Canonical Allele Identifier: CA351502007

Gene: RAF1

Linked Data

• MyVariant Identifiers: chr3:g.12632369A>T (hg19) ; chr3:g.12590870A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12590870A>T , CM000665.2:g.12590870A>T	GRCh38
NC_000003.11:g.12632369A>T , CM000665.1:g.12632369A>T	GRCh37
NC_000003.10:g.12607369A>T	NCBI36
NG_007467.1:g.78310T>A , LRG_413:g.78310T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*963T>A	ENSP00000401088.1:n.*963T>A
ENST00000432427.3:c.615T>A
ENST00000460610.2:n.92T>A
ENST00000465826.6:n.889T>A
ENST00000475353.2:n.1220T>A
ENST00000494557.2:n.1109T>A
ENST00000684903.1:c.*975T>A	ENSP00000508612.1:n.*975T>A
ENST00000685348.1:c.*975T>A	ENSP00000510285.1:n.*975T>A
ENST00000685437.1:c.1199T>A	ENSP00000508794.1:p.Leu400Gln
ENST00000685653.1:c.1298T>A	ENSP00000509968.1:p.Leu433Gln
ENST00000685738.1:c.*262T>A	ENSP00000510156.1:n.*262T>A
ENST00000686409.1:n.2349T>A
ENST00000686455.1:n.1661T>A
ENST00000686762.1:c.1298T>A	ENSP00000509767.1:p.Leu433Gln
ENST00000687257.1:n.1534T>A
ENST00000687326.1:c.*232T>A	ENSP00000509665.1:n.*232T>A
ENST00000687505.1:n.1416T>A
ENST00000687923.1:c.1187T>A	ENSP00000510255.1:p.Leu396Gln
ENST00000687940.1:n.1675T>A
ENST00000688269.1:n.1894T>A
ENST00000688326.1:c.731T>A
ENST00000688444.1:n.1624T>A
ENST00000688543.1:c.1199T>A	ENSP00000509612.1:p.Leu400Gln
ENST00000688625.1:c.*876T>A	ENSP00000509522.1:n.*876T>A
ENST00000688803.1:n.1529T>A
ENST00000688914.1:n.284T>A
ENST00000689097.1:c.*975T>A	ENSP00000509756.1:n.*975T>A
ENST00000689389.1:c.1193+838T>A	ENSP00000510213.1:n.1193+838T>A
ENST00000689418.1:c.*975T>A	ENSP00000509467.1:n.*975T>A
ENST00000689481.1:c.*975T>A	ENSP00000510248.1:n.*975T>A
ENST00000689540.1:n.1448T>A
ENST00000689876.1:c.1298T>A	ENSP00000508535.1:p.Leu433Gln
ENST00000689914.1:c.*232T>A	ENSP00000509847.1:n.*232T>A
ENST00000690397.1:c.1187T>A	ENSP00000508730.1:p.Leu396Gln
ENST00000690460.1:c.1286T>A	ENSP00000509106.1:p.Leu429Gln
ENST00000690585.1:c.190T>A
ENST00000690625.1:n.2334T>A
ENST00000691396.1:c.*1150T>A	ENSP00000510712.1:n.*1150T>A
ENST00000691724.1:c.*255T>A	ENSP00000509255.1:n.*255T>A
ENST00000691779.1:c.*876T>A	ENSP00000508592.1:n.*876T>A
ENST00000691888.1:c.190T>A
ENST00000691899.1:c.1298T>A	ENSP00000508763.1:p.Leu433Gln
ENST00000692069.1:n.1864T>A
ENST00000692093.1:c.1199T>A	ENSP00000509669.1:p.Leu400Gln
ENST00000692311.1:n.2122T>A
ENST00000692558.1:n.1663T>A
ENST00000692773.1:c.*1035T>A	ENSP00000509055.1:n.*1035T>A
ENST00000692830.1:c.*1043T>A	ENSP00000509461.1:n.*1043T>A
