Canonical Allele Identifier: CA351501800

Gene: RAF1

Linked Data

• MyVariant Identifiers: chr3:g.12632334G>C (hg19) ; chr3:g.12590835G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12590835G>C , CM000665.2:g.12590835G>C	GRCh38
NC_000003.11:g.12632334G>C , CM000665.1:g.12632334G>C	GRCh37
NC_000003.10:g.12607334G>C	NCBI36
NG_007467.1:g.78345C>G , LRG_413:g.78345C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*998C>G	ENSP00000401088.1:n.*998C>G
ENST00000432427.3:c.650C>G
ENST00000460610.2:n.127C>G
ENST00000465826.6:n.924C>G
ENST00000475353.2:n.1255C>G
ENST00000494557.2:n.1144C>G
ENST00000684903.1:c.*1010C>G	ENSP00000508612.1:n.*1010C>G
ENST00000685348.1:c.*1010C>G	ENSP00000510285.1:n.*1010C>G
ENST00000685437.1:c.1234C>G	ENSP00000508794.1:p.Leu412Val
ENST00000685653.1:c.1333C>G	ENSP00000509968.1:p.Leu445Val
ENST00000685738.1:c.*297C>G	ENSP00000510156.1:n.*297C>G
ENST00000686409.1:n.2384C>G
ENST00000686455.1:n.1696C>G
ENST00000686762.1:c.1333C>G	ENSP00000509767.1:p.Leu445Val
ENST00000687257.1:n.1569C>G
ENST00000687326.1:c.*267C>G	ENSP00000509665.1:n.*267C>G
ENST00000687505.1:n.1451C>G
ENST00000687923.1:c.1222C>G	ENSP00000510255.1:p.Leu408Val
ENST00000687940.1:n.1710C>G
ENST00000688269.1:n.1929C>G
ENST00000688326.1:c.766C>G
ENST00000688444.1:n.1659C>G
ENST00000688543.1:c.1234C>G	ENSP00000509612.1:p.Leu412Val
ENST00000688625.1:c.*911C>G	ENSP00000509522.1:n.*911C>G
ENST00000688803.1:n.1564C>G
ENST00000688914.1:n.319C>G
ENST00000689097.1:c.*1010C>G	ENSP00000509756.1:n.*1010C>G
ENST00000689389.1:c.1193+873C>G	ENSP00000510213.1:n.1193+873C>G
ENST00000689418.1:c.*1010C>G	ENSP00000509467.1:n.*1010C>G
ENST00000689481.1:c.*1010C>G	ENSP00000510248.1:n.*1010C>G
ENST00000689540.1:n.1483C>G
ENST00000689876.1:c.1333C>G	ENSP00000508535.1:p.Leu445Val
ENST00000689914.1:c.*267C>G	ENSP00000509847.1:n.*267C>G
ENST00000690397.1:c.1222C>G	ENSP00000508730.1:p.Leu408Val
ENST00000690460.1:c.1321C>G	ENSP00000509106.1:p.Leu441Val
ENST00000690585.1:c.225C>G
ENST00000690625.1:n.2369C>G
ENST00000691396.1:c.*1185C>G	ENSP00000510712.1:n.*1185C>G
ENST00000691724.1:c.*290C>G	ENSP00000509255.1:n.*290C>G
ENST00000691779.1:c.*911C>G	ENSP00000508592.1:n.*911C>G
ENST00000691888.1:c.225C>G
ENST00000691899.1:c.1333C>G	ENSP00000508763.1:p.Leu445Val
ENST00000692069.1:n.1899C>G
ENST00000692093.1:c.1234C>G	ENSP00000509669.1:p.Leu412Val
ENST00000692311.1:n.2157C>G
ENST00000692558.1:n.1698C>G
ENST00000692773.1:c.*1070C>G	ENSP00000509055.1:n.*1070C>G
ENST00000692830.1:c.*1078C>G	ENSP00000509461.1:n.*1078C>G
