Canonical Allele Identifier: CA2577511331
Gene: RAF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12600236dup , CM000665.2:g.12600236dup GRCh38
NC_000003.11:g.12641735dup , CM000665.1:g.12641735dup GRCh37
NC_000003.10:g.12616735dup NCBI36
NG_007467.1:g.68945dup , LRG_413:g.68945dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000423275.6:c.*572dup ENSP00000401088.1:n.*572dup
ENST00000432427.3:c.227dup
ENST00000465826.6:n.498dup
ENST00000491290.2:n.1284dup
ENST00000684903.1:c.*584dup ENSP00000508612.1:n.*584dup
ENST00000685348.1:c.*584dup ENSP00000510285.1:n.*584dup
ENST00000685437.1:c.808dup ENSP00000508794.1:p.Thr270AsnfsTer29
ENST00000685438.1:n.671dup
ENST00000685653.1:c.907dup ENSP00000509968.1:p.Thr303AsnfsTer29
ENST00000685738.1:c.907dup ENSP00000510156.1:p.Thr303AsnfsTer29
ENST00000686409.1:n.1615dup
ENST00000686455.1:n.1270dup
ENST00000686479.1:n.1278dup
ENST00000686762.1:c.907dup ENSP00000509767.1:p.Thr303AsnfsTer29
ENST00000687257.1:n.1143dup
ENST00000687326.1:c.907dup ENSP00000509665.1:p.Thr303AsnfsTer29
ENST00000687486.1:c.182+153dup
ENST00000687505.1:n.1025dup
ENST00000687923.1:c.808dup ENSP00000510255.1:p.Thr270AsnfsTer29
ENST00000687940.1:n.1284dup
ENST00000688269.1:n.1503dup
ENST00000688326.1:c.227dup
ENST00000688444.1:n.1233dup
ENST00000688543.1:c.808dup ENSP00000509612.1:p.Thr270AsnfsTer29
ENST00000688625.1:c.*485dup ENSP00000509522.1:n.*485dup
ENST00000688803.1:n.1138dup
ENST00000689097.1:c.*584dup ENSP00000509756.1:n.*584dup
ENST00000689389.1:c.907dup ENSP00000510213.1:p.Thr303AsnfsTer29
ENST00000689418.1:c.*584dup ENSP00000509467.1:n.*584dup
ENST00000689481.1:c.*584dup ENSP00000510248.1:n.*584dup
ENST00000689540.1:n.1057dup
ENST00000689876.1:c.907dup ENSP00000508535.1:p.Thr303AsnfsTer29
ENST00000689914.1:c.907dup ENSP00000509847.1:p.Thr303AsnfsTer29
ENST00000690397.1:c.796dup ENSP00000508730.1:p.Thr266AsnfsTer29
ENST00000690460.1:c.895dup ENSP00000509106.1:p.Thr299AsnfsTer29
ENST00000690625.1:n.1210dup
ENST00000691268.1:c.334dup
ENST00000691396.1:c.*700dup ENSP00000510712.1:n.*700dup
ENST00000691724.1:c.907dup ENSP00000509255.1:p.Thr303AsnfsTer?
