Canonical Allele Identifier: CA351495706

Gene: RAF1 MKRN2

Linked Data

• dbSNP Id: rs1440964132
• MyVariant Identifiers: chr3:g.12626068G>A (hg19) ; chr3:g.12584569G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584569G>A , CM000665.2:g.12584569G>A	GRCh38
NC_000003.11:g.12626068G>A , CM000665.1:g.12626068G>A	GRCh37
NC_000003.10:g.12601068G>A	NCBI36
NG_007467.1:g.84611C>T , LRG_413:g.84611C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1557C>T (RAF1)	ENSP00000401088.1:n.*1557C>T
ENST00000432427.3:c.1209C>T (RAF1)
ENST00000460610.2:n.6204C>T (RAF1)
ENST00000471449.2:n.702C>T (RAF1)
ENST00000475353.2:n.4172C>T (RAF1)
ENST00000684903.1:c.*1569C>T (RAF1)	ENSP00000508612.1:n.*1569C>T
ENST00000685348.1:c.*1603C>T (RAF1)	ENSP00000510285.1:n.*1603C>T
ENST00000685437.1:c.1793C>T (RAF1)	ENSP00000508794.1:p.Thr598Ile
ENST00000685653.1:c.1892C>T (RAF1)	ENSP00000509968.1:p.Thr631Ile
ENST00000685697.1:n.2627C>T (RAF1)
ENST00000685738.1:c.*856C>T (RAF1)	ENSP00000510156.1:n.*856C>T
ENST00000686409.1:n.5301C>T (RAF1)
ENST00000686455.1:n.4613C>T (RAF1)
ENST00000686762.1:c.*451C>T (RAF1)	ENSP00000509767.1:n.*451C>T
ENST00000687257.1:n.4346C>T (RAF1)
ENST00000687326.1:c.*3184C>T (RAF1)	ENSP00000509665.1:n.*3184C>T
ENST00000687505.1:n.2010C>T (RAF1)
ENST00000687923.1:c.1781C>T (RAF1)	ENSP00000510255.1:p.Thr594Ile
ENST00000688269.1:n.2488C>T (RAF1)
ENST00000688444.1:n.4009C>T (RAF1)
ENST00000688543.1:c.1793C>T (RAF1)	ENSP00000509612.1:p.Thr598Ile
ENST00000688625.1:c.*3261C>T (RAF1)	ENSP00000509522.1:n.*3261C>T
ENST00000688803.1:n.3320C>T (RAF1)
ENST00000689097.1:c.*1569C>T (RAF1)	ENSP00000509756.1:n.*1569C>T
ENST00000689389.1:c.1715C>T (RAF1)	ENSP00000510213.1:p.Thr572Ile
ENST00000689418.1:c.*3787C>T (RAF1)	ENSP00000509467.1:n.*3787C>T
ENST00000689540.1:n.4260C>T (RAF1)
ENST00000689876.1:c.*441C>T (RAF1)	ENSP00000508535.1:n.*441C>T
ENST00000689914.1:c.*826C>T (RAF1)	ENSP00000509847.1:n.*826C>T
ENST00000690397.1:c.1781C>T (RAF1)	ENSP00000508730.1:p.Thr594Ile
ENST00000690460.1:c.1880C>T (RAF1)	ENSP00000509106.1:p.Thr627Ile
ENST00000690585.1:c.618C>T (RAF1)
ENST00000690625.1:n.2928C>T (RAF1)
ENST00000691396.1:c.*1764C>T (RAF1)	ENSP00000510712.1:n.*1764C>T
ENST00000691643.1:n.2945C>T (RAF1)
ENST00000691724.1:c.*849C>T (RAF1)	ENSP00000509255.1:n.*849C>T
ENST00000691779.1:c.*1470C>T (RAF1)	ENSP00000508592.1:n.*1470C>T
ENST00000691888.1:c.766C>T (RAF1)
ENST00000691899.1:c.1892C>T (RAF1)	ENSP00000508763.1:p.Thr631Ile
ENST00000692069.1:n.4816C>T (RAF1)
ENST00000692093.1:c.1793C>T (RAF1)	ENSP00000509669.1:p.Thr598Ile
ENST00000692311.1:n.2716C>T (RAF1)
ENST00000692558.1:n.4475C>T (RAF1)
ENST00000692773.1:c.*1629C>T (RAF1)	ENSP00000509055.1:n.*1629C>T
ENST00000692830.1:c.*1637C>T (RAF1)	ENSP00000509461.1:n.*1637C>T
ENST00000693312.1:c.1667C>T (RAF1)	ENSP00000508686.1:p.Thr556Ile
