Canonical Allele Identifier: CA351501645

Gene: RAF1

Linked Data

• MyVariant Identifiers: chr3:g.12632303C>A (hg19) ; chr3:g.12590804C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12590804C>A , CM000665.2:g.12590804C>A	GRCh38
NC_000003.11:g.12632303C>A , CM000665.1:g.12632303C>A	GRCh37
NC_000003.10:g.12607303C>A	NCBI36
NG_007467.1:g.78376G>T , LRG_413:g.78376G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000423275.6:c.*1029G>T	ENSP00000401088.1:n.*1029G>T
ENST00000432427.3:c.681G>T
ENST00000460610.2:n.158G>T
ENST00000465826.6:n.955G>T
ENST00000475353.2:n.1286G>T
ENST00000494557.2:n.1175G>T
ENST00000684903.1:c.*1041G>T	ENSP00000508612.1:n.*1041G>T
ENST00000685348.1:c.*1041G>T	ENSP00000510285.1:n.*1041G>T
ENST00000685437.1:c.1265G>T	ENSP00000508794.1:p.Gly422Val
ENST00000685653.1:c.1364G>T	ENSP00000509968.1:p.Gly455Val
ENST00000685738.1:c.*328G>T	ENSP00000510156.1:n.*328G>T
ENST00000686409.1:n.2415G>T
ENST00000686455.1:n.1727G>T
ENST00000686762.1:c.1364G>T	ENSP00000509767.1:p.Gly455Val
ENST00000687257.1:n.1600G>T
ENST00000687326.1:c.*298G>T	ENSP00000509665.1:n.*298G>T
ENST00000687505.1:n.1482G>T
ENST00000687923.1:c.1253G>T	ENSP00000510255.1:p.Gly418Val
ENST00000687940.1:n.1741G>T
ENST00000688269.1:n.1960G>T
ENST00000688326.1:c.797G>T
ENST00000688444.1:n.1690G>T
ENST00000688543.1:c.1265G>T	ENSP00000509612.1:p.Gly422Val
ENST00000688625.1:c.*942G>T	ENSP00000509522.1:n.*942G>T
ENST00000688803.1:n.1595G>T
ENST00000688914.1:n.350G>T
ENST00000689097.1:c.*1041G>T	ENSP00000509756.1:n.*1041G>T
ENST00000689389.1:c.1193+904G>T	ENSP00000510213.1:n.1193+904G>T
ENST00000689418.1:c.*1041G>T	ENSP00000509467.1:n.*1041G>T
ENST00000689481.1:c.*1041G>T	ENSP00000510248.1:n.*1041G>T
ENST00000689540.1:n.1514G>T
ENST00000689876.1:c.1364G>T	ENSP00000508535.1:p.Gly455Val
ENST00000689914.1:c.*298G>T	ENSP00000509847.1:n.*298G>T
ENST00000690397.1:c.1253G>T	ENSP00000508730.1:p.Gly418Val
ENST00000690460.1:c.1352G>T	ENSP00000509106.1:p.Gly451Val
ENST00000690585.1:c.256G>T
ENST00000690625.1:n.2400G>T
ENST00000691396.1:c.*1216G>T	ENSP00000510712.1:n.*1216G>T
ENST00000691724.1:c.*321G>T	ENSP00000509255.1:n.*321G>T
ENST00000691779.1:c.*942G>T	ENSP00000508592.1:n.*942G>T
ENST00000691888.1:c.256G>T
ENST00000691899.1:c.1364G>T	ENSP00000508763.1:p.Gly455Val
ENST00000692069.1:n.1930G>T
ENST00000692093.1:c.1265G>T	ENSP00000509669.1:p.Gly422Val
ENST00000692311.1:n.2188G>T
ENST00000692558.1:n.1729G>T
ENST00000692773.1:c.*1101G>T	ENSP00000509055.1:n.*1101G>T
ENST00000692830.1:c.*1109G>T	ENSP00000509461.1:n.*1109G>T
