Canonical Allele Identifier: CA351496553

Gene: RAF1 MKRN2

Linked Data

• MyVariant Identifiers: chr3:g.12626374A>G (hg19) ; chr3:g.12584875A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584875A>G , CM000665.2:g.12584875A>G	GRCh38
NC_000003.11:g.12626374A>G , CM000665.1:g.12626374A>G	GRCh37
NC_000003.10:g.12601374A>G	NCBI36
NG_007467.1:g.84305T>C , LRG_413:g.84305T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1440T>C (RAF1)	ENSP00000401088.1:n.*1440T>C
ENST00000432427.3:c.1092T>C (RAF1)
ENST00000460610.2:n.6087T>C (RAF1)
ENST00000471449.2:n.585T>C (RAF1)
ENST00000475353.2:n.4055T>C (RAF1)
ENST00000684903.1:c.*1452T>C (RAF1)	ENSP00000508612.1:n.*1452T>C
ENST00000685348.1:c.*1486T>C (RAF1)	ENSP00000510285.1:n.*1486T>C
ENST00000685437.1:c.1676T>C (RAF1)	ENSP00000508794.1:p.Val559Ala
ENST00000685653.1:c.1775T>C (RAF1)	ENSP00000509968.1:p.Val592Ala
ENST00000685697.1:n.2510T>C (RAF1)
ENST00000685738.1:c.*739T>C (RAF1)	ENSP00000510156.1:n.*739T>C
ENST00000686409.1:n.5184T>C (RAF1)
ENST00000686455.1:n.4496T>C (RAF1)
ENST00000686762.1:c.*334T>C (RAF1)	ENSP00000509767.1:n.*334T>C
ENST00000687257.1:n.4229T>C (RAF1)
ENST00000687326.1:c.*3067T>C (RAF1)	ENSP00000509665.1:n.*3067T>C
ENST00000687505.1:n.1893T>C (RAF1)
ENST00000687923.1:c.1664T>C (RAF1)	ENSP00000510255.1:p.Val555Ala
ENST00000688269.1:n.2371T>C (RAF1)
ENST00000688444.1:n.3892T>C (RAF1)
ENST00000688543.1:c.1676T>C (RAF1)	ENSP00000509612.1:p.Val559Ala
ENST00000688625.1:c.*3144T>C (RAF1)	ENSP00000509522.1:n.*3144T>C
ENST00000688803.1:n.3203T>C (RAF1)
ENST00000689097.1:c.*1452T>C (RAF1)	ENSP00000509756.1:n.*1452T>C
ENST00000689389.1:c.1598T>C (RAF1)	ENSP00000510213.1:p.Val533Ala
ENST00000689418.1:c.*3670T>C (RAF1)	ENSP00000509467.1:n.*3670T>C
ENST00000689540.1:n.4143T>C (RAF1)
ENST00000689876.1:c.*324T>C (RAF1)	ENSP00000508535.1:n.*324T>C
ENST00000689914.1:c.*709T>C (RAF1)	ENSP00000509847.1:n.*709T>C
ENST00000690397.1:c.1664T>C (RAF1)	ENSP00000508730.1:p.Val555Ala
ENST00000690460.1:c.1763T>C (RAF1)	ENSP00000509106.1:p.Val588Ala
ENST00000690585.1:c.501T>C (RAF1)
ENST00000690625.1:n.2811T>C (RAF1)
ENST00000691396.1:c.*1647T>C (RAF1)	ENSP00000510712.1:n.*1647T>C
ENST00000691643.1:n.2828T>C (RAF1)
ENST00000691724.1:c.*732T>C (RAF1)	ENSP00000509255.1:n.*732T>C
ENST00000691779.1:c.*1353T>C (RAF1)	ENSP00000508592.1:n.*1353T>C
ENST00000691888.1:c.649T>C (RAF1)
ENST00000691899.1:c.1775T>C (RAF1)	ENSP00000508763.1:p.Val592Ala
ENST00000692069.1:n.4699T>C (RAF1)
ENST00000692093.1:c.1676T>C (RAF1)	ENSP00000509669.1:p.Val559Ala
ENST00000692311.1:n.2599T>C (RAF1)
ENST00000692558.1:n.4358T>C (RAF1)
ENST00000692773.1:c.*1512T>C (RAF1)	ENSP00000509055.1:n.*1512T>C
ENST00000692830.1:c.*1520T>C (RAF1)	ENSP00000509461.1:n.*1520T>C
ENST00000693312.1:c.1550T>C (RAF1)	ENSP00000508686.1:p.Val517Ala
ENST00000693664.1:c.*226T>C (RAF1)	ENSP00000509614.1:n.*226T>C
