Canonical Allele Identifier: CA432272632

Gene: RAF1 MKRN2

Linked Data

• dbSNP Id: rs151027203
• MyVariant Identifiers: chr3:g.12626043C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584544C>G , CM000665.2:g.12584544C>G	GRCh38
NC_000003.11:g.12626043C>G , CM000665.1:g.12626043C>G	GRCh37
NC_000003.10:g.12601043C>G	NCBI36
NG_007467.1:g.84636G>C , LRG_413:g.84636G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000423275.6:c.*1582G>C (RAF1)	ENSP00000401088.1:n.*1582G>C
ENST00000432427.3:c.1234G>C (RAF1)
ENST00000460610.2:n.6229G>C (RAF1)
ENST00000471449.2:n.727G>C (RAF1)
ENST00000475353.2:n.4197G>C (RAF1)
ENST00000684903.1:c.*1594G>C (RAF1)	ENSP00000508612.1:n.*1594G>C
ENST00000685348.1:c.*1628G>C (RAF1)	ENSP00000510285.1:n.*1628G>C
ENST00000685437.1:c.1818G>C (RAF1)	ENSP00000508794.1:p.Leu606=
ENST00000685653.1:c.1917G>C (RAF1)	ENSP00000509968.1:p.Leu639=
ENST00000685697.1:n.2652G>C (RAF1)
ENST00000685738.1:c.*881G>C (RAF1)	ENSP00000510156.1:n.*881G>C
ENST00000686409.1:n.5326G>C (RAF1)
ENST00000686455.1:n.4638G>C (RAF1)
ENST00000686762.1:c.*476G>C (RAF1)	ENSP00000509767.1:n.*476G>C
ENST00000687257.1:n.4371G>C (RAF1)
ENST00000687326.1:c.*3209G>C (RAF1)	ENSP00000509665.1:n.*3209G>C
ENST00000687505.1:n.2035G>C (RAF1)
ENST00000687923.1:c.1806G>C (RAF1)	ENSP00000510255.1:p.Leu602=
ENST00000688269.1:n.2513G>C (RAF1)
ENST00000688444.1:n.4034G>C (RAF1)
ENST00000688543.1:c.1818G>C (RAF1)	ENSP00000509612.1:p.Leu606=
ENST00000688625.1:c.*3286G>C (RAF1)	ENSP00000509522.1:n.*3286G>C
ENST00000688803.1:n.3345G>C (RAF1)
ENST00000689097.1:c.*1594G>C (RAF1)	ENSP00000509756.1:n.*1594G>C
ENST00000689389.1:c.1740G>C (RAF1)	ENSP00000510213.1:p.Leu580=
ENST00000689418.1:c.*3812G>C (RAF1)	ENSP00000509467.1:n.*3812G>C
ENST00000689540.1:n.4285G>C (RAF1)
ENST00000689876.1:c.*466G>C (RAF1)	ENSP00000508535.1:n.*466G>C
ENST00000689914.1:c.*851G>C (RAF1)	ENSP00000509847.1:n.*851G>C
ENST00000690397.1:c.1806G>C (RAF1)	ENSP00000508730.1:p.Leu602=
ENST00000690460.1:c.1905G>C (RAF1)	ENSP00000509106.1:p.Leu635=
ENST00000690585.1:c.643G>C (RAF1)
ENST00000690625.1:n.2953G>C (RAF1)
ENST00000691396.1:c.*1789G>C (RAF1)	ENSP00000510712.1:n.*1789G>C
ENST00000691643.1:n.2970G>C (RAF1)
ENST00000691724.1:c.*874G>C (RAF1)	ENSP00000509255.1:n.*874G>C
ENST00000691779.1:c.*1495G>C (RAF1)	ENSP00000508592.1:n.*1495G>C
ENST00000691888.1:c.791G>C (RAF1)
ENST00000691899.1:c.1917G>C (RAF1)	ENSP00000508763.1:p.Leu639=
ENST00000692069.1:n.4841G>C (RAF1)
ENST00000692093.1:c.1818G>C (RAF1)	ENSP00000509669.1:p.Leu606=
ENST00000692311.1:n.2741G>C (RAF1)
ENST00000692558.1:n.4500G>C (RAF1)
ENST00000692773.1:c.*1654G>C (RAF1)	ENSP00000509055.1:n.*1654G>C
ENST00000692830.1:c.*1662G>C (RAF1)	ENSP00000509461.1:n.*1662G>C
ENST00000693312.1:c.1692G>C (RAF1)	ENSP00000508686.1:p.Leu564=
