Canonical Allele Identifier: CA351497029

Gene: RAF1 MKRN2

Linked Data

• MyVariant Identifiers: chr3:g.12626469C>A (hg19) ; chr3:g.12584970C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584970C>A , CM000665.2:g.12584970C>A	GRCh38
NC_000003.11:g.12626469C>A , CM000665.1:g.12626469C>A	GRCh37
NC_000003.10:g.12601469C>A	NCBI36
NG_007467.1:g.84210G>T , LRG_413:g.84210G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1345G>T (RAF1)	ENSP00000401088.1:n.*1345G>T
ENST00000432427.3:c.997G>T (RAF1)
ENST00000460610.2:n.5992G>T (RAF1)
ENST00000471449.2:n.490G>T (RAF1)
ENST00000475353.2:n.3960G>T (RAF1)
ENST00000684903.1:c.*1357G>T (RAF1)	ENSP00000508612.1:n.*1357G>T
ENST00000685348.1:c.*1391G>T (RAF1)	ENSP00000510285.1:n.*1391G>T
ENST00000685437.1:c.1581G>T (RAF1)	ENSP00000508794.1:p.Met527Ile
ENST00000685653.1:c.1680G>T (RAF1)	ENSP00000509968.1:p.Met560Ile
ENST00000685697.1:n.2415G>T (RAF1)
ENST00000685738.1:c.*644G>T (RAF1)	ENSP00000510156.1:n.*644G>T
ENST00000686409.1:n.5089G>T (RAF1)
ENST00000686455.1:n.4401G>T (RAF1)
ENST00000686762.1:c.*239G>T (RAF1)	ENSP00000509767.1:n.*239G>T
ENST00000687257.1:n.4134G>T (RAF1)
ENST00000687326.1:c.*2972G>T (RAF1)	ENSP00000509665.1:n.*2972G>T
ENST00000687505.1:n.1798G>T (RAF1)
ENST00000687923.1:c.1569G>T (RAF1)	ENSP00000510255.1:p.Met523Ile
ENST00000688269.1:n.2276G>T (RAF1)
ENST00000688444.1:n.3797G>T (RAF1)
ENST00000688543.1:c.1581G>T (RAF1)	ENSP00000509612.1:p.Met527Ile
ENST00000688625.1:c.*3049G>T (RAF1)	ENSP00000509522.1:n.*3049G>T
ENST00000688803.1:n.3108G>T (RAF1)
ENST00000688914.1:n.1093G>T (RAF1)
ENST00000689097.1:c.*1357G>T (RAF1)	ENSP00000509756.1:n.*1357G>T
ENST00000689389.1:c.1503G>T (RAF1)	ENSP00000510213.1:p.Met501Ile
ENST00000689418.1:c.*3575G>T (RAF1)	ENSP00000509467.1:n.*3575G>T
ENST00000689540.1:n.4048G>T (RAF1)
ENST00000689876.1:c.*229G>T (RAF1)	ENSP00000508535.1:n.*229G>T
ENST00000689914.1:c.*614G>T (RAF1)	ENSP00000509847.1:n.*614G>T
ENST00000690397.1:c.1569G>T (RAF1)	ENSP00000508730.1:p.Met523Ile
ENST00000690460.1:c.1668G>T (RAF1)	ENSP00000509106.1:p.Met556Ile
ENST00000690585.1:c.406G>T (RAF1)
ENST00000690625.1:n.2716G>T (RAF1)
ENST00000691396.1:c.*1552G>T (RAF1)	ENSP00000510712.1:n.*1552G>T
ENST00000691643.1:n.2733G>T (RAF1)
ENST00000691724.1:c.*637G>T (RAF1)	ENSP00000509255.1:n.*637G>T
ENST00000691779.1:c.*1258G>T (RAF1)	ENSP00000508592.1:n.*1258G>T
ENST00000691888.1:c.554G>T (RAF1)
ENST00000691899.1:c.1680G>T (RAF1)	ENSP00000508763.1:p.Met560Ile
ENST00000692069.1:n.4604G>T (RAF1)
ENST00000692093.1:c.1581G>T (RAF1)	ENSP00000509669.1:p.Met527Ile
ENST00000692311.1:n.2504G>T (RAF1)
ENST00000692558.1:n.4263G>T (RAF1)
ENST00000692773.1:c.*1417G>T (RAF1)	ENSP00000509055.1:n.*1417G>T
ENST00000692830.1:c.*1425G>T (RAF1)	ENSP00000509461.1:n.*1425G>T
ENST00000693312.1:c.1455G>T (RAF1)	ENSP00000508686.1:p.Met485Ile
