Canonical Allele Identifier: CA351501613
Gene: RAF1 HGNC NCBI

Linked Data

gnomAD v4: 3-12590798-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12590798T>C , CM000665.2:g.12590798T>C GRCh38
NC_000003.11:g.12632297T>C , CM000665.1:g.12632297T>C GRCh37
NC_000003.10:g.12607297T>C NCBI36
NG_007467.1:g.78382A>G , LRG_413:g.78382A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000423275.6:c.*1035A>G ENSP00000401088.1:n.*1035A>G
ENST00000432427.3:c.687A>G
ENST00000460610.2:n.164A>G
ENST00000465826.6:n.961A>G
ENST00000475353.2:n.1292A>G
ENST00000494557.2:n.1181A>G
ENST00000684903.1:c.*1047A>G ENSP00000508612.1:n.*1047A>G
ENST00000685348.1:c.*1047A>G ENSP00000510285.1:n.*1047A>G
ENST00000685437.1:c.1271A>G ENSP00000508794.1:p.Asp424Gly
ENST00000685653.1:c.1370A>G ENSP00000509968.1:p.Asp457Gly
ENST00000685738.1:c.*334A>G ENSP00000510156.1:n.*334A>G
ENST00000686409.1:n.2421A>G
ENST00000686455.1:n.1733A>G
ENST00000686762.1:c.1370A>G ENSP00000509767.1:p.Asp457Gly
ENST00000687257.1:n.1606A>G
ENST00000687326.1:c.*304A>G ENSP00000509665.1:n.*304A>G
ENST00000687505.1:n.1488A>G
ENST00000687923.1:c.1259A>G ENSP00000510255.1:p.Asp420Gly
ENST00000687940.1:n.1747A>G
ENST00000688269.1:n.1966A>G
ENST00000688326.1:c.803A>G
ENST00000688444.1:n.1696A>G
ENST00000688543.1:c.1271A>G ENSP00000509612.1:p.Asp424Gly
ENST00000688625.1:c.*948A>G ENSP00000509522.1:n.*948A>G
ENST00000688803.1:n.1601A>G
ENST00000688914.1:n.356A>G
ENST00000689097.1:c.*1047A>G ENSP00000509756.1:n.*1047A>G
ENST00000689389.1:c.1193+910A>G ENSP00000510213.1:n.1193+910A>G
ENST00000689418.1:c.*1047A>G ENSP00000509467.1:n.*1047A>G
ENST00000689481.1:c.*1047A>G ENSP00000510248.1:n.*1047A>G
ENST00000689540.1:n.1520A>G
ENST00000689876.1:c.1370A>G ENSP00000508535.1:p.Asp457Gly
ENST00000689914.1:c.*304A>G ENSP00000509847.1:n.*304A>G
ENST00000690397.1:c.1259A>G ENSP00000508730.1:p.Asp420Gly
ENST00000690460.1:c.1358A>G ENSP00000509106.1:p.Asp453Gly
ENST00000690585.1:c.262A>G
ENST00000690625.1:n.2406A>G
ENST00000691396.1:c.*1222A>G ENSP00000510712.1:n.*1222A>G
ENST00000691724.1:c.*327A>G ENSP00000509255.1:n.*327A>G
ENST00000691779.1:c.*948A>G ENSP00000508592.1:n.*948A>G
ENST00000691888.1:c.262A>G
ENST00000691899.1:c.1370A>G ENSP00000508763.1:p.Asp457Gly
ENST00000692069.1:n.1936A>G
ENST00000692093.1:c.1271A>G ENSP00000509669.1:p.Asp424Gly
ENST00000692311.1:n.2194A>G
ENST00000692558.1:n.1735A>G
ENST00000692773.1:c.*1107A>G ENSP00000509055.1:n.*1107A>G
ENST00000692830.1:c.*1115A>G ENSP00000509461.1:n.*1115A>G
