Canonical Allele Identifier: CA351510111

Gene: RAF1

Linked Data

• MyVariant Identifiers: chr3:g.12641907A>G (hg19) ; chr3:g.12600408A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12600408A>G , CM000665.2:g.12600408A>G	GRCh38
NC_000003.11:g.12641907A>G , CM000665.1:g.12641907A>G	GRCh37
NC_000003.10:g.12616907A>G	NCBI36
NG_007467.1:g.68772T>C , LRG_413:g.68772T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000423275.6:c.*519T>C	ENSP00000401088.1:n.*519T>C
ENST00000432427.3:c.162T>C
ENST00000465826.6:n.433T>C
ENST00000491290.2:n.1219T>C
ENST00000684903.1:c.*519T>C	ENSP00000508612.1:n.*519T>C
ENST00000685348.1:c.*519T>C	ENSP00000510285.1:n.*519T>C
ENST00000685437.1:c.743T>C	ENSP00000508794.1:p.Ile248Thr
ENST00000685438.1:n.606T>C
ENST00000685653.1:c.842T>C	ENSP00000509968.1:p.Ile281Thr
ENST00000685738.1:c.842T>C	ENSP00000510156.1:p.Ile281Thr
ENST00000686409.1:n.1442T>C
ENST00000686455.1:n.1205T>C
ENST00000686479.1:n.1213T>C
ENST00000686762.1:c.842T>C	ENSP00000509767.1:p.Ile281Thr
ENST00000687257.1:n.1078T>C
ENST00000687326.1:c.842T>C	ENSP00000509665.1:p.Ile281Thr
ENST00000687486.1:c.162T>C
ENST00000687505.1:n.960T>C
ENST00000687923.1:c.743T>C	ENSP00000510255.1:p.Ile248Thr
ENST00000687940.1:n.1219T>C
ENST00000688269.1:n.1450T>C
ENST00000688326.1:c.162T>C
ENST00000688444.1:n.1168T>C
ENST00000688543.1:c.743T>C	ENSP00000509612.1:p.Ile248Thr
ENST00000688625.1:c.*420T>C	ENSP00000509522.1:n.*420T>C
ENST00000688803.1:n.1073T>C
ENST00000689097.1:c.*519T>C	ENSP00000509756.1:n.*519T>C
ENST00000689389.1:c.842T>C	ENSP00000510213.1:p.Ile281Thr
ENST00000689418.1:c.*519T>C	ENSP00000509467.1:n.*519T>C
ENST00000689481.1:c.*519T>C	ENSP00000510248.1:n.*519T>C
ENST00000689540.1:n.992T>C
ENST00000689876.1:c.842T>C	ENSP00000508535.1:p.Ile281Thr
ENST00000689914.1:c.842T>C	ENSP00000509847.1:p.Ile281Thr
ENST00000690397.1:c.743T>C	ENSP00000508730.1:p.Ile248Thr
ENST00000690460.1:c.842T>C	ENSP00000509106.1:p.Ile281Thr
ENST00000690625.1:n.1145T>C
ENST00000691268.1:c.269T>C
ENST00000691396.1:c.*635T>C	ENSP00000510712.1:n.*635T>C
ENST00000691724.1:c.842T>C	ENSP00000509255.1:p.Ile281Thr
ENST00000691779.1:c.*420T>C	ENSP00000508592.1:n.*420T>C
ENST00000691899.1:c.842T>C	ENSP00000508763.1:p.Ile281Thr
ENST00000692069.1:n.957T>C
ENST00000692093.1:c.743T>C	ENSP00000509669.1:p.Ile248Thr
ENST00000692311.1:n.1215T>C
ENST00000692558.1:n.1207T>C
ENST00000692773.1:c.*579T>C	ENSP00000509055.1:n.*579T>C
ENST00000692830.1:c.*587T>C	ENSP00000509461.1:n.*587T>C
