Canonical Allele Identifier: CA432272704

Gene: RAF1 MKRN2

Linked Data

• dbSNP Id: rs1057523409
• MyVariant Identifiers: chr3:g.12626136C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584637C>G , CM000665.2:g.12584637C>G	GRCh38
NC_000003.11:g.12626136C>G , CM000665.1:g.12626136C>G	GRCh37
NC_000003.10:g.12601136C>G	NCBI36
NG_007467.1:g.84543G>C , LRG_413:g.84543G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1489G>C (RAF1)	ENSP00000401088.1:n.*1489G>C
ENST00000432427.3:c.1141G>C (RAF1)
ENST00000460610.2:n.6136G>C (RAF1)
ENST00000471449.2:n.634G>C (RAF1)
ENST00000475353.2:n.4104G>C (RAF1)
ENST00000684903.1:c.*1501G>C (RAF1)	ENSP00000508612.1:n.*1501G>C
ENST00000685348.1:c.*1535G>C (RAF1)	ENSP00000510285.1:n.*1535G>C
ENST00000685437.1:c.1725G>C (RAF1)	ENSP00000508794.1:p.Leu575=
ENST00000685653.1:c.1824G>C (RAF1)	ENSP00000509968.1:p.Leu608=
ENST00000685697.1:n.2559G>C (RAF1)
ENST00000685738.1:c.*788G>C (RAF1)	ENSP00000510156.1:n.*788G>C
ENST00000686409.1:n.5233G>C (RAF1)
ENST00000686455.1:n.4545G>C (RAF1)
ENST00000686762.1:c.*383G>C (RAF1)	ENSP00000509767.1:n.*383G>C
ENST00000687257.1:n.4278G>C (RAF1)
ENST00000687326.1:c.*3116G>C (RAF1)	ENSP00000509665.1:n.*3116G>C
ENST00000687505.1:n.1942G>C (RAF1)
ENST00000687923.1:c.1713G>C (RAF1)	ENSP00000510255.1:p.Leu571=
ENST00000688269.1:n.2420G>C (RAF1)
ENST00000688444.1:n.3941G>C (RAF1)
ENST00000688543.1:c.1725G>C (RAF1)	ENSP00000509612.1:p.Leu575=
ENST00000688625.1:c.*3193G>C (RAF1)	ENSP00000509522.1:n.*3193G>C
ENST00000688803.1:n.3252G>C (RAF1)
ENST00000689097.1:c.*1501G>C (RAF1)	ENSP00000509756.1:n.*1501G>C
ENST00000689389.1:c.1647G>C (RAF1)	ENSP00000510213.1:p.Leu549=
ENST00000689418.1:c.*3719G>C (RAF1)	ENSP00000509467.1:n.*3719G>C
ENST00000689540.1:n.4192G>C (RAF1)
ENST00000689876.1:c.*373G>C (RAF1)	ENSP00000508535.1:n.*373G>C
ENST00000689914.1:c.*758G>C (RAF1)	ENSP00000509847.1:n.*758G>C
ENST00000690397.1:c.1713G>C (RAF1)	ENSP00000508730.1:p.Leu571=
ENST00000690460.1:c.1812G>C (RAF1)	ENSP00000509106.1:p.Leu604=
ENST00000690585.1:c.550G>C (RAF1)
ENST00000690625.1:n.2860G>C (RAF1)
ENST00000691396.1:c.*1696G>C (RAF1)	ENSP00000510712.1:n.*1696G>C
ENST00000691643.1:n.2877G>C (RAF1)
ENST00000691724.1:c.*781G>C (RAF1)	ENSP00000509255.1:n.*781G>C
ENST00000691779.1:c.*1402G>C (RAF1)	ENSP00000508592.1:n.*1402G>C
ENST00000691888.1:c.698G>C (RAF1)
ENST00000691899.1:c.1824G>C (RAF1)	ENSP00000508763.1:p.Leu608=
ENST00000692069.1:n.4748G>C (RAF1)
ENST00000692093.1:c.1725G>C (RAF1)	ENSP00000509669.1:p.Leu575=
ENST00000692311.1:n.2648G>C (RAF1)
ENST00000692558.1:n.4407G>C (RAF1)
ENST00000692773.1:c.*1561G>C (RAF1)	ENSP00000509055.1:n.*1561G>C
ENST00000692830.1:c.*1569G>C (RAF1)	ENSP00000509461.1:n.*1569G>C
ENST00000693312.1:c.1599G>C (RAF1)	ENSP00000508686.1:p.Leu533=
