Canonical Allele Identifier: CA351508108
Gene: RAF1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.12641650C>A (hg19) chr3:g.12600151C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12600151C>A , CM000665.2:g.12600151C>A GRCh38
NC_000003.11:g.12641650C>A , CM000665.1:g.12641650C>A GRCh37
NC_000003.10:g.12616650C>A NCBI36
NG_007467.1:g.69029G>T , LRG_413:g.69029G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000423275.6:c.*655+1G>T ENSP00000401088.1:n.*655+1G>T
ENST00000432427.3:c.310+1G>T
ENST00000465826.6:n.581+1G>T
ENST00000491290.2:n.1367+1G>T
ENST00000684903.1:c.*667+1G>T ENSP00000508612.1:n.*667+1G>T
ENST00000685348.1:c.*667+1G>T ENSP00000510285.1:n.*667+1G>T
ENST00000685437.1:c.891+1G>T ENSP00000508794.1:n.891+1G>T
ENST00000685653.1:c.990+1G>T ENSP00000509968.1:n.990+1G>T
ENST00000685738.1:c.990+1G>T ENSP00000510156.1:n.990+1G>T
ENST00000686409.1:n.1699G>T
ENST00000686455.1:n.1353+1G>T
ENST00000686479.1:n.1361+1G>T
ENST00000686762.1:c.990+1G>T ENSP00000509767.1:n.990+1G>T
ENST00000687257.1:n.1226+1G>T
ENST00000687326.1:c.990+1G>T ENSP00000509665.1:n.990+1G>T
ENST00000687486.1:c.182+237G>T
ENST00000687505.1:n.1108+1G>T
ENST00000687923.1:c.891+1G>T ENSP00000510255.1:n.891+1G>T
ENST00000687940.1:n.1367+1G>T
ENST00000688269.1:n.1586+1G>T
ENST00000688326.1:c.310+1G>T
ENST00000688444.1:n.1316+1G>T
ENST00000688543.1:c.891+1G>T ENSP00000509612.1:n.891+1G>T
ENST00000688625.1:c.*568+1G>T ENSP00000509522.1:n.*568+1G>T
ENST00000688803.1:n.1221+1G>T
ENST00000689097.1:c.*667+1G>T ENSP00000509756.1:n.*667+1G>T
ENST00000689389.1:c.990+1G>T ENSP00000510213.1:n.990+1G>T
ENST00000689418.1:c.*667+1G>T ENSP00000509467.1:n.*667+1G>T
ENST00000689481.1:c.*667+1G>T ENSP00000510248.1:n.*667+1G>T
ENST00000689540.1:n.1140+1G>T
ENST00000689876.1:c.990+1G>T ENSP00000508535.1:n.990+1G>T
ENST00000689914.1:c.990+1G>T ENSP00000509847.1:n.990+1G>T
ENST00000690397.1:c.879+1G>T ENSP00000508730.1:n.879+1G>T
ENST00000690460.1:c.978+1G>T ENSP00000509106.1:n.978+1G>T
ENST00000690625.1:n.1293+1G>T
ENST00000691268.1:c.417+1G>T
ENST00000691396.1:c.*783+1G>T ENSP00000510712.1:n.*783+1G>T
ENST00000691724.1:c.990+1G>T ENSP00000509255.1:n.990+1G>T
ENST00000691779.1:c.*568+1G>T ENSP00000508592.1:n.*568+1G>T
ENST00000691899.1:c.990+1G>T ENSP00000508763.1:n.990+1G>T
ENST00000692069.1:n.1214G>T
ENST00000692093.1:c.891+1G>T ENSP00000509669.1:n.891+1G>T
ENST00000692311.1:n.1472G>T
ENST00000692558.1:n.1355+1G>T
ENST00000692773.1:c.*727+1G>T ENSP00000509055.1:n.*727+1G>T
ENST00000692830.1:c.*735+1G>T ENSP00000509461.1:n.*735+1G>T
