Canonical Allele Identifier: CA351496164

Gene: RAF1 MKRN2

Linked Data

• MyVariant Identifiers: chr3:g.12626135G>T (hg19) ; chr3:g.12584636G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584636G>T , CM000665.2:g.12584636G>T	GRCh38
NC_000003.11:g.12626135G>T , CM000665.1:g.12626135G>T	GRCh37
NC_000003.10:g.12601135G>T	NCBI36
NG_007467.1:g.84544C>A , LRG_413:g.84544C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1490C>A (RAF1)	ENSP00000401088.1:n.*1490C>A
ENST00000432427.3:c.1142C>A (RAF1)
ENST00000460610.2:n.6137C>A (RAF1)
ENST00000471449.2:n.635C>A (RAF1)
ENST00000475353.2:n.4105C>A (RAF1)
ENST00000684903.1:c.*1502C>A (RAF1)	ENSP00000508612.1:n.*1502C>A
ENST00000685348.1:c.*1536C>A (RAF1)	ENSP00000510285.1:n.*1536C>A
ENST00000685437.1:c.1726C>A (RAF1)	ENSP00000508794.1:p.Leu576Ile
ENST00000685653.1:c.1825C>A (RAF1)	ENSP00000509968.1:p.Leu609Ile
ENST00000685697.1:n.2560C>A (RAF1)
ENST00000685738.1:c.*789C>A (RAF1)	ENSP00000510156.1:n.*789C>A
ENST00000686409.1:n.5234C>A (RAF1)
ENST00000686455.1:n.4546C>A (RAF1)
ENST00000686762.1:c.*384C>A (RAF1)	ENSP00000509767.1:n.*384C>A
ENST00000687257.1:n.4279C>A (RAF1)
ENST00000687326.1:c.*3117C>A (RAF1)	ENSP00000509665.1:n.*3117C>A
ENST00000687505.1:n.1943C>A (RAF1)
ENST00000687923.1:c.1714C>A (RAF1)	ENSP00000510255.1:p.Leu572Ile
ENST00000688269.1:n.2421C>A (RAF1)
ENST00000688444.1:n.3942C>A (RAF1)
ENST00000688543.1:c.1726C>A (RAF1)	ENSP00000509612.1:p.Leu576Ile
ENST00000688625.1:c.*3194C>A (RAF1)	ENSP00000509522.1:n.*3194C>A
ENST00000688803.1:n.3253C>A (RAF1)
ENST00000689097.1:c.*1502C>A (RAF1)	ENSP00000509756.1:n.*1502C>A
ENST00000689389.1:c.1648C>A (RAF1)	ENSP00000510213.1:p.Leu550Ile
ENST00000689418.1:c.*3720C>A (RAF1)	ENSP00000509467.1:n.*3720C>A
ENST00000689540.1:n.4193C>A (RAF1)
ENST00000689876.1:c.*374C>A (RAF1)	ENSP00000508535.1:n.*374C>A
ENST00000689914.1:c.*759C>A (RAF1)	ENSP00000509847.1:n.*759C>A
ENST00000690397.1:c.1714C>A (RAF1)	ENSP00000508730.1:p.Leu572Ile
ENST00000690460.1:c.1813C>A (RAF1)	ENSP00000509106.1:p.Leu605Ile
ENST00000690585.1:c.551C>A (RAF1)
ENST00000690625.1:n.2861C>A (RAF1)
ENST00000691396.1:c.*1697C>A (RAF1)	ENSP00000510712.1:n.*1697C>A
ENST00000691643.1:n.2878C>A (RAF1)
ENST00000691724.1:c.*782C>A (RAF1)	ENSP00000509255.1:n.*782C>A
ENST00000691779.1:c.*1403C>A (RAF1)	ENSP00000508592.1:n.*1403C>A
ENST00000691888.1:c.699C>A (RAF1)
ENST00000691899.1:c.1825C>A (RAF1)	ENSP00000508763.1:p.Leu609Ile
ENST00000692069.1:n.4749C>A (RAF1)
ENST00000692093.1:c.1726C>A (RAF1)	ENSP00000509669.1:p.Leu576Ile
ENST00000692311.1:n.2649C>A (RAF1)
ENST00000692558.1:n.4408C>A (RAF1)
ENST00000692773.1:c.*1562C>A (RAF1)	ENSP00000509055.1:n.*1562C>A
ENST00000692830.1:c.*1570C>A (RAF1)	ENSP00000509461.1:n.*1570C>A
ENST00000693312.1:c.1600C>A (RAF1)	ENSP00000508686.1:p.Leu534Ile
ENST00000693664.1:c.*276C>A (RAF1)	ENSP00000509614.1:n.*276C>A
