Canonical Allele Identifier: CA351501903

Gene: RAF1

Linked Data

• MyVariant Identifiers: chr3:g.12632352T>G (hg19) ; chr3:g.12590853T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12590853T>G , CM000665.2:g.12590853T>G	GRCh38
NC_000003.11:g.12632352T>G , CM000665.1:g.12632352T>G	GRCh37
NC_000003.10:g.12607352T>G	NCBI36
NG_007467.1:g.78327A>C , LRG_413:g.78327A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*980A>C	ENSP00000401088.1:n.*980A>C
ENST00000432427.3:c.632A>C
ENST00000460610.2:n.109A>C
ENST00000465826.6:n.906A>C
ENST00000475353.2:n.1237A>C
ENST00000494557.2:n.1126A>C
ENST00000684903.1:c.*992A>C	ENSP00000508612.1:n.*992A>C
ENST00000685348.1:c.*992A>C	ENSP00000510285.1:n.*992A>C
ENST00000685437.1:c.1216A>C	ENSP00000508794.1:p.Lys406Gln
ENST00000685653.1:c.1315A>C	ENSP00000509968.1:p.Lys439Gln
ENST00000685738.1:c.*279A>C	ENSP00000510156.1:n.*279A>C
ENST00000686409.1:n.2366A>C
ENST00000686455.1:n.1678A>C
ENST00000686762.1:c.1315A>C	ENSP00000509767.1:p.Lys439Gln
ENST00000687257.1:n.1551A>C
ENST00000687326.1:c.*249A>C	ENSP00000509665.1:n.*249A>C
ENST00000687505.1:n.1433A>C
ENST00000687923.1:c.1204A>C	ENSP00000510255.1:p.Lys402Gln
ENST00000687940.1:n.1692A>C
ENST00000688269.1:n.1911A>C
ENST00000688326.1:c.748A>C
ENST00000688444.1:n.1641A>C
ENST00000688543.1:c.1216A>C	ENSP00000509612.1:p.Lys406Gln
ENST00000688625.1:c.*893A>C	ENSP00000509522.1:n.*893A>C
ENST00000688803.1:n.1546A>C
ENST00000688914.1:n.301A>C
ENST00000689097.1:c.*992A>C	ENSP00000509756.1:n.*992A>C
ENST00000689389.1:c.1193+855A>C	ENSP00000510213.1:n.1193+855A>C
ENST00000689418.1:c.*992A>C	ENSP00000509467.1:n.*992A>C
ENST00000689481.1:c.*992A>C	ENSP00000510248.1:n.*992A>C
ENST00000689540.1:n.1465A>C
ENST00000689876.1:c.1315A>C	ENSP00000508535.1:p.Lys439Gln
ENST00000689914.1:c.*249A>C	ENSP00000509847.1:n.*249A>C
ENST00000690397.1:c.1204A>C	ENSP00000508730.1:p.Lys402Gln
ENST00000690460.1:c.1303A>C	ENSP00000509106.1:p.Lys435Gln
ENST00000690585.1:c.207A>C
ENST00000690625.1:n.2351A>C
ENST00000691396.1:c.*1167A>C	ENSP00000510712.1:n.*1167A>C
ENST00000691724.1:c.*272A>C	ENSP00000509255.1:n.*272A>C
ENST00000691779.1:c.*893A>C	ENSP00000508592.1:n.*893A>C
ENST00000691888.1:c.207A>C
ENST00000691899.1:c.1315A>C	ENSP00000508763.1:p.Lys439Gln
ENST00000692069.1:n.1881A>C
ENST00000692093.1:c.1216A>C	ENSP00000509669.1:p.Lys406Gln
ENST00000692311.1:n.2139A>C
ENST00000692558.1:n.1680A>C
ENST00000692773.1:c.*1052A>C	ENSP00000509055.1:n.*1052A>C
ENST00000692830.1:c.*1060A>C	ENSP00000509461.1:n.*1060A>C