ENST00000693069.1:c.*232T>A	ENSP00000510072.1:n.*232T>A
ENST00000693312.1:c.1073T>A	ENSP00000508686.1:p.Leu358Gln
ENST00000693664.1:c.1298T>A	ENSP00000509614.1:p.Leu433Gln
ENST00000693705.1:c.*975T>A	ENSP00000510697.1:n.*975T>A
ENST00000251849.9:c.1298T>A MANE Select	ENSP00000251849.4:p.Leu433Gln
ENST00000442415.7:c.1358T>A	ENSP00000401888.2:p.Leu453Gln
ENST00000251849.8:c.1298T>A	ENSP00000251849.4:p.Leu433Gln
ENST00000423275.5:c.*975T>A	ENSP00000401088.1:n.*975T>A
ENST00000432427.2:c.935T>A	ENSP00000398591.2:p.Leu312Gln
ENST00000442415.6:c.1358T>A	ENSP00000401888.2:p.Leu453Gln
ENST00000460610.1:n.255T>A
ENST00000465826.5:n.655T>A
ENST00000475353.1:n.466T>A
ENST00000494557.1:n.314T>A
NM_002880.3:c.1298T>A , LRG_413t1:c.1298T>A	NP_002871.1:p.Leu433Gln
XM_005265355.1:c.1298T>A	XP_005265412.1:p.Leu433Gln
XM_005265357.1:c.1199T>A	XP_005265414.1:p.Leu400Gln
XM_005265358.3:c.1055T>A	XP_005265415.1:p.Leu352Gln
XM_005265359.3:c.956T>A	XP_005265416.1:p.Leu319Gln
XM_005265360.1:c.1298T>A	XP_005265417.1:p.Leu433Gln
XM_011533974.1:c.1298T>A	XP_011532276.1:p.Leu433Gln
XM_011533975.1:c.1055T>A	XP_011532277.1:p.Leu352Gln
NM_001354689.1:c.1358T>A	NP_001341618.1:p.Leu453Gln
NM_001354690.1:c.1298T>A	NP_001341619.1:p.Leu433Gln
NM_001354691.1:c.1055T>A	NP_001341620.1:p.Leu352Gln
NM_001354692.1:c.1055T>A	NP_001341621.1:p.Leu352Gln
NM_001354693.1:c.1199T>A	NP_001341622.1:p.Leu400Gln
NM_001354694.1:c.1115T>A	NP_001341623.1:p.Leu372Gln
NM_001354695.1:c.956T>A	NP_001341624.1:p.Leu319Gln
NR_148940.1:n.1826T>A
NR_148941.1:n.1772T>A
NR_148942.1:n.1711T>A
XM_011533974.3:c.1298T>A	XP_011532276.1:p.Leu433Gln
XM_017006966.1:c.1199T>A	XP_016862455.1:p.Leu400Gln
NM_001354689.3:c.1358T>A	NP_001341618.1:p.Leu453Gln
NM_001354690.2:c.1298T>A	NP_001341619.1:p.Leu433Gln
NM_001354691.2:c.1055T>A	NP_001341620.1:p.Leu352Gln
NM_001354692.2:c.1055T>A	NP_001341621.1:p.Leu352Gln
NM_001354693.2:c.1199T>A	NP_001341622.1:p.Leu400Gln
NM_001354694.2:c.1115T>A	NP_001341623.1:p.Leu372Gln
NM_001354695.2:c.956T>A	NP_001341624.1:p.Leu319Gln
NR_148940.2:n.1742T>A
NR_148941.2:n.1688T>A
NR_148942.2:n.1627T>A
NM_001354690.3:c.1298T>A	NP_001341619.1:p.Leu433Gln
NM_001354691.3:c.1055T>A	NP_001341620.1:p.Leu352Gln
NM_001354692.3:c.1055T>A	NP_001341621.1:p.Leu352Gln
NM_001354693.3:c.1199T>A	NP_001341622.1:p.Leu400Gln
NM_001354694.3:c.1115T>A	NP_001341623.1:p.Leu372Gln
NM_001354695.3:c.956T>A	NP_001341624.1:p.Leu319Gln
NM_002880.4:c.1298T>A MANE Select	NP_002871.1:p.Leu433Gln
NR_148940.3:n.1742T>A
NR_148941.3:n.1688T>A
NR_148942.3:n.1627T>A