Canonical Allele Identifier: CA351497103

Gene: RAF1 MKRN2

Linked Data

• MyVariant Identifiers: chr3:g.12626479A>C (hg19) ; chr3:g.12584980A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584980A>C , CM000665.2:g.12584980A>C	GRCh38
NC_000003.11:g.12626479A>C , CM000665.1:g.12626479A>C	GRCh37
NC_000003.10:g.12601479A>C	NCBI36
NG_007467.1:g.84200T>G , LRG_413:g.84200T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1335T>G (RAF1)	ENSP00000401088.1:n.*1335T>G
ENST00000432427.3:c.987T>G (RAF1)
ENST00000460610.2:n.5982T>G (RAF1)
ENST00000471449.2:n.480T>G (RAF1)
ENST00000475353.2:n.3950T>G (RAF1)
ENST00000684903.1:c.*1347T>G (RAF1)	ENSP00000508612.1:n.*1347T>G
ENST00000685348.1:c.*1381T>G (RAF1)	ENSP00000510285.1:n.*1381T>G
ENST00000685437.1:c.1571T>G (RAF1)	ENSP00000508794.1:p.Ile524Ser
ENST00000685653.1:c.1670T>G (RAF1)	ENSP00000509968.1:p.Ile557Ser
ENST00000685697.1:n.2405T>G (RAF1)
ENST00000685738.1:c.*634T>G (RAF1)	ENSP00000510156.1:n.*634T>G
ENST00000686409.1:n.5079T>G (RAF1)
ENST00000686455.1:n.4391T>G (RAF1)
ENST00000686762.1:c.*229T>G (RAF1)	ENSP00000509767.1:n.*229T>G
ENST00000687257.1:n.4124T>G (RAF1)
ENST00000687326.1:c.*2962T>G (RAF1)	ENSP00000509665.1:n.*2962T>G
ENST00000687505.1:n.1788T>G (RAF1)
ENST00000687923.1:c.1559T>G (RAF1)	ENSP00000510255.1:p.Ile520Ser
ENST00000688269.1:n.2266T>G (RAF1)
ENST00000688444.1:n.3787T>G (RAF1)
ENST00000688543.1:c.1571T>G (RAF1)	ENSP00000509612.1:p.Ile524Ser
ENST00000688625.1:c.*3039T>G (RAF1)	ENSP00000509522.1:n.*3039T>G
ENST00000688803.1:n.3098T>G (RAF1)
ENST00000688914.1:n.1083T>G (RAF1)
ENST00000689097.1:c.*1347T>G (RAF1)	ENSP00000509756.1:n.*1347T>G
ENST00000689389.1:c.1493T>G (RAF1)	ENSP00000510213.1:p.Ile498Ser
ENST00000689418.1:c.*3565T>G (RAF1)	ENSP00000509467.1:n.*3565T>G
ENST00000689540.1:n.4038T>G (RAF1)
ENST00000689876.1:c.*219T>G (RAF1)	ENSP00000508535.1:n.*219T>G
ENST00000689914.1:c.*604T>G (RAF1)	ENSP00000509847.1:n.*604T>G
ENST00000690397.1:c.1559T>G (RAF1)	ENSP00000508730.1:p.Ile520Ser
ENST00000690460.1:c.1658T>G (RAF1)	ENSP00000509106.1:p.Ile553Ser
ENST00000690585.1:c.396T>G (RAF1)
ENST00000690625.1:n.2706T>G (RAF1)
ENST00000691396.1:c.*1542T>G (RAF1)	ENSP00000510712.1:n.*1542T>G
ENST00000691643.1:n.2723T>G (RAF1)
ENST00000691724.1:c.*627T>G (RAF1)	ENSP00000509255.1:n.*627T>G
ENST00000691779.1:c.*1248T>G (RAF1)	ENSP00000508592.1:n.*1248T>G
ENST00000691888.1:c.544T>G (RAF1)
ENST00000691899.1:c.1670T>G (RAF1)	ENSP00000508763.1:p.Ile557Ser
ENST00000692069.1:n.4594T>G (RAF1)
ENST00000692093.1:c.1571T>G (RAF1)	ENSP00000509669.1:p.Ile524Ser
ENST00000692311.1:n.2494T>G (RAF1)
ENST00000692558.1:n.4253T>G (RAF1)
ENST00000692773.1:c.*1407T>G (RAF1)	ENSP00000509055.1:n.*1407T>G
ENST00000692830.1:c.*1415T>G (RAF1)	ENSP00000509461.1:n.*1415T>G
ENST00000693312.1:c.1445T>G (RAF1)	ENSP00000508686.1:p.Ile482Ser