ENST00000693705.1:c.*1204C>A (RAF1)	ENSP00000510697.1:n.*1204C>A
ENST00000251849.9:c.1825C>A (RAF1) MANE Select	ENSP00000251849.4:p.Leu609Ile
ENST00000442415.7:c.1885C>A (RAF1)	ENSP00000401888.2:p.Leu629Ile
ENST00000676541.1:c.*2383G>T (MKRN2)	ENSP00000503730.1:n.*2383G>T
ENST00000677142.1:c.*2383G>T (MKRN2)	ENSP00000504455.1:n.*2383G>T
ENST00000677816.1:c.*938G>T (MKRN2)	ENSP00000502893.1:n.*938G>T
ENST00000677941.1:n.2446G>T (MKRN2)
ENST00000251849.8:c.1825C>A (RAF1)	ENSP00000251849.4:p.Leu609Ile
ENST00000423275.5:c.*1502C>A (RAF1)	ENSP00000401088.1:n.*1502C>A
ENST00000432427.2:c.1462C>A (RAF1)	ENSP00000398591.2:p.Leu488Ile
ENST00000442415.6:c.1885C>A (RAF1)	ENSP00000401888.2:p.Leu629Ile
ENST00000471449.1:n.514C>A (RAF1)
NM_002880.3:c.1825C>A , LRG_413t1:c.1825C>A (RAF1)	NP_002871.1:p.Leu609Ile
XM_005265355.1:c.1825C>A (RAF1)	XP_005265412.1:p.Leu609Ile
XM_005265357.1:c.1726C>A (RAF1)	XP_005265414.1:p.Leu576Ile
XM_005265358.3:c.1582C>A (RAF1)	XP_005265415.1:p.Leu528Ile
XM_005265359.3:c.1483C>A (RAF1)	XP_005265416.1:p.Leu495Ile
XM_011533974.1:c.1825C>A (RAF1)	XP_011532276.1:p.Leu609Ile
XM_011533975.1:c.1582C>A (RAF1)	XP_011532277.1:p.Leu528Ile
NM_001354689.1:c.1885C>A (RAF1)	NP_001341618.1:p.Leu629Ile
NM_001354690.1:c.1825C>A (RAF1)	NP_001341619.1:p.Leu609Ile
NM_001354691.1:c.1582C>A (RAF1)	NP_001341620.1:p.Leu528Ile
NM_001354692.1:c.1582C>A (RAF1)	NP_001341621.1:p.Leu528Ile
NM_001354693.1:c.1726C>A (RAF1)	NP_001341622.1:p.Leu576Ile
NM_001354694.1:c.1642C>A (RAF1)	NP_001341623.1:p.Leu548Ile
NM_001354695.1:c.1483C>A (RAF1)	NP_001341624.1:p.Leu495Ile
NR_148940.1:n.2353C>A (RAF1)
NR_148941.1:n.2299C>A (RAF1)
NR_148942.1:n.2238C>A (RAF1)
XM_011533974.3:c.1825C>A (RAF1)	XP_011532276.1:p.Leu609Ile
XM_017006966.1:c.1726C>A (RAF1)	XP_016862455.1:p.Leu576Ile
NM_001354689.3:c.1885C>A (RAF1)	NP_001341618.1:p.Leu629Ile
NM_001354690.2:c.1825C>A (RAF1)	NP_001341619.1:p.Leu609Ile
NM_001354691.2:c.1582C>A (RAF1)	NP_001341620.1:p.Leu528Ile
NM_001354692.2:c.1582C>A (RAF1)	NP_001341621.1:p.Leu528Ile
NM_001354693.2:c.1726C>A (RAF1)	NP_001341622.1:p.Leu576Ile
NM_001354694.2:c.1642C>A (RAF1)	NP_001341623.1:p.Leu548Ile
NM_001354695.2:c.1483C>A (RAF1)	NP_001341624.1:p.Leu495Ile
NR_148940.2:n.2269C>A (RAF1)
NR_148941.2:n.2215C>A (RAF1)
NR_148942.2:n.2154C>A (RAF1)
NM_001354690.3:c.1825C>A (RAF1)	NP_001341619.1:p.Leu609Ile
NM_001354691.3:c.1582C>A (RAF1)	NP_001341620.1:p.Leu528Ile
NM_001354692.3:c.1582C>A (RAF1)	NP_001341621.1:p.Leu528Ile
NM_001354693.3:c.1726C>A (RAF1)	NP_001341622.1:p.Leu576Ile
NM_001354694.3:c.1642C>A (RAF1)	NP_001341623.1:p.Leu548Ile
NM_001354695.3:c.1483C>A (RAF1)	NP_001341624.1:p.Leu495Ile
NM_002880.4:c.1825C>A (RAF1) MANE Select	NP_002871.1:p.Leu609Ile
NR_148940.3:n.2269C>A (RAF1)
NR_148941.3:n.2215C>A (RAF1)
NR_148942.3:n.2154C>A (RAF1)