ENST00000693069.1:c.*298G>T	ENSP00000510072.1:n.*298G>T
ENST00000693312.1:c.1139G>T	ENSP00000508686.1:p.Gly380Val
ENST00000693664.1:c.1364G>T	ENSP00000509614.1:p.Gly455Val
ENST00000693705.1:c.*1041G>T	ENSP00000510697.1:n.*1041G>T
ENST00000251849.9:c.1364G>T MANE Select	ENSP00000251849.4:p.Gly455Val
ENST00000442415.7:c.1424G>T	ENSP00000401888.2:p.Gly475Val
ENST00000251849.8:c.1364G>T	ENSP00000251849.4:p.Gly455Val
ENST00000423275.5:c.*1041G>T	ENSP00000401088.1:n.*1041G>T
ENST00000432427.2:c.1001G>T	ENSP00000398591.2:p.Gly334Val
ENST00000442415.6:c.1424G>T	ENSP00000401888.2:p.Gly475Val
ENST00000460610.1:n.321G>T
ENST00000465826.5:n.721G>T
ENST00000475353.1:n.532G>T
ENST00000494557.1:n.380G>T
NM_002880.3:c.1364G>T , LRG_413t1:c.1364G>T	NP_002871.1:p.Gly455Val
XM_005265355.1:c.1364G>T	XP_005265412.1:p.Gly455Val
XM_005265357.1:c.1265G>T	XP_005265414.1:p.Gly422Val
XM_005265358.3:c.1121G>T	XP_005265415.1:p.Gly374Val
XM_005265359.3:c.1022G>T	XP_005265416.1:p.Gly341Val
XM_005265360.1:c.1364G>T	XP_005265417.1:p.Gly455Val
XM_011533974.1:c.1364G>T	XP_011532276.1:p.Gly455Val
XM_011533975.1:c.1121G>T	XP_011532277.1:p.Gly374Val
NM_001354689.1:c.1424G>T	NP_001341618.1:p.Gly475Val
NM_001354690.1:c.1364G>T	NP_001341619.1:p.Gly455Val
NM_001354691.1:c.1121G>T	NP_001341620.1:p.Gly374Val
NM_001354692.1:c.1121G>T	NP_001341621.1:p.Gly374Val
NM_001354693.1:c.1265G>T	NP_001341622.1:p.Gly422Val
NM_001354694.1:c.1181G>T	NP_001341623.1:p.Gly394Val
NM_001354695.1:c.1022G>T	NP_001341624.1:p.Gly341Val
NR_148940.1:n.1892G>T
NR_148941.1:n.1838G>T
NR_148942.1:n.1777G>T
XM_011533974.3:c.1364G>T	XP_011532276.1:p.Gly455Val
XM_017006966.1:c.1265G>T	XP_016862455.1:p.Gly422Val
NM_001354689.3:c.1424G>T	NP_001341618.1:p.Gly475Val
NM_001354690.2:c.1364G>T	NP_001341619.1:p.Gly455Val
NM_001354691.2:c.1121G>T	NP_001341620.1:p.Gly374Val
NM_001354692.2:c.1121G>T	NP_001341621.1:p.Gly374Val
NM_001354693.2:c.1265G>T	NP_001341622.1:p.Gly422Val
NM_001354694.2:c.1181G>T	NP_001341623.1:p.Gly394Val
NM_001354695.2:c.1022G>T	NP_001341624.1:p.Gly341Val
NR_148940.2:n.1808G>T
NR_148941.2:n.1754G>T
NR_148942.2:n.1693G>T
NM_001354690.3:c.1364G>T	NP_001341619.1:p.Gly455Val
NM_001354691.3:c.1121G>T	NP_001341620.1:p.Gly374Val
NM_001354692.3:c.1121G>T	NP_001341621.1:p.Gly374Val
NM_001354693.3:c.1265G>T	NP_001341622.1:p.Gly422Val
NM_001354694.3:c.1181G>T	NP_001341623.1:p.Gly394Val
NM_001354695.3:c.1022G>T	NP_001341624.1:p.Gly341Val
NM_002880.4:c.1364G>T MANE Select	NP_002871.1:p.Gly455Val
NR_148940.3:n.1808G>T
NR_148941.3:n.1754G>T
NR_148942.3:n.1693G>T