Canonical Allele Identifier: CA351502139

Gene: RAF1

Linked Data

• MyVariant Identifiers: chr3:g.12632391C>A (hg19) ; chr3:g.12590892C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12590892C>A , CM000665.2:g.12590892C>A	GRCh38
NC_000003.11:g.12632391C>A , CM000665.1:g.12632391C>A	GRCh37
NC_000003.10:g.12607391C>A	NCBI36
NG_007467.1:g.78288G>T , LRG_413:g.78288G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000423275.6:c.*941G>T	ENSP00000401088.1:n.*941G>T
ENST00000432427.3:c.593G>T
ENST00000460610.2:n.70G>T
ENST00000465826.6:n.867G>T
ENST00000475353.2:n.1198G>T
ENST00000494557.2:n.1087G>T
ENST00000684903.1:c.*953G>T	ENSP00000508612.1:n.*953G>T
ENST00000685348.1:c.*953G>T	ENSP00000510285.1:n.*953G>T
ENST00000685437.1:c.1177G>T	ENSP00000508794.1:p.Gly393Cys
ENST00000685653.1:c.1276G>T	ENSP00000509968.1:p.Gly426Cys
ENST00000685738.1:c.*240G>T	ENSP00000510156.1:n.*240G>T
ENST00000686409.1:n.2327G>T
ENST00000686455.1:n.1639G>T
ENST00000686762.1:c.1276G>T	ENSP00000509767.1:p.Gly426Cys
ENST00000687257.1:n.1512G>T
ENST00000687326.1:c.*210G>T	ENSP00000509665.1:n.*210G>T
ENST00000687505.1:n.1394G>T
ENST00000687923.1:c.1165G>T	ENSP00000510255.1:p.Gly389Cys
ENST00000687940.1:n.1653G>T
ENST00000688269.1:n.1872G>T
ENST00000688326.1:c.709G>T
ENST00000688444.1:n.1602G>T
ENST00000688543.1:c.1177G>T	ENSP00000509612.1:p.Gly393Cys
ENST00000688625.1:c.*854G>T	ENSP00000509522.1:n.*854G>T
ENST00000688803.1:n.1507G>T
ENST00000688914.1:n.262G>T
ENST00000689097.1:c.*953G>T	ENSP00000509756.1:n.*953G>T
ENST00000689389.1:c.1193+816G>T	ENSP00000510213.1:n.1193+816G>T
ENST00000689418.1:c.*953G>T	ENSP00000509467.1:n.*953G>T
ENST00000689481.1:c.*953G>T	ENSP00000510248.1:n.*953G>T
ENST00000689540.1:n.1426G>T
ENST00000689876.1:c.1276G>T	ENSP00000508535.1:p.Gly426Cys
ENST00000689914.1:c.*210G>T	ENSP00000509847.1:n.*210G>T
ENST00000690397.1:c.1165G>T	ENSP00000508730.1:p.Gly389Cys
ENST00000690460.1:c.1264G>T	ENSP00000509106.1:p.Gly422Cys
ENST00000690585.1:c.168G>T
ENST00000690625.1:n.2312G>T
ENST00000691396.1:c.*1128G>T	ENSP00000510712.1:n.*1128G>T
ENST00000691724.1:c.*233G>T	ENSP00000509255.1:n.*233G>T
ENST00000691779.1:c.*854G>T	ENSP00000508592.1:n.*854G>T
ENST00000691888.1:c.168G>T
ENST00000691899.1:c.1276G>T	ENSP00000508763.1:p.Gly426Cys
ENST00000692069.1:n.1842G>T
ENST00000692093.1:c.1177G>T	ENSP00000509669.1:p.Gly393Cys
ENST00000692311.1:n.2100G>T
ENST00000692558.1:n.1641G>T
ENST00000692773.1:c.*1013G>T	ENSP00000509055.1:n.*1013G>T
ENST00000692830.1:c.*1021G>T	ENSP00000509461.1:n.*1021G>T
