Canonical Allele Identifier: CA351495662

Gene: RAF1 MKRN2

Linked Data

• dbSNP Id: rs1013186582
• MyVariant Identifiers: chr3:g.12626059A>T (hg19) ; chr3:g.12584560A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584560A>T , CM000665.2:g.12584560A>T	GRCh38
NC_000003.11:g.12626059A>T , CM000665.1:g.12626059A>T	GRCh37
NC_000003.10:g.12601059A>T	NCBI36
NG_007467.1:g.84620T>A , LRG_413:g.84620T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1566T>A (RAF1)	ENSP00000401088.1:n.*1566T>A
ENST00000432427.3:c.1218T>A (RAF1)
ENST00000460610.2:n.6213T>A (RAF1)
ENST00000471449.2:n.711T>A (RAF1)
ENST00000475353.2:n.4181T>A (RAF1)
ENST00000684903.1:c.*1578T>A (RAF1)	ENSP00000508612.1:n.*1578T>A
ENST00000685348.1:c.*1612T>A (RAF1)	ENSP00000510285.1:n.*1612T>A
ENST00000685437.1:c.1802T>A (RAF1)	ENSP00000508794.1:p.Ile601Asn
ENST00000685653.1:c.1901T>A (RAF1)	ENSP00000509968.1:p.Ile634Asn
ENST00000685697.1:n.2636T>A (RAF1)
ENST00000685738.1:c.*865T>A (RAF1)	ENSP00000510156.1:n.*865T>A
ENST00000686409.1:n.5310T>A (RAF1)
ENST00000686455.1:n.4622T>A (RAF1)
ENST00000686762.1:c.*460T>A (RAF1)	ENSP00000509767.1:n.*460T>A
ENST00000687257.1:n.4355T>A (RAF1)
ENST00000687326.1:c.*3193T>A (RAF1)	ENSP00000509665.1:n.*3193T>A
ENST00000687505.1:n.2019T>A (RAF1)
ENST00000687923.1:c.1790T>A (RAF1)	ENSP00000510255.1:p.Ile597Asn
ENST00000688269.1:n.2497T>A (RAF1)
ENST00000688444.1:n.4018T>A (RAF1)
ENST00000688543.1:c.1802T>A (RAF1)	ENSP00000509612.1:p.Ile601Asn
ENST00000688625.1:c.*3270T>A (RAF1)	ENSP00000509522.1:n.*3270T>A
ENST00000688803.1:n.3329T>A (RAF1)
ENST00000689097.1:c.*1578T>A (RAF1)	ENSP00000509756.1:n.*1578T>A
ENST00000689389.1:c.1724T>A (RAF1)	ENSP00000510213.1:p.Ile575Asn
ENST00000689418.1:c.*3796T>A (RAF1)	ENSP00000509467.1:n.*3796T>A
ENST00000689540.1:n.4269T>A (RAF1)
ENST00000689876.1:c.*450T>A (RAF1)	ENSP00000508535.1:n.*450T>A
ENST00000689914.1:c.*835T>A (RAF1)	ENSP00000509847.1:n.*835T>A
ENST00000690397.1:c.1790T>A (RAF1)	ENSP00000508730.1:p.Ile597Asn
ENST00000690460.1:c.1889T>A (RAF1)	ENSP00000509106.1:p.Ile630Asn
ENST00000690585.1:c.627T>A (RAF1)
ENST00000690625.1:n.2937T>A (RAF1)
ENST00000691396.1:c.*1773T>A (RAF1)	ENSP00000510712.1:n.*1773T>A
ENST00000691643.1:n.2954T>A (RAF1)
ENST00000691724.1:c.*858T>A (RAF1)	ENSP00000509255.1:n.*858T>A
ENST00000691779.1:c.*1479T>A (RAF1)	ENSP00000508592.1:n.*1479T>A
ENST00000691888.1:c.775T>A (RAF1)
ENST00000691899.1:c.1901T>A (RAF1)	ENSP00000508763.1:p.Ile634Asn
ENST00000692069.1:n.4825T>A (RAF1)
ENST00000692093.1:c.1802T>A (RAF1)	ENSP00000509669.1:p.Ile601Asn
ENST00000692311.1:n.2725T>A (RAF1)
ENST00000692558.1:n.4484T>A (RAF1)
ENST00000692773.1:c.*1638T>A (RAF1)	ENSP00000509055.1:n.*1638T>A
ENST00000692830.1:c.*1646T>A (RAF1)	ENSP00000509461.1:n.*1646T>A
ENST00000693312.1:c.1676T>A (RAF1)	ENSP00000508686.1:p.Ile559Asn
