Canonical Allele Identifier: CA1346233153
Gene: RAF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12590829C= , CM000665.2:g.12590829C= GRCh38
NC_000003.11:g.12632328C= , CM000665.1:g.12632328C= GRCh37
NC_000003.10:g.12607328C= NCBI36
NG_007467.1:g.78351G= , LRG_413:g.78351G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000423275.6:c.*1004G= ENSP00000401088.1:n.*1004G=
ENST00000432427.3:c.656G=
ENST00000460610.2:n.133G=
ENST00000465826.6:n.930G=
ENST00000475353.2:n.1261G=
ENST00000494557.2:n.1150G=
ENST00000684903.1:c.*1016G= ENSP00000508612.1:n.*1016G=
ENST00000685348.1:c.*1016G= ENSP00000510285.1:n.*1016G=
ENST00000685437.1:c.1240G= ENSP00000508794.1:p.Asp414=
ENST00000685653.1:c.1339G= ENSP00000509968.1:p.Asp447=
ENST00000685738.1:c.*303G= ENSP00000510156.1:n.*303G=
ENST00000686409.1:n.2390G=
ENST00000686455.1:n.1702G=
ENST00000686762.1:c.1339G= ENSP00000509767.1:p.Asp447=
ENST00000687257.1:n.1575G=
ENST00000687326.1:c.*273G= ENSP00000509665.1:n.*273G=
ENST00000687505.1:n.1457G=
ENST00000687923.1:c.1228G= ENSP00000510255.1:p.Asp410=
ENST00000687940.1:n.1716G=
ENST00000688269.1:n.1935G=
ENST00000688326.1:c.772G=
ENST00000688444.1:n.1665G=
ENST00000688543.1:c.1240G= ENSP00000509612.1:p.Asp414=
ENST00000688625.1:c.*917G= ENSP00000509522.1:n.*917G=
ENST00000688803.1:n.1570G=
ENST00000688914.1:n.325G=
ENST00000689097.1:c.*1016G= ENSP00000509756.1:n.*1016G=
ENST00000689389.1:c.1193+879G= ENSP00000510213.1:n.1193+879G=
ENST00000689418.1:c.*1016G= ENSP00000509467.1:n.*1016G=
ENST00000689481.1:c.*1016G= ENSP00000510248.1:n.*1016G=
ENST00000689540.1:n.1489G=
ENST00000689876.1:c.1339G= ENSP00000508535.1:p.Asp447=
ENST00000689914.1:c.*273G= ENSP00000509847.1:n.*273G=
ENST00000690397.1:c.1228G= ENSP00000508730.1:p.Asp410=
ENST00000690460.1:c.1327G= ENSP00000509106.1:p.Asp443=
ENST00000690585.1:c.231G=
ENST00000690625.1:n.2375G=
ENST00000691396.1:c.*1191G= ENSP00000510712.1:n.*1191G=
ENST00000691724.1:c.*296G= ENSP00000509255.1:n.*296G=
ENST00000691779.1:c.*917G= ENSP00000508592.1:n.*917G=
ENST00000691888.1:c.231G=
ENST00000691899.1:c.1339G= ENSP00000508763.1:p.Asp447=
ENST00000692069.1:n.1905G=
ENST00000692093.1:c.1240G= ENSP00000509669.1:p.Asp414=
ENST00000692311.1:n.2163G=
ENST00000692558.1:n.1704G=
ENST00000692773.1:c.*1076G= ENSP00000509055.1:n.*1076G=
ENST00000692830.1:c.*1084G= ENSP00000509461.1:n.*1084G=
ENST00000693069.1:c.*273G= ENSP00000510072.1:n.*273G=
ENST00000693312.1:c.1114G= ENSP00000508686.1:p.Asp372=
ENST00000693664.1:c.1339G= ENSP00000509614.1:p.Asp447=
ENST00000693705.1:c.*1016G= ENSP00000510697.1:n.*1016G=
ENST00000251849.9:c.1339G= MANE Select ENSP00000251849.4:p.Asp447=
ENST00000442415.7:c.1399G= ENSP00000401888.2:p.Asp467=
ENST00000251849.8:c.1339G= ENSP00000251849.4:p.Asp447=
ENST00000423275.5:c.*1016G= ENSP00000401088.1:n.*1016G=
ENST00000432427.2:c.976G= ENSP00000398591.2:p.Asp326=
ENST00000442415.6:c.1399G= ENSP00000401888.2:p.Asp467=
ENST00000460610.1:n.296G=
ENST00000465826.5:n.696G=
ENST00000475353.1:n.507G=
ENST00000494557.1:n.355G=
NM_002880.3:c.1339G= , LRG_413t1:c.1339G= NP_002871.1:p.Asp447=
XM_005265355.1:c.1339G= XP_005265412.1:p.Asp447=
XM_005265357.1:c.1240G= XP_005265414.1:p.Asp414=
XM_005265358.3:c.1096G= XP_005265415.1:p.Asp366=
XM_005265359.3:c.997G= XP_005265416.1:p.Asp333=
XM_005265360.1:c.1339G= XP_005265417.1:p.Asp447=
XM_011533974.1:c.1339G= XP_011532276.1:p.Asp447=
XM_011533975.1:c.1096G= XP_011532277.1:p.Asp366=
NM_001354689.1:c.1399G= NP_001341618.1:p.Asp467=
NM_001354690.1:c.1339G= NP_001341619.1:p.Asp447=
NM_001354691.1:c.1096G= NP_001341620.1:p.Asp366=
NM_001354692.1:c.1096G= NP_001341621.1:p.Asp366=
NM_001354693.1:c.1240G= NP_001341622.1:p.Asp414=
NM_001354694.1:c.1156G= NP_001341623.1:p.Asp386=
NM_001354695.1:c.997G= NP_001341624.1:p.Asp333=
NR_148940.1:n.1867G=
NR_148941.1:n.1813G=
NR_148942.1:n.1752G=
XM_011533974.3:c.1339G= XP_011532276.1:p.Asp447=
XM_017006966.1:c.1240G= XP_016862455.1:p.Asp414=
NM_001354689.3:c.1399G= NP_001341618.1:p.Asp467=
NM_001354690.2:c.1339G= NP_001341619.1:p.Asp447=
NM_001354691.2:c.1096G= NP_001341620.1:p.Asp366=
NM_001354692.2:c.1096G= NP_001341621.1:p.Asp366=
NM_001354693.2:c.1240G= NP_001341622.1:p.Asp414=
NM_001354694.2:c.1156G= NP_001341623.1:p.Asp386=
NM_001354695.2:c.997G= NP_001341624.1:p.Asp333=
NR_148940.2:n.1783G=
NR_148941.2:n.1729G=
NR_148942.2:n.1668G=
NM_001354690.3:c.1339G= NP_001341619.1:p.Asp447=
NM_001354691.3:c.1096G= NP_001341620.1:p.Asp366=
NM_001354692.3:c.1096G= NP_001341621.1:p.Asp366=
NM_001354693.3:c.1240G= NP_001341622.1:p.Asp414=
NM_001354694.3:c.1156G= NP_001341623.1:p.Asp386=
NM_001354695.3:c.997G= NP_001341624.1:p.Asp333=
NM_002880.4:c.1339G= MANE Select NP_002871.1:p.Asp447=
NR_148940.3:n.1783G=
NR_148941.3:n.1729G=
NR_148942.3:n.1668G=