Canonical Allele Identifier: CA351495586

Gene: RAF1 MKRN2

Linked Data

• MyVariant Identifiers: chr3:g.12626049G>T (hg19) ; chr3:g.12584550G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584550G>T , CM000665.2:g.12584550G>T	GRCh38
NC_000003.11:g.12626049G>T , CM000665.1:g.12626049G>T	GRCh37
NC_000003.10:g.12601049G>T	NCBI36
NG_007467.1:g.84630C>A , LRG_413:g.84630C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000423275.6:c.*1576C>A (RAF1)	ENSP00000401088.1:n.*1576C>A
ENST00000432427.3:c.1228C>A (RAF1)
ENST00000460610.2:n.6223C>A (RAF1)
ENST00000471449.2:n.721C>A (RAF1)
ENST00000475353.2:n.4191C>A (RAF1)
ENST00000684903.1:c.*1588C>A (RAF1)	ENSP00000508612.1:n.*1588C>A
ENST00000685348.1:c.*1622C>A (RAF1)	ENSP00000510285.1:n.*1622C>A
ENST00000685437.1:c.1812C>A (RAF1)	ENSP00000508794.1:p.Cys604Ter
ENST00000685653.1:c.1911C>A (RAF1)	ENSP00000509968.1:p.Cys637Ter
ENST00000685697.1:n.2646C>A (RAF1)
ENST00000685738.1:c.*875C>A (RAF1)	ENSP00000510156.1:n.*875C>A
ENST00000686409.1:n.5320C>A (RAF1)
ENST00000686455.1:n.4632C>A (RAF1)
ENST00000686762.1:c.*470C>A (RAF1)	ENSP00000509767.1:n.*470C>A
ENST00000687257.1:n.4365C>A (RAF1)
ENST00000687326.1:c.*3203C>A (RAF1)	ENSP00000509665.1:n.*3203C>A
ENST00000687505.1:n.2029C>A (RAF1)
ENST00000687923.1:c.1800C>A (RAF1)	ENSP00000510255.1:p.Cys600Ter
ENST00000688269.1:n.2507C>A (RAF1)
ENST00000688444.1:n.4028C>A (RAF1)
ENST00000688543.1:c.1812C>A (RAF1)	ENSP00000509612.1:p.Cys604Ter
ENST00000688625.1:c.*3280C>A (RAF1)	ENSP00000509522.1:n.*3280C>A
ENST00000688803.1:n.3339C>A (RAF1)
ENST00000689097.1:c.*1588C>A (RAF1)	ENSP00000509756.1:n.*1588C>A
ENST00000689389.1:c.1734C>A (RAF1)	ENSP00000510213.1:p.Cys578Ter
ENST00000689418.1:c.*3806C>A (RAF1)	ENSP00000509467.1:n.*3806C>A
ENST00000689540.1:n.4279C>A (RAF1)
ENST00000689876.1:c.*460C>A (RAF1)	ENSP00000508535.1:n.*460C>A
ENST00000689914.1:c.*845C>A (RAF1)	ENSP00000509847.1:n.*845C>A
ENST00000690397.1:c.1800C>A (RAF1)	ENSP00000508730.1:p.Cys600Ter
ENST00000690460.1:c.1899C>A (RAF1)	ENSP00000509106.1:p.Cys633Ter
ENST00000690585.1:c.637C>A (RAF1)
ENST00000690625.1:n.2947C>A (RAF1)
ENST00000691396.1:c.*1783C>A (RAF1)	ENSP00000510712.1:n.*1783C>A
ENST00000691643.1:n.2964C>A (RAF1)
ENST00000691724.1:c.*868C>A (RAF1)	ENSP00000509255.1:n.*868C>A
ENST00000691779.1:c.*1489C>A (RAF1)	ENSP00000508592.1:n.*1489C>A
ENST00000691888.1:c.785C>A (RAF1)
ENST00000691899.1:c.1911C>A (RAF1)	ENSP00000508763.1:p.Cys637Ter
ENST00000692069.1:n.4835C>A (RAF1)
ENST00000692093.1:c.1812C>A (RAF1)	ENSP00000509669.1:p.Cys604Ter
ENST00000692311.1:n.2735C>A (RAF1)
ENST00000692558.1:n.4494C>A (RAF1)
ENST00000692773.1:c.*1648C>A (RAF1)	ENSP00000509055.1:n.*1648C>A
ENST00000692830.1:c.*1656C>A (RAF1)	ENSP00000509461.1:n.*1656C>A
ENST00000693312.1:c.1686C>A (RAF1)	ENSP00000508686.1:p.Cys562Ter
