Canonical Allele Identifier: CA2607829386
Gene: RAF1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12600175dup , CM000665.2:g.12600175dup GRCh38
NC_000003.11:g.12641674dup , CM000665.1:g.12641674dup GRCh37
NC_000003.10:g.12616674dup NCBI36
NG_007467.1:g.69007dup , LRG_413:g.69007dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000423275.6:c.*634dup ENSP00000401088.1:n.*634dup
ENST00000432427.3:c.289dup
ENST00000465826.6:n.560dup
ENST00000491290.2:n.1346dup
ENST00000684903.1:c.*646dup ENSP00000508612.1:n.*646dup
ENST00000685348.1:c.*646dup ENSP00000510285.1:n.*646dup
ENST00000685437.1:c.870dup ENSP00000508794.1:p.Thr291AspfsTer8
ENST00000685653.1:c.969dup ENSP00000509968.1:p.Thr324AspfsTer8
ENST00000685738.1:c.969dup ENSP00000510156.1:p.Thr324AspfsTer8
ENST00000686409.1:n.1677dup
ENST00000686455.1:n.1332dup
ENST00000686479.1:n.1340dup
ENST00000686762.1:c.969dup ENSP00000509767.1:p.Thr324AspfsTer8
ENST00000687257.1:n.1205dup
ENST00000687326.1:c.969dup ENSP00000509665.1:p.Thr324AspfsTer8
ENST00000687486.1:c.182+215dup
ENST00000687505.1:n.1087dup
ENST00000687923.1:c.870dup ENSP00000510255.1:p.Thr291AspfsTer8
ENST00000687940.1:n.1346dup
ENST00000688269.1:n.1565dup
ENST00000688326.1:c.289dup
ENST00000688444.1:n.1295dup
ENST00000688543.1:c.870dup ENSP00000509612.1:p.Thr291AspfsTer8
ENST00000688625.1:c.*547dup ENSP00000509522.1:n.*547dup
ENST00000688803.1:n.1200dup
ENST00000689097.1:c.*646dup ENSP00000509756.1:n.*646dup
ENST00000689389.1:c.969dup ENSP00000510213.1:p.Thr324AspfsTer8
ENST00000689418.1:c.*646dup ENSP00000509467.1:n.*646dup
ENST00000689481.1:c.*646dup ENSP00000510248.1:n.*646dup
ENST00000689540.1:n.1119dup
ENST00000689876.1:c.969dup ENSP00000508535.1:p.Thr324AspfsTer8
ENST00000689914.1:c.969dup ENSP00000509847.1:p.Thr324AspfsTer8
ENST00000690397.1:c.858dup ENSP00000508730.1:p.Thr287AspfsTer8
ENST00000690460.1:c.957dup ENSP00000509106.1:p.Thr320AspfsTer8
ENST00000690625.1:n.1272dup
ENST00000691268.1:c.396dup
ENST00000691396.1:c.*762dup ENSP00000510712.1:n.*762dup
ENST00000691724.1:c.969dup ENSP00000509255.1:p.Thr324AspfsTer21
ENST00000691779.1:c.*547dup ENSP00000508592.1:n.*547dup
ENST00000691899.1:c.969dup ENSP00000508763.1:p.Thr324AspfsTer8
ENST00000692069.1:n.1192dup
ENST00000692093.1:c.870dup ENSP00000509669.1:p.Thr291AspfsTer8
ENST00000692311.1:n.1450dup
ENST00000692558.1:n.1334dup
ENST00000692773.1:c.*706dup ENSP00000509055.1:n.*706dup
ENST00000692830.1:c.*714dup ENSP00000509461.1:n.*714dup
ENST00000693069.1:c.870dup ENSP00000510072.1:p.Thr291AspfsTer8
ENST00000693312.1:c.744dup ENSP00000508686.1:p.Thr249AspfsTer8
