>A (RAF1)	NP_001341622.1:p.Phe526Leu
NM_001354694.2:c.1494C>A (RAF1)	NP_001341623.1:p.Phe498Leu
NM_001354695.2:c.1335C>A (RAF1)	NP_001341624.1:p.Phe445Leu
NR_148940.2:n.2121C>A (RAF1)
NR_148941.2:n.2067C>A (RAF1)
NR_148942.2:n.2006C>A (RAF1)
NM_001354690.3:c.1677C>A (RAF1)	NP_001341619.1:p.Phe559Leu
NM_001354691.3:c.1434C>A (RAF1)	NP_001341620.1:p.Phe478Leu
NM_001354692.3:c.1434C>A (RAF1)	NP_001341621.1:p.Phe478Leu
NM_001354693.3:c.1578C>A (RAF1)	NP_001341622.1:p.Phe526Leu
NM_001354694.3:c.1494C>A (RAF1)	NP_001341623.1:p.Phe498Leu
NM_001354695.3:c.1335C>A (RAF1)	NP_001341624.1:p.Phe445Leu
NM_002880.4:c.1677C>A (RAF1) MANE Select	NP_002871.1:p.Phe559Leu
NR_148940.3:n.2121C>A (RAF1)
NR_148941.3:n.2067C>A (RAF1)
NR_148942.3:n.2006C>A (RAF1)