Canonical Allele Identifier: CA432273067

Gene: RAF1

Linked Data

• MyVariant Identifiers: chr3:g.12632302T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12590803T>C , CM000665.2:g.12590803T>C	GRCh38
NC_000003.11:g.12632302T>C , CM000665.1:g.12632302T>C	GRCh37
NC_000003.10:g.12607302T>C	NCBI36
NG_007467.1:g.78377A>G , LRG_413:g.78377A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000423275.6:c.*1030A>G	ENSP00000401088.1:n.*1030A>G
ENST00000432427.3:c.682A>G
ENST00000460610.2:n.159A>G
ENST00000465826.6:n.956A>G
ENST00000475353.2:n.1287A>G
ENST00000494557.2:n.1176A>G
ENST00000684903.1:c.*1042A>G	ENSP00000508612.1:n.*1042A>G
ENST00000685348.1:c.*1042A>G	ENSP00000510285.1:n.*1042A>G
ENST00000685437.1:c.1266A>G	ENSP00000508794.1:p.Gly422=
ENST00000685653.1:c.1365A>G	ENSP00000509968.1:p.Gly455=
ENST00000685738.1:c.*329A>G	ENSP00000510156.1:n.*329A>G
ENST00000686409.1:n.2416A>G
ENST00000686455.1:n.1728A>G
ENST00000686762.1:c.1365A>G	ENSP00000509767.1:p.Gly455=
ENST00000687257.1:n.1601A>G
ENST00000687326.1:c.*299A>G	ENSP00000509665.1:n.*299A>G
ENST00000687505.1:n.1483A>G
ENST00000687923.1:c.1254A>G	ENSP00000510255.1:p.Gly418=
ENST00000687940.1:n.1742A>G
ENST00000688269.1:n.1961A>G
ENST00000688326.1:c.798A>G
ENST00000688444.1:n.1691A>G
ENST00000688543.1:c.1266A>G	ENSP00000509612.1:p.Gly422=
ENST00000688625.1:c.*943A>G	ENSP00000509522.1:n.*943A>G
ENST00000688803.1:n.1596A>G
ENST00000688914.1:n.351A>G
ENST00000689097.1:c.*1042A>G	ENSP00000509756.1:n.*1042A>G
ENST00000689389.1:c.1193+905A>G	ENSP00000510213.1:n.1193+905A>G
ENST00000689418.1:c.*1042A>G	ENSP00000509467.1:n.*1042A>G
ENST00000689481.1:c.*1042A>G	ENSP00000510248.1:n.*1042A>G
ENST00000689540.1:n.1515A>G
ENST00000689876.1:c.1365A>G	ENSP00000508535.1:p.Gly455=
ENST00000689914.1:c.*299A>G	ENSP00000509847.1:n.*299A>G
ENST00000690397.1:c.1254A>G	ENSP00000508730.1:p.Gly418=
ENST00000690460.1:c.1353A>G	ENSP00000509106.1:p.Gly451=
ENST00000690585.1:c.257A>G
ENST00000690625.1:n.2401A>G
ENST00000691396.1:c.*1217A>G	ENSP00000510712.1:n.*1217A>G
ENST00000691724.1:c.*322A>G	ENSP00000509255.1:n.*322A>G
ENST00000691779.1:c.*943A>G	ENSP00000508592.1:n.*943A>G
ENST00000691888.1:c.257A>G
ENST00000691899.1:c.1365A>G	ENSP00000508763.1:p.Gly455=
ENST00000692069.1:n.1931A>G
ENST00000692093.1:c.1266A>G	ENSP00000509669.1:p.Gly422=
ENST00000692311.1:n.2189A>G
ENST00000692558.1:n.1730A>G
ENST00000692773.1:c.*1102A>G	ENSP00000509055.1:n.*1102A>G
ENST00000692830.1:c.*1110A>G	ENSP00000509461.1:n.*1110A>G
