Canonical Allele Identifier: CA351496999

Gene: RAF1 MKRN2

Linked Data

• MyVariant Identifiers: chr3:g.12626465C>A (hg19) ; chr3:g.12584966C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584966C>A , CM000665.2:g.12584966C>A	GRCh38
NC_000003.11:g.12626465C>A , CM000665.1:g.12626465C>A	GRCh37
NC_000003.10:g.12601465C>A	NCBI36
NG_007467.1:g.84214G>T , LRG_413:g.84214G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1349G>T (RAF1)	ENSP00000401088.1:n.*1349G>T
ENST00000432427.3:c.1001G>T (RAF1)
ENST00000460610.2:n.5996G>T (RAF1)
ENST00000471449.2:n.494G>T (RAF1)
ENST00000475353.2:n.3964G>T (RAF1)
ENST00000684903.1:c.*1361G>T (RAF1)	ENSP00000508612.1:n.*1361G>T
ENST00000685348.1:c.*1395G>T (RAF1)	ENSP00000510285.1:n.*1395G>T
ENST00000685437.1:c.1585G>T (RAF1)	ENSP00000508794.1:p.Gly529Cys
ENST00000685653.1:c.1684G>T (RAF1)	ENSP00000509968.1:p.Gly562Cys
ENST00000685697.1:n.2419G>T (RAF1)
ENST00000685738.1:c.*648G>T (RAF1)	ENSP00000510156.1:n.*648G>T
ENST00000686409.1:n.5093G>T (RAF1)
ENST00000686455.1:n.4405G>T (RAF1)
ENST00000686762.1:c.*243G>T (RAF1)	ENSP00000509767.1:n.*243G>T
ENST00000687257.1:n.4138G>T (RAF1)
ENST00000687326.1:c.*2976G>T (RAF1)	ENSP00000509665.1:n.*2976G>T
ENST00000687505.1:n.1802G>T (RAF1)
ENST00000687923.1:c.1573G>T (RAF1)	ENSP00000510255.1:p.Gly525Cys
ENST00000688269.1:n.2280G>T (RAF1)
ENST00000688444.1:n.3801G>T (RAF1)
ENST00000688543.1:c.1585G>T (RAF1)	ENSP00000509612.1:p.Gly529Cys
ENST00000688625.1:c.*3053G>T (RAF1)	ENSP00000509522.1:n.*3053G>T
ENST00000688803.1:n.3112G>T (RAF1)
ENST00000688914.1:n.1097G>T (RAF1)
ENST00000689097.1:c.*1361G>T (RAF1)	ENSP00000509756.1:n.*1361G>T
ENST00000689389.1:c.1507G>T (RAF1)	ENSP00000510213.1:p.Gly503Cys
ENST00000689418.1:c.*3579G>T (RAF1)	ENSP00000509467.1:n.*3579G>T
ENST00000689540.1:n.4052G>T (RAF1)
ENST00000689876.1:c.*233G>T (RAF1)	ENSP00000508535.1:n.*233G>T
ENST00000689914.1:c.*618G>T (RAF1)	ENSP00000509847.1:n.*618G>T
ENST00000690397.1:c.1573G>T (RAF1)	ENSP00000508730.1:p.Gly525Cys
ENST00000690460.1:c.1672G>T (RAF1)	ENSP00000509106.1:p.Gly558Cys
ENST00000690585.1:c.410G>T (RAF1)
ENST00000690625.1:n.2720G>T (RAF1)
ENST00000691396.1:c.*1556G>T (RAF1)	ENSP00000510712.1:n.*1556G>T
ENST00000691643.1:n.2737G>T (RAF1)
ENST00000691724.1:c.*641G>T (RAF1)	ENSP00000509255.1:n.*641G>T
ENST00000691779.1:c.*1262G>T (RAF1)	ENSP00000508592.1:n.*1262G>T
ENST00000691888.1:c.558G>T (RAF1)
ENST00000691899.1:c.1684G>T (RAF1)	ENSP00000508763.1:p.Gly562Cys
ENST00000692069.1:n.4608G>T (RAF1)
ENST00000692093.1:c.1585G>T (RAF1)	ENSP00000509669.1:p.Gly529Cys
ENST00000692311.1:n.2508G>T (RAF1)
ENST00000692558.1:n.4267G>T (RAF1)
ENST00000692773.1:c.*1421G>T (RAF1)	ENSP00000509055.1:n.*1421G>T
ENST00000692830.1:c.*1429G>T (RAF1)	ENSP00000509461.1:n.*1429G>T
ENST00000693312.1:c.1459G>T (RAF1)	ENSP00000508686.1:p.Gly487Cys
