Canonical Allele Identifier: CA1346242062
Gene: RAF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12599692G= , CM000665.2:g.12599692G= GRCh38
NC_000003.11:g.12641191G= , CM000665.1:g.12641191G= GRCh37
NC_000003.10:g.12616191G= NCBI36
NG_007467.1:g.69488C= , LRG_413:g.69488C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000423275.6:c.*772C= ENSP00000401088.1:n.*772C=
ENST00000432427.3:c.427C=
ENST00000465826.6:n.698C=
ENST00000491290.2:n.1484C=
ENST00000684903.1:c.*784C= ENSP00000508612.1:n.*784C=
ENST00000685348.1:c.*784C= ENSP00000510285.1:n.*784C=
ENST00000685437.1:c.1008C= ENSP00000508794.1:p.His336=
ENST00000685653.1:c.1107C= ENSP00000509968.1:p.His369=
ENST00000685738.1:c.1107C= ENSP00000510156.1:p.His369=
ENST00000686409.1:n.2158C=
ENST00000686455.1:n.1470C=
ENST00000686479.1:n.1478C=
ENST00000686762.1:c.1107C= ENSP00000509767.1:p.His369=
ENST00000687257.1:n.1343C=
ENST00000687326.1:c.1107C= ENSP00000509665.1:p.His369=
ENST00000687486.1:c.299C=
ENST00000687505.1:n.1225C=
ENST00000687923.1:c.997+11C= ENSP00000510255.1:n.997+11C=
ENST00000687940.1:n.1484C=
ENST00000688269.1:n.1703C=
ENST00000688326.1:c.427C=
ENST00000688444.1:n.1433C=
ENST00000688543.1:c.1008C= ENSP00000509612.1:p.His336=
ENST00000688625.1:c.*685C= ENSP00000509522.1:n.*685C=
ENST00000688803.1:n.1338C=
ENST00000688914.1:n.93C=
ENST00000689097.1:c.*784C= ENSP00000509756.1:n.*784C=
ENST00000689389.1:c.1107C= ENSP00000510213.1:p.His369=
ENST00000689418.1:c.*784C= ENSP00000509467.1:n.*784C=
ENST00000689481.1:c.*784C= ENSP00000510248.1:n.*784C=
ENST00000689540.1:n.1257C=
ENST00000689876.1:c.1107C= ENSP00000508535.1:p.His369=
ENST00000689914.1:c.1107C= ENSP00000509847.1:p.His369=
ENST00000690397.1:c.996C= ENSP00000508730.1:p.His332=
ENST00000690460.1:c.1095C= ENSP00000509106.1:p.His365=
ENST00000690625.1:n.1410C=
ENST00000691268.1:c.534C=
ENST00000691396.1:c.*900C= ENSP00000510712.1:n.*900C=
ENST00000691724.1:c.*64C= ENSP00000509255.1:n.*64C=
ENST00000691779.1:c.*685C= ENSP00000508592.1:n.*685C=
ENST00000691899.1:c.1107C= ENSP00000508763.1:p.His369=
ENST00000692069.1:n.1673C=
ENST00000692093.1:c.1008C= ENSP00000509669.1:p.His336=
ENST00000692311.1:n.1931C=
ENST00000692558.1:n.1472C=
ENST00000692773.1:c.*844C= ENSP00000509055.1:n.*844C=
ENST00000692830.1:c.*852C= ENSP00000509461.1:n.*852C=
ENST00000693069.1:c.1008C= ENSP00000510072.1:p.His336=
ENST00000693312.1:c.882C= ENSP00000508686.1:p.His294=
ENST00000693664.1:c.1107C= ENSP00000509614.1:p.His369=
ENST00000693705.1:c.*784C= ENSP00000510697.1:n.*784C=
ENST00000251849.9:c.1107C= MANE Select ENSP00000251849.4:p.His369=
ENST00000442415.7:c.1167C= ENSP00000401888.2:p.His389=
ENST00000251849.8:c.1107C= ENSP00000251849.4:p.His369=
ENST00000423275.5:c.*784C= ENSP00000401088.1:n.*784C=
ENST00000432427.2:c.744C= ENSP00000398591.2:p.His248=
ENST00000442415.6:c.1167C= ENSP00000401888.2:p.His389=
ENST00000460610.1:n.64C=
ENST00000465826.5:n.351C=
NM_002880.3:c.1107C= , LRG_413t1:c.1107C= NP_002871.1:p.His369=
XM_005265355.1:c.1107C= XP_005265412.1:p.His369=
XM_005265357.1:c.1008C= XP_005265414.1:p.His336=
XM_005265358.3:c.864C= XP_005265415.1:p.His288=
XM_005265359.3:c.765C= XP_005265416.1:p.His255=
XM_005265360.1:c.1107C= XP_005265417.1:p.His369=
XM_011533974.1:c.1107C= XP_011532276.1:p.His369=
XM_011533975.1:c.864C= XP_011532277.1:p.His288=
NM_001354689.1:c.1167C= NP_001341618.1:p.His389=
NM_001354690.1:c.1107C= NP_001341619.1:p.His369=
NM_001354691.1:c.864C= NP_001341620.1:p.His288=
NM_001354692.1:c.864C= NP_001341621.1:p.His288=
NM_001354693.1:c.1008C= NP_001341622.1:p.His336=
NM_001354694.1:c.924C= NP_001341623.1:p.His308=
NM_001354695.1:c.765C= NP_001341624.1:p.His255=
NR_148940.1:n.1522C=
NR_148941.1:n.1522C=
NR_148942.1:n.1520C=
XM_011533974.3:c.1107C= XP_011532276.1:p.His369=
XM_017006966.1:c.1008C= XP_016862455.1:p.His336=
XR_001740227.1:n.1339C=
NM_001354689.3:c.1167C= NP_001341618.1:p.His389=
NM_001354690.2:c.1107C= NP_001341619.1:p.His369=
NM_001354691.2:c.864C= NP_001341620.1:p.His288=
NM_001354692.2:c.864C= NP_001341621.1:p.His288=
NM_001354693.2:c.1008C= NP_001341622.1:p.His336=
NM_001354694.2:c.924C= NP_001341623.1:p.His308=
NM_001354695.2:c.765C= NP_001341624.1:p.His255=
NR_148940.2:n.1438C=
NR_148941.2:n.1438C=
NR_148942.2:n.1436C=
NM_001354690.3:c.1107C= NP_001341619.1:p.His369=
NM_001354691.3:c.864C= NP_001341620.1:p.His288=
NM_001354692.3:c.864C= NP_001341621.1:p.His288=
NM_001354693.3:c.1008C= NP_001341622.1:p.His336=
NM_001354694.3:c.924C= NP_001341623.1:p.His308=
NM_001354695.3:c.765C= NP_001341624.1:p.His255=
NM_002880.4:c.1107C= MANE Select NP_002871.1:p.His369=
NR_148940.3:n.1438C=
NR_148941.3:n.1438C=
NR_148942.3:n.1436C=