ENST00000693664.1:c.*362C>A (RAF1)	ENSP00000509614.1:n.*362C>A
ENST00000693705.1:c.*1290C>A (RAF1)	ENSP00000510697.1:n.*1290C>A
ENST00000251849.9:c.1911C>A (RAF1) MANE Select	ENSP00000251849.4:p.Cys637Ter
ENST00000442415.7:c.1971C>A (RAF1)	ENSP00000401888.2:p.Cys657Ter
ENST00000676541.1:c.*2297G>T (MKRN2)	ENSP00000503730.1:n.*2297G>T
ENST00000677142.1:c.*2297G>T (MKRN2)	ENSP00000504455.1:n.*2297G>T
ENST00000677816.1:c.*852G>T (MKRN2)	ENSP00000502893.1:n.*852G>T
ENST00000677941.1:n.2360G>T (MKRN2)
ENST00000251849.8:c.1911C>A (RAF1)	ENSP00000251849.4:p.Cys637Ter
ENST00000423275.5:c.*1588C>A (RAF1)	ENSP00000401088.1:n.*1588C>A
ENST00000432427.2:c.1548C>A (RAF1)	ENSP00000398591.2:p.Cys516Ter
ENST00000442415.6:c.1971C>A (RAF1)	ENSP00000401888.2:p.Cys657Ter
ENST00000471449.1:n.600C>A (RAF1)
NM_002880.3:c.1911C>A , LRG_413t1:c.1911C>A (RAF1)	NP_002871.1:p.Cys637Ter
XM_005265355.1:c.1911C>A (RAF1)	XP_005265412.1:p.Cys637Ter
XM_005265357.1:c.1812C>A (RAF1)	XP_005265414.1:p.Cys604Ter
XM_005265358.3:c.1668C>A (RAF1)	XP_005265415.1:p.Cys556Ter
XM_005265359.3:c.1569C>A (RAF1)	XP_005265416.1:p.Cys523Ter
XM_011533974.1:c.1911C>A (RAF1)	XP_011532276.1:p.Cys637Ter
XM_011533975.1:c.1668C>A (RAF1)	XP_011532277.1:p.Cys556Ter
NM_001354689.1:c.1971C>A (RAF1)	NP_001341618.1:p.Cys657Ter
NM_001354690.1:c.1911C>A (RAF1)	NP_001341619.1:p.Cys637Ter
NM_001354691.1:c.1668C>A (RAF1)	NP_001341620.1:p.Cys556Ter
NM_001354692.1:c.1668C>A (RAF1)	NP_001341621.1:p.Cys556Ter
NM_001354693.1:c.1812C>A (RAF1)	NP_001341622.1:p.Cys604Ter
NM_001354694.1:c.1728C>A (RAF1)	NP_001341623.1:p.Cys576Ter
NM_001354695.1:c.1569C>A (RAF1)	NP_001341624.1:p.Cys523Ter
NR_148940.1:n.2439C>A (RAF1)
NR_148941.1:n.2385C>A (RAF1)
NR_148942.1:n.2324C>A (RAF1)
XM_011533974.3:c.1911C>A (RAF1)	XP_011532276.1:p.Cys637Ter
XM_017006966.1:c.1812C>A (RAF1)	XP_016862455.1:p.Cys604Ter
NM_001354689.3:c.1971C>A (RAF1)	NP_001341618.1:p.Cys657Ter
NM_001354690.2:c.1911C>A (RAF1)	NP_001341619.1:p.Cys637Ter
NM_001354691.2:c.1668C>A (RAF1)	NP_001341620.1:p.Cys556Ter
NM_001354692.2:c.1668C>A (RAF1)	NP_001341621.1:p.Cys556Ter
NM_001354693.2:c.1812C>A (RAF1)	NP_001341622.1:p.Cys604Ter
NM_001354694.2:c.1728C>A (RAF1)	NP_001341623.1:p.Cys576Ter
NM_001354695.2:c.1569C>A (RAF1)	NP_001341624.1:p.Cys523Ter
NR_148940.2:n.2355C>A (RAF1)
NR_148941.2:n.2301C>A (RAF1)
NR_148942.2:n.2240C>A (RAF1)
NM_001354690.3:c.1911C>A (RAF1)	NP_001341619.1:p.Cys637Ter
NM_001354691.3:c.1668C>A (RAF1)	NP_001341620.1:p.Cys556Ter
NM_001354692.3:c.1668C>A (RAF1)	NP_001341621.1:p.Cys556Ter
NM_001354693.3:c.1812C>A (RAF1)	NP_001341622.1:p.Cys604Ter
NM_001354694.3:c.1728C>A (RAF1)	NP_001341623.1:p.Cys576Ter
NM_001354695.3:c.1569C>A (RAF1)	NP_001341624.1:p.Cys523Ter
NM_002880.4:c.1911C>A (RAF1) MANE Select	NP_002871.1:p.Cys637Ter
NR_148940.3:n.2355C>A (RAF1)
NR_148941.3:n.2301C>A (RAF1)
NR_148942.3:n.2240C>A (RAF1)