Canonical Allele Identifier: CA351496626

Gene: RAF1 MKRN2

Linked Data

• MyVariant Identifiers: chr3:g.12626387A>C (hg19) ; chr3:g.12584888A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584888A>C , CM000665.2:g.12584888A>C	GRCh38
NC_000003.11:g.12626387A>C , CM000665.1:g.12626387A>C	GRCh37
NC_000003.10:g.12601387A>C	NCBI36
NG_007467.1:g.84292T>G , LRG_413:g.84292T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1427T>G (RAF1)	ENSP00000401088.1:n.*1427T>G
ENST00000432427.3:c.1079T>G (RAF1)
ENST00000460610.2:n.6074T>G (RAF1)
ENST00000471449.2:n.572T>G (RAF1)
ENST00000475353.2:n.4042T>G (RAF1)
ENST00000684903.1:c.*1439T>G (RAF1)	ENSP00000508612.1:n.*1439T>G
ENST00000685348.1:c.*1473T>G (RAF1)	ENSP00000510285.1:n.*1473T>G
ENST00000685437.1:c.1663T>G (RAF1)	ENSP00000508794.1:p.Cys555Gly
ENST00000685653.1:c.1762T>G (RAF1)	ENSP00000509968.1:p.Cys588Gly
ENST00000685697.1:n.2497T>G (RAF1)
ENST00000685738.1:c.*726T>G (RAF1)	ENSP00000510156.1:n.*726T>G
ENST00000686409.1:n.5171T>G (RAF1)
ENST00000686455.1:n.4483T>G (RAF1)
ENST00000686762.1:c.*321T>G (RAF1)	ENSP00000509767.1:n.*321T>G
ENST00000687257.1:n.4216T>G (RAF1)
ENST00000687326.1:c.*3054T>G (RAF1)	ENSP00000509665.1:n.*3054T>G
ENST00000687505.1:n.1880T>G (RAF1)
ENST00000687923.1:c.1651T>G (RAF1)	ENSP00000510255.1:p.Cys551Gly
ENST00000688269.1:n.2358T>G (RAF1)
ENST00000688444.1:n.3879T>G (RAF1)
ENST00000688543.1:c.1663T>G (RAF1)	ENSP00000509612.1:p.Cys555Gly
ENST00000688625.1:c.*3131T>G (RAF1)	ENSP00000509522.1:n.*3131T>G
ENST00000688803.1:n.3190T>G (RAF1)
ENST00000689097.1:c.*1439T>G (RAF1)	ENSP00000509756.1:n.*1439T>G
ENST00000689389.1:c.1585T>G (RAF1)	ENSP00000510213.1:p.Cys529Gly
ENST00000689418.1:c.*3657T>G (RAF1)	ENSP00000509467.1:n.*3657T>G
ENST00000689540.1:n.4130T>G (RAF1)
ENST00000689876.1:c.*311T>G (RAF1)	ENSP00000508535.1:n.*311T>G
ENST00000689914.1:c.*696T>G (RAF1)	ENSP00000509847.1:n.*696T>G
ENST00000690397.1:c.1651T>G (RAF1)	ENSP00000508730.1:p.Cys551Gly
ENST00000690460.1:c.1750T>G (RAF1)	ENSP00000509106.1:p.Cys584Gly
ENST00000690585.1:c.488T>G (RAF1)
ENST00000690625.1:n.2798T>G (RAF1)
ENST00000691396.1:c.*1634T>G (RAF1)	ENSP00000510712.1:n.*1634T>G
ENST00000691643.1:n.2815T>G (RAF1)
ENST00000691724.1:c.*719T>G (RAF1)	ENSP00000509255.1:n.*719T>G
ENST00000691779.1:c.*1340T>G (RAF1)	ENSP00000508592.1:n.*1340T>G
ENST00000691888.1:c.636T>G (RAF1)
ENST00000691899.1:c.1762T>G (RAF1)	ENSP00000508763.1:p.Cys588Gly
ENST00000692069.1:n.4686T>G (RAF1)
ENST00000692093.1:c.1663T>G (RAF1)	ENSP00000509669.1:p.Cys555Gly
ENST00000692311.1:n.2586T>G (RAF1)
ENST00000692558.1:n.4345T>G (RAF1)
ENST00000692773.1:c.*1499T>G (RAF1)	ENSP00000509055.1:n.*1499T>G
ENST00000692830.1:c.*1507T>G (RAF1)	ENSP00000509461.1:n.*1507T>G
ENST00000693312.1:c.1537T>G (RAF1)	ENSP00000508686.1:p.Cys513Gly
ENST00000693664.1:c.*213T>G (RAF1)	ENSP00000509614.1:n.*213T>G
