Canonical Allele Identifier: CA432273161

Gene: RAF1

Linked Data

• COSMIC: COSM3673833 ; COSM3673834
• MyVariant Identifiers: chr3:g.12632413T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12590914T>G , CM000665.2:g.12590914T>G	GRCh38
NC_000003.11:g.12632413T>G , CM000665.1:g.12632413T>G	GRCh37
NC_000003.10:g.12607413T>G	NCBI36
NG_007467.1:g.78266A>C , LRG_413:g.78266A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000423275.6:c.*919A>C	ENSP00000401088.1:n.*919A>C
ENST00000432427.3:c.571A>C
ENST00000460610.2:n.48A>C
ENST00000465826.6:n.845A>C
ENST00000475353.2:n.1176A>C
ENST00000494557.2:n.1065A>C
ENST00000684903.1:c.*931A>C	ENSP00000508612.1:n.*931A>C
ENST00000685348.1:c.*931A>C	ENSP00000510285.1:n.*931A>C
ENST00000685437.1:c.1155A>C	ENSP00000508794.1:p.Ala385=
ENST00000685653.1:c.1254A>C	ENSP00000509968.1:p.Ala418=
ENST00000685738.1:c.*218A>C	ENSP00000510156.1:n.*218A>C
ENST00000686409.1:n.2305A>C
ENST00000686455.1:n.1617A>C
ENST00000686762.1:c.1254A>C	ENSP00000509767.1:p.Ala418=
ENST00000687257.1:n.1490A>C
ENST00000687326.1:c.*188A>C	ENSP00000509665.1:n.*188A>C
ENST00000687505.1:n.1372A>C
ENST00000687923.1:c.1143A>C	ENSP00000510255.1:p.Ala381=
ENST00000687940.1:n.1631A>C
ENST00000688269.1:n.1850A>C
ENST00000688326.1:c.687A>C
ENST00000688444.1:n.1580A>C
ENST00000688543.1:c.1155A>C	ENSP00000509612.1:p.Ala385=
ENST00000688625.1:c.*832A>C	ENSP00000509522.1:n.*832A>C
ENST00000688803.1:n.1485A>C
ENST00000688914.1:n.240A>C
ENST00000689097.1:c.*931A>C	ENSP00000509756.1:n.*931A>C
ENST00000689389.1:c.1193+794A>C	ENSP00000510213.1:n.1193+794A>C
ENST00000689418.1:c.*931A>C	ENSP00000509467.1:n.*931A>C
ENST00000689481.1:c.*931A>C	ENSP00000510248.1:n.*931A>C
ENST00000689540.1:n.1404A>C
ENST00000689876.1:c.1254A>C	ENSP00000508535.1:p.Ala418=
ENST00000689914.1:c.*188A>C	ENSP00000509847.1:n.*188A>C
ENST00000690397.1:c.1143A>C	ENSP00000508730.1:p.Ala381=
ENST00000690460.1:c.1242A>C	ENSP00000509106.1:p.Ala414=
ENST00000690585.1:c.146A>C
ENST00000690625.1:n.2290A>C
ENST00000691396.1:c.*1106A>C	ENSP00000510712.1:n.*1106A>C
ENST00000691724.1:c.*211A>C	ENSP00000509255.1:n.*211A>C
ENST00000691779.1:c.*832A>C	ENSP00000508592.1:n.*832A>C
ENST00000691888.1:c.146A>C
ENST00000691899.1:c.1254A>C	ENSP00000508763.1:p.Ala418=
ENST00000692069.1:n.1820A>C
ENST00000692093.1:c.1155A>C	ENSP00000509669.1:p.Ala385=
ENST00000692311.1:n.2078A>C
ENST00000692558.1:n.1619A>C
ENST00000692773.1:c.*991A>C	ENSP00000509055.1:n.*991A>C
