Canonical Allele Identifier: CA351496069

Gene: RAF1 MKRN2

Linked Data

• MyVariant Identifiers: chr3:g.12626120G>T (hg19) ; chr3:g.12584621G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584621G>T , CM000665.2:g.12584621G>T	GRCh38
NC_000003.11:g.12626120G>T , CM000665.1:g.12626120G>T	GRCh37
NC_000003.10:g.12601120G>T	NCBI36
NG_007467.1:g.84559C>A , LRG_413:g.84559C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1505C>A (RAF1)	ENSP00000401088.1:n.*1505C>A
ENST00000432427.3:c.1157C>A (RAF1)
ENST00000460610.2:n.6152C>A (RAF1)
ENST00000471449.2:n.650C>A (RAF1)
ENST00000475353.2:n.4120C>A (RAF1)
ENST00000684903.1:c.*1517C>A (RAF1)	ENSP00000508612.1:n.*1517C>A
ENST00000685348.1:c.*1551C>A (RAF1)	ENSP00000510285.1:n.*1551C>A
ENST00000685437.1:c.1741C>A (RAF1)	ENSP00000508794.1:p.Pro581Thr
ENST00000685653.1:c.1840C>A (RAF1)	ENSP00000509968.1:p.Pro614Thr
ENST00000685697.1:n.2575C>A (RAF1)
ENST00000685738.1:c.*804C>A (RAF1)	ENSP00000510156.1:n.*804C>A
ENST00000686409.1:n.5249C>A (RAF1)
ENST00000686455.1:n.4561C>A (RAF1)
ENST00000686762.1:c.*399C>A (RAF1)	ENSP00000509767.1:n.*399C>A
ENST00000687257.1:n.4294C>A (RAF1)
ENST00000687326.1:c.*3132C>A (RAF1)	ENSP00000509665.1:n.*3132C>A
ENST00000687505.1:n.1958C>A (RAF1)
ENST00000687923.1:c.1729C>A (RAF1)	ENSP00000510255.1:p.Pro577Thr
ENST00000688269.1:n.2436C>A (RAF1)
ENST00000688444.1:n.3957C>A (RAF1)
ENST00000688543.1:c.1741C>A (RAF1)	ENSP00000509612.1:p.Pro581Thr
ENST00000688625.1:c.*3209C>A (RAF1)	ENSP00000509522.1:n.*3209C>A
ENST00000688803.1:n.3268C>A (RAF1)
ENST00000689097.1:c.*1517C>A (RAF1)	ENSP00000509756.1:n.*1517C>A
ENST00000689389.1:c.1663C>A (RAF1)	ENSP00000510213.1:p.Pro555Thr
ENST00000689418.1:c.*3735C>A (RAF1)	ENSP00000509467.1:n.*3735C>A
ENST00000689540.1:n.4208C>A (RAF1)
ENST00000689876.1:c.*389C>A (RAF1)	ENSP00000508535.1:n.*389C>A
ENST00000689914.1:c.*774C>A (RAF1)	ENSP00000509847.1:n.*774C>A
ENST00000690397.1:c.1729C>A (RAF1)	ENSP00000508730.1:p.Pro577Thr
ENST00000690460.1:c.1828C>A (RAF1)	ENSP00000509106.1:p.Pro610Thr
ENST00000690585.1:c.566C>A (RAF1)
ENST00000690625.1:n.2876C>A (RAF1)
ENST00000691396.1:c.*1712C>A (RAF1)	ENSP00000510712.1:n.*1712C>A
ENST00000691643.1:n.2893C>A (RAF1)
ENST00000691724.1:c.*797C>A (RAF1)	ENSP00000509255.1:n.*797C>A
ENST00000691779.1:c.*1418C>A (RAF1)	ENSP00000508592.1:n.*1418C>A
ENST00000691888.1:c.714C>A (RAF1)
ENST00000691899.1:c.1840C>A (RAF1)	ENSP00000508763.1:p.Pro614Thr
ENST00000692069.1:n.4764C>A (RAF1)
ENST00000692093.1:c.1741C>A (RAF1)	ENSP00000509669.1:p.Pro581Thr
ENST00000692311.1:n.2664C>A (RAF1)
ENST00000692558.1:n.4423C>A (RAF1)
ENST00000692773.1:c.*1577C>A (RAF1)	ENSP00000509055.1:n.*1577C>A
ENST00000692830.1:c.*1585C>A (RAF1)	ENSP00000509461.1:n.*1585C>A
ENST00000693312.1:c.1615C>A (RAF1)	ENSP00000508686.1:p.Pro539Thr
ENST00000693664.1:c.*291C>A (RAF1)	ENSP00000509614.1:n.*291C>A
