Canonical Allele Identifier: CA351497074

Gene: RAF1 MKRN2

Linked Data

• MyVariant Identifiers: chr3:g.12626476A>T (hg19) ; chr3:g.12584977A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584977A>T , CM000665.2:g.12584977A>T	GRCh38
NC_000003.11:g.12626476A>T , CM000665.1:g.12626476A>T	GRCh37
NC_000003.10:g.12601476A>T	NCBI36
NG_007467.1:g.84203T>A , LRG_413:g.84203T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1338T>A (RAF1)	ENSP00000401088.1:n.*1338T>A
ENST00000432427.3:c.990T>A (RAF1)
ENST00000460610.2:n.5985T>A (RAF1)
ENST00000471449.2:n.483T>A (RAF1)
ENST00000475353.2:n.3953T>A (RAF1)
ENST00000684903.1:c.*1350T>A (RAF1)	ENSP00000508612.1:n.*1350T>A
ENST00000685348.1:c.*1384T>A (RAF1)	ENSP00000510285.1:n.*1384T>A
ENST00000685437.1:c.1574T>A (RAF1)	ENSP00000508794.1:p.Ile525Asn
ENST00000685653.1:c.1673T>A (RAF1)	ENSP00000509968.1:p.Ile558Asn
ENST00000685697.1:n.2408T>A (RAF1)
ENST00000685738.1:c.*637T>A (RAF1)	ENSP00000510156.1:n.*637T>A
ENST00000686409.1:n.5082T>A (RAF1)
ENST00000686455.1:n.4394T>A (RAF1)
ENST00000686762.1:c.*232T>A (RAF1)	ENSP00000509767.1:n.*232T>A
ENST00000687257.1:n.4127T>A (RAF1)
ENST00000687326.1:c.*2965T>A (RAF1)	ENSP00000509665.1:n.*2965T>A
ENST00000687505.1:n.1791T>A (RAF1)
ENST00000687923.1:c.1562T>A (RAF1)	ENSP00000510255.1:p.Ile521Asn
ENST00000688269.1:n.2269T>A (RAF1)
ENST00000688444.1:n.3790T>A (RAF1)
ENST00000688543.1:c.1574T>A (RAF1)	ENSP00000509612.1:p.Ile525Asn
ENST00000688625.1:c.*3042T>A (RAF1)	ENSP00000509522.1:n.*3042T>A
ENST00000688803.1:n.3101T>A (RAF1)
ENST00000688914.1:n.1086T>A (RAF1)
ENST00000689097.1:c.*1350T>A (RAF1)	ENSP00000509756.1:n.*1350T>A
ENST00000689389.1:c.1496T>A (RAF1)	ENSP00000510213.1:p.Ile499Asn
ENST00000689418.1:c.*3568T>A (RAF1)	ENSP00000509467.1:n.*3568T>A
ENST00000689540.1:n.4041T>A (RAF1)
ENST00000689876.1:c.*222T>A (RAF1)	ENSP00000508535.1:n.*222T>A
ENST00000689914.1:c.*607T>A (RAF1)	ENSP00000509847.1:n.*607T>A
ENST00000690397.1:c.1562T>A (RAF1)	ENSP00000508730.1:p.Ile521Asn
ENST00000690460.1:c.1661T>A (RAF1)	ENSP00000509106.1:p.Ile554Asn
ENST00000690585.1:c.399T>A (RAF1)
ENST00000690625.1:n.2709T>A (RAF1)
ENST00000691396.1:c.*1545T>A (RAF1)	ENSP00000510712.1:n.*1545T>A
ENST00000691643.1:n.2726T>A (RAF1)
ENST00000691724.1:c.*630T>A (RAF1)	ENSP00000509255.1:n.*630T>A
ENST00000691779.1:c.*1251T>A (RAF1)	ENSP00000508592.1:n.*1251T>A
ENST00000691888.1:c.547T>A (RAF1)
ENST00000691899.1:c.1673T>A (RAF1)	ENSP00000508763.1:p.Ile558Asn
ENST00000692069.1:n.4597T>A (RAF1)
ENST00000692093.1:c.1574T>A (RAF1)	ENSP00000509669.1:p.Ile525Asn
ENST00000692311.1:n.2497T>A (RAF1)
ENST00000692558.1:n.4256T>A (RAF1)
ENST00000692773.1:c.*1410T>A (RAF1)	ENSP00000509055.1:n.*1410T>A
ENST00000692830.1:c.*1418T>A (RAF1)	ENSP00000509461.1:n.*1418T>A
ENST00000693312.1:c.1448T>A (RAF1)	ENSP00000508686.1:p.Ile483Asn