ENST00000693069.1:c.*299A>G	ENSP00000510072.1:n.*299A>G
ENST00000693312.1:c.1140A>G	ENSP00000508686.1:p.Gly380=
ENST00000693664.1:c.1365A>G	ENSP00000509614.1:p.Gly455=
ENST00000693705.1:c.*1042A>G	ENSP00000510697.1:n.*1042A>G
ENST00000251849.9:c.1365A>G MANE Select	ENSP00000251849.4:p.Gly455=
ENST00000442415.7:c.1425A>G	ENSP00000401888.2:p.Gly475=
ENST00000251849.8:c.1365A>G	ENSP00000251849.4:p.Gly455=
ENST00000423275.5:c.*1042A>G	ENSP00000401088.1:n.*1042A>G
ENST00000432427.2:c.1002A>G	ENSP00000398591.2:p.Gly334=
ENST00000442415.6:c.1425A>G	ENSP00000401888.2:p.Gly475=
ENST00000460610.1:n.322A>G
ENST00000465826.5:n.722A>G
ENST00000475353.1:n.533A>G
ENST00000494557.1:n.381A>G
NM_002880.3:c.1365A>G , LRG_413t1:c.1365A>G	NP_002871.1:p.Gly455=
XM_005265355.1:c.1365A>G	XP_005265412.1:p.Gly455=
XM_005265357.1:c.1266A>G	XP_005265414.1:p.Gly422=
XM_005265358.3:c.1122A>G	XP_005265415.1:p.Gly374=
XM_005265359.3:c.1023A>G	XP_005265416.1:p.Gly341=
XM_005265360.1:c.1365A>G	XP_005265417.1:p.Gly455=
XM_011533974.1:c.1365A>G	XP_011532276.1:p.Gly455=
XM_011533975.1:c.1122A>G	XP_011532277.1:p.Gly374=
NM_001354689.1:c.1425A>G	NP_001341618.1:p.Gly475=
NM_001354690.1:c.1365A>G	NP_001341619.1:p.Gly455=
NM_001354691.1:c.1122A>G	NP_001341620.1:p.Gly374=
NM_001354692.1:c.1122A>G	NP_001341621.1:p.Gly374=
NM_001354693.1:c.1266A>G	NP_001341622.1:p.Gly422=
NM_001354694.1:c.1182A>G	NP_001341623.1:p.Gly394=
NM_001354695.1:c.1023A>G	NP_001341624.1:p.Gly341=
NR_148940.1:n.1893A>G
NR_148941.1:n.1839A>G
NR_148942.1:n.1778A>G
XM_011533974.3:c.1365A>G	XP_011532276.1:p.Gly455=
XM_017006966.1:c.1266A>G	XP_016862455.1:p.Gly422=
NM_001354689.3:c.1425A>G	NP_001341618.1:p.Gly475=
NM_001354690.2:c.1365A>G	NP_001341619.1:p.Gly455=
NM_001354691.2:c.1122A>G	NP_001341620.1:p.Gly374=
NM_001354692.2:c.1122A>G	NP_001341621.1:p.Gly374=
NM_001354693.2:c.1266A>G	NP_001341622.1:p.Gly422=
NM_001354694.2:c.1182A>G	NP_001341623.1:p.Gly394=
NM_001354695.2:c.1023A>G	NP_001341624.1:p.Gly341=
NR_148940.2:n.1809A>G
NR_148941.2:n.1755A>G
NR_148942.2:n.1694A>G
NM_001354690.3:c.1365A>G	NP_001341619.1:p.Gly455=
NM_001354691.3:c.1122A>G	NP_001341620.1:p.Gly374=
NM_001354692.3:c.1122A>G	NP_001341621.1:p.Gly374=
NM_001354693.3:c.1266A>G	NP_001341622.1:p.Gly422=
NM_001354694.3:c.1182A>G	NP_001341623.1:p.Gly394=
NM_001354695.3:c.1023A>G	NP_001341624.1:p.Gly341=
NM_002880.4:c.1365A>G MANE Select	NP_002871.1:p.Gly455=
NR_148940.3:n.1809A>G
NR_148941.3:n.1755A>G
NR_148942.3:n.1694A>G