ENST00000693664.1:c.*131G>T (RAF1)	ENSP00000509614.1:n.*131G>T
ENST00000693705.1:c.*1059G>T (RAF1)	ENSP00000510697.1:n.*1059G>T
ENST00000251849.9:c.1680G>T (RAF1) MANE Select	ENSP00000251849.4:p.Met560Ile
ENST00000442415.7:c.1740G>T (RAF1)	ENSP00000401888.2:p.Met580Ile
ENST00000676541.1:c.*2717C>A (MKRN2)	ENSP00000503730.1:n.*2717C>A
ENST00000677142.1:c.*2717C>A (MKRN2)	ENSP00000504455.1:n.*2717C>A
ENST00000677816.1:c.*1272C>A (MKRN2)	ENSP00000502893.1:n.*1272C>A
ENST00000677941.1:n.2780C>A (MKRN2)
ENST00000251849.8:c.1680G>T (RAF1)	ENSP00000251849.4:p.Met560Ile
ENST00000423275.5:c.*1357G>T (RAF1)	ENSP00000401088.1:n.*1357G>T
ENST00000432427.2:c.1317G>T (RAF1)	ENSP00000398591.2:p.Met439Ile
ENST00000442415.6:c.1740G>T (RAF1)	ENSP00000401888.2:p.Met580Ile
ENST00000471449.1:n.369G>T (RAF1)
NM_002880.3:c.1680G>T , LRG_413t1:c.1680G>T (RAF1)	NP_002871.1:p.Met560Ile
XM_005265355.1:c.1680G>T (RAF1)	XP_005265412.1:p.Met560Ile
XM_005265357.1:c.1581G>T (RAF1)	XP_005265414.1:p.Met527Ile
XM_005265358.3:c.1437G>T (RAF1)	XP_005265415.1:p.Met479Ile
XM_005265359.3:c.1338G>T (RAF1)	XP_005265416.1:p.Met446Ile
XM_011533974.1:c.1680G>T (RAF1)	XP_011532276.1:p.Met560Ile
XM_011533975.1:c.1437G>T (RAF1)	XP_011532277.1:p.Met479Ile
NM_001354689.1:c.1740G>T (RAF1)	NP_001341618.1:p.Met580Ile
NM_001354690.1:c.1680G>T (RAF1)	NP_001341619.1:p.Met560Ile
NM_001354691.1:c.1437G>T (RAF1)	NP_001341620.1:p.Met479Ile
NM_001354692.1:c.1437G>T (RAF1)	NP_001341621.1:p.Met479Ile
NM_001354693.1:c.1581G>T (RAF1)	NP_001341622.1:p.Met527Ile
NM_001354694.1:c.1497G>T (RAF1)	NP_001341623.1:p.Met499Ile
NM_001354695.1:c.1338G>T (RAF1)	NP_001341624.1:p.Met446Ile
NR_148940.1:n.2208G>T (RAF1)
NR_148941.1:n.2154G>T (RAF1)
NR_148942.1:n.2093G>T (RAF1)
XM_011533974.3:c.1680G>T (RAF1)	XP_011532276.1:p.Met560Ile
XM_017006966.1:c.1581G>T (RAF1)	XP_016862455.1:p.Met527Ile
NM_001354689.3:c.1740G>T (RAF1)	NP_001341618.1:p.Met580Ile
NM_001354690.2:c.1680G>T (RAF1)	NP_001341619.1:p.Met560Ile
NM_001354691.2:c.1437G>T (RAF1)	NP_001341620.1:p.Met479Ile
NM_001354692.2:c.1437G>T (RAF1)	NP_001341621.1:p.Met479Ile
NM_001354693.2:c.1581G>T (RAF1)	NP_001341622.1:p.Met527Ile
NM_001354694.2:c.1497G>T (RAF1)	NP_001341623.1:p.Met499Ile
NM_001354695.2:c.1338G>T (RAF1)	NP_001341624.1:p.Met446Ile
NR_148940.2:n.2124G>T (RAF1)
NR_148941.2:n.2070G>T (RAF1)
NR_148942.2:n.2009G>T (RAF1)
NM_001354690.3:c.1680G>T (RAF1)	NP_001341619.1:p.Met560Ile
NM_001354691.3:c.1437G>T (RAF1)	NP_001341620.1:p.Met479Ile
NM_001354692.3:c.1437G>T (RAF1)	NP_001341621.1:p.Met479Ile
NM_001354693.3:c.1581G>T (RAF1)	NP_001341622.1:p.Met527Ile
NM_001354694.3:c.1497G>T (RAF1)	NP_001341623.1:p.Met499Ile
NM_001354695.3:c.1338G>T (RAF1)	NP_001341624.1:p.Met446Ile
NM_002880.4:c.1680G>T (RAF1) MANE Select	NP_002871.1:p.Met560Ile
NR_148940.3:n.2124G>T (RAF1)
NR_148941.3:n.2070G>T (RAF1)
NR_148942.3:n.2009G>T (RAF1)