ENST00000693664.1:c.*352T>A (RAF1)	ENSP00000509614.1:n.*352T>A
ENST00000693705.1:c.*1280T>A (RAF1)	ENSP00000510697.1:n.*1280T>A
ENST00000251849.9:c.1901T>A (RAF1) MANE Select	ENSP00000251849.4:p.Ile634Asn
ENST00000442415.7:c.1961T>A (RAF1)	ENSP00000401888.2:p.Ile654Asn
ENST00000676541.1:c.*2307A>T (MKRN2)	ENSP00000503730.1:n.*2307A>T
ENST00000677142.1:c.*2307A>T (MKRN2)	ENSP00000504455.1:n.*2307A>T
ENST00000677816.1:c.*862A>T (MKRN2)	ENSP00000502893.1:n.*862A>T
ENST00000677941.1:n.2370A>T (MKRN2)
ENST00000251849.8:c.1901T>A (RAF1)	ENSP00000251849.4:p.Ile634Asn
ENST00000423275.5:c.*1578T>A (RAF1)	ENSP00000401088.1:n.*1578T>A
ENST00000432427.2:c.1538T>A (RAF1)	ENSP00000398591.2:p.Ile513Asn
ENST00000442415.6:c.1961T>A (RAF1)	ENSP00000401888.2:p.Ile654Asn
ENST00000471449.1:n.590T>A (RAF1)
NM_002880.3:c.1901T>A , LRG_413t1:c.1901T>A (RAF1)	NP_002871.1:p.Ile634Asn
XM_005265355.1:c.1901T>A (RAF1)	XP_005265412.1:p.Ile634Asn
XM_005265357.1:c.1802T>A (RAF1)	XP_005265414.1:p.Ile601Asn
XM_005265358.3:c.1658T>A (RAF1)	XP_005265415.1:p.Ile553Asn
XM_005265359.3:c.1559T>A (RAF1)	XP_005265416.1:p.Ile520Asn
XM_011533974.1:c.1901T>A (RAF1)	XP_011532276.1:p.Ile634Asn
XM_011533975.1:c.1658T>A (RAF1)	XP_011532277.1:p.Ile553Asn
NM_001354689.1:c.1961T>A (RAF1)	NP_001341618.1:p.Ile654Asn
NM_001354690.1:c.1901T>A (RAF1)	NP_001341619.1:p.Ile634Asn
NM_001354691.1:c.1658T>A (RAF1)	NP_001341620.1:p.Ile553Asn
NM_001354692.1:c.1658T>A (RAF1)	NP_001341621.1:p.Ile553Asn
NM_001354693.1:c.1802T>A (RAF1)	NP_001341622.1:p.Ile601Asn
NM_001354694.1:c.1718T>A (RAF1)	NP_001341623.1:p.Ile573Asn
NM_001354695.1:c.1559T>A (RAF1)	NP_001341624.1:p.Ile520Asn
NR_148940.1:n.2429T>A (RAF1)
NR_148941.1:n.2375T>A (RAF1)
NR_148942.1:n.2314T>A (RAF1)
XM_011533974.3:c.1901T>A (RAF1)	XP_011532276.1:p.Ile634Asn
XM_017006966.1:c.1802T>A (RAF1)	XP_016862455.1:p.Ile601Asn
NM_001354689.3:c.1961T>A (RAF1)	NP_001341618.1:p.Ile654Asn
NM_001354690.2:c.1901T>A (RAF1)	NP_001341619.1:p.Ile634Asn
NM_001354691.2:c.1658T>A (RAF1)	NP_001341620.1:p.Ile553Asn
NM_001354692.2:c.1658T>A (RAF1)	NP_001341621.1:p.Ile553Asn
NM_001354693.2:c.1802T>A (RAF1)	NP_001341622.1:p.Ile601Asn
NM_001354694.2:c.1718T>A (RAF1)	NP_001341623.1:p.Ile573Asn
NM_001354695.2:c.1559T>A (RAF1)	NP_001341624.1:p.Ile520Asn
NR_148940.2:n.2345T>A (RAF1)
NR_148941.2:n.2291T>A (RAF1)
NR_148942.2:n.2230T>A (RAF1)
NM_001354690.3:c.1901T>A (RAF1)	NP_001341619.1:p.Ile634Asn
NM_001354691.3:c.1658T>A (RAF1)	NP_001341620.1:p.Ile553Asn
NM_001354692.3:c.1658T>A (RAF1)	NP_001341621.1:p.Ile553Asn
NM_001354693.3:c.1802T>A (RAF1)	NP_001341622.1:p.Ile601Asn
NM_001354694.3:c.1718T>A (RAF1)	NP_001341623.1:p.Ile573Asn
NM_001354695.3:c.1559T>A (RAF1)	NP_001341624.1:p.Ile520Asn
NM_002880.4:c.1901T>A (RAF1) MANE Select	NP_002871.1:p.Ile634Asn
NR_148940.3:n.2345T>A (RAF1)
NR_148941.3:n.2291T>A (RAF1)
NR_148942.3:n.2230T>A (RAF1)