Canonical Allele Identifier: CA351502207
Gene: RAF1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12590899C>G , CM000665.2:g.12590899C>G GRCh38
NC_000003.11:g.12632398C>G , CM000665.1:g.12632398C>G GRCh37
NC_000003.10:g.12607398C>G NCBI36
NG_007467.1:g.78281G>C , LRG_413:g.78281G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000251849.9:c.1269G>C ENSP00000251849.4:p.Trp423Cys
ENST00000442415.7:c.1329G>C MANE Select ENSP00000401888.2:p.Trp443Cys
ENST00000251849.8:c.1269G>C ENSP00000251849.4:p.Trp423Cys
ENST00000423275.5:c.*946G>C ENSP00000401088.1:p.=
ENST00000432427.2:n.906G>C ENSP00000398591.2:p.Trp302Cys
ENST00000442415.6:c.1329G>C ENSP00000401888.2:p.Trp443Cys
ENST00000460610.1:n.226G>C
ENST00000465826.5:n.626G>C
ENST00000475353.1:n.437G>C
ENST00000494557.1:n.285G>C
NM_002880.3:c.1269G>C , LRG_413t1:c.1269G>C NP_002871.1:p.Trp423Cys
XM_005265355.1:c.1269G>C XP_005265412.1:p.Trp423Cys
XM_005265357.1:c.1170G>C XP_005265414.1:p.Trp390Cys
XM_005265358.3:c.1026G>C XP_005265415.1:p.Trp342Cys
XM_005265359.3:c.927G>C XP_005265416.1:p.Trp309Cys
XM_005265360.1:c.1269G>C XP_005265417.1:p.Trp423Cys
XM_011533974.1:c.1269G>C XP_011532276.1:p.Trp423Cys
XM_011533975.1:c.1026G>C XP_011532277.1:p.Trp342Cys
NM_001354689.1:c.1329G>C NP_001341618.1:p.Trp443Cys
NM_001354690.1:c.1269G>C NP_001341619.1:p.Trp423Cys
NM_001354691.1:c.1026G>C NP_001341620.1:p.Trp342Cys
NM_001354692.1:c.1026G>C NP_001341621.1:p.Trp342Cys
NM_001354693.1:c.1170G>C NP_001341622.1:p.Trp390Cys
NM_001354694.1:c.1086G>C NP_001341623.1:p.Trp362Cys
NM_001354695.1:c.927G>C NP_001341624.1:p.Trp309Cys
NR_148940.1:n.1797G>C
NR_148941.1:n.1743G>C
NR_148942.1:n.1682G>C
XM_011533974.3:c.1269G>C XP_011532276.1:p.Trp423Cys
XM_017006966.1:c.1170G>C XP_016862455.1:p.Trp390Cys
NM_001354689.3:c.1329G>C MANE Select NP_001341618.1:p.Trp443Cys
NM_001354690.2:c.1269G>C NP_001341619.1:p.Trp423Cys
NM_001354691.2:c.1026G>C NP_001341620.1:p.Trp342Cys
NM_001354692.2:c.1026G>C NP_001341621.1:p.Trp342Cys
NM_001354693.2:c.1170G>C NP_001341622.1:p.Trp390Cys
NM_001354694.2:c.1086G>C NP_001341623.1:p.Trp362Cys
NM_001354695.2:c.927G>C NP_001341624.1:p.Trp309Cys
NR_148940.2:n.1713G>C
NR_148941.2:n.1659G>C
NR_148942.2:n.1598G>C
NM_001354690.3:c.1269G>C NP_001341619.1:p.Trp423Cys
NM_001354691.3:c.1026G>C NP_001341620.1:p.Trp342Cys
NM_001354692.3:c.1026G>C NP_001341621.1:p.Trp342Cys
NM_001354693.3:c.1170G>C NP_001341622.1:p.Trp390Cys
NM_001354694.3:c.1086G>C NP_001341623.1:p.Trp362Cys
NM_001354695.3:c.927G>C NP_001341624.1:p.Trp309Cys
NM_002880.4:c.1269G>C NP_002871.1:p.Trp423Cys
NR_148940.3:n.1713G>C
NR_148941.3:n.1659G>C
NR_148942.3:n.1598G>C