Canonical Allele Identifier: CA351509557
Gene: RAF1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12600264A>C , CM000665.2:g.12600264A>C GRCh38
NC_000003.11:g.12641763A>C , CM000665.1:g.12641763A>C GRCh37
NC_000003.10:g.12616763A>C NCBI36
NG_007467.1:g.68916T>G , LRG_413:g.68916T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000423275.6:c.*543T>G ENSP00000401088.1:n.*543T>G
ENST00000432427.3:c.198T>G
ENST00000465826.6:n.469T>G
ENST00000491290.2:n.1255T>G
ENST00000684903.1:c.*555T>G ENSP00000508612.1:n.*555T>G
ENST00000685348.1:c.*555T>G ENSP00000510285.1:n.*555T>G
ENST00000685437.1:c.779T>G ENSP00000508794.1:p.Leu260Arg
ENST00000685438.1:n.642T>G
ENST00000685653.1:c.878T>G ENSP00000509968.1:p.Leu293Arg
ENST00000685738.1:c.878T>G ENSP00000510156.1:p.Leu293Arg
ENST00000686409.1:n.1586T>G
ENST00000686455.1:n.1241T>G
ENST00000686479.1:n.1249T>G
ENST00000686762.1:c.878T>G ENSP00000509767.1:p.Leu293Arg
ENST00000687257.1:n.1114T>G
ENST00000687326.1:c.878T>G ENSP00000509665.1:p.Leu293Arg
ENST00000687486.1:c.182+124T>G
ENST00000687505.1:n.996T>G
ENST00000687923.1:c.779T>G ENSP00000510255.1:p.Leu260Arg
ENST00000687940.1:n.1255T>G
ENST00000688269.1:n.1474T>G
ENST00000688326.1:c.198T>G
ENST00000688444.1:n.1204T>G
ENST00000688543.1:c.779T>G ENSP00000509612.1:p.Leu260Arg
ENST00000688625.1:c.*456T>G ENSP00000509522.1:n.*456T>G
ENST00000688803.1:n.1109T>G
ENST00000689097.1:c.*555T>G ENSP00000509756.1:n.*555T>G
ENST00000689389.1:c.878T>G ENSP00000510213.1:p.Leu293Arg
ENST00000689418.1:c.*555T>G ENSP00000509467.1:n.*555T>G
ENST00000689481.1:c.*555T>G ENSP00000510248.1:n.*555T>G
ENST00000689540.1:n.1028T>G
ENST00000689876.1:c.878T>G ENSP00000508535.1:p.Leu293Arg
ENST00000689914.1:c.878T>G ENSP00000509847.1:p.Leu293Arg
ENST00000690397.1:c.767T>G ENSP00000508730.1:p.Leu256Arg
ENST00000690460.1:c.866T>G ENSP00000509106.1:p.Leu289Arg
ENST00000690625.1:n.1181T>G
ENST00000691268.1:c.305T>G
ENST00000691396.1:c.*671T>G ENSP00000510712.1:n.*671T>G
ENST00000691724.1:c.878T>G ENSP00000509255.1:p.Leu293Arg
ENST00000691779.1:c.*456T>G ENSP00000508592.1:n.*456T>G
ENST00000691899.1:c.878T>G ENSP00000508763.1:p.Leu293Arg
ENST00000692069.1:n.1101T>G
ENST00000692093.1:c.779T>G ENSP00000509669.1:p.Leu260Arg
ENST00000692311.1:n.1359T>G
ENST00000692558.1:n.1243T>G
ENST00000692773.1:c.*615T>G ENSP00000509055.1:n.*615T>G
ENST00000692830.1:c.*623T>G ENSP00000509461.1:n.*623T>G
ENST00000693069.1:c.779T>G ENSP00000510072.1:p.Leu260Arg