ENST00000693705.1:c.*1219C>A (RAF1)	ENSP00000510697.1:n.*1219C>A
ENST00000251849.9:c.1840C>A (RAF1) MANE Select	ENSP00000251849.4:p.Pro614Thr
ENST00000442415.7:c.1900C>A (RAF1)	ENSP00000401888.2:p.Pro634Thr
ENST00000676541.1:c.*2368G>T (MKRN2)	ENSP00000503730.1:n.*2368G>T
ENST00000677142.1:c.*2368G>T (MKRN2)	ENSP00000504455.1:n.*2368G>T
ENST00000677816.1:c.*923G>T (MKRN2)	ENSP00000502893.1:n.*923G>T
ENST00000677941.1:n.2431G>T (MKRN2)
ENST00000251849.8:c.1840C>A (RAF1)	ENSP00000251849.4:p.Pro614Thr
ENST00000423275.5:c.*1517C>A (RAF1)	ENSP00000401088.1:n.*1517C>A
ENST00000432427.2:c.1477C>A (RAF1)	ENSP00000398591.2:p.Pro493Thr
ENST00000442415.6:c.1900C>A (RAF1)	ENSP00000401888.2:p.Pro634Thr
ENST00000471449.1:n.529C>A (RAF1)
NM_002880.3:c.1840C>A , LRG_413t1:c.1840C>A (RAF1)	NP_002871.1:p.Pro614Thr
XM_005265355.1:c.1840C>A (RAF1)	XP_005265412.1:p.Pro614Thr
XM_005265357.1:c.1741C>A (RAF1)	XP_005265414.1:p.Pro581Thr
XM_005265358.3:c.1597C>A (RAF1)	XP_005265415.1:p.Pro533Thr
XM_005265359.3:c.1498C>A (RAF1)	XP_005265416.1:p.Pro500Thr
XM_011533974.1:c.1840C>A (RAF1)	XP_011532276.1:p.Pro614Thr
XM_011533975.1:c.1597C>A (RAF1)	XP_011532277.1:p.Pro533Thr
NM_001354689.1:c.1900C>A (RAF1)	NP_001341618.1:p.Pro634Thr
NM_001354690.1:c.1840C>A (RAF1)	NP_001341619.1:p.Pro614Thr
NM_001354691.1:c.1597C>A (RAF1)	NP_001341620.1:p.Pro533Thr
NM_001354692.1:c.1597C>A (RAF1)	NP_001341621.1:p.Pro533Thr
NM_001354693.1:c.1741C>A (RAF1)	NP_001341622.1:p.Pro581Thr
NM_001354694.1:c.1657C>A (RAF1)	NP_001341623.1:p.Pro553Thr
NM_001354695.1:c.1498C>A (RAF1)	NP_001341624.1:p.Pro500Thr
NR_148940.1:n.2368C>A (RAF1)
NR_148941.1:n.2314C>A (RAF1)
NR_148942.1:n.2253C>A (RAF1)
XM_011533974.3:c.1840C>A (RAF1)	XP_011532276.1:p.Pro614Thr
XM_017006966.1:c.1741C>A (RAF1)	XP_016862455.1:p.Pro581Thr
NM_001354689.3:c.1900C>A (RAF1)	NP_001341618.1:p.Pro634Thr
NM_001354690.2:c.1840C>A (RAF1)	NP_001341619.1:p.Pro614Thr
NM_001354691.2:c.1597C>A (RAF1)	NP_001341620.1:p.Pro533Thr
NM_001354692.2:c.1597C>A (RAF1)	NP_001341621.1:p.Pro533Thr
NM_001354693.2:c.1741C>A (RAF1)	NP_001341622.1:p.Pro581Thr
NM_001354694.2:c.1657C>A (RAF1)	NP_001341623.1:p.Pro553Thr
NM_001354695.2:c.1498C>A (RAF1)	NP_001341624.1:p.Pro500Thr
NR_148940.2:n.2284C>A (RAF1)
NR_148941.2:n.2230C>A (RAF1)
NR_148942.2:n.2169C>A (RAF1)
NM_001354690.3:c.1840C>A (RAF1)	NP_001341619.1:p.Pro614Thr
NM_001354691.3:c.1597C>A (RAF1)	NP_001341620.1:p.Pro533Thr
NM_001354692.3:c.1597C>A (RAF1)	NP_001341621.1:p.Pro533Thr
NM_001354693.3:c.1741C>A (RAF1)	NP_001341622.1:p.Pro581Thr
NM_001354694.3:c.1657C>A (RAF1)	NP_001341623.1:p.Pro553Thr
NM_001354695.3:c.1498C>A (RAF1)	NP_001341624.1:p.Pro500Thr
NM_002880.4:c.1840C>A (RAF1) MANE Select	NP_002871.1:p.Pro614Thr
NR_148940.3:n.2284C>A (RAF1)
NR_148941.3:n.2230C>A (RAF1)
NR_148942.3:n.2169C>A (RAF1)