Canonical Allele Identifier: CA2664499564
Gene: RAF1 HGNC NCBI

Linked Data

gnomAD v4: 3-12587435-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12587435C>T , CM000665.2:g.12587435C>T GRCh38
NC_000003.11:g.12628934C>T , CM000665.1:g.12628934C>T GRCh37
NC_000003.10:g.12603934C>T NCBI36
NG_007467.1:g.81745G>A , LRG_413:g.81745G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000423275.6:c.*1082+156G>A ENSP00000401088.1:n.*1082+156G>A
ENST00000432427.3:c.734+156G>A
ENST00000460610.2:n.3527G>A
ENST00000465826.6:n.1164G>A
ENST00000471449.2:n.227+156G>A
ENST00000475353.2:n.1495G>A
ENST00000684903.1:c.*1094+156G>A ENSP00000508612.1:n.*1094+156G>A
ENST00000685348.1:c.*1094+156G>A ENSP00000510285.1:n.*1094+156G>A
ENST00000685437.1:c.1318+156G>A ENSP00000508794.1:n.1318+156G>A
ENST00000685653.1:c.1417+156G>A ENSP00000509968.1:n.1417+156G>A
ENST00000685697.1:n.517G>A
ENST00000685738.1:c.*381+156G>A ENSP00000510156.1:n.*381+156G>A
ENST00000686409.1:n.2624G>A
ENST00000686455.1:n.1936G>A
ENST00000686762.1:c.1417+156G>A ENSP00000509767.1:n.1417+156G>A
ENST00000687257.1:n.1809G>A
ENST00000687326.1:c.*507G>A ENSP00000509665.1:n.*507G>A
ENST00000687505.1:n.1535+156G>A
ENST00000687923.1:c.1306+156G>A ENSP00000510255.1:n.1306+156G>A
ENST00000688269.1:n.2013+156G>A
ENST00000688326.1:c.1006G>A
ENST00000688444.1:n.1899G>A
ENST00000688543.1:c.1318+156G>A ENSP00000509612.1:n.1318+156G>A
ENST00000688625.1:c.*1151G>A ENSP00000509522.1:n.*1151G>A
ENST00000688803.1:n.1804G>A
ENST00000688914.1:n.403+156G>A
ENST00000689097.1:c.*1094+156G>A ENSP00000509756.1:n.*1094+156G>A
ENST00000689389.1:c.1240+156G>A ENSP00000510213.1:n.1240+156G>A
ENST00000689418.1:c.*1250G>A ENSP00000509467.1:n.*1250G>A
ENST00000689540.1:n.1723G>A
ENST00000689876.1:c.1417+156G>A ENSP00000508535.1:n.1417+156G>A
ENST00000689914.1:c.*351+156G>A ENSP00000509847.1:n.*351+156G>A
ENST00000690397.1:c.1306+156G>A ENSP00000508730.1:n.1306+156G>A
ENST00000690460.1:c.1405+156G>A ENSP00000509106.1:n.1405+156G>A
ENST00000690585.1:c.263-2182G>A
ENST00000690625.1:n.2453+156G>A
ENST00000691396.1:c.*1269+156G>A ENSP00000510712.1:n.*1269+156G>A
ENST00000691643.1:n.408G>A
ENST00000691724.1:c.*374+156G>A ENSP00000509255.1:n.*374+156G>A
ENST00000691779.1:c.*995+156G>A ENSP00000508592.1:n.*995+156G>A
ENST00000691888.1:c.309+156G>A
ENST00000691899.1:c.1417+156G>A ENSP00000508763.1:n.1417+156G>A
ENST00000692069.1:n.2139G>A
ENST00000692093.1:c.1318+156G>A ENSP00000509669.1:n.1318+156G>A
ENST00000692311.1:n.2241+156G>A
ENST00000692558.1:n.1938G>A
ENST00000692773.1:c.*1154+156G>A ENSP00000509055.1:n.*1154+156G>A
ENST00000692830.1:c.*1162+156G>A ENSP00000509461.1:n.*1162+156G>A