ENST00000693069.1:c.891+1G>T ENSP00000510072.1:n.891+1G>T
ENST00000693312.1:c.765+1G>T ENSP00000508686.1:n.765+1G>T
ENST00000693664.1:c.990+1G>T ENSP00000509614.1:n.990+1G>T
ENST00000693705.1:c.*667+1G>T ENSP00000510697.1:n.*667+1G>T
ENST00000251849.9:c.990+1G>T MANE Select ENSP00000251849.4:n.990+1G>T
ENST00000442415.7:c.1050+1G>T ENSP00000401888.2:n.1050+1G>T
ENST00000251849.8:c.990+1G>T ENSP00000251849.4:n.990+1G>T
ENST00000423275.5:c.*667+1G>T ENSP00000401088.1:n.*667+1G>T
ENST00000432427.2:c.627+1G>T ENSP00000398591.2:n.627+1G>T
ENST00000442415.6:c.1050+1G>T ENSP00000401888.2:n.1050+1G>T
ENST00000465826.5:n.234+1G>T
NM_002880.3:c.990+1G>T , LRG_413t1:c.990+1G>T NP_002871.1:n.990+1G>T
XM_005265355.1:c.990+1G>T XP_005265412.1:n.990+1G>T
XM_005265357.1:c.891+1G>T XP_005265414.1:n.891+1G>T
XM_005265358.3:c.747+1G>T XP_005265415.1:n.747+1G>T
XM_005265359.3:c.648+1G>T XP_005265416.1:n.648+1G>T
XM_005265360.1:c.990+1G>T XP_005265417.1:n.990+1G>T
XM_011533974.1:c.990+1G>T XP_011532276.1:n.990+1G>T
XM_011533975.1:c.747+1G>T XP_011532277.1:n.747+1G>T
NM_001354689.1:c.1050+1G>T NP_001341618.1:n.1050+1G>T
NM_001354690.1:c.990+1G>T NP_001341619.1:n.990+1G>T
NM_001354691.1:c.747+1G>T NP_001341620.1:n.747+1G>T
NM_001354692.1:c.747+1G>T NP_001341621.1:n.747+1G>T
NM_001354693.1:c.891+1G>T NP_001341622.1:n.891+1G>T
NM_001354694.1:c.807+1G>T NP_001341623.1:n.807+1G>T
NM_001354695.1:c.648+1G>T NP_001341624.1:n.648+1G>T
NR_148940.1:n.1405+1G>T
NR_148941.1:n.1405+1G>T
NR_148942.1:n.1405+1G>T
XM_011533974.3:c.990+1G>T XP_011532276.1:n.990+1G>T
XM_017006966.1:c.891+1G>T XP_016862455.1:n.891+1G>T
XR_001740227.1:n.1222+1G>T
NM_001354689.3:c.1050+1G>T NP_001341618.1:n.1050+1G>T
NM_001354690.2:c.990+1G>T NP_001341619.1:n.990+1G>T
NM_001354691.2:c.747+1G>T NP_001341620.1:n.747+1G>T
NM_001354692.2:c.747+1G>T NP_001341621.1:n.747+1G>T
NM_001354693.2:c.891+1G>T NP_001341622.1:n.891+1G>T
NM_001354694.2:c.807+1G>T NP_001341623.1:n.807+1G>T
NM_001354695.2:c.648+1G>T NP_001341624.1:n.648+1G>T
NR_148940.2:n.1321+1G>T
NR_148941.2:n.1321+1G>T
NR_148942.2:n.1321+1G>T
NM_001354690.3:c.990+1G>T NP_001341619.1:n.990+1G>T
NM_001354691.3:c.747+1G>T NP_001341620.1:n.747+1G>T
NM_001354692.3:c.747+1G>T NP_001341621.1:n.747+1G>T
NM_001354693.3:c.891+1G>T NP_001341622.1:n.891+1G>T
NM_001354694.3:c.807+1G>T NP_001341623.1:n.807+1G>T
NM_001354695.3:c.648+1G>T NP_001341624.1:n.648+1G>T
NM_002880.4:c.990+1G>T MANE Select NP_002871.1:n.990+1G>T
NR_148940.3:n.1321+1G>T
NR_148941.3:n.1321+1G>T
NR_148942.3:n.1321+1G>T
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