ENST00000691779.1:c.*485dup ENSP00000508592.1:n.*485dup
ENST00000691899.1:c.907dup ENSP00000508763.1:p.Thr303AsnfsTer29
ENST00000692069.1:n.1130dup
ENST00000692093.1:c.808dup ENSP00000509669.1:p.Thr270AsnfsTer29
ENST00000692311.1:n.1388dup
ENST00000692558.1:n.1272dup
ENST00000692773.1:c.*644dup ENSP00000509055.1:n.*644dup
ENST00000692830.1:c.*652dup ENSP00000509461.1:n.*652dup
ENST00000693069.1:c.808dup ENSP00000510072.1:p.Thr270AsnfsTer29
ENST00000693312.1:c.682dup ENSP00000508686.1:p.Thr228AsnfsTer29
ENST00000693664.1:c.907dup ENSP00000509614.1:p.Thr303AsnfsTer29
ENST00000693705.1:c.*584dup ENSP00000510697.1:n.*584dup
ENST00000251849.9:c.907dup MANE Select ENSP00000251849.4:p.Thr303AsnfsTer29
ENST00000442415.7:c.967dup ENSP00000401888.2:p.Thr323AsnfsTer29
ENST00000251849.8:c.907dup ENSP00000251849.4:p.Thr303AsnfsTer29
ENST00000423275.5:c.*584dup ENSP00000401088.1:n.*584dup
ENST00000432427.2:c.544dup ENSP00000398591.2:p.Thr182AsnfsTer29
ENST00000442415.6:c.967dup ENSP00000401888.2:p.Thr323AsnfsTer29
ENST00000465826.5:n.151dup
ENST00000491290.1:n.536dup
NM_002880.3:c.907dup , LRG_413t1:c.907dup NP_002871.1:p.Thr303AsnfsTer29
XM_005265355.1:c.907dup XP_005265412.1:p.Thr303AsnfsTer29
XM_005265357.1:c.808dup XP_005265414.1:p.Thr270AsnfsTer29
XM_005265358.3:c.664dup XP_005265415.1:p.Thr222AsnfsTer29
XM_005265359.3:c.565dup XP_005265416.1:p.Thr189AsnfsTer29
XM_005265360.1:c.907dup XP_005265417.1:p.Thr303AsnfsTer29
XM_011533974.1:c.907dup XP_011532276.1:p.Thr303AsnfsTer29
XM_011533975.1:c.664dup XP_011532277.1:p.Thr222AsnfsTer29
NM_001354689.1:c.967dup NP_001341618.1:p.Thr323AsnfsTer29
NM_001354690.1:c.907dup NP_001341619.1:p.Thr303AsnfsTer29
NM_001354691.1:c.664dup NP_001341620.1:p.Thr222AsnfsTer29
NM_001354692.1:c.664dup NP_001341621.1:p.Thr222AsnfsTer29
NM_001354693.1:c.808dup NP_001341622.1:p.Thr270AsnfsTer29
NM_001354694.1:c.724dup NP_001341623.1:p.Thr242AsnfsTer29
NM_001354695.1:c.565dup NP_001341624.1:p.Thr189AsnfsTer29
NR_148940.1:n.1322dup
NR_148941.1:n.1322dup
NR_148942.1:n.1322dup
XM_011533974.3:c.907dup XP_011532276.1:p.Thr303AsnfsTer29
XM_017006966.1:c.808dup XP_016862455.1:p.Thr270AsnfsTer29
XR_001740227.1:n.1139dup
NM_001354689.3:c.967dup NP_001341618.1:p.Thr323AsnfsTer29
NM_001354690.2:c.907dup NP_001341619.1:p.Thr303AsnfsTer29
NM_001354691.2:c.664dup NP_001341620.1:p.Thr222AsnfsTer29
NM_001354692.2:c.664dup NP_001341621.1:p.Thr222AsnfsTer29
NM_001354693.2:c.808dup NP_001341622.1:p.Thr270AsnfsTer29
NM_001354694.2:c.724dup NP_001341623.1:p.Thr242AsnfsTer29
NM_001354695.2:c.565dup NP_001341624.1:p.Thr189AsnfsTer29
NR_148940.2:n.1238dup
NR_148941.2:n.1238dup
NR_148942.2:n.1238dup
NM_001354690.3:c.907dup NP_001341619.1:p.Thr303AsnfsTer29
NM_001354691.3:c.664dup NP_001341620.1:p.Thr222AsnfsTer29
NM_001354692.3:c.664dup NP_001341621.1:p.Thr222AsnfsTer29
NM_001354693.3:c.808dup NP_001341622.1:p.Thr270AsnfsTer29
NM_001354694.3:c.724dup NP_001341623.1:p.Thr242AsnfsTer29
NM_001354695.3:c.565dup NP_001341624.1:p.Thr189AsnfsTer29
NM_002880.4:c.907dup MANE Select NP_002871.1:p.Thr303AsnfsTer29
NR_148940.3:n.1238dup
NR_148941.3:n.1238dup
NR_148942.3:n.1238dup