Canonical Allele Identifier: CA134696
Gene: RAF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 44619
dbSNP Id: rs147547744
gnomAD v4: 3-12590854-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12590854G>A , CM000665.2:g.12590854G>A GRCh38
NC_000003.11:g.12632353G>A , CM000665.1:g.12632353G>A GRCh37
NC_000003.10:g.12607353G>A NCBI36
NG_007467.1:g.78326C>T , LRG_413:g.78326C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000423275.6:c.*979C>T ENSP00000401088.1:n.*979C>T
ENST00000432427.3:c.631C>T
ENST00000460610.2:n.108C>T
ENST00000465826.6:n.905C>T
ENST00000475353.2:n.1236C>T
ENST00000494557.2:n.1125C>T
ENST00000684903.1:c.*991C>T ENSP00000508612.1:n.*991C>T
ENST00000685348.1:c.*991C>T ENSP00000510285.1:n.*991C>T
ENST00000685437.1:c.1215C>T ENSP00000508794.1:p.Thr405=
ENST00000685653.1:c.1314C>T ENSP00000509968.1:p.Thr438=
ENST00000685738.1:c.*278C>T ENSP00000510156.1:n.*278C>T
ENST00000686409.1:n.2365C>T
ENST00000686455.1:n.1677C>T
ENST00000686762.1:c.1314C>T ENSP00000509767.1:p.Thr438=
ENST00000687257.1:n.1550C>T
ENST00000687326.1:c.*248C>T ENSP00000509665.1:n.*248C>T
ENST00000687505.1:n.1432C>T
ENST00000687923.1:c.1203C>T ENSP00000510255.1:p.Thr401=
ENST00000687940.1:n.1691C>T
ENST00000688269.1:n.1910C>T
ENST00000688326.1:c.747C>T
ENST00000688444.1:n.1640C>T
ENST00000688543.1:c.1215C>T ENSP00000509612.1:p.Thr405=
ENST00000688625.1:c.*892C>T ENSP00000509522.1:n.*892C>T
ENST00000688803.1:n.1545C>T
ENST00000688914.1:n.300C>T
ENST00000689097.1:c.*991C>T ENSP00000509756.1:n.*991C>T
ENST00000689389.1:c.1193+854C>T ENSP00000510213.1:n.1193+854C>T
ENST00000689418.1:c.*991C>T ENSP00000509467.1:n.*991C>T
ENST00000689481.1:c.*991C>T ENSP00000510248.1:n.*991C>T
ENST00000689540.1:n.1464C>T
ENST00000689876.1:c.1314C>T ENSP00000508535.1:p.Thr438=
ENST00000689914.1:c.*248C>T ENSP00000509847.1:n.*248C>T
ENST00000690397.1:c.1203C>T ENSP00000508730.1:p.Thr401=
ENST00000690460.1:c.1302C>T ENSP00000509106.1:p.Thr434=
ENST00000690585.1:c.206C>T
ENST00000690625.1:n.2350C>T
ENST00000691396.1:c.*1166C>T ENSP00000510712.1:n.*1166C>T
ENST00000691724.1:c.*271C>T ENSP00000509255.1:n.*271C>T
ENST00000691779.1:c.*892C>T ENSP00000508592.1:n.*892C>T
ENST00000691888.1:c.206C>T
ENST00000691899.1:c.1314C>T ENSP00000508763.1:p.Thr438=
ENST00000692069.1:n.1880C>T
ENST00000692093.1:c.1215C>T ENSP00000509669.1:p.Thr405=
ENST00000692311.1:n.2138C>T
ENST00000692558.1:n.1679C>T
ENST00000692773.1:c.*1051C>T ENSP00000509055.1:n.*1051C>T