ENST00000693069.1:c.*304A>G ENSP00000510072.1:n.*304A>G
ENST00000693312.1:c.1145A>G ENSP00000508686.1:p.Asp382Gly
ENST00000693664.1:c.1370A>G ENSP00000509614.1:p.Asp457Gly
ENST00000693705.1:c.*1047A>G ENSP00000510697.1:n.*1047A>G
ENST00000251849.9:c.1370A>G MANE Select ENSP00000251849.4:p.Asp457Gly
ENST00000442415.7:c.1430A>G ENSP00000401888.2:p.Asp477Gly
ENST00000251849.8:c.1370A>G ENSP00000251849.4:p.Asp457Gly
ENST00000423275.5:c.*1047A>G ENSP00000401088.1:n.*1047A>G
ENST00000432427.2:c.1007A>G ENSP00000398591.2:p.Asp336Gly
ENST00000442415.6:c.1430A>G ENSP00000401888.2:p.Asp477Gly
ENST00000460610.1:n.327A>G
ENST00000465826.5:n.727A>G
ENST00000475353.1:n.538A>G
ENST00000494557.1:n.386A>G
NM_002880.3:c.1370A>G , LRG_413t1:c.1370A>G NP_002871.1:p.Asp457Gly
XM_005265355.1:c.1370A>G XP_005265412.1:p.Asp457Gly
XM_005265357.1:c.1271A>G XP_005265414.1:p.Asp424Gly
XM_005265358.3:c.1127A>G XP_005265415.1:p.Asp376Gly
XM_005265359.3:c.1028A>G XP_005265416.1:p.Asp343Gly
XM_005265360.1:c.1370A>G XP_005265417.1:p.Asp457Gly
XM_011533974.1:c.1370A>G XP_011532276.1:p.Asp457Gly
XM_011533975.1:c.1127A>G XP_011532277.1:p.Asp376Gly
NM_001354689.1:c.1430A>G NP_001341618.1:p.Asp477Gly
NM_001354690.1:c.1370A>G NP_001341619.1:p.Asp457Gly
NM_001354691.1:c.1127A>G NP_001341620.1:p.Asp376Gly
NM_001354692.1:c.1127A>G NP_001341621.1:p.Asp376Gly
NM_001354693.1:c.1271A>G NP_001341622.1:p.Asp424Gly
NM_001354694.1:c.1187A>G NP_001341623.1:p.Asp396Gly
NM_001354695.1:c.1028A>G NP_001341624.1:p.Asp343Gly
NR_148940.1:n.1898A>G
NR_148941.1:n.1844A>G
NR_148942.1:n.1783A>G
XM_011533974.3:c.1370A>G XP_011532276.1:p.Asp457Gly
XM_017006966.1:c.1271A>G XP_016862455.1:p.Asp424Gly
NM_001354689.3:c.1430A>G NP_001341618.1:p.Asp477Gly
NM_001354690.2:c.1370A>G NP_001341619.1:p.Asp457Gly
NM_001354691.2:c.1127A>G NP_001341620.1:p.Asp376Gly
NM_001354692.2:c.1127A>G NP_001341621.1:p.Asp376Gly
NM_001354693.2:c.1271A>G NP_001341622.1:p.Asp424Gly
NM_001354694.2:c.1187A>G NP_001341623.1:p.Asp396Gly
NM_001354695.2:c.1028A>G NP_001341624.1:p.Asp343Gly
NR_148940.2:n.1814A>G
NR_148941.2:n.1760A>G
NR_148942.2:n.1699A>G
NM_001354690.3:c.1370A>G NP_001341619.1:p.Asp457Gly
NM_001354691.3:c.1127A>G NP_001341620.1:p.Asp376Gly
NM_001354692.3:c.1127A>G NP_001341621.1:p.Asp376Gly
NM_001354693.3:c.1271A>G NP_001341622.1:p.Asp424Gly
NM_001354694.3:c.1187A>G NP_001341623.1:p.Asp396Gly
NM_001354695.3:c.1028A>G NP_001341624.1:p.Asp343Gly
NM_002880.4:c.1370A>G MANE Select NP_002871.1:p.Asp457Gly
NR_148940.3:n.1814A>G
NR_148941.3:n.1760A>G
NR_148942.3:n.1699A>G