ENST00000693069.1:c.*249A>C	ENSP00000510072.1:n.*249A>C
ENST00000693312.1:c.1090A>C	ENSP00000508686.1:p.Lys364Gln
ENST00000693664.1:c.1315A>C	ENSP00000509614.1:p.Lys439Gln
ENST00000693705.1:c.*992A>C	ENSP00000510697.1:n.*992A>C
ENST00000251849.9:c.1315A>C MANE Select	ENSP00000251849.4:p.Lys439Gln
ENST00000442415.7:c.1375A>C	ENSP00000401888.2:p.Lys459Gln
ENST00000251849.8:c.1315A>C	ENSP00000251849.4:p.Lys439Gln
ENST00000423275.5:c.*992A>C	ENSP00000401088.1:n.*992A>C
ENST00000432427.2:c.952A>C	ENSP00000398591.2:p.Lys318Gln
ENST00000442415.6:c.1375A>C	ENSP00000401888.2:p.Lys459Gln
ENST00000460610.1:n.272A>C
ENST00000465826.5:n.672A>C
ENST00000475353.1:n.483A>C
ENST00000494557.1:n.331A>C
NM_002880.3:c.1315A>C , LRG_413t1:c.1315A>C	NP_002871.1:p.Lys439Gln
XM_005265355.1:c.1315A>C	XP_005265412.1:p.Lys439Gln
XM_005265357.1:c.1216A>C	XP_005265414.1:p.Lys406Gln
XM_005265358.3:c.1072A>C	XP_005265415.1:p.Lys358Gln
XM_005265359.3:c.973A>C	XP_005265416.1:p.Lys325Gln
XM_005265360.1:c.1315A>C	XP_005265417.1:p.Lys439Gln
XM_011533974.1:c.1315A>C	XP_011532276.1:p.Lys439Gln
XM_011533975.1:c.1072A>C	XP_011532277.1:p.Lys358Gln
NM_001354689.1:c.1375A>C	NP_001341618.1:p.Lys459Gln
NM_001354690.1:c.1315A>C	NP_001341619.1:p.Lys439Gln
NM_001354691.1:c.1072A>C	NP_001341620.1:p.Lys358Gln
NM_001354692.1:c.1072A>C	NP_001341621.1:p.Lys358Gln
NM_001354693.1:c.1216A>C	NP_001341622.1:p.Lys406Gln
NM_001354694.1:c.1132A>C	NP_001341623.1:p.Lys378Gln
NM_001354695.1:c.973A>C	NP_001341624.1:p.Lys325Gln
NR_148940.1:n.1843A>C
NR_148941.1:n.1789A>C
NR_148942.1:n.1728A>C
XM_011533974.3:c.1315A>C	XP_011532276.1:p.Lys439Gln
XM_017006966.1:c.1216A>C	XP_016862455.1:p.Lys406Gln
NM_001354689.3:c.1375A>C	NP_001341618.1:p.Lys459Gln
NM_001354690.2:c.1315A>C	NP_001341619.1:p.Lys439Gln
NM_001354691.2:c.1072A>C	NP_001341620.1:p.Lys358Gln
NM_001354692.2:c.1072A>C	NP_001341621.1:p.Lys358Gln
NM_001354693.2:c.1216A>C	NP_001341622.1:p.Lys406Gln
NM_001354694.2:c.1132A>C	NP_001341623.1:p.Lys378Gln
NM_001354695.2:c.973A>C	NP_001341624.1:p.Lys325Gln
NR_148940.2:n.1759A>C
NR_148941.2:n.1705A>C
NR_148942.2:n.1644A>C
NM_001354690.3:c.1315A>C	NP_001341619.1:p.Lys439Gln
NM_001354691.3:c.1072A>C	NP_001341620.1:p.Lys358Gln
NM_001354692.3:c.1072A>C	NP_001341621.1:p.Lys358Gln
NM_001354693.3:c.1216A>C	NP_001341622.1:p.Lys406Gln
NM_001354694.3:c.1132A>C	NP_001341623.1:p.Lys378Gln
NM_001354695.3:c.973A>C	NP_001341624.1:p.Lys325Gln
NM_002880.4:c.1315A>C MANE Select	NP_002871.1:p.Lys439Gln
NR_148940.3:n.1759A>C
NR_148941.3:n.1705A>C
NR_148942.3:n.1644A>C