ENST00000693664.1:c.*275G>C (RAF1)	ENSP00000509614.1:n.*275G>C
ENST00000693705.1:c.*1203G>C (RAF1)	ENSP00000510697.1:n.*1203G>C
ENST00000251849.9:c.1824G>C (RAF1) MANE Select	ENSP00000251849.4:p.Leu608=
ENST00000442415.7:c.1884G>C (RAF1)	ENSP00000401888.2:p.Leu628=
ENST00000676541.1:c.*2384C>G (MKRN2)	ENSP00000503730.1:n.*2384C>G
ENST00000677142.1:c.*2384C>G (MKRN2)	ENSP00000504455.1:n.*2384C>G
ENST00000677816.1:c.*939C>G (MKRN2)	ENSP00000502893.1:n.*939C>G
ENST00000677941.1:n.2447C>G (MKRN2)
ENST00000251849.8:c.1824G>C (RAF1)	ENSP00000251849.4:p.Leu608=
ENST00000423275.5:c.*1501G>C (RAF1)	ENSP00000401088.1:n.*1501G>C
ENST00000432427.2:c.1461G>C (RAF1)	ENSP00000398591.2:p.Leu487=
ENST00000442415.6:c.1884G>C (RAF1)	ENSP00000401888.2:p.Leu628=
ENST00000471449.1:n.513G>C (RAF1)
NM_002880.3:c.1824G>C , LRG_413t1:c.1824G>C (RAF1)	NP_002871.1:p.Leu608=
XM_005265355.1:c.1824G>C (RAF1)	XP_005265412.1:p.Leu608=
XM_005265357.1:c.1725G>C (RAF1)	XP_005265414.1:p.Leu575=
XM_005265358.3:c.1581G>C (RAF1)	XP_005265415.1:p.Leu527=
XM_005265359.3:c.1482G>C (RAF1)	XP_005265416.1:p.Leu494=
XM_011533974.1:c.1824G>C (RAF1)	XP_011532276.1:p.Leu608=
XM_011533975.1:c.1581G>C (RAF1)	XP_011532277.1:p.Leu527=
NM_001354689.1:c.1884G>C (RAF1)	NP_001341618.1:p.Leu628=
NM_001354690.1:c.1824G>C (RAF1)	NP_001341619.1:p.Leu608=
NM_001354691.1:c.1581G>C (RAF1)	NP_001341620.1:p.Leu527=
NM_001354692.1:c.1581G>C (RAF1)	NP_001341621.1:p.Leu527=
NM_001354693.1:c.1725G>C (RAF1)	NP_001341622.1:p.Leu575=
NM_001354694.1:c.1641G>C (RAF1)	NP_001341623.1:p.Leu547=
NM_001354695.1:c.1482G>C (RAF1)	NP_001341624.1:p.Leu494=
NR_148940.1:n.2352G>C (RAF1)
NR_148941.1:n.2298G>C (RAF1)
NR_148942.1:n.2237G>C (RAF1)
XM_011533974.3:c.1824G>C (RAF1)	XP_011532276.1:p.Leu608=
XM_017006966.1:c.1725G>C (RAF1)	XP_016862455.1:p.Leu575=
NM_001354689.3:c.1884G>C (RAF1)	NP_001341618.1:p.Leu628=
NM_001354690.2:c.1824G>C (RAF1)	NP_001341619.1:p.Leu608=
NM_001354691.2:c.1581G>C (RAF1)	NP_001341620.1:p.Leu527=
NM_001354692.2:c.1581G>C (RAF1)	NP_001341621.1:p.Leu527=
NM_001354693.2:c.1725G>C (RAF1)	NP_001341622.1:p.Leu575=
NM_001354694.2:c.1641G>C (RAF1)	NP_001341623.1:p.Leu547=
NM_001354695.2:c.1482G>C (RAF1)	NP_001341624.1:p.Leu494=
NR_148940.2:n.2268G>C (RAF1)
NR_148941.2:n.2214G>C (RAF1)
NR_148942.2:n.2153G>C (RAF1)
NM_001354690.3:c.1824G>C (RAF1)	NP_001341619.1:p.Leu608=
NM_001354691.3:c.1581G>C (RAF1)	NP_001341620.1:p.Leu527=
NM_001354692.3:c.1581G>C (RAF1)	NP_001341621.1:p.Leu527=
NM_001354693.3:c.1725G>C (RAF1)	NP_001341622.1:p.Leu575=
NM_001354694.3:c.1641G>C (RAF1)	NP_001341623.1:p.Leu547=
NM_001354695.3:c.1482G>C (RAF1)	NP_001341624.1:p.Leu494=
NM_002880.4:c.1824G>C (RAF1) MANE Select	NP_002871.1:p.Leu608=
NR_148940.3:n.2268G>C (RAF1)
NR_148941.3:n.2214G>C (RAF1)
NR_148942.3:n.2153G>C (RAF1)