Canonical Allele Identifier: CA351507186

Gene: RAF1

Linked Data

• MyVariant Identifiers: chr3:g.12641198T>A (hg19) ; chr3:g.12599699T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12599699T>A , CM000665.2:g.12599699T>A	GRCh38
NC_000003.11:g.12641198T>A , CM000665.1:g.12641198T>A	GRCh37
NC_000003.10:g.12616198T>A	NCBI36
NG_007467.1:g.69481A>T , LRG_413:g.69481A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000423275.6:c.*765A>T	ENSP00000401088.1:n.*765A>T
ENST00000432427.3:c.420A>T
ENST00000465826.6:n.691A>T
ENST00000491290.2:n.1477A>T
ENST00000684903.1:c.*777A>T	ENSP00000508612.1:n.*777A>T
ENST00000685348.1:c.*777A>T	ENSP00000510285.1:n.*777A>T
ENST00000685437.1:c.1001A>T	ENSP00000508794.1:p.Lys334Ile
ENST00000685653.1:c.1100A>T	ENSP00000509968.1:p.Lys367Ile
ENST00000685738.1:c.1100A>T	ENSP00000510156.1:p.Lys367Ile
ENST00000686409.1:n.2151A>T
ENST00000686455.1:n.1463A>T
ENST00000686479.1:n.1471A>T
ENST00000686762.1:c.1100A>T	ENSP00000509767.1:p.Lys367Ile
ENST00000687257.1:n.1336A>T
ENST00000687326.1:c.1100A>T	ENSP00000509665.1:p.Lys367Ile
ENST00000687486.1:c.292A>T
ENST00000687505.1:n.1218A>T
ENST00000687923.1:c.997+4A>T	ENSP00000510255.1:n.997+4A>T
ENST00000687940.1:n.1477A>T
ENST00000688269.1:n.1696A>T
ENST00000688326.1:c.420A>T
ENST00000688444.1:n.1426A>T
ENST00000688543.1:c.1001A>T	ENSP00000509612.1:p.Lys334Ile
ENST00000688625.1:c.*678A>T	ENSP00000509522.1:n.*678A>T
ENST00000688803.1:n.1331A>T
ENST00000688914.1:n.86A>T
ENST00000689097.1:c.*777A>T	ENSP00000509756.1:n.*777A>T
ENST00000689389.1:c.1100A>T	ENSP00000510213.1:p.Lys367Ile
ENST00000689418.1:c.*777A>T	ENSP00000509467.1:n.*777A>T
ENST00000689481.1:c.*777A>T	ENSP00000510248.1:n.*777A>T
ENST00000689540.1:n.1250A>T
ENST00000689876.1:c.1100A>T	ENSP00000508535.1:p.Lys367Ile
ENST00000689914.1:c.1100A>T	ENSP00000509847.1:p.Lys367Ile
ENST00000690397.1:c.989A>T	ENSP00000508730.1:p.Lys330Ile
ENST00000690460.1:c.1088A>T	ENSP00000509106.1:p.Lys363Ile
ENST00000690625.1:n.1403A>T
ENST00000691268.1:c.527A>T
ENST00000691396.1:c.*893A>T	ENSP00000510712.1:n.*893A>T
ENST00000691724.1:c.*57A>T	ENSP00000509255.1:n.*57A>T
ENST00000691779.1:c.*678A>T	ENSP00000508592.1:n.*678A>T
ENST00000691899.1:c.1100A>T	ENSP00000508763.1:p.Lys367Ile
ENST00000692069.1:n.1666A>T
ENST00000692093.1:c.1001A>T	ENSP00000509669.1:p.Lys334Ile
ENST00000692311.1:n.1924A>T
ENST00000692558.1:n.1465A>T
ENST00000692773.1:c.*837A>T	ENSP00000509055.1:n.*837A>T
ENST00000692830.1:c.*845A>T	ENSP00000509461.1:n.*845A>T