ENST00000693664.1:c.*368G>C (RAF1)	ENSP00000509614.1:n.*368G>C
ENST00000693705.1:c.*1296G>C (RAF1)	ENSP00000510697.1:n.*1296G>C
ENST00000251849.9:c.1917G>C (RAF1) MANE Select	ENSP00000251849.4:p.Leu639=
ENST00000442415.7:c.1977G>C (RAF1)	ENSP00000401888.2:p.Leu659=
ENST00000676541.1:c.*2291C>G (MKRN2)	ENSP00000503730.1:n.*2291C>G
ENST00000677142.1:c.*2291C>G (MKRN2)	ENSP00000504455.1:n.*2291C>G
ENST00000677816.1:c.*846C>G (MKRN2)	ENSP00000502893.1:n.*846C>G
ENST00000677941.1:n.2354C>G (MKRN2)
ENST00000251849.8:c.1917G>C (RAF1)	ENSP00000251849.4:p.Leu639=
ENST00000423275.5:c.*1594G>C (RAF1)	ENSP00000401088.1:n.*1594G>C
ENST00000432427.2:c.1554G>C (RAF1)	ENSP00000398591.2:p.Leu518=
ENST00000442415.6:c.1977G>C (RAF1)	ENSP00000401888.2:p.Leu659=
ENST00000471449.1:n.606G>C (RAF1)
NM_002880.3:c.1917G>C , LRG_413t1:c.1917G>C (RAF1)	NP_002871.1:p.Leu639=
XM_005265355.1:c.1917G>C (RAF1)	XP_005265412.1:p.Leu639=
XM_005265357.1:c.1818G>C (RAF1)	XP_005265414.1:p.Leu606=
XM_005265358.3:c.1674G>C (RAF1)	XP_005265415.1:p.Leu558=
XM_005265359.3:c.1575G>C (RAF1)	XP_005265416.1:p.Leu525=
XM_011533974.1:c.1917G>C (RAF1)	XP_011532276.1:p.Leu639=
XM_011533975.1:c.1674G>C (RAF1)	XP_011532277.1:p.Leu558=
NM_001354689.1:c.1977G>C (RAF1)	NP_001341618.1:p.Leu659=
NM_001354690.1:c.1917G>C (RAF1)	NP_001341619.1:p.Leu639=
NM_001354691.1:c.1674G>C (RAF1)	NP_001341620.1:p.Leu558=
NM_001354692.1:c.1674G>C (RAF1)	NP_001341621.1:p.Leu558=
NM_001354693.1:c.1818G>C (RAF1)	NP_001341622.1:p.Leu606=
NM_001354694.1:c.1734G>C (RAF1)	NP_001341623.1:p.Leu578=
NM_001354695.1:c.1575G>C (RAF1)	NP_001341624.1:p.Leu525=
NR_148940.1:n.2445G>C (RAF1)
NR_148941.1:n.2391G>C (RAF1)
NR_148942.1:n.2330G>C (RAF1)
XM_011533974.3:c.1917G>C (RAF1)	XP_011532276.1:p.Leu639=
XM_017006966.1:c.1818G>C (RAF1)	XP_016862455.1:p.Leu606=
NM_001354689.3:c.1977G>C (RAF1)	NP_001341618.1:p.Leu659=
NM_001354690.2:c.1917G>C (RAF1)	NP_001341619.1:p.Leu639=
NM_001354691.2:c.1674G>C (RAF1)	NP_001341620.1:p.Leu558=
NM_001354692.2:c.1674G>C (RAF1)	NP_001341621.1:p.Leu558=
NM_001354693.2:c.1818G>C (RAF1)	NP_001341622.1:p.Leu606=
NM_001354694.2:c.1734G>C (RAF1)	NP_001341623.1:p.Leu578=
NM_001354695.2:c.1575G>C (RAF1)	NP_001341624.1:p.Leu525=
NR_148940.2:n.2361G>C (RAF1)
NR_148941.2:n.2307G>C (RAF1)
NR_148942.2:n.2246G>C (RAF1)
NM_001354690.3:c.1917G>C (RAF1)	NP_001341619.1:p.Leu639=
NM_001354691.3:c.1674G>C (RAF1)	NP_001341620.1:p.Leu558=
NM_001354692.3:c.1674G>C (RAF1)	NP_001341621.1:p.Leu558=
NM_001354693.3:c.1818G>C (RAF1)	NP_001341622.1:p.Leu606=
NM_001354694.3:c.1734G>C (RAF1)	NP_001341623.1:p.Leu578=
NM_001354695.3:c.1575G>C (RAF1)	NP_001341624.1:p.Leu525=
NM_002880.4:c.1917G>C (RAF1) MANE Select	NP_002871.1:p.Leu639=
NR_148940.3:n.2361G>C (RAF1)
NR_148941.3:n.2307G>C (RAF1)
NR_148942.3:n.2246G>C (RAF1)