Canonical Allele Identifier: CA351496674

Gene: RAF1 MKRN2

Linked Data

• MyVariant Identifiers: chr3:g.12626400C>A (hg19) ; chr3:g.12584901C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584901C>A , CM000665.2:g.12584901C>A	GRCh38
NC_000003.11:g.12626400C>A , CM000665.1:g.12626400C>A	GRCh37
NC_000003.10:g.12601400C>A	NCBI36
NG_007467.1:g.84279G>T , LRG_413:g.84279G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1414G>T (RAF1)	ENSP00000401088.1:n.*1414G>T
ENST00000432427.3:c.1066G>T (RAF1)
ENST00000460610.2:n.6061G>T (RAF1)
ENST00000471449.2:n.559G>T (RAF1)
ENST00000475353.2:n.4029G>T (RAF1)
ENST00000684903.1:c.*1426G>T (RAF1)	ENSP00000508612.1:n.*1426G>T
ENST00000685348.1:c.*1460G>T (RAF1)	ENSP00000510285.1:n.*1460G>T
ENST00000685437.1:c.1650G>T (RAF1)	ENSP00000508794.1:p.Arg550Ser
ENST00000685653.1:c.1749G>T (RAF1)	ENSP00000509968.1:p.Arg583Ser
ENST00000685697.1:n.2484G>T (RAF1)
ENST00000685738.1:c.*713G>T (RAF1)	ENSP00000510156.1:n.*713G>T
ENST00000686409.1:n.5158G>T (RAF1)
ENST00000686455.1:n.4470G>T (RAF1)
ENST00000686762.1:c.*308G>T (RAF1)	ENSP00000509767.1:n.*308G>T
ENST00000687257.1:n.4203G>T (RAF1)
ENST00000687326.1:c.*3041G>T (RAF1)	ENSP00000509665.1:n.*3041G>T
ENST00000687505.1:n.1867G>T (RAF1)
ENST00000687923.1:c.1638G>T (RAF1)	ENSP00000510255.1:p.Arg546Ser
ENST00000688269.1:n.2345G>T (RAF1)
ENST00000688444.1:n.3866G>T (RAF1)
ENST00000688543.1:c.1650G>T (RAF1)	ENSP00000509612.1:p.Arg550Ser
ENST00000688625.1:c.*3118G>T (RAF1)	ENSP00000509522.1:n.*3118G>T
ENST00000688803.1:n.3177G>T (RAF1)
ENST00000688914.1:n.1162G>T (RAF1)
ENST00000689097.1:c.*1426G>T (RAF1)	ENSP00000509756.1:n.*1426G>T
ENST00000689389.1:c.1572G>T (RAF1)	ENSP00000510213.1:p.Arg524Ser
ENST00000689418.1:c.*3644G>T (RAF1)	ENSP00000509467.1:n.*3644G>T
ENST00000689540.1:n.4117G>T (RAF1)
ENST00000689876.1:c.*298G>T (RAF1)	ENSP00000508535.1:n.*298G>T
ENST00000689914.1:c.*683G>T (RAF1)	ENSP00000509847.1:n.*683G>T
ENST00000690397.1:c.1638G>T (RAF1)	ENSP00000508730.1:p.Arg546Ser
ENST00000690460.1:c.1737G>T (RAF1)	ENSP00000509106.1:p.Arg579Ser
ENST00000690585.1:c.475G>T (RAF1)
ENST00000690625.1:n.2785G>T (RAF1)
ENST00000691396.1:c.*1621G>T (RAF1)	ENSP00000510712.1:n.*1621G>T
ENST00000691643.1:n.2802G>T (RAF1)
ENST00000691724.1:c.*706G>T (RAF1)	ENSP00000509255.1:n.*706G>T
ENST00000691779.1:c.*1327G>T (RAF1)	ENSP00000508592.1:n.*1327G>T
ENST00000691888.1:c.623G>T (RAF1)
ENST00000691899.1:c.1749G>T (RAF1)	ENSP00000508763.1:p.Arg583Ser
ENST00000692069.1:n.4673G>T (RAF1)
ENST00000692093.1:c.1650G>T (RAF1)	ENSP00000509669.1:p.Arg550Ser
ENST00000692311.1:n.2573G>T (RAF1)
ENST00000692558.1:n.4332G>T (RAF1)
ENST00000692773.1:c.*1486G>T (RAF1)	ENSP00000509055.1:n.*1486G>T
ENST00000692830.1:c.*1494G>T (RAF1)	ENSP00000509461.1:n.*1494G>T
ENST00000693312.1:c.1524G>T (RAF1)	ENSP00000508686.1:p.Arg508Ser
