Canonical Allele Identifier: CA351495303

Gene: RAF1 MKRN2

Linked Data

• MyVariant Identifiers: chr3:g.12626018A>G (hg19) ; chr3:g.12584519A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584519A>G , CM000665.2:g.12584519A>G	GRCh38
NC_000003.11:g.12626018A>G , CM000665.1:g.12626018A>G	GRCh37
NC_000003.10:g.12601018A>G	NCBI36
NG_007467.1:g.84661T>C , LRG_413:g.84661T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1607T>C (RAF1)	ENSP00000401088.1:n.*1607T>C
ENST00000432427.3:c.1259T>C (RAF1)
ENST00000460610.2:n.6254T>C (RAF1)
ENST00000471449.2:n.752T>C (RAF1)
ENST00000475353.2:n.4222T>C (RAF1)
ENST00000684903.1:c.*1619T>C (RAF1)	ENSP00000508612.1:n.*1619T>C
ENST00000685348.1:c.*1653T>C (RAF1)	ENSP00000510285.1:n.*1653T>C
ENST00000685437.1:c.1843T>C (RAF1)	ENSP00000508794.1:p.Phe615Leu
ENST00000685653.1:c.1942T>C (RAF1)	ENSP00000509968.1:p.Phe648Leu
ENST00000685697.1:n.2677T>C (RAF1)
ENST00000685738.1:c.*906T>C (RAF1)	ENSP00000510156.1:n.*906T>C
ENST00000686409.1:n.5351T>C (RAF1)
ENST00000686455.1:n.4663T>C (RAF1)
ENST00000686762.1:c.*501T>C (RAF1)	ENSP00000509767.1:n.*501T>C
ENST00000687257.1:n.4396T>C (RAF1)
ENST00000687326.1:c.*3234T>C (RAF1)	ENSP00000509665.1:n.*3234T>C
ENST00000687505.1:n.2060T>C (RAF1)
ENST00000687923.1:c.1831T>C (RAF1)	ENSP00000510255.1:p.Phe611Leu
ENST00000688269.1:n.2538T>C (RAF1)
ENST00000688444.1:n.4059T>C (RAF1)
ENST00000688543.1:c.1843T>C (RAF1)	ENSP00000509612.1:p.Phe615Leu
ENST00000688625.1:c.*3311T>C (RAF1)	ENSP00000509522.1:n.*3311T>C
ENST00000688803.1:n.3370T>C (RAF1)
ENST00000689097.1:c.*1619T>C (RAF1)	ENSP00000509756.1:n.*1619T>C
ENST00000689389.1:c.1765T>C (RAF1)	ENSP00000510213.1:p.Phe589Leu
ENST00000689418.1:c.*3837T>C (RAF1)	ENSP00000509467.1:n.*3837T>C
ENST00000689540.1:n.4310T>C (RAF1)
ENST00000689876.1:c.*491T>C (RAF1)	ENSP00000508535.1:n.*491T>C
ENST00000689914.1:c.*876T>C (RAF1)	ENSP00000509847.1:n.*876T>C
ENST00000690397.1:c.1831T>C (RAF1)	ENSP00000508730.1:p.Phe611Leu
ENST00000690460.1:c.1930T>C (RAF1)	ENSP00000509106.1:p.Phe644Leu
ENST00000690585.1:c.668T>C (RAF1)
ENST00000690625.1:n.2978T>C (RAF1)
ENST00000691396.1:c.*1814T>C (RAF1)	ENSP00000510712.1:n.*1814T>C
ENST00000691643.1:n.2995T>C (RAF1)
ENST00000691724.1:c.*899T>C (RAF1)	ENSP00000509255.1:n.*899T>C
ENST00000691779.1:c.*1520T>C (RAF1)	ENSP00000508592.1:n.*1520T>C
ENST00000691888.1:c.816T>C (RAF1)
ENST00000691899.1:c.1942T>C (RAF1)	ENSP00000508763.1:p.Phe648Leu
ENST00000692069.1:n.4866T>C (RAF1)
ENST00000692093.1:c.1843T>C (RAF1)	ENSP00000509669.1:p.Phe615Leu
ENST00000692311.1:n.2766T>C (RAF1)
ENST00000692558.1:n.4525T>C (RAF1)
ENST00000692773.1:c.*1679T>C (RAF1)	ENSP00000509055.1:n.*1679T>C
ENST00000692830.1:c.*1687T>C (RAF1)	ENSP00000509461.1:n.*1687T>C
ENST00000693312.1:c.1717T>C (RAF1)	ENSP00000508686.1:p.Phe573Leu
ENST00000693664.1:c.*393T>C (RAF1)	ENSP00000509614.1:n.*393T>C