ENST00000693069.1:c.743T>C	ENSP00000510072.1:p.Ile248Thr
ENST00000693312.1:c.617T>C	ENSP00000508686.1:p.Ile206Thr
ENST00000693664.1:c.842T>C	ENSP00000509614.1:p.Ile281Thr
ENST00000693705.1:c.*519T>C	ENSP00000510697.1:n.*519T>C
ENST00000251849.9:c.842T>C MANE Select	ENSP00000251849.4:p.Ile281Thr
ENST00000442415.7:c.902T>C	ENSP00000401888.2:p.Ile301Thr
ENST00000251849.8:c.842T>C	ENSP00000251849.4:p.Ile281Thr
ENST00000423275.5:c.*519T>C	ENSP00000401088.1:n.*519T>C
ENST00000432427.2:c.479T>C	ENSP00000398591.2:p.Ile160Thr
ENST00000442415.6:c.902T>C	ENSP00000401888.2:p.Ile301Thr
ENST00000465826.5:n.86T>C
ENST00000491290.1:n.363T>C
NM_002880.3:c.842T>C , LRG_413t1:c.842T>C	NP_002871.1:p.Ile281Thr
XM_005265355.1:c.842T>C	XP_005265412.1:p.Ile281Thr
XM_005265357.1:c.743T>C	XP_005265414.1:p.Ile248Thr
XM_005265358.3:c.599T>C	XP_005265415.1:p.Ile200Thr
XM_005265359.3:c.500T>C	XP_005265416.1:p.Ile167Thr
XM_005265360.1:c.842T>C	XP_005265417.1:p.Ile281Thr
XM_011533974.1:c.842T>C	XP_011532276.1:p.Ile281Thr
XM_011533975.1:c.599T>C	XP_011532277.1:p.Ile200Thr
NM_001354689.1:c.902T>C	NP_001341618.1:p.Ile301Thr
NM_001354690.1:c.842T>C	NP_001341619.1:p.Ile281Thr
NM_001354691.1:c.599T>C	NP_001341620.1:p.Ile200Thr
NM_001354692.1:c.599T>C	NP_001341621.1:p.Ile200Thr
NM_001354693.1:c.743T>C	NP_001341622.1:p.Ile248Thr
NM_001354694.1:c.659T>C	NP_001341623.1:p.Ile220Thr
NM_001354695.1:c.500T>C	NP_001341624.1:p.Ile167Thr
NR_148940.1:n.1257T>C
NR_148941.1:n.1257T>C
NR_148942.1:n.1257T>C
XM_011533974.3:c.842T>C	XP_011532276.1:p.Ile281Thr
XM_017006966.1:c.743T>C	XP_016862455.1:p.Ile248Thr
XR_001740227.1:n.1074T>C
NM_001354689.3:c.902T>C	NP_001341618.1:p.Ile301Thr
NM_001354690.2:c.842T>C	NP_001341619.1:p.Ile281Thr
NM_001354691.2:c.599T>C	NP_001341620.1:p.Ile200Thr
NM_001354692.2:c.599T>C	NP_001341621.1:p.Ile200Thr
NM_001354693.2:c.743T>C	NP_001341622.1:p.Ile248Thr
NM_001354694.2:c.659T>C	NP_001341623.1:p.Ile220Thr
NM_001354695.2:c.500T>C	NP_001341624.1:p.Ile167Thr
NR_148940.2:n.1173T>C
NR_148941.2:n.1173T>C
NR_148942.2:n.1173T>C
NM_001354690.3:c.842T>C	NP_001341619.1:p.Ile281Thr
NM_001354691.3:c.599T>C	NP_001341620.1:p.Ile200Thr
NM_001354692.3:c.599T>C	NP_001341621.1:p.Ile200Thr
NM_001354693.3:c.743T>C	NP_001341622.1:p.Ile248Thr
NM_001354694.3:c.659T>C	NP_001341623.1:p.Ile220Thr
NM_001354695.3:c.500T>C	NP_001341624.1:p.Ile167Thr
NM_002880.4:c.842T>C MANE Select	NP_002871.1:p.Ile281Thr
NR_148940.3:n.1173T>C
NR_148941.3:n.1173T>C
NR_148942.3:n.1173T>C