Canonical Allele Identifier: CA432522055

Gene: RAF1 MKRN2

Linked Data

• MyVariant Identifiers: chr3:g.12626457T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584958T>A , CM000665.2:g.12584958T>A	GRCh38
NC_000003.11:g.12626457T>A , CM000665.1:g.12626457T>A	GRCh37
NC_000003.10:g.12601457T>A	NCBI36
NG_007467.1:g.84222A>T , LRG_413:g.84222A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1357A>T (RAF1)	ENSP00000401088.1:n.*1357A>T
ENST00000432427.3:c.1009A>T (RAF1)
ENST00000460610.2:n.6004A>T (RAF1)
ENST00000471449.2:n.502A>T (RAF1)
ENST00000475353.2:n.3972A>T (RAF1)
ENST00000684903.1:c.*1369A>T (RAF1)	ENSP00000508612.1:n.*1369A>T
ENST00000685348.1:c.*1403A>T (RAF1)	ENSP00000510285.1:n.*1403A>T
ENST00000685437.1:c.1593A>T (RAF1)	ENSP00000508794.1:p.Gly531=
ENST00000685653.1:c.1692A>T (RAF1)	ENSP00000509968.1:p.Gly564=
ENST00000685697.1:n.2427A>T (RAF1)
ENST00000685738.1:c.*656A>T (RAF1)	ENSP00000510156.1:n.*656A>T
ENST00000686409.1:n.5101A>T (RAF1)
ENST00000686455.1:n.4413A>T (RAF1)
ENST00000686762.1:c.*251A>T (RAF1)	ENSP00000509767.1:n.*251A>T
ENST00000687257.1:n.4146A>T (RAF1)
ENST00000687326.1:c.*2984A>T (RAF1)	ENSP00000509665.1:n.*2984A>T
ENST00000687505.1:n.1810A>T (RAF1)
ENST00000687923.1:c.1581A>T (RAF1)	ENSP00000510255.1:p.Gly527=
ENST00000688269.1:n.2288A>T (RAF1)
ENST00000688444.1:n.3809A>T (RAF1)
ENST00000688543.1:c.1593A>T (RAF1)	ENSP00000509612.1:p.Gly531=
ENST00000688625.1:c.*3061A>T (RAF1)	ENSP00000509522.1:n.*3061A>T
ENST00000688803.1:n.3120A>T (RAF1)
ENST00000688914.1:n.1105A>T (RAF1)
ENST00000689097.1:c.*1369A>T (RAF1)	ENSP00000509756.1:n.*1369A>T
ENST00000689389.1:c.1515A>T (RAF1)	ENSP00000510213.1:p.Gly505=
ENST00000689418.1:c.*3587A>T (RAF1)	ENSP00000509467.1:n.*3587A>T
ENST00000689540.1:n.4060A>T (RAF1)
ENST00000689876.1:c.*241A>T (RAF1)	ENSP00000508535.1:n.*241A>T
ENST00000689914.1:c.*626A>T (RAF1)	ENSP00000509847.1:n.*626A>T
ENST00000690397.1:c.1581A>T (RAF1)	ENSP00000508730.1:p.Gly527=
ENST00000690460.1:c.1680A>T (RAF1)	ENSP00000509106.1:p.Gly560=
ENST00000690585.1:c.418A>T (RAF1)
ENST00000690625.1:n.2728A>T (RAF1)
ENST00000691396.1:c.*1564A>T (RAF1)	ENSP00000510712.1:n.*1564A>T
ENST00000691643.1:n.2745A>T (RAF1)
ENST00000691724.1:c.*649A>T (RAF1)	ENSP00000509255.1:n.*649A>T
ENST00000691779.1:c.*1270A>T (RAF1)	ENSP00000508592.1:n.*1270A>T
ENST00000691888.1:c.566A>T (RAF1)
ENST00000691899.1:c.1692A>T (RAF1)	ENSP00000508763.1:p.Gly564=
ENST00000692069.1:n.4616A>T (RAF1)
ENST00000692093.1:c.1593A>T (RAF1)	ENSP00000509669.1:p.Gly531=
ENST00000692311.1:n.2516A>T (RAF1)
ENST00000692558.1:n.4275A>T (RAF1)
ENST00000692773.1:c.*1429A>T (RAF1)	ENSP00000509055.1:n.*1429A>T
ENST00000692830.1:c.*1437A>T (RAF1)	ENSP00000509461.1:n.*1437A>T
ENST00000693312.1:c.1467A>T (RAF1)	ENSP00000508686.1:p.Gly489=
