Canonical Allele Identifier: CA351512400
Gene: RAF1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12604191G>C , CM000665.2:g.12604191G>C GRCh38
NC_000003.11:g.12645690G>C , CM000665.1:g.12645690G>C GRCh37
NC_000003.10:g.12620690G>C NCBI36
NG_007467.1:g.64989C>G , LRG_413:g.64989C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000251849.9:c.779C>G ENSP00000251849.4:p.Thr260Arg
ENST00000442415.7:c.779C>G MANE Select ENSP00000401888.2:p.Thr260Arg
ENST00000251849.8:c.779C>G ENSP00000251849.4:p.Thr260Arg
ENST00000416093.1:c.*357C>G ENSP00000391265.1:p.=
ENST00000423275.5:c.*456C>G ENSP00000401088.1:p.=
ENST00000432427.2:n.416C>G ENSP00000398591.2:p.Thr139Arg
ENST00000442415.6:c.779C>G ENSP00000401888.2:p.Thr260Arg
ENST00000465826.5:n.23C>G
ENST00000491290.1:n.300C>G
NM_002880.3:c.779C>G , LRG_413t1:c.779C>G NP_002871.1:p.Thr260Arg
XM_005265355.1:c.779C>G XP_005265412.1:p.Thr260Arg
XM_005265357.1:c.680C>G XP_005265414.1:p.Thr227Arg
XM_005265358.3:c.536C>G XP_005265415.1:p.Thr179Arg
XM_005265359.3:c.437C>G XP_005265416.1:p.Thr146Arg
XM_005265360.1:c.779C>G XP_005265417.1:p.Thr260Arg
XM_011533974.1:c.779C>G XP_011532276.1:p.Thr260Arg
XM_011533975.1:c.536C>G XP_011532277.1:p.Thr179Arg
NM_001354689.1:c.779C>G NP_001341618.1:p.Thr260Arg
NM_001354690.1:c.779C>G NP_001341619.1:p.Thr260Arg
NM_001354691.1:c.536C>G NP_001341620.1:p.Thr179Arg
NM_001354692.1:c.536C>G NP_001341621.1:p.Thr179Arg
NM_001354693.1:c.680C>G NP_001341622.1:p.Thr227Arg
NM_001354694.1:c.536C>G NP_001341623.1:p.Thr179Arg
NM_001354695.1:c.437C>G NP_001341624.1:p.Thr146Arg
NR_148940.1:n.1194C>G
NR_148941.1:n.1194C>G
NR_148942.1:n.1194C>G
XM_011533974.3:c.779C>G XP_011532276.1:p.Thr260Arg
XM_017006966.1:c.680C>G XP_016862455.1:p.Thr227Arg
XR_001740227.1:n.1011C>G
NM_001354689.3:c.779C>G MANE Select NP_001341618.1:p.Thr260Arg
NM_001354690.2:c.779C>G NP_001341619.1:p.Thr260Arg
NM_001354691.2:c.536C>G NP_001341620.1:p.Thr179Arg
NM_001354692.2:c.536C>G NP_001341621.1:p.Thr179Arg
NM_001354693.2:c.680C>G NP_001341622.1:p.Thr227Arg
NM_001354694.2:c.536C>G NP_001341623.1:p.Thr179Arg
NM_001354695.2:c.437C>G NP_001341624.1:p.Thr146Arg
NR_148940.2:n.1110C>G
NR_148941.2:n.1110C>G
NR_148942.2:n.1110C>G
NM_001354690.3:c.779C>G NP_001341619.1:p.Thr260Arg
NM_001354691.3:c.536C>G NP_001341620.1:p.Thr179Arg
NM_001354692.3:c.536C>G NP_001341621.1:p.Thr179Arg
NM_001354693.3:c.680C>G NP_001341622.1:p.Thr227Arg
NM_001354694.3:c.536C>G NP_001341623.1:p.Thr179Arg
NM_001354695.3:c.437C>G NP_001341624.1:p.Thr146Arg
NM_002880.4:c.779C>G NP_002871.1:p.Thr260Arg
NR_148940.3:n.1110C>G
NR_148941.3:n.1110C>G
NR_148942.3:n.1110C>G