ENST00000692830.1:c.*999A>C	ENSP00000509461.1:n.*999A>C
ENST00000693069.1:c.*188A>C	ENSP00000510072.1:n.*188A>C
ENST00000693312.1:c.1029A>C	ENSP00000508686.1:p.Ala343=
ENST00000693664.1:c.1254A>C	ENSP00000509614.1:p.Ala418=
ENST00000693705.1:c.*931A>C	ENSP00000510697.1:n.*931A>C
ENST00000251849.9:c.1254A>C MANE Select	ENSP00000251849.4:p.Ala418=
ENST00000442415.7:c.1314A>C	ENSP00000401888.2:p.Ala438=
ENST00000251849.8:c.1254A>C	ENSP00000251849.4:p.Ala418=
ENST00000423275.5:c.*931A>C	ENSP00000401088.1:n.*931A>C
ENST00000432427.2:c.891A>C	ENSP00000398591.2:p.Ala297=
ENST00000442415.6:c.1314A>C	ENSP00000401888.2:p.Ala438=
ENST00000460610.1:n.211A>C
ENST00000465826.5:n.611A>C
ENST00000475353.1:n.422A>C
ENST00000494557.1:n.270A>C
NM_002880.3:c.1254A>C , LRG_413t1:c.1254A>C	NP_002871.1:p.Ala418=
XM_005265355.1:c.1254A>C	XP_005265412.1:p.Ala418=
XM_005265357.1:c.1155A>C	XP_005265414.1:p.Ala385=
XM_005265358.3:c.1011A>C	XP_005265415.1:p.Ala337=
XM_005265359.3:c.912A>C	XP_005265416.1:p.Ala304=
XM_005265360.1:c.1254A>C	XP_005265417.1:p.Ala418=
XM_011533974.1:c.1254A>C	XP_011532276.1:p.Ala418=
XM_011533975.1:c.1011A>C	XP_011532277.1:p.Ala337=
NM_001354689.1:c.1314A>C	NP_001341618.1:p.Ala438=
NM_001354690.1:c.1254A>C	NP_001341619.1:p.Ala418=
NM_001354691.1:c.1011A>C	NP_001341620.1:p.Ala337=
NM_001354692.1:c.1011A>C	NP_001341621.1:p.Ala337=
NM_001354693.1:c.1155A>C	NP_001341622.1:p.Ala385=
NM_001354694.1:c.1071A>C	NP_001341623.1:p.Ala357=
NM_001354695.1:c.912A>C	NP_001341624.1:p.Ala304=
NR_148940.1:n.1782A>C
NR_148941.1:n.1728A>C
NR_148942.1:n.1667A>C
XM_011533974.3:c.1254A>C	XP_011532276.1:p.Ala418=
XM_017006966.1:c.1155A>C	XP_016862455.1:p.Ala385=
NM_001354689.3:c.1314A>C	NP_001341618.1:p.Ala438=
NM_001354690.2:c.1254A>C	NP_001341619.1:p.Ala418=
NM_001354691.2:c.1011A>C	NP_001341620.1:p.Ala337=
NM_001354692.2:c.1011A>C	NP_001341621.1:p.Ala337=
NM_001354693.2:c.1155A>C	NP_001341622.1:p.Ala385=
NM_001354694.2:c.1071A>C	NP_001341623.1:p.Ala357=
NM_001354695.2:c.912A>C	NP_001341624.1:p.Ala304=
NR_148940.2:n.1698A>C
NR_148941.2:n.1644A>C
NR_148942.2:n.1583A>C
NM_001354690.3:c.1254A>C	NP_001341619.1:p.Ala418=
NM_001354691.3:c.1011A>C	NP_001341620.1:p.Ala337=
NM_001354692.3:c.1011A>C	NP_001341621.1:p.Ala337=
NM_001354693.3:c.1155A>C	NP_001341622.1:p.Ala385=
NM_001354694.3:c.1071A>C	NP_001341623.1:p.Ala357=
NM_001354695.3:c.912A>C	NP_001341624.1:p.Ala304=
NM_002880.4:c.1254A>C MANE Select	NP_002871.1:p.Ala418=
NR_148940.3:n.1698A>C
NR_148941.3:n.1644A>C
NR_148942.3:n.1583A>C