ENST00000693664.1:c.*143A>T (RAF1)	ENSP00000509614.1:n.*143A>T
ENST00000693705.1:c.*1071A>T (RAF1)	ENSP00000510697.1:n.*1071A>T
ENST00000251849.9:c.1692A>T (RAF1) MANE Select	ENSP00000251849.4:p.Gly564=
ENST00000442415.7:c.1752A>T (RAF1)	ENSP00000401888.2:p.Gly584=
ENST00000676541.1:c.*2705T>A (MKRN2)	ENSP00000503730.1:n.*2705T>A
ENST00000677142.1:c.*2705T>A (MKRN2)	ENSP00000504455.1:n.*2705T>A
ENST00000677816.1:c.*1260T>A (MKRN2)	ENSP00000502893.1:n.*1260T>A
ENST00000677941.1:n.2768T>A (MKRN2)
ENST00000251849.8:c.1692A>T (RAF1)	ENSP00000251849.4:p.Gly564=
ENST00000423275.5:c.*1369A>T (RAF1)	ENSP00000401088.1:n.*1369A>T
ENST00000432427.2:c.1329A>T (RAF1)	ENSP00000398591.2:p.Gly443=
ENST00000442415.6:c.1752A>T (RAF1)	ENSP00000401888.2:p.Gly584=
ENST00000471449.1:n.381A>T (RAF1)
NM_002880.3:c.1692A>T , LRG_413t1:c.1692A>T (RAF1)	NP_002871.1:p.Gly564=
XM_005265355.1:c.1692A>T (RAF1)	XP_005265412.1:p.Gly564=
XM_005265357.1:c.1593A>T (RAF1)	XP_005265414.1:p.Gly531=
XM_005265358.3:c.1449A>T (RAF1)	XP_005265415.1:p.Gly483=
XM_005265359.3:c.1350A>T (RAF1)	XP_005265416.1:p.Gly450=
XM_011533974.1:c.1692A>T (RAF1)	XP_011532276.1:p.Gly564=
XM_011533975.1:c.1449A>T (RAF1)	XP_011532277.1:p.Gly483=
NM_001354689.1:c.1752A>T (RAF1)	NP_001341618.1:p.Gly584=
NM_001354690.1:c.1692A>T (RAF1)	NP_001341619.1:p.Gly564=
NM_001354691.1:c.1449A>T (RAF1)	NP_001341620.1:p.Gly483=
NM_001354692.1:c.1449A>T (RAF1)	NP_001341621.1:p.Gly483=
NM_001354693.1:c.1593A>T (RAF1)	NP_001341622.1:p.Gly531=
NM_001354694.1:c.1509A>T (RAF1)	NP_001341623.1:p.Gly503=
NM_001354695.1:c.1350A>T (RAF1)	NP_001341624.1:p.Gly450=
NR_148940.1:n.2220A>T (RAF1)
NR_148941.1:n.2166A>T (RAF1)
NR_148942.1:n.2105A>T (RAF1)
XM_011533974.3:c.1692A>T (RAF1)	XP_011532276.1:p.Gly564=
XM_017006966.1:c.1593A>T (RAF1)	XP_016862455.1:p.Gly531=
NM_001354689.3:c.1752A>T (RAF1)	NP_001341618.1:p.Gly584=
NM_001354690.2:c.1692A>T (RAF1)	NP_001341619.1:p.Gly564=
NM_001354691.2:c.1449A>T (RAF1)	NP_001341620.1:p.Gly483=
NM_001354692.2:c.1449A>T (RAF1)	NP_001341621.1:p.Gly483=
NM_001354693.2:c.1593A>T (RAF1)	NP_001341622.1:p.Gly531=
NM_001354694.2:c.1509A>T (RAF1)	NP_001341623.1:p.Gly503=
NM_001354695.2:c.1350A>T (RAF1)	NP_001341624.1:p.Gly450=
NR_148940.2:n.2136A>T (RAF1)
NR_148941.2:n.2082A>T (RAF1)
NR_148942.2:n.2021A>T (RAF1)
NM_001354690.3:c.1692A>T (RAF1)	NP_001341619.1:p.Gly564=
NM_001354691.3:c.1449A>T (RAF1)	NP_001341620.1:p.Gly483=
NM_001354692.3:c.1449A>T (RAF1)	NP_001341621.1:p.Gly483=
NM_001354693.3:c.1593A>T (RAF1)	NP_001341622.1:p.Gly531=
NM_001354694.3:c.1509A>T (RAF1)	NP_001341623.1:p.Gly503=
NM_001354695.3:c.1350A>T (RAF1)	NP_001341624.1:p.Gly450=
NM_002880.4:c.1692A>T (RAF1) MANE Select	NP_002871.1:p.Gly564=
NR_148940.3:n.2136A>T (RAF1)
NR_148941.3:n.2082A>T (RAF1)
NR_148942.3:n.2021A>T (RAF1)