Canonical Allele Identifier: CA351496786

Gene: RAF1 MKRN2

Linked Data

• MyVariant Identifiers: chr3:g.12626423T>A (hg19) ; chr3:g.12584924T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584924T>A , CM000665.2:g.12584924T>A	GRCh38
NC_000003.11:g.12626423T>A , CM000665.1:g.12626423T>A	GRCh37
NC_000003.10:g.12601423T>A	NCBI36
NG_007467.1:g.84256A>T , LRG_413:g.84256A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1391A>T (RAF1)	ENSP00000401088.1:n.*1391A>T
ENST00000432427.3:c.1043A>T (RAF1)
ENST00000460610.2:n.6038A>T (RAF1)
ENST00000471449.2:n.536A>T (RAF1)
ENST00000475353.2:n.4006A>T (RAF1)
ENST00000684903.1:c.*1403A>T (RAF1)	ENSP00000508612.1:n.*1403A>T
ENST00000685348.1:c.*1437A>T (RAF1)	ENSP00000510285.1:n.*1437A>T
ENST00000685437.1:c.1627A>T (RAF1)	ENSP00000508794.1:p.Asn543Tyr
ENST00000685653.1:c.1726A>T (RAF1)	ENSP00000509968.1:p.Asn576Tyr
ENST00000685697.1:n.2461A>T (RAF1)
ENST00000685738.1:c.*690A>T (RAF1)	ENSP00000510156.1:n.*690A>T
ENST00000686409.1:n.5135A>T (RAF1)
ENST00000686455.1:n.4447A>T (RAF1)
ENST00000686762.1:c.*285A>T (RAF1)	ENSP00000509767.1:n.*285A>T
ENST00000687257.1:n.4180A>T (RAF1)
ENST00000687326.1:c.*3018A>T (RAF1)	ENSP00000509665.1:n.*3018A>T
ENST00000687505.1:n.1844A>T (RAF1)
ENST00000687923.1:c.1615A>T (RAF1)	ENSP00000510255.1:p.Asn539Tyr
ENST00000688269.1:n.2322A>T (RAF1)
ENST00000688444.1:n.3843A>T (RAF1)
ENST00000688543.1:c.1627A>T (RAF1)	ENSP00000509612.1:p.Asn543Tyr
ENST00000688625.1:c.*3095A>T (RAF1)	ENSP00000509522.1:n.*3095A>T
ENST00000688803.1:n.3154A>T (RAF1)
ENST00000688914.1:n.1139A>T (RAF1)
ENST00000689097.1:c.*1403A>T (RAF1)	ENSP00000509756.1:n.*1403A>T
ENST00000689389.1:c.1549A>T (RAF1)	ENSP00000510213.1:p.Asn517Tyr
ENST00000689418.1:c.*3621A>T (RAF1)	ENSP00000509467.1:n.*3621A>T
ENST00000689540.1:n.4094A>T (RAF1)
ENST00000689876.1:c.*275A>T (RAF1)	ENSP00000508535.1:n.*275A>T
ENST00000689914.1:c.*660A>T (RAF1)	ENSP00000509847.1:n.*660A>T
ENST00000690397.1:c.1615A>T (RAF1)	ENSP00000508730.1:p.Asn539Tyr
ENST00000690460.1:c.1714A>T (RAF1)	ENSP00000509106.1:p.Asn572Tyr
ENST00000690585.1:c.452A>T (RAF1)
ENST00000690625.1:n.2762A>T (RAF1)
ENST00000691396.1:c.*1598A>T (RAF1)	ENSP00000510712.1:n.*1598A>T
ENST00000691643.1:n.2779A>T (RAF1)
ENST00000691724.1:c.*683A>T (RAF1)	ENSP00000509255.1:n.*683A>T
ENST00000691779.1:c.*1304A>T (RAF1)	ENSP00000508592.1:n.*1304A>T
ENST00000691888.1:c.600A>T (RAF1)
ENST00000691899.1:c.1726A>T (RAF1)	ENSP00000508763.1:p.Asn576Tyr
ENST00000692069.1:n.4650A>T (RAF1)
ENST00000692093.1:c.1627A>T (RAF1)	ENSP00000509669.1:p.Asn543Tyr
ENST00000692311.1:n.2550A>T (RAF1)
ENST00000692558.1:n.4309A>T (RAF1)
ENST00000692773.1:c.*1463A>T (RAF1)	ENSP00000509055.1:n.*1463A>T
ENST00000692830.1:c.*1471A>T (RAF1)	ENSP00000509461.1:n.*1471A>T
ENST00000693312.1:c.1501A>T (RAF1)	ENSP00000508686.1:p.Asn501Tyr
