Canonical Allele Identifier: CA351496640

Gene: RAF1 MKRN2

Linked Data

• MyVariant Identifiers: chr3:g.12626389T>G (hg19) ; chr3:g.12584890T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584890T>G , CM000665.2:g.12584890T>G	GRCh38
NC_000003.11:g.12626389T>G , CM000665.1:g.12626389T>G	GRCh37
NC_000003.10:g.12601389T>G	NCBI36
NG_007467.1:g.84290A>C , LRG_413:g.84290A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1425A>C (RAF1)	ENSP00000401088.1:n.*1425A>C
ENST00000432427.3:c.1077A>C (RAF1)
ENST00000460610.2:n.6072A>C (RAF1)
ENST00000471449.2:n.570A>C (RAF1)
ENST00000475353.2:n.4040A>C (RAF1)
ENST00000684903.1:c.*1437A>C (RAF1)	ENSP00000508612.1:n.*1437A>C
ENST00000685348.1:c.*1471A>C (RAF1)	ENSP00000510285.1:n.*1471A>C
ENST00000685437.1:c.1661A>C (RAF1)	ENSP00000508794.1:p.Asp554Ala
ENST00000685653.1:c.1760A>C (RAF1)	ENSP00000509968.1:p.Asp587Ala
ENST00000685697.1:n.2495A>C (RAF1)
ENST00000685738.1:c.*724A>C (RAF1)	ENSP00000510156.1:n.*724A>C
ENST00000686409.1:n.5169A>C (RAF1)
ENST00000686455.1:n.4481A>C (RAF1)
ENST00000686762.1:c.*319A>C (RAF1)	ENSP00000509767.1:n.*319A>C
ENST00000687257.1:n.4214A>C (RAF1)
ENST00000687326.1:c.*3052A>C (RAF1)	ENSP00000509665.1:n.*3052A>C
ENST00000687505.1:n.1878A>C (RAF1)
ENST00000687923.1:c.1649A>C (RAF1)	ENSP00000510255.1:p.Asp550Ala
ENST00000688269.1:n.2356A>C (RAF1)
ENST00000688444.1:n.3877A>C (RAF1)
ENST00000688543.1:c.1661A>C (RAF1)	ENSP00000509612.1:p.Asp554Ala
ENST00000688625.1:c.*3129A>C (RAF1)	ENSP00000509522.1:n.*3129A>C
ENST00000688803.1:n.3188A>C (RAF1)
ENST00000688914.1:n.1173A>C (RAF1)
ENST00000689097.1:c.*1437A>C (RAF1)	ENSP00000509756.1:n.*1437A>C
ENST00000689389.1:c.1583A>C (RAF1)	ENSP00000510213.1:p.Asp528Ala
ENST00000689418.1:c.*3655A>C (RAF1)	ENSP00000509467.1:n.*3655A>C
ENST00000689540.1:n.4128A>C (RAF1)
ENST00000689876.1:c.*309A>C (RAF1)	ENSP00000508535.1:n.*309A>C
ENST00000689914.1:c.*694A>C (RAF1)	ENSP00000509847.1:n.*694A>C
ENST00000690397.1:c.1649A>C (RAF1)	ENSP00000508730.1:p.Asp550Ala
ENST00000690460.1:c.1748A>C (RAF1)	ENSP00000509106.1:p.Asp583Ala
ENST00000690585.1:c.486A>C (RAF1)
ENST00000690625.1:n.2796A>C (RAF1)
ENST00000691396.1:c.*1632A>C (RAF1)	ENSP00000510712.1:n.*1632A>C
ENST00000691643.1:n.2813A>C (RAF1)
ENST00000691724.1:c.*717A>C (RAF1)	ENSP00000509255.1:n.*717A>C
ENST00000691779.1:c.*1338A>C (RAF1)	ENSP00000508592.1:n.*1338A>C
ENST00000691888.1:c.634A>C (RAF1)
ENST00000691899.1:c.1760A>C (RAF1)	ENSP00000508763.1:p.Asp587Ala
ENST00000692069.1:n.4684A>C (RAF1)
ENST00000692093.1:c.1661A>C (RAF1)	ENSP00000509669.1:p.Asp554Ala
ENST00000692311.1:n.2584A>C (RAF1)
ENST00000692558.1:n.4343A>C (RAF1)
ENST00000692773.1:c.*1497A>C (RAF1)	ENSP00000509055.1:n.*1497A>C
ENST00000692830.1:c.*1505A>C (RAF1)	ENSP00000509461.1:n.*1505A>C
ENST00000693312.1:c.1535A>C (RAF1)	ENSP00000508686.1:p.Asp512Ala