ENST00000692830.1:c.*1059C>T ENSP00000509461.1:n.*1059C>T
ENST00000693069.1:c.*248C>T ENSP00000510072.1:n.*248C>T
ENST00000693312.1:c.1089C>T ENSP00000508686.1:p.Thr363=
ENST00000693664.1:c.1314C>T ENSP00000509614.1:p.Thr438=
ENST00000693705.1:c.*991C>T ENSP00000510697.1:n.*991C>T
ENST00000251849.9:c.1314C>T MANE Select ENSP00000251849.4:p.Thr438=
ENST00000442415.7:c.1374C>T ENSP00000401888.2:p.Thr458=
ENST00000251849.8:c.1314C>T ENSP00000251849.4:p.Thr438=
ENST00000423275.5:c.*991C>T ENSP00000401088.1:n.*991C>T
ENST00000432427.2:c.951C>T ENSP00000398591.2:p.Thr317=
ENST00000442415.6:c.1374C>T ENSP00000401888.2:p.Thr458=
ENST00000460610.1:n.271C>T
ENST00000465826.5:n.671C>T
ENST00000475353.1:n.482C>T
ENST00000494557.1:n.330C>T
NM_002880.3:c.1314C>T , LRG_413t1:c.1314C>T NP_002871.1:p.Thr438=
XM_005265355.1:c.1314C>T XP_005265412.1:p.Thr438=
XM_005265357.1:c.1215C>T XP_005265414.1:p.Thr405=
XM_005265358.3:c.1071C>T XP_005265415.1:p.Thr357=
XM_005265359.3:c.972C>T XP_005265416.1:p.Thr324=
XM_005265360.1:c.1314C>T XP_005265417.1:p.Thr438=
XM_011533974.1:c.1314C>T XP_011532276.1:p.Thr438=
XM_011533975.1:c.1071C>T XP_011532277.1:p.Thr357=
NM_001354689.1:c.1374C>T NP_001341618.1:p.Thr458=
NM_001354690.1:c.1314C>T NP_001341619.1:p.Thr438=
NM_001354691.1:c.1071C>T NP_001341620.1:p.Thr357=
NM_001354692.1:c.1071C>T NP_001341621.1:p.Thr357=
NM_001354693.1:c.1215C>T NP_001341622.1:p.Thr405=
NM_001354694.1:c.1131C>T NP_001341623.1:p.Thr377=
NM_001354695.1:c.972C>T NP_001341624.1:p.Thr324=
NR_148940.1:n.1842C>T
NR_148941.1:n.1788C>T
NR_148942.1:n.1727C>T
XM_011533974.3:c.1314C>T XP_011532276.1:p.Thr438=
XM_017006966.1:c.1215C>T XP_016862455.1:p.Thr405=
NM_001354689.3:c.1374C>T NP_001341618.1:p.Thr458=
NM_001354690.2:c.1314C>T NP_001341619.1:p.Thr438=
NM_001354691.2:c.1071C>T NP_001341620.1:p.Thr357=
NM_001354692.2:c.1071C>T NP_001341621.1:p.Thr357=
NM_001354693.2:c.1215C>T NP_001341622.1:p.Thr405=
NM_001354694.2:c.1131C>T NP_001341623.1:p.Thr377=
NM_001354695.2:c.972C>T NP_001341624.1:p.Thr324=
NR_148940.2:n.1758C>T
NR_148941.2:n.1704C>T
NR_148942.2:n.1643C>T
NM_001354690.3:c.1314C>T NP_001341619.1:p.Thr438=
NM_001354691.3:c.1071C>T NP_001341620.1:p.Thr357=
NM_001354692.3:c.1071C>T NP_001341621.1:p.Thr357=
NM_001354693.3:c.1215C>T NP_001341622.1:p.Thr405=
NM_001354694.3:c.1131C>T NP_001341623.1:p.Thr377=
NM_001354695.3:c.972C>T NP_001341624.1:p.Thr324=
NM_002880.4:c.1314C>T MANE Select NP_002871.1:p.Thr438=
NR_148940.3:n.1758C>T
NR_148941.3:n.1704C>T
NR_148942.3:n.1643C>T