ENST00000693664.1:c.*177A>T (RAF1)	ENSP00000509614.1:n.*177A>T
ENST00000693705.1:c.*1105A>T (RAF1)	ENSP00000510697.1:n.*1105A>T
ENST00000251849.9:c.1726A>T (RAF1) MANE Select	ENSP00000251849.4:p.Asn576Tyr
ENST00000442415.7:c.1786A>T (RAF1)	ENSP00000401888.2:p.Asn596Tyr
ENST00000676541.1:c.*2671T>A (MKRN2)	ENSP00000503730.1:n.*2671T>A
ENST00000677142.1:c.*2671T>A (MKRN2)	ENSP00000504455.1:n.*2671T>A
ENST00000677816.1:c.*1226T>A (MKRN2)	ENSP00000502893.1:n.*1226T>A
ENST00000677941.1:n.2734T>A (MKRN2)
ENST00000251849.8:c.1726A>T (RAF1)	ENSP00000251849.4:p.Asn576Tyr
ENST00000423275.5:c.*1403A>T (RAF1)	ENSP00000401088.1:n.*1403A>T
ENST00000432427.2:c.1363A>T (RAF1)	ENSP00000398591.2:p.Asn455Tyr
ENST00000442415.6:c.1786A>T (RAF1)	ENSP00000401888.2:p.Asn596Tyr
ENST00000471449.1:n.415A>T (RAF1)
NM_002880.3:c.1726A>T , LRG_413t1:c.1726A>T (RAF1)	NP_002871.1:p.Asn576Tyr
XM_005265355.1:c.1726A>T (RAF1)	XP_005265412.1:p.Asn576Tyr
XM_005265357.1:c.1627A>T (RAF1)	XP_005265414.1:p.Asn543Tyr
XM_005265358.3:c.1483A>T (RAF1)	XP_005265415.1:p.Asn495Tyr
XM_005265359.3:c.1384A>T (RAF1)	XP_005265416.1:p.Asn462Tyr
XM_011533974.1:c.1726A>T (RAF1)	XP_011532276.1:p.Asn576Tyr
XM_011533975.1:c.1483A>T (RAF1)	XP_011532277.1:p.Asn495Tyr
NM_001354689.1:c.1786A>T (RAF1)	NP_001341618.1:p.Asn596Tyr
NM_001354690.1:c.1726A>T (RAF1)	NP_001341619.1:p.Asn576Tyr
NM_001354691.1:c.1483A>T (RAF1)	NP_001341620.1:p.Asn495Tyr
NM_001354692.1:c.1483A>T (RAF1)	NP_001341621.1:p.Asn495Tyr
NM_001354693.1:c.1627A>T (RAF1)	NP_001341622.1:p.Asn543Tyr
NM_001354694.1:c.1543A>T (RAF1)	NP_001341623.1:p.Asn515Tyr
NM_001354695.1:c.1384A>T (RAF1)	NP_001341624.1:p.Asn462Tyr
NR_148940.1:n.2254A>T (RAF1)
NR_148941.1:n.2200A>T (RAF1)
NR_148942.1:n.2139A>T (RAF1)
XM_011533974.3:c.1726A>T (RAF1)	XP_011532276.1:p.Asn576Tyr
XM_017006966.1:c.1627A>T (RAF1)	XP_016862455.1:p.Asn543Tyr
NM_001354689.3:c.1786A>T (RAF1)	NP_001341618.1:p.Asn596Tyr
NM_001354690.2:c.1726A>T (RAF1)	NP_001341619.1:p.Asn576Tyr
NM_001354691.2:c.1483A>T (RAF1)	NP_001341620.1:p.Asn495Tyr
NM_001354692.2:c.1483A>T (RAF1)	NP_001341621.1:p.Asn495Tyr
NM_001354693.2:c.1627A>T (RAF1)	NP_001341622.1:p.Asn543Tyr
NM_001354694.2:c.1543A>T (RAF1)	NP_001341623.1:p.Asn515Tyr
NM_001354695.2:c.1384A>T (RAF1)	NP_001341624.1:p.Asn462Tyr
NR_148940.2:n.2170A>T (RAF1)
NR_148941.2:n.2116A>T (RAF1)
NR_148942.2:n.2055A>T (RAF1)
NM_001354690.3:c.1726A>T (RAF1)	NP_001341619.1:p.Asn576Tyr
NM_001354691.3:c.1483A>T (RAF1)	NP_001341620.1:p.Asn495Tyr
NM_001354692.3:c.1483A>T (RAF1)	NP_001341621.1:p.Asn495Tyr
NM_001354693.3:c.1627A>T (RAF1)	NP_001341622.1:p.Asn543Tyr
NM_001354694.3:c.1543A>T (RAF1)	NP_001341623.1:p.Asn515Tyr
NM_001354695.3:c.1384A>T (RAF1)	NP_001341624.1:p.Asn462Tyr
NM_002880.4:c.1726A>T (RAF1) MANE Select	NP_002871.1:p.Asn576Tyr
NR_148940.3:n.2170A>T (RAF1)
NR_148941.3:n.2116A>T (RAF1)
NR_148942.3:n.2055A>T (RAF1)