ENST00000693664.1:c.*124T>A (RAF1)	ENSP00000509614.1:n.*124T>A
ENST00000693705.1:c.*1052T>A (RAF1)	ENSP00000510697.1:n.*1052T>A
ENST00000251849.9:c.1673T>A (RAF1) MANE Select	ENSP00000251849.4:p.Ile558Asn
ENST00000442415.7:c.1733T>A (RAF1)	ENSP00000401888.2:p.Ile578Asn
ENST00000676541.1:c.*2724A>T (MKRN2)	ENSP00000503730.1:n.*2724A>T
ENST00000677142.1:c.*2724A>T (MKRN2)	ENSP00000504455.1:n.*2724A>T
ENST00000677816.1:c.*1279A>T (MKRN2)	ENSP00000502893.1:n.*1279A>T
ENST00000677941.1:n.2787A>T (MKRN2)
ENST00000251849.8:c.1673T>A (RAF1)	ENSP00000251849.4:p.Ile558Asn
ENST00000423275.5:c.*1350T>A (RAF1)	ENSP00000401088.1:n.*1350T>A
ENST00000432427.2:c.1310T>A (RAF1)	ENSP00000398591.2:p.Ile437Asn
ENST00000442415.6:c.1733T>A (RAF1)	ENSP00000401888.2:p.Ile578Asn
ENST00000471449.1:n.362T>A (RAF1)
NM_002880.3:c.1673T>A , LRG_413t1:c.1673T>A (RAF1)	NP_002871.1:p.Ile558Asn
XM_005265355.1:c.1673T>A (RAF1)	XP_005265412.1:p.Ile558Asn
XM_005265357.1:c.1574T>A (RAF1)	XP_005265414.1:p.Ile525Asn
XM_005265358.3:c.1430T>A (RAF1)	XP_005265415.1:p.Ile477Asn
XM_005265359.3:c.1331T>A (RAF1)	XP_005265416.1:p.Ile444Asn
XM_011533974.1:c.1673T>A (RAF1)	XP_011532276.1:p.Ile558Asn
XM_011533975.1:c.1430T>A (RAF1)	XP_011532277.1:p.Ile477Asn
NM_001354689.1:c.1733T>A (RAF1)	NP_001341618.1:p.Ile578Asn
NM_001354690.1:c.1673T>A (RAF1)	NP_001341619.1:p.Ile558Asn
NM_001354691.1:c.1430T>A (RAF1)	NP_001341620.1:p.Ile477Asn
NM_001354692.1:c.1430T>A (RAF1)	NP_001341621.1:p.Ile477Asn
NM_001354693.1:c.1574T>A (RAF1)	NP_001341622.1:p.Ile525Asn
NM_001354694.1:c.1490T>A (RAF1)	NP_001341623.1:p.Ile497Asn
NM_001354695.1:c.1331T>A (RAF1)	NP_001341624.1:p.Ile444Asn
NR_148940.1:n.2201T>A (RAF1)
NR_148941.1:n.2147T>A (RAF1)
NR_148942.1:n.2086T>A (RAF1)
XM_011533974.3:c.1673T>A (RAF1)	XP_011532276.1:p.Ile558Asn
XM_017006966.1:c.1574T>A (RAF1)	XP_016862455.1:p.Ile525Asn
NM_001354689.3:c.1733T>A (RAF1)	NP_001341618.1:p.Ile578Asn
NM_001354690.2:c.1673T>A (RAF1)	NP_001341619.1:p.Ile558Asn
NM_001354691.2:c.1430T>A (RAF1)	NP_001341620.1:p.Ile477Asn
NM_001354692.2:c.1430T>A (RAF1)	NP_001341621.1:p.Ile477Asn
NM_001354693.2:c.1574T>A (RAF1)	NP_001341622.1:p.Ile525Asn
NM_001354694.2:c.1490T>A (RAF1)	NP_001341623.1:p.Ile497Asn
NM_001354695.2:c.1331T>A (RAF1)	NP_001341624.1:p.Ile444Asn
NR_148940.2:n.2117T>A (RAF1)
NR_148941.2:n.2063T>A (RAF1)
NR_148942.2:n.2002T>A (RAF1)
NM_001354690.3:c.1673T>A (RAF1)	NP_001341619.1:p.Ile558Asn
NM_001354691.3:c.1430T>A (RAF1)	NP_001341620.1:p.Ile477Asn
NM_001354692.3:c.1430T>A (RAF1)	NP_001341621.1:p.Ile477Asn
NM_001354693.3:c.1574T>A (RAF1)	NP_001341622.1:p.Ile525Asn
NM_001354694.3:c.1490T>A (RAF1)	NP_001341623.1:p.Ile497Asn
NM_001354695.3:c.1331T>A (RAF1)	NP_001341624.1:p.Ile444Asn
NM_002880.4:c.1673T>A (RAF1) MANE Select	NP_002871.1:p.Ile558Asn
NR_148940.3:n.2117T>A (RAF1)
NR_148941.3:n.2063T>A (RAF1)
NR_148942.3:n.2002T>A (RAF1)