ENST00000693664.1:c.969dup ENSP00000509614.1:p.Thr324AspfsTer8
ENST00000693705.1:c.*646dup ENSP00000510697.1:n.*646dup
ENST00000251849.9:c.969dup MANE Select ENSP00000251849.4:p.Thr324AspfsTer8
ENST00000442415.7:c.1029dup ENSP00000401888.2:p.Thr344AspfsTer8
ENST00000251849.8:c.969dup ENSP00000251849.4:p.Thr324AspfsTer8
ENST00000423275.5:c.*646dup ENSP00000401088.1:n.*646dup
ENST00000432427.2:c.606dup ENSP00000398591.2:p.Thr203AspfsTer8
ENST00000442415.6:c.1029dup ENSP00000401888.2:p.Thr344AspfsTer8
ENST00000465826.5:n.213dup
NM_002880.3:c.969dup , LRG_413t1:c.969dup NP_002871.1:p.Thr324AspfsTer8
XM_005265355.1:c.969dup XP_005265412.1:p.Thr324AspfsTer8
XM_005265357.1:c.870dup XP_005265414.1:p.Thr291AspfsTer8
XM_005265358.3:c.726dup XP_005265415.1:p.Thr243AspfsTer8
XM_005265359.3:c.627dup XP_005265416.1:p.Thr210AspfsTer8
XM_005265360.1:c.969dup XP_005265417.1:p.Thr324AspfsTer8
XM_011533974.1:c.969dup XP_011532276.1:p.Thr324AspfsTer8
XM_011533975.1:c.726dup XP_011532277.1:p.Thr243AspfsTer8
NM_001354689.1:c.1029dup NP_001341618.1:p.Thr344AspfsTer8
NM_001354690.1:c.969dup NP_001341619.1:p.Thr324AspfsTer8
NM_001354691.1:c.726dup NP_001341620.1:p.Thr243AspfsTer8
NM_001354692.1:c.726dup NP_001341621.1:p.Thr243AspfsTer8
NM_001354693.1:c.870dup NP_001341622.1:p.Thr291AspfsTer8
NM_001354694.1:c.786dup NP_001341623.1:p.Thr263AspfsTer8
NM_001354695.1:c.627dup NP_001341624.1:p.Thr210AspfsTer8
NR_148940.1:n.1384dup
NR_148941.1:n.1384dup
NR_148942.1:n.1384dup
XM_011533974.3:c.969dup XP_011532276.1:p.Thr324AspfsTer8
XM_017006966.1:c.870dup XP_016862455.1:p.Thr291AspfsTer8
XR_001740227.1:n.1201dup
NM_001354689.3:c.1029dup NP_001341618.1:p.Thr344AspfsTer8
NM_001354690.2:c.969dup NP_001341619.1:p.Thr324AspfsTer8
NM_001354691.2:c.726dup NP_001341620.1:p.Thr243AspfsTer8
NM_001354692.2:c.726dup NP_001341621.1:p.Thr243AspfsTer8
NM_001354693.2:c.870dup NP_001341622.1:p.Thr291AspfsTer8
NM_001354694.2:c.786dup NP_001341623.1:p.Thr263AspfsTer8
NM_001354695.2:c.627dup NP_001341624.1:p.Thr210AspfsTer8
NR_148940.2:n.1300dup
NR_148941.2:n.1300dup
NR_148942.2:n.1300dup
NM_001354690.3:c.969dup NP_001341619.1:p.Thr324AspfsTer8
NM_001354691.3:c.726dup NP_001341620.1:p.Thr243AspfsTer8
NM_001354692.3:c.726dup NP_001341621.1:p.Thr243AspfsTer8
NM_001354693.3:c.870dup NP_001341622.1:p.Thr291AspfsTer8
NM_001354694.3:c.786dup NP_001341623.1:p.Thr263AspfsTer8
NM_001354695.3:c.627dup NP_001341624.1:p.Thr210AspfsTer8
NM_002880.4:c.969dup MANE Select NP_002871.1:p.Thr324AspfsTer8
NR_148940.3:n.1300dup
NR_148941.3:n.1300dup
NR_148942.3:n.1300dup