ENST00000693705.1:c.*1154T>C (RAF1)	ENSP00000510697.1:n.*1154T>C
ENST00000251849.9:c.1775T>C (RAF1) MANE Select	ENSP00000251849.4:p.Val592Ala
ENST00000442415.7:c.1835T>C (RAF1)	ENSP00000401888.2:p.Val612Ala
ENST00000676541.1:c.*2622A>G (MKRN2)	ENSP00000503730.1:n.*2622A>G
ENST00000677142.1:c.*2622A>G (MKRN2)	ENSP00000504455.1:n.*2622A>G
ENST00000677816.1:c.*1177A>G (MKRN2)	ENSP00000502893.1:n.*1177A>G
ENST00000677941.1:n.2685A>G (MKRN2)
ENST00000251849.8:c.1775T>C (RAF1)	ENSP00000251849.4:p.Val592Ala
ENST00000423275.5:c.*1452T>C (RAF1)	ENSP00000401088.1:n.*1452T>C
ENST00000432427.2:c.1412T>C (RAF1)	ENSP00000398591.2:p.Val471Ala
ENST00000442415.6:c.1835T>C (RAF1)	ENSP00000401888.2:p.Val612Ala
ENST00000471449.1:n.464T>C (RAF1)
NM_002880.3:c.1775T>C , LRG_413t1:c.1775T>C (RAF1)	NP_002871.1:p.Val592Ala
XM_005265355.1:c.1775T>C (RAF1)	XP_005265412.1:p.Val592Ala
XM_005265357.1:c.1676T>C (RAF1)	XP_005265414.1:p.Val559Ala
XM_005265358.3:c.1532T>C (RAF1)	XP_005265415.1:p.Val511Ala
XM_005265359.3:c.1433T>C (RAF1)	XP_005265416.1:p.Val478Ala
XM_011533974.1:c.1775T>C (RAF1)	XP_011532276.1:p.Val592Ala
XM_011533975.1:c.1532T>C (RAF1)	XP_011532277.1:p.Val511Ala
NM_001354689.1:c.1835T>C (RAF1)	NP_001341618.1:p.Val612Ala
NM_001354690.1:c.1775T>C (RAF1)	NP_001341619.1:p.Val592Ala
NM_001354691.1:c.1532T>C (RAF1)	NP_001341620.1:p.Val511Ala
NM_001354692.1:c.1532T>C (RAF1)	NP_001341621.1:p.Val511Ala
NM_001354693.1:c.1676T>C (RAF1)	NP_001341622.1:p.Val559Ala
NM_001354694.1:c.1592T>C (RAF1)	NP_001341623.1:p.Val531Ala
NM_001354695.1:c.1433T>C (RAF1)	NP_001341624.1:p.Val478Ala
NR_148940.1:n.2303T>C (RAF1)
NR_148941.1:n.2249T>C (RAF1)
NR_148942.1:n.2188T>C (RAF1)
XM_011533974.3:c.1775T>C (RAF1)	XP_011532276.1:p.Val592Ala
XM_017006966.1:c.1676T>C (RAF1)	XP_016862455.1:p.Val559Ala
NM_001354689.3:c.1835T>C (RAF1)	NP_001341618.1:p.Val612Ala
NM_001354690.2:c.1775T>C (RAF1)	NP_001341619.1:p.Val592Ala
NM_001354691.2:c.1532T>C (RAF1)	NP_001341620.1:p.Val511Ala
NM_001354692.2:c.1532T>C (RAF1)	NP_001341621.1:p.Val511Ala
NM_001354693.2:c.1676T>C (RAF1)	NP_001341622.1:p.Val559Ala
NM_001354694.2:c.1592T>C (RAF1)	NP_001341623.1:p.Val531Ala
NM_001354695.2:c.1433T>C (RAF1)	NP_001341624.1:p.Val478Ala
NR_148940.2:n.2219T>C (RAF1)
NR_148941.2:n.2165T>C (RAF1)
NR_148942.2:n.2104T>C (RAF1)
NM_001354690.3:c.1775T>C (RAF1)	NP_001341619.1:p.Val592Ala
NM_001354691.3:c.1532T>C (RAF1)	NP_001341620.1:p.Val511Ala
NM_001354692.3:c.1532T>C (RAF1)	NP_001341621.1:p.Val511Ala
NM_001354693.3:c.1676T>C (RAF1)	NP_001341622.1:p.Val559Ala
NM_001354694.3:c.1592T>C (RAF1)	NP_001341623.1:p.Val531Ala
NM_001354695.3:c.1433T>C (RAF1)	NP_001341624.1:p.Val478Ala
NM_002880.4:c.1775T>C (RAF1) MANE Select	NP_002871.1:p.Val592Ala
NR_148940.3:n.2219T>C (RAF1)
NR_148941.3:n.2165T>C (RAF1)
NR_148942.3:n.2104T>C (RAF1)