Canonical Allele Identifier: CA432272684

Gene: RAF1 MKRN2

Linked Data

• MyVariant Identifiers: chr3:g.12626121T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584622T>G , CM000665.2:g.12584622T>G	GRCh38
NC_000003.11:g.12626121T>G , CM000665.1:g.12626121T>G	GRCh37
NC_000003.10:g.12601121T>G	NCBI36
NG_007467.1:g.84558A>C , LRG_413:g.84558A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1504A>C (RAF1)	ENSP00000401088.1:n.*1504A>C
ENST00000432427.3:c.1156A>C (RAF1)
ENST00000460610.2:n.6151A>C (RAF1)
ENST00000471449.2:n.649A>C (RAF1)
ENST00000475353.2:n.4119A>C (RAF1)
ENST00000684903.1:c.*1516A>C (RAF1)	ENSP00000508612.1:n.*1516A>C
ENST00000685348.1:c.*1550A>C (RAF1)	ENSP00000510285.1:n.*1550A>C
ENST00000685437.1:c.1740A>C (RAF1)	ENSP00000508794.1:p.Leu580=
ENST00000685653.1:c.1839A>C (RAF1)	ENSP00000509968.1:p.Leu613=
ENST00000685697.1:n.2574A>C (RAF1)
ENST00000685738.1:c.*803A>C (RAF1)	ENSP00000510156.1:n.*803A>C
ENST00000686409.1:n.5248A>C (RAF1)
ENST00000686455.1:n.4560A>C (RAF1)
ENST00000686762.1:c.*398A>C (RAF1)	ENSP00000509767.1:n.*398A>C
ENST00000687257.1:n.4293A>C (RAF1)
ENST00000687326.1:c.*3131A>C (RAF1)	ENSP00000509665.1:n.*3131A>C
ENST00000687505.1:n.1957A>C (RAF1)
ENST00000687923.1:c.1728A>C (RAF1)	ENSP00000510255.1:p.Leu576=
ENST00000688269.1:n.2435A>C (RAF1)
ENST00000688444.1:n.3956A>C (RAF1)
ENST00000688543.1:c.1740A>C (RAF1)	ENSP00000509612.1:p.Leu580=
ENST00000688625.1:c.*3208A>C (RAF1)	ENSP00000509522.1:n.*3208A>C
ENST00000688803.1:n.3267A>C (RAF1)
ENST00000689097.1:c.*1516A>C (RAF1)	ENSP00000509756.1:n.*1516A>C
ENST00000689389.1:c.1662A>C (RAF1)	ENSP00000510213.1:p.Leu554=
ENST00000689418.1:c.*3734A>C (RAF1)	ENSP00000509467.1:n.*3734A>C
ENST00000689540.1:n.4207A>C (RAF1)
ENST00000689876.1:c.*388A>C (RAF1)	ENSP00000508535.1:n.*388A>C
ENST00000689914.1:c.*773A>C (RAF1)	ENSP00000509847.1:n.*773A>C
ENST00000690397.1:c.1728A>C (RAF1)	ENSP00000508730.1:p.Leu576=
ENST00000690460.1:c.1827A>C (RAF1)	ENSP00000509106.1:p.Leu609=
ENST00000690585.1:c.565A>C (RAF1)
ENST00000690625.1:n.2875A>C (RAF1)
ENST00000691396.1:c.*1711A>C (RAF1)	ENSP00000510712.1:n.*1711A>C
ENST00000691643.1:n.2892A>C (RAF1)
ENST00000691724.1:c.*796A>C (RAF1)	ENSP00000509255.1:n.*796A>C
ENST00000691779.1:c.*1417A>C (RAF1)	ENSP00000508592.1:n.*1417A>C
ENST00000691888.1:c.713A>C (RAF1)
ENST00000691899.1:c.1839A>C (RAF1)	ENSP00000508763.1:p.Leu613=
ENST00000692069.1:n.4763A>C (RAF1)
ENST00000692093.1:c.1740A>C (RAF1)	ENSP00000509669.1:p.Leu580=
ENST00000692311.1:n.2663A>C (RAF1)
ENST00000692558.1:n.4422A>C (RAF1)
ENST00000692773.1:c.*1576A>C (RAF1)	ENSP00000509055.1:n.*1576A>C
ENST00000692830.1:c.*1584A>C (RAF1)	ENSP00000509461.1:n.*1584A>C
ENST00000693312.1:c.1614A>C (RAF1)	ENSP00000508686.1:p.Leu538=
