Canonical Allele Identifier: CA432274301

Gene: RAF1

Linked Data

• MyVariant Identifiers: chr3:g.12645689T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12604190T>G , CM000665.2:g.12604190T>G	GRCh38
NC_000003.11:g.12645689T>G , CM000665.1:g.12645689T>G	GRCh37
NC_000003.10:g.12620689T>G	NCBI36
NG_007467.1:g.64990A>C , LRG_413:g.64990A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000416093.2:c.*457A>C	ENSP00000391265.2:n.*457A>C
ENST00000423275.6:c.*457A>C	ENSP00000401088.1:n.*457A>C
ENST00000432427.3:c.100A>C
ENST00000465826.6:n.371A>C
ENST00000491290.2:n.1157A>C
ENST00000684903.1:c.*457A>C	ENSP00000508612.1:n.*457A>C
ENST00000685348.1:c.*457A>C	ENSP00000510285.1:n.*457A>C
ENST00000685437.1:c.681A>C	ENSP00000508794.1:p.Thr227=
ENST00000685653.1:c.780A>C	ENSP00000509968.1:p.Thr260=
ENST00000685738.1:c.780A>C	ENSP00000510156.1:p.Thr260=
ENST00000685959.1:c.780A>C	ENSP00000510452.1:p.Thr260=
ENST00000686409.1:n.1380A>C
ENST00000686455.1:n.1143A>C
ENST00000686479.1:n.1151A>C
ENST00000686762.1:c.780A>C	ENSP00000509767.1:p.Thr260=
ENST00000687257.1:n.1016A>C
ENST00000687326.1:c.780A>C	ENSP00000509665.1:p.Thr260=
ENST00000687486.1:c.100A>C
ENST00000687505.1:n.898A>C
ENST00000687923.1:c.681A>C	ENSP00000510255.1:p.Thr227=
ENST00000687940.1:n.1157A>C
ENST00000688269.1:n.1388A>C
ENST00000688326.1:c.100A>C
ENST00000688444.1:n.1106A>C
ENST00000688543.1:c.681A>C	ENSP00000509612.1:p.Thr227=
ENST00000688625.1:c.*358A>C	ENSP00000509522.1:n.*358A>C
ENST00000688803.1:n.1011A>C
ENST00000689033.1:c.780A>C	ENSP00000508983.1:p.Thr260=
ENST00000689097.1:c.*457A>C	ENSP00000509756.1:n.*457A>C
ENST00000689389.1:c.780A>C	ENSP00000510213.1:p.Thr260=
ENST00000689418.1:c.*457A>C	ENSP00000509467.1:n.*457A>C
ENST00000689481.1:c.*457A>C	ENSP00000510248.1:n.*457A>C
ENST00000689540.1:n.930A>C
ENST00000689876.1:c.780A>C	ENSP00000508535.1:p.Thr260=
ENST00000689914.1:c.780A>C	ENSP00000509847.1:p.Thr260=
ENST00000690397.1:c.681A>C	ENSP00000508730.1:p.Thr227=
ENST00000690460.1:c.780A>C	ENSP00000509106.1:p.Thr260=
ENST00000690625.1:n.1083A>C
ENST00000691268.1:c.262-3775A>C
ENST00000691396.1:c.*573A>C	ENSP00000510712.1:n.*573A>C
ENST00000691724.1:c.780A>C	ENSP00000509255.1:p.Thr260=
ENST00000691779.1:c.*358A>C	ENSP00000508592.1:n.*358A>C
ENST00000691899.1:c.780A>C	ENSP00000508763.1:p.Thr260=
ENST00000692093.1:c.681A>C	ENSP00000509669.1:p.Thr227=
ENST00000692311.1:n.1153A>C
ENST00000692558.1:n.1145A>C
ENST00000692773.1:c.*457A>C	ENSP00000509055.1:n.*457A>C