ENST00000693664.1:c.*211A>C (RAF1)	ENSP00000509614.1:n.*211A>C
ENST00000693705.1:c.*1139A>C (RAF1)	ENSP00000510697.1:n.*1139A>C
ENST00000251849.9:c.1760A>C (RAF1) MANE Select	ENSP00000251849.4:p.Asp587Ala
ENST00000442415.7:c.1820A>C (RAF1)	ENSP00000401888.2:p.Asp607Ala
ENST00000676541.1:c.*2637T>G (MKRN2)	ENSP00000503730.1:n.*2637T>G
ENST00000677142.1:c.*2637T>G (MKRN2)	ENSP00000504455.1:n.*2637T>G
ENST00000677816.1:c.*1192T>G (MKRN2)	ENSP00000502893.1:n.*1192T>G
ENST00000677941.1:n.2700T>G (MKRN2)
ENST00000251849.8:c.1760A>C (RAF1)	ENSP00000251849.4:p.Asp587Ala
ENST00000423275.5:c.*1437A>C (RAF1)	ENSP00000401088.1:n.*1437A>C
ENST00000432427.2:c.1397A>C (RAF1)	ENSP00000398591.2:p.Asp466Ala
ENST00000442415.6:c.1820A>C (RAF1)	ENSP00000401888.2:p.Asp607Ala
ENST00000471449.1:n.449A>C (RAF1)
NM_002880.3:c.1760A>C , LRG_413t1:c.1760A>C (RAF1)	NP_002871.1:p.Asp587Ala
XM_005265355.1:c.1760A>C (RAF1)	XP_005265412.1:p.Asp587Ala
XM_005265357.1:c.1661A>C (RAF1)	XP_005265414.1:p.Asp554Ala
XM_005265358.3:c.1517A>C (RAF1)	XP_005265415.1:p.Asp506Ala
XM_005265359.3:c.1418A>C (RAF1)	XP_005265416.1:p.Asp473Ala
XM_011533974.1:c.1760A>C (RAF1)	XP_011532276.1:p.Asp587Ala
XM_011533975.1:c.1517A>C (RAF1)	XP_011532277.1:p.Asp506Ala
NM_001354689.1:c.1820A>C (RAF1)	NP_001341618.1:p.Asp607Ala
NM_001354690.1:c.1760A>C (RAF1)	NP_001341619.1:p.Asp587Ala
NM_001354691.1:c.1517A>C (RAF1)	NP_001341620.1:p.Asp506Ala
NM_001354692.1:c.1517A>C (RAF1)	NP_001341621.1:p.Asp506Ala
NM_001354693.1:c.1661A>C (RAF1)	NP_001341622.1:p.Asp554Ala
NM_001354694.1:c.1577A>C (RAF1)	NP_001341623.1:p.Asp526Ala
NM_001354695.1:c.1418A>C (RAF1)	NP_001341624.1:p.Asp473Ala
NR_148940.1:n.2288A>C (RAF1)
NR_148941.1:n.2234A>C (RAF1)
NR_148942.1:n.2173A>C (RAF1)
XM_011533974.3:c.1760A>C (RAF1)	XP_011532276.1:p.Asp587Ala
XM_017006966.1:c.1661A>C (RAF1)	XP_016862455.1:p.Asp554Ala
NM_001354689.3:c.1820A>C (RAF1)	NP_001341618.1:p.Asp607Ala
NM_001354690.2:c.1760A>C (RAF1)	NP_001341619.1:p.Asp587Ala
NM_001354691.2:c.1517A>C (RAF1)	NP_001341620.1:p.Asp506Ala
NM_001354692.2:c.1517A>C (RAF1)	NP_001341621.1:p.Asp506Ala
NM_001354693.2:c.1661A>C (RAF1)	NP_001341622.1:p.Asp554Ala
NM_001354694.2:c.1577A>C (RAF1)	NP_001341623.1:p.Asp526Ala
NM_001354695.2:c.1418A>C (RAF1)	NP_001341624.1:p.Asp473Ala
NR_148940.2:n.2204A>C (RAF1)
NR_148941.2:n.2150A>C (RAF1)
NR_148942.2:n.2089A>C (RAF1)
NM_001354690.3:c.1760A>C (RAF1)	NP_001341619.1:p.Asp587Ala
NM_001354691.3:c.1517A>C (RAF1)	NP_001341620.1:p.Asp506Ala
NM_001354692.3:c.1517A>C (RAF1)	NP_001341621.1:p.Asp506Ala
NM_001354693.3:c.1661A>C (RAF1)	NP_001341622.1:p.Asp554Ala
NM_001354694.3:c.1577A>C (RAF1)	NP_001341623.1:p.Asp526Ala
NM_001354695.3:c.1418A>C (RAF1)	NP_001341624.1:p.Asp473Ala
NM_002880.4:c.1760A>C (RAF1) MANE Select	NP_002871.1:p.Asp587Ala
NR_148940.3:n.2204A>C (RAF1)
NR_148941.3:n.2150A>C (RAF1)
NR_148942.3:n.2089A>C (RAF1)