Canonical Allele Identifier: CA1346242583
Gene: RAF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12600161T= , CM000665.2:g.12600161T= GRCh38
NC_000003.11:g.12641660T= , CM000665.1:g.12641660T= GRCh37
NC_000003.10:g.12616660T= NCBI36
NG_007467.1:g.69019A= , LRG_413:g.69019A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000423275.6:c.*646A= ENSP00000401088.1:n.*646A=
ENST00000432427.3:c.301A=
ENST00000465826.6:n.572A=
ENST00000491290.2:n.1358A=
ENST00000684903.1:c.*658A= ENSP00000508612.1:n.*658A=
ENST00000685348.1:c.*658A= ENSP00000510285.1:n.*658A=
ENST00000685437.1:c.882A= ENSP00000508794.1:p.Lys294=
ENST00000685653.1:c.981A= ENSP00000509968.1:p.Lys327=
ENST00000685738.1:c.981A= ENSP00000510156.1:p.Lys327=
ENST00000686409.1:n.1689A=
ENST00000686455.1:n.1344A=
ENST00000686479.1:n.1352A=
ENST00000686762.1:c.981A= ENSP00000509767.1:p.Lys327=
ENST00000687257.1:n.1217A=
ENST00000687326.1:c.981A= ENSP00000509665.1:p.Lys327=
ENST00000687486.1:c.182+227A=
ENST00000687505.1:n.1099A=
ENST00000687923.1:c.882A= ENSP00000510255.1:p.Lys294=
ENST00000687940.1:n.1358A=
ENST00000688269.1:n.1577A=
ENST00000688326.1:c.301A=
ENST00000688444.1:n.1307A=
ENST00000688543.1:c.882A= ENSP00000509612.1:p.Lys294=
ENST00000688625.1:c.*559A= ENSP00000509522.1:n.*559A=
ENST00000688803.1:n.1212A=
ENST00000689097.1:c.*658A= ENSP00000509756.1:n.*658A=
ENST00000689389.1:c.981A= ENSP00000510213.1:p.Lys327=
ENST00000689418.1:c.*658A= ENSP00000509467.1:n.*658A=
ENST00000689481.1:c.*658A= ENSP00000510248.1:n.*658A=
ENST00000689540.1:n.1131A=
ENST00000689876.1:c.981A= ENSP00000508535.1:p.Lys327=
ENST00000689914.1:c.981A= ENSP00000509847.1:p.Lys327=
ENST00000690397.1:c.870A= ENSP00000508730.1:p.Lys290=
ENST00000690460.1:c.969A= ENSP00000509106.1:p.Lys323=
ENST00000690625.1:n.1284A=
ENST00000691268.1:c.408A=
ENST00000691396.1:c.*774A= ENSP00000510712.1:n.*774A=
ENST00000691724.1:c.981A= ENSP00000509255.1:p.Lys327=
ENST00000691779.1:c.*559A= ENSP00000508592.1:n.*559A=
ENST00000691899.1:c.981A= ENSP00000508763.1:p.Lys327=
ENST00000692069.1:n.1204A=
ENST00000692093.1:c.882A= ENSP00000509669.1:p.Lys294=
ENST00000692311.1:n.1462A=
ENST00000692558.1:n.1346A=
ENST00000692773.1:c.*718A= ENSP00000509055.1:n.*718A=
ENST00000692830.1:c.*726A= ENSP00000509461.1:n.*726A=
ENST00000693069.1:c.882A= ENSP00000510072.1:p.Lys294=
ENST00000693312.1:c.756A= ENSP00000508686.1:p.Lys252=
ENST00000693664.1:c.981A= ENSP00000509614.1:p.Lys327=
ENST00000693705.1:c.*658A= ENSP00000510697.1:n.*658A=
ENST00000251849.9:c.981A= MANE Select ENSP00000251849.4:p.Lys327=
ENST00000442415.7:c.1041A= ENSP00000401888.2:p.Lys347=
ENST00000251849.8:c.981A= ENSP00000251849.4:p.Lys327=
ENST00000423275.5:c.*658A= ENSP00000401088.1:n.*658A=
ENST00000432427.2:c.618A= ENSP00000398591.2:p.Lys206=
ENST00000442415.6:c.1041A= ENSP00000401888.2:p.Lys347=
ENST00000465826.5:n.225A=
NM_002880.3:c.981A= , LRG_413t1:c.981A= NP_002871.1:p.Lys327=
XM_005265355.1:c.981A= XP_005265412.1:p.Lys327=
XM_005265357.1:c.882A= XP_005265414.1:p.Lys294=
XM_005265358.3:c.738A= XP_005265415.1:p.Lys246=
XM_005265359.3:c.639A= XP_005265416.1:p.Lys213=
XM_005265360.1:c.981A= XP_005265417.1:p.Lys327=
XM_011533974.1:c.981A= XP_011532276.1:p.Lys327=
XM_011533975.1:c.738A= XP_011532277.1:p.Lys246=
NM_001354689.1:c.1041A= NP_001341618.1:p.Lys347=
NM_001354690.1:c.981A= NP_001341619.1:p.Lys327=
NM_001354691.1:c.738A= NP_001341620.1:p.Lys246=
NM_001354692.1:c.738A= NP_001341621.1:p.Lys246=
NM_001354693.1:c.882A= NP_001341622.1:p.Lys294=
NM_001354694.1:c.798A= NP_001341623.1:p.Lys266=
NM_001354695.1:c.639A= NP_001341624.1:p.Lys213=
NR_148940.1:n.1396A=
NR_148941.1:n.1396A=
NR_148942.1:n.1396A=
XM_011533974.3:c.981A= XP_011532276.1:p.Lys327=
XM_017006966.1:c.882A= XP_016862455.1:p.Lys294=
XR_001740227.1:n.1213A=
NM_001354689.3:c.1041A= NP_001341618.1:p.Lys347=
NM_001354690.2:c.981A= NP_001341619.1:p.Lys327=
NM_001354691.2:c.738A= NP_001341620.1:p.Lys246=
NM_001354692.2:c.738A= NP_001341621.1:p.Lys246=
NM_001354693.2:c.882A= NP_001341622.1:p.Lys294=
NM_001354694.2:c.798A= NP_001341623.1:p.Lys266=
NM_001354695.2:c.639A= NP_001341624.1:p.Lys213=
NR_148940.2:n.1312A=
NR_148941.2:n.1312A=
NR_148942.2:n.1312A=
NM_001354690.3:c.981A= NP_001341619.1:p.Lys327=
NM_001354691.3:c.738A= NP_001341620.1:p.Lys246=
NM_001354692.3:c.738A= NP_001341621.1:p.Lys246=
NM_001354693.3:c.882A= NP_001341622.1:p.Lys294=
NM_001354694.3:c.798A= NP_001341623.1:p.Lys266=
NM_001354695.3:c.639A= NP_001341624.1:p.Lys213=
NM_002880.4:c.981A= MANE Select NP_002871.1:p.Lys327=
NR_148940.3:n.1312A=
NR_148941.3:n.1312A=
NR_148942.3:n.1312A=