Canonical Allele Identifier: CA351508797
Gene: RAF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2775483
ClinVar RCV Id: RCV003655431
dbSNP Id: rs2058817795

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12600213G>A , CM000665.2:g.12600213G>A GRCh38
NC_000003.11:g.12641712G>A , CM000665.1:g.12641712G>A GRCh37
NC_000003.10:g.12616712G>A NCBI36
NG_007467.1:g.68967C>T , LRG_413:g.68967C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000423275.6:c.*594C>T ENSP00000401088.1:n.*594C>T
ENST00000432427.3:c.249C>T
ENST00000465826.6:n.520C>T
ENST00000491290.2:n.1306C>T
ENST00000684903.1:c.*606C>T ENSP00000508612.1:n.*606C>T
ENST00000685348.1:c.*606C>T ENSP00000510285.1:n.*606C>T
ENST00000685437.1:c.830C>T ENSP00000508794.1:p.Thr277Ile
ENST00000685438.1:n.693C>T
ENST00000685653.1:c.929C>T ENSP00000509968.1:p.Thr310Ile
ENST00000685738.1:c.929C>T ENSP00000510156.1:p.Thr310Ile
ENST00000686409.1:n.1637C>T
ENST00000686455.1:n.1292C>T
ENST00000686479.1:n.1300C>T
ENST00000686762.1:c.929C>T ENSP00000509767.1:p.Thr310Ile
ENST00000687257.1:n.1165C>T
ENST00000687326.1:c.929C>T ENSP00000509665.1:p.Thr310Ile
ENST00000687486.1:c.182+175C>T
ENST00000687505.1:n.1047C>T
ENST00000687923.1:c.830C>T ENSP00000510255.1:p.Thr277Ile
ENST00000687940.1:n.1306C>T
ENST00000688269.1:n.1525C>T
ENST00000688326.1:c.249C>T
ENST00000688444.1:n.1255C>T
ENST00000688543.1:c.830C>T ENSP00000509612.1:p.Thr277Ile
ENST00000688625.1:c.*507C>T ENSP00000509522.1:n.*507C>T
ENST00000688803.1:n.1160C>T
ENST00000689097.1:c.*606C>T ENSP00000509756.1:n.*606C>T
ENST00000689389.1:c.929C>T ENSP00000510213.1:p.Thr310Ile
ENST00000689418.1:c.*606C>T ENSP00000509467.1:n.*606C>T
ENST00000689481.1:c.*606C>T ENSP00000510248.1:n.*606C>T
ENST00000689540.1:n.1079C>T
ENST00000689876.1:c.929C>T ENSP00000508535.1:p.Thr310Ile
ENST00000689914.1:c.929C>T ENSP00000509847.1:p.Thr310Ile
ENST00000690397.1:c.818C>T ENSP00000508730.1:p.Thr273Ile
ENST00000690460.1:c.917C>T ENSP00000509106.1:p.Thr306Ile
ENST00000690625.1:n.1232C>T
ENST00000691268.1:c.356C>T
ENST00000691396.1:c.*722C>T ENSP00000510712.1:n.*722C>T
ENST00000691724.1:c.929C>T ENSP00000509255.1:p.Thr310Ile
ENST00000691779.1:c.*507C>T ENSP00000508592.1:n.*507C>T
ENST00000691899.1:c.929C>T ENSP00000508763.1:p.Thr310Ile
ENST00000692069.1:n.1152C>T
ENST00000692093.1:c.830C>T ENSP00000509669.1:p.Thr277Ile
ENST00000692311.1:n.1410C>T
ENST00000692558.1:n.1294C>T
ENST00000692773.1:c.*666C>T ENSP00000509055.1:n.*666C>T
ENST00000692830.1:c.*674C>T ENSP00000509461.1:n.*674C>T