ENST00000693664.1:c.*200G>T (RAF1)	ENSP00000509614.1:n.*200G>T
ENST00000693705.1:c.*1128G>T (RAF1)	ENSP00000510697.1:n.*1128G>T
ENST00000251849.9:c.1749G>T (RAF1) MANE Select	ENSP00000251849.4:p.Arg583Ser
ENST00000442415.7:c.1809G>T (RAF1)	ENSP00000401888.2:p.Arg603Ser
ENST00000676541.1:c.*2648C>A (MKRN2)	ENSP00000503730.1:n.*2648C>A
ENST00000677142.1:c.*2648C>A (MKRN2)	ENSP00000504455.1:n.*2648C>A
ENST00000677816.1:c.*1203C>A (MKRN2)	ENSP00000502893.1:n.*1203C>A
ENST00000677941.1:n.2711C>A (MKRN2)
ENST00000251849.8:c.1749G>T (RAF1)	ENSP00000251849.4:p.Arg583Ser
ENST00000423275.5:c.*1426G>T (RAF1)	ENSP00000401088.1:n.*1426G>T
ENST00000432427.2:c.1386G>T (RAF1)	ENSP00000398591.2:p.Arg462Ser
ENST00000442415.6:c.1809G>T (RAF1)	ENSP00000401888.2:p.Arg603Ser
ENST00000471449.1:n.438G>T (RAF1)
NM_002880.3:c.1749G>T , LRG_413t1:c.1749G>T (RAF1)	NP_002871.1:p.Arg583Ser
XM_005265355.1:c.1749G>T (RAF1)	XP_005265412.1:p.Arg583Ser
XM_005265357.1:c.1650G>T (RAF1)	XP_005265414.1:p.Arg550Ser
XM_005265358.3:c.1506G>T (RAF1)	XP_005265415.1:p.Arg502Ser
XM_005265359.3:c.1407G>T (RAF1)	XP_005265416.1:p.Arg469Ser
XM_011533974.1:c.1749G>T (RAF1)	XP_011532276.1:p.Arg583Ser
XM_011533975.1:c.1506G>T (RAF1)	XP_011532277.1:p.Arg502Ser
NM_001354689.1:c.1809G>T (RAF1)	NP_001341618.1:p.Arg603Ser
NM_001354690.1:c.1749G>T (RAF1)	NP_001341619.1:p.Arg583Ser
NM_001354691.1:c.1506G>T (RAF1)	NP_001341620.1:p.Arg502Ser
NM_001354692.1:c.1506G>T (RAF1)	NP_001341621.1:p.Arg502Ser
NM_001354693.1:c.1650G>T (RAF1)	NP_001341622.1:p.Arg550Ser
NM_001354694.1:c.1566G>T (RAF1)	NP_001341623.1:p.Arg522Ser
NM_001354695.1:c.1407G>T (RAF1)	NP_001341624.1:p.Arg469Ser
NR_148940.1:n.2277G>T (RAF1)
NR_148941.1:n.2223G>T (RAF1)
NR_148942.1:n.2162G>T (RAF1)
XM_011533974.3:c.1749G>T (RAF1)	XP_011532276.1:p.Arg583Ser
XM_017006966.1:c.1650G>T (RAF1)	XP_016862455.1:p.Arg550Ser
NM_001354689.3:c.1809G>T (RAF1)	NP_001341618.1:p.Arg603Ser
NM_001354690.2:c.1749G>T (RAF1)	NP_001341619.1:p.Arg583Ser
NM_001354691.2:c.1506G>T (RAF1)	NP_001341620.1:p.Arg502Ser
NM_001354692.2:c.1506G>T (RAF1)	NP_001341621.1:p.Arg502Ser
NM_001354693.2:c.1650G>T (RAF1)	NP_001341622.1:p.Arg550Ser
NM_001354694.2:c.1566G>T (RAF1)	NP_001341623.1:p.Arg522Ser
NM_001354695.2:c.1407G>T (RAF1)	NP_001341624.1:p.Arg469Ser
NR_148940.2:n.2193G>T (RAF1)
NR_148941.2:n.2139G>T (RAF1)
NR_148942.2:n.2078G>T (RAF1)
NM_001354690.3:c.1749G>T (RAF1)	NP_001341619.1:p.Arg583Ser
NM_001354691.3:c.1506G>T (RAF1)	NP_001341620.1:p.Arg502Ser
NM_001354692.3:c.1506G>T (RAF1)	NP_001341621.1:p.Arg502Ser
NM_001354693.3:c.1650G>T (RAF1)	NP_001341622.1:p.Arg550Ser
NM_001354694.3:c.1566G>T (RAF1)	NP_001341623.1:p.Arg522Ser
NM_001354695.3:c.1407G>T (RAF1)	NP_001341624.1:p.Arg469Ser
NM_002880.4:c.1749G>T (RAF1) MANE Select	NP_002871.1:p.Arg583Ser
NR_148940.3:n.2193G>T (RAF1)
NR_148941.3:n.2139G>T (RAF1)
NR_148942.3:n.2078G>T (RAF1)