ENST00000693069.1:c.1001A>T	ENSP00000510072.1:p.Lys334Ile
ENST00000693312.1:c.875A>T	ENSP00000508686.1:p.Lys292Ile
ENST00000693664.1:c.1100A>T	ENSP00000509614.1:p.Lys367Ile
ENST00000693705.1:c.*777A>T	ENSP00000510697.1:n.*777A>T
ENST00000251849.9:c.1100A>T MANE Select	ENSP00000251849.4:p.Lys367Ile
ENST00000442415.7:c.1160A>T	ENSP00000401888.2:p.Lys387Ile
ENST00000251849.8:c.1100A>T	ENSP00000251849.4:p.Lys367Ile
ENST00000423275.5:c.*777A>T	ENSP00000401088.1:n.*777A>T
ENST00000432427.2:c.737A>T	ENSP00000398591.2:p.Lys246Ile
ENST00000442415.6:c.1160A>T	ENSP00000401888.2:p.Lys387Ile
ENST00000460610.1:n.57A>T
ENST00000465826.5:n.344A>T
NM_002880.3:c.1100A>T , LRG_413t1:c.1100A>T	NP_002871.1:p.Lys367Ile
XM_005265355.1:c.1100A>T	XP_005265412.1:p.Lys367Ile
XM_005265357.1:c.1001A>T	XP_005265414.1:p.Lys334Ile
XM_005265358.3:c.857A>T	XP_005265415.1:p.Lys286Ile
XM_005265359.3:c.758A>T	XP_005265416.1:p.Lys253Ile
XM_005265360.1:c.1100A>T	XP_005265417.1:p.Lys367Ile
XM_011533974.1:c.1100A>T	XP_011532276.1:p.Lys367Ile
XM_011533975.1:c.857A>T	XP_011532277.1:p.Lys286Ile
NM_001354689.1:c.1160A>T	NP_001341618.1:p.Lys387Ile
NM_001354690.1:c.1100A>T	NP_001341619.1:p.Lys367Ile
NM_001354691.1:c.857A>T	NP_001341620.1:p.Lys286Ile
NM_001354692.1:c.857A>T	NP_001341621.1:p.Lys286Ile
NM_001354693.1:c.1001A>T	NP_001341622.1:p.Lys334Ile
NM_001354694.1:c.917A>T	NP_001341623.1:p.Lys306Ile
NM_001354695.1:c.758A>T	NP_001341624.1:p.Lys253Ile
NR_148940.1:n.1515A>T
NR_148941.1:n.1515A>T
NR_148942.1:n.1513A>T
XM_011533974.3:c.1100A>T	XP_011532276.1:p.Lys367Ile
XM_017006966.1:c.1001A>T	XP_016862455.1:p.Lys334Ile
XR_001740227.1:n.1332A>T
NM_001354689.3:c.1160A>T	NP_001341618.1:p.Lys387Ile
NM_001354690.2:c.1100A>T	NP_001341619.1:p.Lys367Ile
NM_001354691.2:c.857A>T	NP_001341620.1:p.Lys286Ile
NM_001354692.2:c.857A>T	NP_001341621.1:p.Lys286Ile
NM_001354693.2:c.1001A>T	NP_001341622.1:p.Lys334Ile
NM_001354694.2:c.917A>T	NP_001341623.1:p.Lys306Ile
NM_001354695.2:c.758A>T	NP_001341624.1:p.Lys253Ile
NR_148940.2:n.1431A>T
NR_148941.2:n.1431A>T
NR_148942.2:n.1429A>T
NM_001354690.3:c.1100A>T	NP_001341619.1:p.Lys367Ile
NM_001354691.3:c.857A>T	NP_001341620.1:p.Lys286Ile
NM_001354692.3:c.857A>T	NP_001341621.1:p.Lys286Ile
NM_001354693.3:c.1001A>T	NP_001341622.1:p.Lys334Ile
NM_001354694.3:c.917A>T	NP_001341623.1:p.Lys306Ile
NM_001354695.3:c.758A>T	NP_001341624.1:p.Lys253Ile
NM_002880.4:c.1100A>T MANE Select	NP_002871.1:p.Lys367Ile
NR_148940.3:n.1431A>T
NR_148941.3:n.1431A>T
NR_148942.3:n.1429A>T