Canonical Allele Identifier: CA351496535

Gene: RAF1 MKRN2

Linked Data

• MyVariant Identifiers: chr3:g.12626370C>A (hg19) ; chr3:g.12584871C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584871C>A , CM000665.2:g.12584871C>A	GRCh38
NC_000003.11:g.12626370C>A , CM000665.1:g.12626370C>A	GRCh37
NC_000003.10:g.12601370C>A	NCBI36
NG_007467.1:g.84309G>T , LRG_413:g.84309G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1444G>T (RAF1)	ENSP00000401088.1:n.*1444G>T
ENST00000432427.3:c.1096G>T (RAF1)
ENST00000460610.2:n.6091G>T (RAF1)
ENST00000471449.2:n.589G>T (RAF1)
ENST00000475353.2:n.4059G>T (RAF1)
ENST00000684903.1:c.*1456G>T (RAF1)	ENSP00000508612.1:n.*1456G>T
ENST00000685348.1:c.*1490G>T (RAF1)	ENSP00000510285.1:n.*1490G>T
ENST00000685437.1:c.1680G>T (RAF1)	ENSP00000508794.1:p.Lys560Asn
ENST00000685653.1:c.1779G>T (RAF1)	ENSP00000509968.1:p.Lys593Asn
ENST00000685697.1:n.2514G>T (RAF1)
ENST00000685738.1:c.*743G>T (RAF1)	ENSP00000510156.1:n.*743G>T
ENST00000686409.1:n.5188G>T (RAF1)
ENST00000686455.1:n.4500G>T (RAF1)
ENST00000686762.1:c.*338G>T (RAF1)	ENSP00000509767.1:n.*338G>T
ENST00000687257.1:n.4233G>T (RAF1)
ENST00000687326.1:c.*3071G>T (RAF1)	ENSP00000509665.1:n.*3071G>T
ENST00000687505.1:n.1897G>T (RAF1)
ENST00000687923.1:c.1668G>T (RAF1)	ENSP00000510255.1:p.Lys556Asn
ENST00000688269.1:n.2375G>T (RAF1)
ENST00000688444.1:n.3896G>T (RAF1)
ENST00000688543.1:c.1680G>T (RAF1)	ENSP00000509612.1:p.Lys560Asn
ENST00000688625.1:c.*3148G>T (RAF1)	ENSP00000509522.1:n.*3148G>T
ENST00000688803.1:n.3207G>T (RAF1)
ENST00000689097.1:c.*1456G>T (RAF1)	ENSP00000509756.1:n.*1456G>T
ENST00000689389.1:c.1602G>T (RAF1)	ENSP00000510213.1:p.Lys534Asn
ENST00000689418.1:c.*3674G>T (RAF1)	ENSP00000509467.1:n.*3674G>T
ENST00000689540.1:n.4147G>T (RAF1)
ENST00000689876.1:c.*328G>T (RAF1)	ENSP00000508535.1:n.*328G>T
ENST00000689914.1:c.*713G>T (RAF1)	ENSP00000509847.1:n.*713G>T
ENST00000690397.1:c.1668G>T (RAF1)	ENSP00000508730.1:p.Lys556Asn
ENST00000690460.1:c.1767G>T (RAF1)	ENSP00000509106.1:p.Lys589Asn
ENST00000690585.1:c.505G>T (RAF1)
ENST00000690625.1:n.2815G>T (RAF1)
ENST00000691396.1:c.*1651G>T (RAF1)	ENSP00000510712.1:n.*1651G>T
ENST00000691643.1:n.2832G>T (RAF1)
ENST00000691724.1:c.*736G>T (RAF1)	ENSP00000509255.1:n.*736G>T
ENST00000691779.1:c.*1357G>T (RAF1)	ENSP00000508592.1:n.*1357G>T
ENST00000691888.1:c.653G>T (RAF1)
ENST00000691899.1:c.1779G>T (RAF1)	ENSP00000508763.1:p.Lys593Asn
ENST00000692069.1:n.4703G>T (RAF1)
ENST00000692093.1:c.1680G>T (RAF1)	ENSP00000509669.1:p.Lys560Asn
ENST00000692311.1:n.2603G>T (RAF1)
ENST00000692558.1:n.4362G>T (RAF1)
ENST00000692773.1:c.*1516G>T (RAF1)	ENSP00000509055.1:n.*1516G>T
ENST00000692830.1:c.*1524G>T (RAF1)	ENSP00000509461.1:n.*1524G>T
ENST00000693312.1:c.1554G>T (RAF1)	ENSP00000508686.1:p.Lys518Asn
ENST00000693664.1:c.*230G>T (RAF1)	ENSP00000509614.1:n.*230G>T
