Canonical Allele Identifier: CA432522061

Gene: RAF1 MKRN2

Linked Data

• dbSNP Id: rs894831042
• COSMIC: COSM6234057 ; COSM6234058
• MyVariant Identifiers: chr3:g.12626463G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584964G>A , CM000665.2:g.12584964G>A	GRCh38
NC_000003.11:g.12626463G>A , CM000665.1:g.12626463G>A	GRCh37
NC_000003.10:g.12601463G>A	NCBI36
NG_007467.1:g.84216C>T , LRG_413:g.84216C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1351C>T (RAF1)	ENSP00000401088.1:n.*1351C>T
ENST00000432427.3:c.1003C>T (RAF1)
ENST00000460610.2:n.5998C>T (RAF1)
ENST00000471449.2:n.496C>T (RAF1)
ENST00000475353.2:n.3966C>T (RAF1)
ENST00000684903.1:c.*1363C>T (RAF1)	ENSP00000508612.1:n.*1363C>T
ENST00000685348.1:c.*1397C>T (RAF1)	ENSP00000510285.1:n.*1397C>T
ENST00000685437.1:c.1587C>T (RAF1)	ENSP00000508794.1:p.Gly529=
ENST00000685653.1:c.1686C>T (RAF1)	ENSP00000509968.1:p.Gly562=
ENST00000685697.1:n.2421C>T (RAF1)
ENST00000685738.1:c.*650C>T (RAF1)	ENSP00000510156.1:n.*650C>T
ENST00000686409.1:n.5095C>T (RAF1)
ENST00000686455.1:n.4407C>T (RAF1)
ENST00000686762.1:c.*245C>T (RAF1)	ENSP00000509767.1:n.*245C>T
ENST00000687257.1:n.4140C>T (RAF1)
ENST00000687326.1:c.*2978C>T (RAF1)	ENSP00000509665.1:n.*2978C>T
ENST00000687505.1:n.1804C>T (RAF1)
ENST00000687923.1:c.1575C>T (RAF1)	ENSP00000510255.1:p.Gly525=
ENST00000688269.1:n.2282C>T (RAF1)
ENST00000688444.1:n.3803C>T (RAF1)
ENST00000688543.1:c.1587C>T (RAF1)	ENSP00000509612.1:p.Gly529=
ENST00000688625.1:c.*3055C>T (RAF1)	ENSP00000509522.1:n.*3055C>T
ENST00000688803.1:n.3114C>T (RAF1)
ENST00000688914.1:n.1099C>T (RAF1)
ENST00000689097.1:c.*1363C>T (RAF1)	ENSP00000509756.1:n.*1363C>T
ENST00000689389.1:c.1509C>T (RAF1)	ENSP00000510213.1:p.Gly503=
ENST00000689418.1:c.*3581C>T (RAF1)	ENSP00000509467.1:n.*3581C>T
ENST00000689540.1:n.4054C>T (RAF1)
ENST00000689876.1:c.*235C>T (RAF1)	ENSP00000508535.1:n.*235C>T
ENST00000689914.1:c.*620C>T (RAF1)	ENSP00000509847.1:n.*620C>T
ENST00000690397.1:c.1575C>T (RAF1)	ENSP00000508730.1:p.Gly525=
ENST00000690460.1:c.1674C>T (RAF1)	ENSP00000509106.1:p.Gly558=
ENST00000690585.1:c.412C>T (RAF1)
ENST00000690625.1:n.2722C>T (RAF1)
ENST00000691396.1:c.*1558C>T (RAF1)	ENSP00000510712.1:n.*1558C>T
ENST00000691643.1:n.2739C>T (RAF1)
ENST00000691724.1:c.*643C>T (RAF1)	ENSP00000509255.1:n.*643C>T
ENST00000691779.1:c.*1264C>T (RAF1)	ENSP00000508592.1:n.*1264C>T
ENST00000691888.1:c.560C>T (RAF1)
ENST00000691899.1:c.1686C>T (RAF1)	ENSP00000508763.1:p.Gly562=
ENST00000692069.1:n.4610C>T (RAF1)
ENST00000692093.1:c.1587C>T (RAF1)	ENSP00000509669.1:p.Gly529=
ENST00000692311.1:n.2510C>T (RAF1)
ENST00000692558.1:n.4269C>T (RAF1)
ENST00000692773.1:c.*1423C>T (RAF1)	ENSP00000509055.1:n.*1423C>T
ENST00000692830.1:c.*1431C>T (RAF1)	ENSP00000509461.1:n.*1431C>T
ENST00000693312.1:c.1461C>T (RAF1)	ENSP00000508686.1:p.Gly487=