ENST00000693312.1:c.1192+156G>A ENSP00000508686.1:n.1192+156G>A
ENST00000693664.1:c.1417+156G>A ENSP00000509614.1:n.1417+156G>A
ENST00000693705.1:c.*1048-2454G>A ENSP00000510697.1:n.*1048-2454G>A
ENST00000251849.9:c.1417+156G>A MANE Select ENSP00000251849.4:n.1417+156G>A
ENST00000442415.7:c.1477+156G>A ENSP00000401888.2:n.1477+156G>A
ENST00000251849.8:c.1417+156G>A ENSP00000251849.4:n.1417+156G>A
ENST00000423275.5:c.*1094+156G>A ENSP00000401088.1:n.*1094+156G>A
ENST00000432427.2:c.1054+156G>A ENSP00000398591.2:n.1054+156G>A
ENST00000442415.6:c.1477+156G>A ENSP00000401888.2:n.1477+156G>A
ENST00000465826.5:n.930G>A
NM_002880.3:c.1417+156G>A , LRG_413t1:c.1417+156G>A NP_002871.1:n.1417+156G>A
XM_005265355.1:c.1417+156G>A XP_005265412.1:n.1417+156G>A
XM_005265357.1:c.1318+156G>A XP_005265414.1:n.1318+156G>A
XM_005265358.3:c.1174+156G>A XP_005265415.1:n.1174+156G>A
XM_005265359.3:c.1075+156G>A XP_005265416.1:n.1075+156G>A
XM_005265360.1:c.1417+156G>A XP_005265417.1:n.1417+156G>A
XM_011533974.1:c.1417+156G>A XP_011532276.1:n.1417+156G>A
XM_011533975.1:c.1174+156G>A XP_011532277.1:n.1174+156G>A
NM_001354689.1:c.1477+156G>A NP_001341618.1:n.1477+156G>A
NM_001354690.1:c.1417+156G>A NP_001341619.1:n.1417+156G>A
NM_001354691.1:c.1174+156G>A NP_001341620.1:n.1174+156G>A
NM_001354692.1:c.1174+156G>A NP_001341621.1:n.1174+156G>A
NM_001354693.1:c.1318+156G>A NP_001341622.1:n.1318+156G>A
NM_001354694.1:c.1234+156G>A NP_001341623.1:n.1234+156G>A
NM_001354695.1:c.1075+156G>A NP_001341624.1:n.1075+156G>A
NR_148940.1:n.1945+156G>A
NR_148941.1:n.1891+156G>A
NR_148942.1:n.1830+156G>A
XM_011533974.3:c.1417+156G>A XP_011532276.1:n.1417+156G>A
XM_017006966.1:c.1318+156G>A XP_016862455.1:n.1318+156G>A
NM_001354689.3:c.1477+156G>A NP_001341618.1:n.1477+156G>A
NM_001354690.2:c.1417+156G>A NP_001341619.1:n.1417+156G>A
NM_001354691.2:c.1174+156G>A NP_001341620.1:n.1174+156G>A
NM_001354692.2:c.1174+156G>A NP_001341621.1:n.1174+156G>A
NM_001354693.2:c.1318+156G>A NP_001341622.1:n.1318+156G>A
NM_001354694.2:c.1234+156G>A NP_001341623.1:n.1234+156G>A
NM_001354695.2:c.1075+156G>A NP_001341624.1:n.1075+156G>A
NR_148940.2:n.1861+156G>A
NR_148941.2:n.1807+156G>A
NR_148942.2:n.1746+156G>A
NM_001354690.3:c.1417+156G>A NP_001341619.1:n.1417+156G>A
NM_001354691.3:c.1174+156G>A NP_001341620.1:n.1174+156G>A
NM_001354692.3:c.1174+156G>A NP_001341621.1:n.1174+156G>A
NM_001354693.3:c.1318+156G>A NP_001341622.1:n.1318+156G>A
NM_001354694.3:c.1234+156G>A NP_001341623.1:n.1234+156G>A
NM_001354695.3:c.1075+156G>A NP_001341624.1:n.1075+156G>A
NM_002880.4:c.1417+156G>A MANE Select NP_002871.1:n.1417+156G>A
NR_148940.3:n.1861+156G>A
NR_148941.3:n.1807+156G>A
NR_148942.3:n.1746+156G>A