ENST00000693069.1:c.830C>T ENSP00000510072.1:p.Thr277Ile
ENST00000693312.1:c.704C>T ENSP00000508686.1:p.Thr235Ile
ENST00000693664.1:c.929C>T ENSP00000509614.1:p.Thr310Ile
ENST00000693705.1:c.*606C>T ENSP00000510697.1:n.*606C>T
ENST00000251849.9:c.929C>T MANE Select ENSP00000251849.4:p.Thr310Ile
ENST00000442415.7:c.989C>T ENSP00000401888.2:p.Thr330Ile
ENST00000251849.8:c.929C>T ENSP00000251849.4:p.Thr310Ile
ENST00000423275.5:c.*606C>T ENSP00000401088.1:n.*606C>T
ENST00000432427.2:c.566C>T ENSP00000398591.2:p.Thr189Ile
ENST00000442415.6:c.989C>T ENSP00000401888.2:p.Thr330Ile
ENST00000465826.5:n.173C>T
ENST00000491290.1:n.558C>T
NM_002880.3:c.929C>T , LRG_413t1:c.929C>T NP_002871.1:p.Thr310Ile
XM_005265355.1:c.929C>T XP_005265412.1:p.Thr310Ile
XM_005265357.1:c.830C>T XP_005265414.1:p.Thr277Ile
XM_005265358.3:c.686C>T XP_005265415.1:p.Thr229Ile
XM_005265359.3:c.587C>T XP_005265416.1:p.Thr196Ile
XM_005265360.1:c.929C>T XP_005265417.1:p.Thr310Ile
XM_011533974.1:c.929C>T XP_011532276.1:p.Thr310Ile
XM_011533975.1:c.686C>T XP_011532277.1:p.Thr229Ile
NM_001354689.1:c.989C>T NP_001341618.1:p.Thr330Ile
NM_001354690.1:c.929C>T NP_001341619.1:p.Thr310Ile
NM_001354691.1:c.686C>T NP_001341620.1:p.Thr229Ile
NM_001354692.1:c.686C>T NP_001341621.1:p.Thr229Ile
NM_001354693.1:c.830C>T NP_001341622.1:p.Thr277Ile
NM_001354694.1:c.746C>T NP_001341623.1:p.Thr249Ile
NM_001354695.1:c.587C>T NP_001341624.1:p.Thr196Ile
NR_148940.1:n.1344C>T
NR_148941.1:n.1344C>T
NR_148942.1:n.1344C>T
XM_011533974.3:c.929C>T XP_011532276.1:p.Thr310Ile
XM_017006966.1:c.830C>T XP_016862455.1:p.Thr277Ile
XR_001740227.1:n.1161C>T
NM_001354689.3:c.989C>T NP_001341618.1:p.Thr330Ile
NM_001354690.2:c.929C>T NP_001341619.1:p.Thr310Ile
NM_001354691.2:c.686C>T NP_001341620.1:p.Thr229Ile
NM_001354692.2:c.686C>T NP_001341621.1:p.Thr229Ile
NM_001354693.2:c.830C>T NP_001341622.1:p.Thr277Ile
NM_001354694.2:c.746C>T NP_001341623.1:p.Thr249Ile
NM_001354695.2:c.587C>T NP_001341624.1:p.Thr196Ile
NR_148940.2:n.1260C>T
NR_148941.2:n.1260C>T
NR_148942.2:n.1260C>T
NM_001354690.3:c.929C>T NP_001341619.1:p.Thr310Ile
NM_001354691.3:c.686C>T NP_001341620.1:p.Thr229Ile
NM_001354692.3:c.686C>T NP_001341621.1:p.Thr229Ile
NM_001354693.3:c.830C>T NP_001341622.1:p.Thr277Ile
NM_001354694.3:c.746C>T NP_001341623.1:p.Thr249Ile
NM_001354695.3:c.587C>T NP_001341624.1:p.Thr196Ile
NM_002880.4:c.929C>T MANE Select NP_002871.1:p.Thr310Ile
NR_148940.3:n.1260C>T
NR_148941.3:n.1260C>T
NR_148942.3:n.1260C>T