ENST00000693312.1:c.653T>G ENSP00000508686.1:p.Leu218Arg
ENST00000693664.1:c.878T>G ENSP00000509614.1:p.Leu293Arg
ENST00000693705.1:c.*555T>G ENSP00000510697.1:n.*555T>G
ENST00000251849.9:c.878T>G MANE Select ENSP00000251849.4:p.Leu293Arg
ENST00000442415.7:c.938T>G ENSP00000401888.2:p.Leu313Arg
ENST00000251849.8:c.878T>G ENSP00000251849.4:p.Leu293Arg
ENST00000423275.5:c.*555T>G ENSP00000401088.1:n.*555T>G
ENST00000432427.2:c.515T>G ENSP00000398591.2:p.Leu172Arg
ENST00000442415.6:c.938T>G ENSP00000401888.2:p.Leu313Arg
ENST00000465826.5:n.122T>G
ENST00000491290.1:n.507T>G
NM_002880.3:c.878T>G , LRG_413t1:c.878T>G NP_002871.1:p.Leu293Arg
XM_005265355.1:c.878T>G XP_005265412.1:p.Leu293Arg
XM_005265357.1:c.779T>G XP_005265414.1:p.Leu260Arg
XM_005265358.3:c.635T>G XP_005265415.1:p.Leu212Arg
XM_005265359.3:c.536T>G XP_005265416.1:p.Leu179Arg
XM_005265360.1:c.878T>G XP_005265417.1:p.Leu293Arg
XM_011533974.1:c.878T>G XP_011532276.1:p.Leu293Arg
XM_011533975.1:c.635T>G XP_011532277.1:p.Leu212Arg
NM_001354689.1:c.938T>G NP_001341618.1:p.Leu313Arg
NM_001354690.1:c.878T>G NP_001341619.1:p.Leu293Arg
NM_001354691.1:c.635T>G NP_001341620.1:p.Leu212Arg
NM_001354692.1:c.635T>G NP_001341621.1:p.Leu212Arg
NM_001354693.1:c.779T>G NP_001341622.1:p.Leu260Arg
NM_001354694.1:c.695T>G NP_001341623.1:p.Leu232Arg
NM_001354695.1:c.536T>G NP_001341624.1:p.Leu179Arg
NR_148940.1:n.1293T>G
NR_148941.1:n.1293T>G
NR_148942.1:n.1293T>G
XM_011533974.3:c.878T>G XP_011532276.1:p.Leu293Arg
XM_017006966.1:c.779T>G XP_016862455.1:p.Leu260Arg
XR_001740227.1:n.1110T>G
NM_001354689.3:c.938T>G NP_001341618.1:p.Leu313Arg
NM_001354690.2:c.878T>G NP_001341619.1:p.Leu293Arg
NM_001354691.2:c.635T>G NP_001341620.1:p.Leu212Arg
NM_001354692.2:c.635T>G NP_001341621.1:p.Leu212Arg
NM_001354693.2:c.779T>G NP_001341622.1:p.Leu260Arg
NM_001354694.2:c.695T>G NP_001341623.1:p.Leu232Arg
NM_001354695.2:c.536T>G NP_001341624.1:p.Leu179Arg
NR_148940.2:n.1209T>G
NR_148941.2:n.1209T>G
NR_148942.2:n.1209T>G
NM_001354690.3:c.878T>G NP_001341619.1:p.Leu293Arg
NM_001354691.3:c.635T>G NP_001341620.1:p.Leu212Arg
NM_001354692.3:c.635T>G NP_001341621.1:p.Leu212Arg
NM_001354693.3:c.779T>G NP_001341622.1:p.Leu260Arg
NM_001354694.3:c.695T>G NP_001341623.1:p.Leu232Arg
NM_001354695.3:c.536T>G NP_001341624.1:p.Leu179Arg
NM_002880.4:c.878T>G MANE Select NP_002871.1:p.Leu293Arg
NR_148940.3:n.1209T>G
NR_148941.3:n.1209T>G
NR_148942.3:n.1209T>G