ENST00000693664.1:c.*343C>T (RAF1)	ENSP00000509614.1:n.*343C>T
ENST00000693705.1:c.*1271C>T (RAF1)	ENSP00000510697.1:n.*1271C>T
ENST00000251849.9:c.1892C>T (RAF1) MANE Select	ENSP00000251849.4:p.Thr631Ile
ENST00000442415.7:c.1952C>T (RAF1)	ENSP00000401888.2:p.Thr651Ile
ENST00000676541.1:c.*2316G>A (MKRN2)	ENSP00000503730.1:n.*2316G>A
ENST00000677142.1:c.*2316G>A (MKRN2)	ENSP00000504455.1:n.*2316G>A
ENST00000677816.1:c.*871G>A (MKRN2)	ENSP00000502893.1:n.*871G>A
ENST00000677941.1:n.2379G>A (MKRN2)
ENST00000251849.8:c.1892C>T (RAF1)	ENSP00000251849.4:p.Thr631Ile
ENST00000423275.5:c.*1569C>T (RAF1)	ENSP00000401088.1:n.*1569C>T
ENST00000432427.2:c.1529C>T (RAF1)	ENSP00000398591.2:p.Thr510Ile
ENST00000442415.6:c.1952C>T (RAF1)	ENSP00000401888.2:p.Thr651Ile
ENST00000471449.1:n.581C>T (RAF1)
NM_002880.3:c.1892C>T , LRG_413t1:c.1892C>T (RAF1)	NP_002871.1:p.Thr631Ile
XM_005265355.1:c.1892C>T (RAF1)	XP_005265412.1:p.Thr631Ile
XM_005265357.1:c.1793C>T (RAF1)	XP_005265414.1:p.Thr598Ile
XM_005265358.3:c.1649C>T (RAF1)	XP_005265415.1:p.Thr550Ile
XM_005265359.3:c.1550C>T (RAF1)	XP_005265416.1:p.Thr517Ile
XM_011533974.1:c.1892C>T (RAF1)	XP_011532276.1:p.Thr631Ile
XM_011533975.1:c.1649C>T (RAF1)	XP_011532277.1:p.Thr550Ile
NM_001354689.1:c.1952C>T (RAF1)	NP_001341618.1:p.Thr651Ile
NM_001354690.1:c.1892C>T (RAF1)	NP_001341619.1:p.Thr631Ile
NM_001354691.1:c.1649C>T (RAF1)	NP_001341620.1:p.Thr550Ile
NM_001354692.1:c.1649C>T (RAF1)	NP_001341621.1:p.Thr550Ile
NM_001354693.1:c.1793C>T (RAF1)	NP_001341622.1:p.Thr598Ile
NM_001354694.1:c.1709C>T (RAF1)	NP_001341623.1:p.Thr570Ile
NM_001354695.1:c.1550C>T (RAF1)	NP_001341624.1:p.Thr517Ile
NR_148940.1:n.2420C>T (RAF1)
NR_148941.1:n.2366C>T (RAF1)
NR_148942.1:n.2305C>T (RAF1)
XM_011533974.3:c.1892C>T (RAF1)	XP_011532276.1:p.Thr631Ile
XM_017006966.1:c.1793C>T (RAF1)	XP_016862455.1:p.Thr598Ile
NM_001354689.3:c.1952C>T (RAF1)	NP_001341618.1:p.Thr651Ile
NM_001354690.2:c.1892C>T (RAF1)	NP_001341619.1:p.Thr631Ile
NM_001354691.2:c.1649C>T (RAF1)	NP_001341620.1:p.Thr550Ile
NM_001354692.2:c.1649C>T (RAF1)	NP_001341621.1:p.Thr550Ile
NM_001354693.2:c.1793C>T (RAF1)	NP_001341622.1:p.Thr598Ile
NM_001354694.2:c.1709C>T (RAF1)	NP_001341623.1:p.Thr570Ile
NM_001354695.2:c.1550C>T (RAF1)	NP_001341624.1:p.Thr517Ile
NR_148940.2:n.2336C>T (RAF1)
NR_148941.2:n.2282C>T (RAF1)
NR_148942.2:n.2221C>T (RAF1)
NM_001354690.3:c.1892C>T (RAF1)	NP_001341619.1:p.Thr631Ile
NM_001354691.3:c.1649C>T (RAF1)	NP_001341620.1:p.Thr550Ile
NM_001354692.3:c.1649C>T (RAF1)	NP_001341621.1:p.Thr550Ile
NM_001354693.3:c.1793C>T (RAF1)	NP_001341622.1:p.Thr598Ile
NM_001354694.3:c.1709C>T (RAF1)	NP_001341623.1:p.Thr570Ile
NM_001354695.3:c.1550C>T (RAF1)	NP_001341624.1:p.Thr517Ile
NM_002880.4:c.1892C>T (RAF1) MANE Select	NP_002871.1:p.Thr631Ile
NR_148940.3:n.2336C>T (RAF1)
NR_148941.3:n.2282C>T (RAF1)
NR_148942.3:n.2221C>T (RAF1)