ENST00000693664.1:c.*121T>G (RAF1)	ENSP00000509614.1:n.*121T>G
ENST00000693705.1:c.*1049T>G (RAF1)	ENSP00000510697.1:n.*1049T>G
ENST00000251849.9:c.1670T>G (RAF1) MANE Select	ENSP00000251849.4:p.Ile557Ser
ENST00000442415.7:c.1730T>G (RAF1)	ENSP00000401888.2:p.Ile577Ser
ENST00000676541.1:c.*2727A>C (MKRN2)	ENSP00000503730.1:n.*2727A>C
ENST00000677142.1:c.*2727A>C (MKRN2)	ENSP00000504455.1:n.*2727A>C
ENST00000677816.1:c.*1282A>C (MKRN2)	ENSP00000502893.1:n.*1282A>C
ENST00000677941.1:n.2790A>C (MKRN2)
ENST00000251849.8:c.1670T>G (RAF1)	ENSP00000251849.4:p.Ile557Ser
ENST00000423275.5:c.*1347T>G (RAF1)	ENSP00000401088.1:n.*1347T>G
ENST00000432427.2:c.1307T>G (RAF1)	ENSP00000398591.2:p.Ile436Ser
ENST00000442415.6:c.1730T>G (RAF1)	ENSP00000401888.2:p.Ile577Ser
ENST00000471449.1:n.359T>G (RAF1)
NM_002880.3:c.1670T>G , LRG_413t1:c.1670T>G (RAF1)	NP_002871.1:p.Ile557Ser
XM_005265355.1:c.1670T>G (RAF1)	XP_005265412.1:p.Ile557Ser
XM_005265357.1:c.1571T>G (RAF1)	XP_005265414.1:p.Ile524Ser
XM_005265358.3:c.1427T>G (RAF1)	XP_005265415.1:p.Ile476Ser
XM_005265359.3:c.1328T>G (RAF1)	XP_005265416.1:p.Ile443Ser
XM_011533974.1:c.1670T>G (RAF1)	XP_011532276.1:p.Ile557Ser
XM_011533975.1:c.1427T>G (RAF1)	XP_011532277.1:p.Ile476Ser
NM_001354689.1:c.1730T>G (RAF1)	NP_001341618.1:p.Ile577Ser
NM_001354690.1:c.1670T>G (RAF1)	NP_001341619.1:p.Ile557Ser
NM_001354691.1:c.1427T>G (RAF1)	NP_001341620.1:p.Ile476Ser
NM_001354692.1:c.1427T>G (RAF1)	NP_001341621.1:p.Ile476Ser
NM_001354693.1:c.1571T>G (RAF1)	NP_001341622.1:p.Ile524Ser
NM_001354694.1:c.1487T>G (RAF1)	NP_001341623.1:p.Ile496Ser
NM_001354695.1:c.1328T>G (RAF1)	NP_001341624.1:p.Ile443Ser
NR_148940.1:n.2198T>G (RAF1)
NR_148941.1:n.2144T>G (RAF1)
NR_148942.1:n.2083T>G (RAF1)
XM_011533974.3:c.1670T>G (RAF1)	XP_011532276.1:p.Ile557Ser
XM_017006966.1:c.1571T>G (RAF1)	XP_016862455.1:p.Ile524Ser
NM_001354689.3:c.1730T>G (RAF1)	NP_001341618.1:p.Ile577Ser
NM_001354690.2:c.1670T>G (RAF1)	NP_001341619.1:p.Ile557Ser
NM_001354691.2:c.1427T>G (RAF1)	NP_001341620.1:p.Ile476Ser
NM_001354692.2:c.1427T>G (RAF1)	NP_001341621.1:p.Ile476Ser
NM_001354693.2:c.1571T>G (RAF1)	NP_001341622.1:p.Ile524Ser
NM_001354694.2:c.1487T>G (RAF1)	NP_001341623.1:p.Ile496Ser
NM_001354695.2:c.1328T>G (RAF1)	NP_001341624.1:p.Ile443Ser
NR_148940.2:n.2114T>G (RAF1)
NR_148941.2:n.2060T>G (RAF1)
NR_148942.2:n.1999T>G (RAF1)
NM_001354690.3:c.1670T>G (RAF1)	NP_001341619.1:p.Ile557Ser
NM_001354691.3:c.1427T>G (RAF1)	NP_001341620.1:p.Ile476Ser
NM_001354692.3:c.1427T>G (RAF1)	NP_001341621.1:p.Ile476Ser
NM_001354693.3:c.1571T>G (RAF1)	NP_001341622.1:p.Ile524Ser
NM_001354694.3:c.1487T>G (RAF1)	NP_001341623.1:p.Ile496Ser
NM_001354695.3:c.1328T>G (RAF1)	NP_001341624.1:p.Ile443Ser
NM_002880.4:c.1670T>G (RAF1) MANE Select	NP_002871.1:p.Ile557Ser
NR_148940.3:n.2114T>G (RAF1)
NR_148941.3:n.2060T>G (RAF1)
NR_148942.3:n.1999T>G (RAF1)