ENST00000693069.1:c.*210G>T	ENSP00000510072.1:n.*210G>T
ENST00000693312.1:c.1051G>T	ENSP00000508686.1:p.Gly351Cys
ENST00000693664.1:c.1276G>T	ENSP00000509614.1:p.Gly426Cys
ENST00000693705.1:c.*953G>T	ENSP00000510697.1:n.*953G>T
ENST00000251849.9:c.1276G>T MANE Select	ENSP00000251849.4:p.Gly426Cys
ENST00000442415.7:c.1336G>T	ENSP00000401888.2:p.Gly446Cys
ENST00000251849.8:c.1276G>T	ENSP00000251849.4:p.Gly426Cys
ENST00000423275.5:c.*953G>T	ENSP00000401088.1:n.*953G>T
ENST00000432427.2:c.913G>T	ENSP00000398591.2:p.Gly305Cys
ENST00000442415.6:c.1336G>T	ENSP00000401888.2:p.Gly446Cys
ENST00000460610.1:n.233G>T
ENST00000465826.5:n.633G>T
ENST00000475353.1:n.444G>T
ENST00000494557.1:n.292G>T
NM_002880.3:c.1276G>T , LRG_413t1:c.1276G>T	NP_002871.1:p.Gly426Cys
XM_005265355.1:c.1276G>T	XP_005265412.1:p.Gly426Cys
XM_005265357.1:c.1177G>T	XP_005265414.1:p.Gly393Cys
XM_005265358.3:c.1033G>T	XP_005265415.1:p.Gly345Cys
XM_005265359.3:c.934G>T	XP_005265416.1:p.Gly312Cys
XM_005265360.1:c.1276G>T	XP_005265417.1:p.Gly426Cys
XM_011533974.1:c.1276G>T	XP_011532276.1:p.Gly426Cys
XM_011533975.1:c.1033G>T	XP_011532277.1:p.Gly345Cys
NM_001354689.1:c.1336G>T	NP_001341618.1:p.Gly446Cys
NM_001354690.1:c.1276G>T	NP_001341619.1:p.Gly426Cys
NM_001354691.1:c.1033G>T	NP_001341620.1:p.Gly345Cys
NM_001354692.1:c.1033G>T	NP_001341621.1:p.Gly345Cys
NM_001354693.1:c.1177G>T	NP_001341622.1:p.Gly393Cys
NM_001354694.1:c.1093G>T	NP_001341623.1:p.Gly365Cys
NM_001354695.1:c.934G>T	NP_001341624.1:p.Gly312Cys
NR_148940.1:n.1804G>T
NR_148941.1:n.1750G>T
NR_148942.1:n.1689G>T
XM_011533974.3:c.1276G>T	XP_011532276.1:p.Gly426Cys
XM_017006966.1:c.1177G>T	XP_016862455.1:p.Gly393Cys
NM_001354689.3:c.1336G>T	NP_001341618.1:p.Gly446Cys
NM_001354690.2:c.1276G>T	NP_001341619.1:p.Gly426Cys
NM_001354691.2:c.1033G>T	NP_001341620.1:p.Gly345Cys
NM_001354692.2:c.1033G>T	NP_001341621.1:p.Gly345Cys
NM_001354693.2:c.1177G>T	NP_001341622.1:p.Gly393Cys
NM_001354694.2:c.1093G>T	NP_001341623.1:p.Gly365Cys
NM_001354695.2:c.934G>T	NP_001341624.1:p.Gly312Cys
NR_148940.2:n.1720G>T
NR_148941.2:n.1666G>T
NR_148942.2:n.1605G>T
NM_001354690.3:c.1276G>T	NP_001341619.1:p.Gly426Cys
NM_001354691.3:c.1033G>T	NP_001341620.1:p.Gly345Cys
NM_001354692.3:c.1033G>T	NP_001341621.1:p.Gly345Cys
NM_001354693.3:c.1177G>T	NP_001341622.1:p.Gly393Cys
NM_001354694.3:c.1093G>T	NP_001341623.1:p.Gly365Cys
NM_001354695.3:c.934G>T	NP_001341624.1:p.Gly312Cys
NM_002880.4:c.1276G>T MANE Select	NP_002871.1:p.Gly426Cys
NR_148940.3:n.1720G>T
NR_148941.3:n.1666G>T
NR_148942.3:n.1605G>T