ENST00000693705.1:c.*1321T>C (RAF1)	ENSP00000510697.1:n.*1321T>C
ENST00000251849.9:c.1942T>C (RAF1) MANE Select	ENSP00000251849.4:p.Phe648Leu
ENST00000442415.7:c.2002T>C (RAF1)	ENSP00000401888.2:p.Phe668Leu
ENST00000676541.1:c.*2266A>G (MKRN2)	ENSP00000503730.1:n.*2266A>G
ENST00000677142.1:c.*2266A>G (MKRN2)	ENSP00000504455.1:n.*2266A>G
ENST00000677816.1:c.*821A>G (MKRN2)	ENSP00000502893.1:n.*821A>G
ENST00000677941.1:n.2329A>G (MKRN2)
ENST00000251849.8:c.1942T>C (RAF1)	ENSP00000251849.4:p.Phe648Leu
ENST00000423275.5:c.*1619T>C (RAF1)	ENSP00000401088.1:n.*1619T>C
ENST00000432427.2:c.1579T>C (RAF1)	ENSP00000398591.2:p.Phe527Leu
ENST00000442415.6:c.2002T>C (RAF1)	ENSP00000401888.2:p.Phe668Leu
ENST00000471449.1:n.631T>C (RAF1)
NM_002880.3:c.1942T>C , LRG_413t1:c.1942T>C (RAF1)	NP_002871.1:p.Phe648Leu
XM_005265355.1:c.1942T>C (RAF1)	XP_005265412.1:p.Phe648Leu
XM_005265357.1:c.1843T>C (RAF1)	XP_005265414.1:p.Phe615Leu
XM_005265358.3:c.1699T>C (RAF1)	XP_005265415.1:p.Phe567Leu
XM_005265359.3:c.1600T>C (RAF1)	XP_005265416.1:p.Phe534Leu
XM_011533974.1:c.1942T>C (RAF1)	XP_011532276.1:p.Phe648Leu
XM_011533975.1:c.1699T>C (RAF1)	XP_011532277.1:p.Phe567Leu
NM_001354689.1:c.2002T>C (RAF1)	NP_001341618.1:p.Phe668Leu
NM_001354690.1:c.1942T>C (RAF1)	NP_001341619.1:p.Phe648Leu
NM_001354691.1:c.1699T>C (RAF1)	NP_001341620.1:p.Phe567Leu
NM_001354692.1:c.1699T>C (RAF1)	NP_001341621.1:p.Phe567Leu
NM_001354693.1:c.1843T>C (RAF1)	NP_001341622.1:p.Phe615Leu
NM_001354694.1:c.1759T>C (RAF1)	NP_001341623.1:p.Phe587Leu
NM_001354695.1:c.1600T>C (RAF1)	NP_001341624.1:p.Phe534Leu
NR_148940.1:n.2470T>C (RAF1)
NR_148941.1:n.2416T>C (RAF1)
NR_148942.1:n.2355T>C (RAF1)
XM_011533974.3:c.1942T>C (RAF1)	XP_011532276.1:p.Phe648Leu
XM_017006966.1:c.1843T>C (RAF1)	XP_016862455.1:p.Phe615Leu
NM_001354689.3:c.2002T>C (RAF1)	NP_001341618.1:p.Phe668Leu
NM_001354690.2:c.1942T>C (RAF1)	NP_001341619.1:p.Phe648Leu
NM_001354691.2:c.1699T>C (RAF1)	NP_001341620.1:p.Phe567Leu
NM_001354692.2:c.1699T>C (RAF1)	NP_001341621.1:p.Phe567Leu
NM_001354693.2:c.1843T>C (RAF1)	NP_001341622.1:p.Phe615Leu
NM_001354694.2:c.1759T>C (RAF1)	NP_001341623.1:p.Phe587Leu
NM_001354695.2:c.1600T>C (RAF1)	NP_001341624.1:p.Phe534Leu
NR_148940.2:n.2386T>C (RAF1)
NR_148941.2:n.2332T>C (RAF1)
NR_148942.2:n.2271T>C (RAF1)
NM_001354690.3:c.1942T>C (RAF1)	NP_001341619.1:p.Phe648Leu
NM_001354691.3:c.1699T>C (RAF1)	NP_001341620.1:p.Phe567Leu
NM_001354692.3:c.1699T>C (RAF1)	NP_001341621.1:p.Phe567Leu
NM_001354693.3:c.1843T>C (RAF1)	NP_001341622.1:p.Phe615Leu
NM_001354694.3:c.1759T>C (RAF1)	NP_001341623.1:p.Phe587Leu
NM_001354695.3:c.1600T>C (RAF1)	NP_001341624.1:p.Phe534Leu
NM_002880.4:c.1942T>C (RAF1) MANE Select	NP_002871.1:p.Phe648Leu
NR_148940.3:n.2386T>C (RAF1)
NR_148941.3:n.2332T>C (RAF1)
NR_148942.3:n.2271T>C (RAF1)