ENST00000693664.1:c.*137C>T (RAF1)	ENSP00000509614.1:n.*137C>T
ENST00000693705.1:c.*1065C>T (RAF1)	ENSP00000510697.1:n.*1065C>T
ENST00000251849.9:c.1686C>T (RAF1) MANE Select	ENSP00000251849.4:p.Gly562=
ENST00000442415.7:c.1746C>T (RAF1)	ENSP00000401888.2:p.Gly582=
ENST00000676541.1:c.*2711G>A (MKRN2)	ENSP00000503730.1:n.*2711G>A
ENST00000677142.1:c.*2711G>A (MKRN2)	ENSP00000504455.1:n.*2711G>A
ENST00000677816.1:c.*1266G>A (MKRN2)	ENSP00000502893.1:n.*1266G>A
ENST00000677941.1:n.2774G>A (MKRN2)
ENST00000251849.8:c.1686C>T (RAF1)	ENSP00000251849.4:p.Gly562=
ENST00000423275.5:c.*1363C>T (RAF1)	ENSP00000401088.1:n.*1363C>T
ENST00000432427.2:c.1323C>T (RAF1)	ENSP00000398591.2:p.Gly441=
ENST00000442415.6:c.1746C>T (RAF1)	ENSP00000401888.2:p.Gly582=
ENST00000471449.1:n.375C>T (RAF1)
NM_002880.3:c.1686C>T , LRG_413t1:c.1686C>T (RAF1)	NP_002871.1:p.Gly562=
XM_005265355.1:c.1686C>T (RAF1)	XP_005265412.1:p.Gly562=
XM_005265357.1:c.1587C>T (RAF1)	XP_005265414.1:p.Gly529=
XM_005265358.3:c.1443C>T (RAF1)	XP_005265415.1:p.Gly481=
XM_005265359.3:c.1344C>T (RAF1)	XP_005265416.1:p.Gly448=
XM_011533974.1:c.1686C>T (RAF1)	XP_011532276.1:p.Gly562=
XM_011533975.1:c.1443C>T (RAF1)	XP_011532277.1:p.Gly481=
NM_001354689.1:c.1746C>T (RAF1)	NP_001341618.1:p.Gly582=
NM_001354690.1:c.1686C>T (RAF1)	NP_001341619.1:p.Gly562=
NM_001354691.1:c.1443C>T (RAF1)	NP_001341620.1:p.Gly481=
NM_001354692.1:c.1443C>T (RAF1)	NP_001341621.1:p.Gly481=
NM_001354693.1:c.1587C>T (RAF1)	NP_001341622.1:p.Gly529=
NM_001354694.1:c.1503C>T (RAF1)	NP_001341623.1:p.Gly501=
NM_001354695.1:c.1344C>T (RAF1)	NP_001341624.1:p.Gly448=
NR_148940.1:n.2214C>T (RAF1)
NR_148941.1:n.2160C>T (RAF1)
NR_148942.1:n.2099C>T (RAF1)
XM_011533974.3:c.1686C>T (RAF1)	XP_011532276.1:p.Gly562=
XM_017006966.1:c.1587C>T (RAF1)	XP_016862455.1:p.Gly529=
NM_001354689.3:c.1746C>T (RAF1)	NP_001341618.1:p.Gly582=
NM_001354690.2:c.1686C>T (RAF1)	NP_001341619.1:p.Gly562=
NM_001354691.2:c.1443C>T (RAF1)	NP_001341620.1:p.Gly481=
NM_001354692.2:c.1443C>T (RAF1)	NP_001341621.1:p.Gly481=
NM_001354693.2:c.1587C>T (RAF1)	NP_001341622.1:p.Gly529=
NM_001354694.2:c.1503C>T (RAF1)	NP_001341623.1:p.Gly501=
NM_001354695.2:c.1344C>T (RAF1)	NP_001341624.1:p.Gly448=
NR_148940.2:n.2130C>T (RAF1)
NR_148941.2:n.2076C>T (RAF1)
NR_148942.2:n.2015C>T (RAF1)
NM_001354690.3:c.1686C>T (RAF1)	NP_001341619.1:p.Gly562=
NM_001354691.3:c.1443C>T (RAF1)	NP_001341620.1:p.Gly481=
NM_001354692.3:c.1443C>T (RAF1)	NP_001341621.1:p.Gly481=
NM_001354693.3:c.1587C>T (RAF1)	NP_001341622.1:p.Gly529=
NM_001354694.3:c.1503C>T (RAF1)	NP_001341623.1:p.Gly501=
NM_001354695.3:c.1344C>T (RAF1)	NP_001341624.1:p.Gly448=
NM_002880.4:c.1686C>T (RAF1) MANE Select	NP_002871.1:p.Gly562=
NR_148940.3:n.2130C>T (RAF1)
NR_148941.3:n.2076C>T (RAF1)
NR_148942.3:n.2015C>T (RAF1)