ENST00000693069.1:c.*267C>G	ENSP00000510072.1:n.*267C>G
ENST00000693312.1:c.1108C>G	ENSP00000508686.1:p.Leu370Val
ENST00000693664.1:c.1333C>G	ENSP00000509614.1:p.Leu445Val
ENST00000693705.1:c.*1010C>G	ENSP00000510697.1:n.*1010C>G
ENST00000251849.9:c.1333C>G MANE Select	ENSP00000251849.4:p.Leu445Val
ENST00000442415.7:c.1393C>G	ENSP00000401888.2:p.Leu465Val
ENST00000251849.8:c.1333C>G	ENSP00000251849.4:p.Leu445Val
ENST00000423275.5:c.*1010C>G	ENSP00000401088.1:n.*1010C>G
ENST00000432427.2:c.970C>G	ENSP00000398591.2:p.Leu324Val
ENST00000442415.6:c.1393C>G	ENSP00000401888.2:p.Leu465Val
ENST00000460610.1:n.290C>G
ENST00000465826.5:n.690C>G
ENST00000475353.1:n.501C>G
ENST00000494557.1:n.349C>G
NM_002880.3:c.1333C>G , LRG_413t1:c.1333C>G	NP_002871.1:p.Leu445Val
XM_005265355.1:c.1333C>G	XP_005265412.1:p.Leu445Val
XM_005265357.1:c.1234C>G	XP_005265414.1:p.Leu412Val
XM_005265358.3:c.1090C>G	XP_005265415.1:p.Leu364Val
XM_005265359.3:c.991C>G	XP_005265416.1:p.Leu331Val
XM_005265360.1:c.1333C>G	XP_005265417.1:p.Leu445Val
XM_011533974.1:c.1333C>G	XP_011532276.1:p.Leu445Val
XM_011533975.1:c.1090C>G	XP_011532277.1:p.Leu364Val
NM_001354689.1:c.1393C>G	NP_001341618.1:p.Leu465Val
NM_001354690.1:c.1333C>G	NP_001341619.1:p.Leu445Val
NM_001354691.1:c.1090C>G	NP_001341620.1:p.Leu364Val
NM_001354692.1:c.1090C>G	NP_001341621.1:p.Leu364Val
NM_001354693.1:c.1234C>G	NP_001341622.1:p.Leu412Val
NM_001354694.1:c.1150C>G	NP_001341623.1:p.Leu384Val
NM_001354695.1:c.991C>G	NP_001341624.1:p.Leu331Val
NR_148940.1:n.1861C>G
NR_148941.1:n.1807C>G
NR_148942.1:n.1746C>G
XM_011533974.3:c.1333C>G	XP_011532276.1:p.Leu445Val
XM_017006966.1:c.1234C>G	XP_016862455.1:p.Leu412Val
NM_001354689.3:c.1393C>G	NP_001341618.1:p.Leu465Val
NM_001354690.2:c.1333C>G	NP_001341619.1:p.Leu445Val
NM_001354691.2:c.1090C>G	NP_001341620.1:p.Leu364Val
NM_001354692.2:c.1090C>G	NP_001341621.1:p.Leu364Val
NM_001354693.2:c.1234C>G	NP_001341622.1:p.Leu412Val
NM_001354694.2:c.1150C>G	NP_001341623.1:p.Leu384Val
NM_001354695.2:c.991C>G	NP_001341624.1:p.Leu331Val
NR_148940.2:n.1777C>G
NR_148941.2:n.1723C>G
NR_148942.2:n.1662C>G
NM_001354690.3:c.1333C>G	NP_001341619.1:p.Leu445Val
NM_001354691.3:c.1090C>G	NP_001341620.1:p.Leu364Val
NM_001354692.3:c.1090C>G	NP_001341621.1:p.Leu364Val
NM_001354693.3:c.1234C>G	NP_001341622.1:p.Leu412Val
NM_001354694.3:c.1150C>G	NP_001341623.1:p.Leu384Val
NM_001354695.3:c.991C>G	NP_001341624.1:p.Leu331Val
NM_002880.4:c.1333C>G MANE Select	NP_002871.1:p.Leu445Val
NR_148940.3:n.1777C>G
NR_148941.3:n.1723C>G
NR_148942.3:n.1662C>G