ENST00000693705.1:c.*1158G>T (RAF1)	ENSP00000510697.1:n.*1158G>T
ENST00000251849.9:c.1779G>T (RAF1) MANE Select	ENSP00000251849.4:p.Lys593Asn
ENST00000442415.7:c.1839G>T (RAF1)	ENSP00000401888.2:p.Lys613Asn
ENST00000676541.1:c.*2618C>A (MKRN2)	ENSP00000503730.1:n.*2618C>A
ENST00000677142.1:c.*2618C>A (MKRN2)	ENSP00000504455.1:n.*2618C>A
ENST00000677816.1:c.*1173C>A (MKRN2)	ENSP00000502893.1:n.*1173C>A
ENST00000677941.1:n.2681C>A (MKRN2)
ENST00000251849.8:c.1779G>T (RAF1)	ENSP00000251849.4:p.Lys593Asn
ENST00000423275.5:c.*1456G>T (RAF1)	ENSP00000401088.1:n.*1456G>T
ENST00000432427.2:c.1416G>T (RAF1)	ENSP00000398591.2:p.Lys472Asn
ENST00000442415.6:c.1839G>T (RAF1)	ENSP00000401888.2:p.Lys613Asn
ENST00000471449.1:n.468G>T (RAF1)
NM_002880.3:c.1779G>T , LRG_413t1:c.1779G>T (RAF1)	NP_002871.1:p.Lys593Asn
XM_005265355.1:c.1779G>T (RAF1)	XP_005265412.1:p.Lys593Asn
XM_005265357.1:c.1680G>T (RAF1)	XP_005265414.1:p.Lys560Asn
XM_005265358.3:c.1536G>T (RAF1)	XP_005265415.1:p.Lys512Asn
XM_005265359.3:c.1437G>T (RAF1)	XP_005265416.1:p.Lys479Asn
XM_011533974.1:c.1779G>T (RAF1)	XP_011532276.1:p.Lys593Asn
XM_011533975.1:c.1536G>T (RAF1)	XP_011532277.1:p.Lys512Asn
NM_001354689.1:c.1839G>T (RAF1)	NP_001341618.1:p.Lys613Asn
NM_001354690.1:c.1779G>T (RAF1)	NP_001341619.1:p.Lys593Asn
NM_001354691.1:c.1536G>T (RAF1)	NP_001341620.1:p.Lys512Asn
NM_001354692.1:c.1536G>T (RAF1)	NP_001341621.1:p.Lys512Asn
NM_001354693.1:c.1680G>T (RAF1)	NP_001341622.1:p.Lys560Asn
NM_001354694.1:c.1596G>T (RAF1)	NP_001341623.1:p.Lys532Asn
NM_001354695.1:c.1437G>T (RAF1)	NP_001341624.1:p.Lys479Asn
NR_148940.1:n.2307G>T (RAF1)
NR_148941.1:n.2253G>T (RAF1)
NR_148942.1:n.2192G>T (RAF1)
XM_011533974.3:c.1779G>T (RAF1)	XP_011532276.1:p.Lys593Asn
XM_017006966.1:c.1680G>T (RAF1)	XP_016862455.1:p.Lys560Asn
NM_001354689.3:c.1839G>T (RAF1)	NP_001341618.1:p.Lys613Asn
NM_001354690.2:c.1779G>T (RAF1)	NP_001341619.1:p.Lys593Asn
NM_001354691.2:c.1536G>T (RAF1)	NP_001341620.1:p.Lys512Asn
NM_001354692.2:c.1536G>T (RAF1)	NP_001341621.1:p.Lys512Asn
NM_001354693.2:c.1680G>T (RAF1)	NP_001341622.1:p.Lys560Asn
NM_001354694.2:c.1596G>T (RAF1)	NP_001341623.1:p.Lys532Asn
NM_001354695.2:c.1437G>T (RAF1)	NP_001341624.1:p.Lys479Asn
NR_148940.2:n.2223G>T (RAF1)
NR_148941.2:n.2169G>T (RAF1)
NR_148942.2:n.2108G>T (RAF1)
NM_001354690.3:c.1779G>T (RAF1)	NP_001341619.1:p.Lys593Asn
NM_001354691.3:c.1536G>T (RAF1)	NP_001341620.1:p.Lys512Asn
NM_001354692.3:c.1536G>T (RAF1)	NP_001341621.1:p.Lys512Asn
NM_001354693.3:c.1680G>T (RAF1)	NP_001341622.1:p.Lys560Asn
NM_001354694.3:c.1596G>T (RAF1)	NP_001341623.1:p.Lys532Asn
NM_001354695.3:c.1437G>T (RAF1)	NP_001341624.1:p.Lys479Asn
NM_002880.4:c.1779G>T (RAF1) MANE Select	NP_002871.1:p.Lys593Asn
NR_148940.3:n.2223G>T (RAF1)
NR_148941.3:n.2169G>T (RAF1)
NR_148942.3:n.2108G>T (RAF1)