ENST00000692830.1:c.*525A>C	ENSP00000509461.1:n.*525A>C
ENST00000693069.1:c.681A>C	ENSP00000510072.1:p.Thr227=
ENST00000693312.1:c.555A>C	ENSP00000508686.1:p.Thr185=
ENST00000693664.1:c.780A>C	ENSP00000509614.1:p.Thr260=
ENST00000693705.1:c.*457A>C	ENSP00000510697.1:n.*457A>C
ENST00000251849.9:c.780A>C MANE Select	ENSP00000251849.4:p.Thr260=
ENST00000442415.7:c.780A>C	ENSP00000401888.2:p.Thr260=
ENST00000251849.8:c.780A>C	ENSP00000251849.4:p.Thr260=
ENST00000416093.1:c.*358A>C	ENSP00000391265.1:n.*358A>C
ENST00000423275.5:c.*457A>C	ENSP00000401088.1:n.*457A>C
ENST00000432427.2:c.417A>C	ENSP00000398591.2:p.Thr139=
ENST00000442415.6:c.780A>C	ENSP00000401888.2:p.Thr260=
ENST00000465826.5:n.24A>C
ENST00000491290.1:n.301A>C
NM_002880.3:c.780A>C , LRG_413t1:c.780A>C	NP_002871.1:p.Thr260=
XM_005265355.1:c.780A>C	XP_005265412.1:p.Thr260=
XM_005265357.1:c.681A>C	XP_005265414.1:p.Thr227=
XM_005265358.3:c.537A>C	XP_005265415.1:p.Thr179=
XM_005265359.3:c.438A>C	XP_005265416.1:p.Thr146=
XM_005265360.1:c.780A>C	XP_005265417.1:p.Thr260=
XM_011533974.1:c.780A>C	XP_011532276.1:p.Thr260=
XM_011533975.1:c.537A>C	XP_011532277.1:p.Thr179=
NM_001354689.1:c.780A>C	NP_001341618.1:p.Thr260=
NM_001354690.1:c.780A>C	NP_001341619.1:p.Thr260=
NM_001354691.1:c.537A>C	NP_001341620.1:p.Thr179=
NM_001354692.1:c.537A>C	NP_001341621.1:p.Thr179=
NM_001354693.1:c.681A>C	NP_001341622.1:p.Thr227=
NM_001354694.1:c.537A>C	NP_001341623.1:p.Thr179=
NM_001354695.1:c.438A>C	NP_001341624.1:p.Thr146=
NR_148940.1:n.1195A>C
NR_148941.1:n.1195A>C
NR_148942.1:n.1195A>C
XM_011533974.3:c.780A>C	XP_011532276.1:p.Thr260=
XM_017006966.1:c.681A>C	XP_016862455.1:p.Thr227=
XR_001740227.1:n.1012A>C
NM_001354689.3:c.780A>C	NP_001341618.1:p.Thr260=
NM_001354690.2:c.780A>C	NP_001341619.1:p.Thr260=
NM_001354691.2:c.537A>C	NP_001341620.1:p.Thr179=
NM_001354692.2:c.537A>C	NP_001341621.1:p.Thr179=
NM_001354693.2:c.681A>C	NP_001341622.1:p.Thr227=
NM_001354694.2:c.537A>C	NP_001341623.1:p.Thr179=
NM_001354695.2:c.438A>C	NP_001341624.1:p.Thr146=
NR_148940.2:n.1111A>C
NR_148941.2:n.1111A>C
NR_148942.2:n.1111A>C
NM_001354690.3:c.780A>C	NP_001341619.1:p.Thr260=
NM_001354691.3:c.537A>C	NP_001341620.1:p.Thr179=
NM_001354692.3:c.537A>C	NP_001341621.1:p.Thr179=
NM_001354693.3:c.681A>C	NP_001341622.1:p.Thr227=
NM_001354694.3:c.537A>C	NP_001341623.1:p.Thr179=
NM_001354695.3:c.438A>C	NP_001341624.1:p.Thr146=
NM_002880.4:c.780A>C MANE Select	NP_002871.1:p.Thr260=
NR_148940.3:n.1111A>C
NR_148941.3:n.1111A>C
NR_148942.3:n.1111A>C