ENST00000693705.1:c.*1141T>G (RAF1)	ENSP00000510697.1:n.*1141T>G
ENST00000251849.9:c.1762T>G (RAF1) MANE Select	ENSP00000251849.4:p.Cys588Gly
ENST00000442415.7:c.1822T>G (RAF1)	ENSP00000401888.2:p.Cys608Gly
ENST00000676541.1:c.*2635A>C (MKRN2)	ENSP00000503730.1:n.*2635A>C
ENST00000677142.1:c.*2635A>C (MKRN2)	ENSP00000504455.1:n.*2635A>C
ENST00000677816.1:c.*1190A>C (MKRN2)	ENSP00000502893.1:n.*1190A>C
ENST00000677941.1:n.2698A>C (MKRN2)
ENST00000251849.8:c.1762T>G (RAF1)	ENSP00000251849.4:p.Cys588Gly
ENST00000423275.5:c.*1439T>G (RAF1)	ENSP00000401088.1:n.*1439T>G
ENST00000432427.2:c.1399T>G (RAF1)	ENSP00000398591.2:p.Cys467Gly
ENST00000442415.6:c.1822T>G (RAF1)	ENSP00000401888.2:p.Cys608Gly
ENST00000471449.1:n.451T>G (RAF1)
NM_002880.3:c.1762T>G , LRG_413t1:c.1762T>G (RAF1)	NP_002871.1:p.Cys588Gly
XM_005265355.1:c.1762T>G (RAF1)	XP_005265412.1:p.Cys588Gly
XM_005265357.1:c.1663T>G (RAF1)	XP_005265414.1:p.Cys555Gly
XM_005265358.3:c.1519T>G (RAF1)	XP_005265415.1:p.Cys507Gly
XM_005265359.3:c.1420T>G (RAF1)	XP_005265416.1:p.Cys474Gly
XM_011533974.1:c.1762T>G (RAF1)	XP_011532276.1:p.Cys588Gly
XM_011533975.1:c.1519T>G (RAF1)	XP_011532277.1:p.Cys507Gly
NM_001354689.1:c.1822T>G (RAF1)	NP_001341618.1:p.Cys608Gly
NM_001354690.1:c.1762T>G (RAF1)	NP_001341619.1:p.Cys588Gly
NM_001354691.1:c.1519T>G (RAF1)	NP_001341620.1:p.Cys507Gly
NM_001354692.1:c.1519T>G (RAF1)	NP_001341621.1:p.Cys507Gly
NM_001354693.1:c.1663T>G (RAF1)	NP_001341622.1:p.Cys555Gly
NM_001354694.1:c.1579T>G (RAF1)	NP_001341623.1:p.Cys527Gly
NM_001354695.1:c.1420T>G (RAF1)	NP_001341624.1:p.Cys474Gly
NR_148940.1:n.2290T>G (RAF1)
NR_148941.1:n.2236T>G (RAF1)
NR_148942.1:n.2175T>G (RAF1)
XM_011533974.3:c.1762T>G (RAF1)	XP_011532276.1:p.Cys588Gly
XM_017006966.1:c.1663T>G (RAF1)	XP_016862455.1:p.Cys555Gly
NM_001354689.3:c.1822T>G (RAF1)	NP_001341618.1:p.Cys608Gly
NM_001354690.2:c.1762T>G (RAF1)	NP_001341619.1:p.Cys588Gly
NM_001354691.2:c.1519T>G (RAF1)	NP_001341620.1:p.Cys507Gly
NM_001354692.2:c.1519T>G (RAF1)	NP_001341621.1:p.Cys507Gly
NM_001354693.2:c.1663T>G (RAF1)	NP_001341622.1:p.Cys555Gly
NM_001354694.2:c.1579T>G (RAF1)	NP_001341623.1:p.Cys527Gly
NM_001354695.2:c.1420T>G (RAF1)	NP_001341624.1:p.Cys474Gly
NR_148940.2:n.2206T>G (RAF1)
NR_148941.2:n.2152T>G (RAF1)
NR_148942.2:n.2091T>G (RAF1)
NM_001354690.3:c.1762T>G (RAF1)	NP_001341619.1:p.Cys588Gly
NM_001354691.3:c.1519T>G (RAF1)	NP_001341620.1:p.Cys507Gly
NM_001354692.3:c.1519T>G (RAF1)	NP_001341621.1:p.Cys507Gly
NM_001354693.3:c.1663T>G (RAF1)	NP_001341622.1:p.Cys555Gly
NM_001354694.3:c.1579T>G (RAF1)	NP_001341623.1:p.Cys527Gly
NM_001354695.3:c.1420T>G (RAF1)	NP_001341624.1:p.Cys474Gly
NM_002880.4:c.1762T>G (RAF1) MANE Select	NP_002871.1:p.Cys588Gly
NR_148940.3:n.2206T>G (RAF1)
NR_148941.3:n.2152T>G (RAF1)
NR_148942.3:n.2091T>G (RAF1)