ENST00000693664.1:c.*290A>C (RAF1)	ENSP00000509614.1:n.*290A>C
ENST00000693705.1:c.*1218A>C (RAF1)	ENSP00000510697.1:n.*1218A>C
ENST00000251849.9:c.1839A>C (RAF1) MANE Select	ENSP00000251849.4:p.Leu613=
ENST00000442415.7:c.1899A>C (RAF1)	ENSP00000401888.2:p.Leu633=
ENST00000676541.1:c.*2369T>G (MKRN2)	ENSP00000503730.1:n.*2369T>G
ENST00000677142.1:c.*2369T>G (MKRN2)	ENSP00000504455.1:n.*2369T>G
ENST00000677816.1:c.*924T>G (MKRN2)	ENSP00000502893.1:n.*924T>G
ENST00000677941.1:n.2432T>G (MKRN2)
ENST00000251849.8:c.1839A>C (RAF1)	ENSP00000251849.4:p.Leu613=
ENST00000423275.5:c.*1516A>C (RAF1)	ENSP00000401088.1:n.*1516A>C
ENST00000432427.2:c.1476A>C (RAF1)	ENSP00000398591.2:p.Leu492=
ENST00000442415.6:c.1899A>C (RAF1)	ENSP00000401888.2:p.Leu633=
ENST00000471449.1:n.528A>C (RAF1)
NM_002880.3:c.1839A>C , LRG_413t1:c.1839A>C (RAF1)	NP_002871.1:p.Leu613=
XM_005265355.1:c.1839A>C (RAF1)	XP_005265412.1:p.Leu613=
XM_005265357.1:c.1740A>C (RAF1)	XP_005265414.1:p.Leu580=
XM_005265358.3:c.1596A>C (RAF1)	XP_005265415.1:p.Leu532=
XM_005265359.3:c.1497A>C (RAF1)	XP_005265416.1:p.Leu499=
XM_011533974.1:c.1839A>C (RAF1)	XP_011532276.1:p.Leu613=
XM_011533975.1:c.1596A>C (RAF1)	XP_011532277.1:p.Leu532=
NM_001354689.1:c.1899A>C (RAF1)	NP_001341618.1:p.Leu633=
NM_001354690.1:c.1839A>C (RAF1)	NP_001341619.1:p.Leu613=
NM_001354691.1:c.1596A>C (RAF1)	NP_001341620.1:p.Leu532=
NM_001354692.1:c.1596A>C (RAF1)	NP_001341621.1:p.Leu532=
NM_001354693.1:c.1740A>C (RAF1)	NP_001341622.1:p.Leu580=
NM_001354694.1:c.1656A>C (RAF1)	NP_001341623.1:p.Leu552=
NM_001354695.1:c.1497A>C (RAF1)	NP_001341624.1:p.Leu499=
NR_148940.1:n.2367A>C (RAF1)
NR_148941.1:n.2313A>C (RAF1)
NR_148942.1:n.2252A>C (RAF1)
XM_011533974.3:c.1839A>C (RAF1)	XP_011532276.1:p.Leu613=
XM_017006966.1:c.1740A>C (RAF1)	XP_016862455.1:p.Leu580=
NM_001354689.3:c.1899A>C (RAF1)	NP_001341618.1:p.Leu633=
NM_001354690.2:c.1839A>C (RAF1)	NP_001341619.1:p.Leu613=
NM_001354691.2:c.1596A>C (RAF1)	NP_001341620.1:p.Leu532=
NM_001354692.2:c.1596A>C (RAF1)	NP_001341621.1:p.Leu532=
NM_001354693.2:c.1740A>C (RAF1)	NP_001341622.1:p.Leu580=
NM_001354694.2:c.1656A>C (RAF1)	NP_001341623.1:p.Leu552=
NM_001354695.2:c.1497A>C (RAF1)	NP_001341624.1:p.Leu499=
NR_148940.2:n.2283A>C (RAF1)
NR_148941.2:n.2229A>C (RAF1)
NR_148942.2:n.2168A>C (RAF1)
NM_001354690.3:c.1839A>C (RAF1)	NP_001341619.1:p.Leu613=
NM_001354691.3:c.1596A>C (RAF1)	NP_001341620.1:p.Leu532=
NM_001354692.3:c.1596A>C (RAF1)	NP_001341621.1:p.Leu532=
NM_001354693.3:c.1740A>C (RAF1)	NP_001341622.1:p.Leu580=
NM_001354694.3:c.1656A>C (RAF1)	NP_001341623.1:p.Leu552=
NM_001354695.3:c.1497A>C (RAF1)	NP_001341624.1:p.Leu499=
NM_002880.4:c.1839A>C (RAF1) MANE Select	NP_002871.1:p.Leu613=
NR_148940.3:n.2283A>C (RAF1)
NR_148941.3:n.2229A>C (RAF1)
NR_148942.3:n.2168A>C (RAF1)