ENST00000693664.1:c.*135G>T (RAF1)	ENSP00000509614.1:n.*135G>T
ENST00000693705.1:c.*1063G>T (RAF1)	ENSP00000510697.1:n.*1063G>T
ENST00000251849.9:c.1684G>T (RAF1) MANE Select	ENSP00000251849.4:p.Gly562Cys
ENST00000442415.7:c.1744G>T (RAF1)	ENSP00000401888.2:p.Gly582Cys
ENST00000676541.1:c.*2713C>A (MKRN2)	ENSP00000503730.1:n.*2713C>A
ENST00000677142.1:c.*2713C>A (MKRN2)	ENSP00000504455.1:n.*2713C>A
ENST00000677816.1:c.*1268C>A (MKRN2)	ENSP00000502893.1:n.*1268C>A
ENST00000677941.1:n.2776C>A (MKRN2)
ENST00000251849.8:c.1684G>T (RAF1)	ENSP00000251849.4:p.Gly562Cys
ENST00000423275.5:c.*1361G>T (RAF1)	ENSP00000401088.1:n.*1361G>T
ENST00000432427.2:c.1321G>T (RAF1)	ENSP00000398591.2:p.Gly441Cys
ENST00000442415.6:c.1744G>T (RAF1)	ENSP00000401888.2:p.Gly582Cys
ENST00000471449.1:n.373G>T (RAF1)
NM_002880.3:c.1684G>T , LRG_413t1:c.1684G>T (RAF1)	NP_002871.1:p.Gly562Cys
XM_005265355.1:c.1684G>T (RAF1)	XP_005265412.1:p.Gly562Cys
XM_005265357.1:c.1585G>T (RAF1)	XP_005265414.1:p.Gly529Cys
XM_005265358.3:c.1441G>T (RAF1)	XP_005265415.1:p.Gly481Cys
XM_005265359.3:c.1342G>T (RAF1)	XP_005265416.1:p.Gly448Cys
XM_011533974.1:c.1684G>T (RAF1)	XP_011532276.1:p.Gly562Cys
XM_011533975.1:c.1441G>T (RAF1)	XP_011532277.1:p.Gly481Cys
NM_001354689.1:c.1744G>T (RAF1)	NP_001341618.1:p.Gly582Cys
NM_001354690.1:c.1684G>T (RAF1)	NP_001341619.1:p.Gly562Cys
NM_001354691.1:c.1441G>T (RAF1)	NP_001341620.1:p.Gly481Cys
NM_001354692.1:c.1441G>T (RAF1)	NP_001341621.1:p.Gly481Cys
NM_001354693.1:c.1585G>T (RAF1)	NP_001341622.1:p.Gly529Cys
NM_001354694.1:c.1501G>T (RAF1)	NP_001341623.1:p.Gly501Cys
NM_001354695.1:c.1342G>T (RAF1)	NP_001341624.1:p.Gly448Cys
NR_148940.1:n.2212G>T (RAF1)
NR_148941.1:n.2158G>T (RAF1)
NR_148942.1:n.2097G>T (RAF1)
XM_011533974.3:c.1684G>T (RAF1)	XP_011532276.1:p.Gly562Cys
XM_017006966.1:c.1585G>T (RAF1)	XP_016862455.1:p.Gly529Cys
NM_001354689.3:c.1744G>T (RAF1)	NP_001341618.1:p.Gly582Cys
NM_001354690.2:c.1684G>T (RAF1)	NP_001341619.1:p.Gly562Cys
NM_001354691.2:c.1441G>T (RAF1)	NP_001341620.1:p.Gly481Cys
NM_001354692.2:c.1441G>T (RAF1)	NP_001341621.1:p.Gly481Cys
NM_001354693.2:c.1585G>T (RAF1)	NP_001341622.1:p.Gly529Cys
NM_001354694.2:c.1501G>T (RAF1)	NP_001341623.1:p.Gly501Cys
NM_001354695.2:c.1342G>T (RAF1)	NP_001341624.1:p.Gly448Cys
NR_148940.2:n.2128G>T (RAF1)
NR_148941.2:n.2074G>T (RAF1)
NR_148942.2:n.2013G>T (RAF1)
NM_001354690.3:c.1684G>T (RAF1)	NP_001341619.1:p.Gly562Cys
NM_001354691.3:c.1441G>T (RAF1)	NP_001341620.1:p.Gly481Cys
NM_001354692.3:c.1441G>T (RAF1)	NP_001341621.1:p.Gly481Cys
NM_001354693.3:c.1585G>T (RAF1)	NP_001341622.1:p.Gly529Cys
NM_001354694.3:c.1501G>T (RAF1)	NP_001341623.1:p.Gly501Cys
NM_001354695.3:c.1342G>T (RAF1)	NP_001341624.1:p.Gly448Cys
NM_002880.4:c.1684G>T (RAF1) MANE Select	NP_002871.1:p.Gly562Cys
NR_148940.3:n.2128G>T (RAF1)
NR_148941.3:n.2074G>T (RAF1)
NR_148942.3:n.2013G>T (RAF1)