Canonical Allele Identifier: CA261623
Gene: RAF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 44632
ClinVar RCV Id: RCV000037700
dbSNP Id: rs397516826

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12604202C>G , CM000665.2:g.12604202C>G GRCh38
NC_000003.11:g.12645701C>G , CM000665.1:g.12645701C>G GRCh37
NC_000003.10:g.12620701C>G NCBI36
NG_007467.1:g.64978G>C , LRG_413:g.64978G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000251849.9:c.768G>C ENSP00000251849.4:p.Arg256Ser
ENST00000442415.7:c.768G>C MANE Select ENSP00000401888.2:p.Arg256Ser
ENST00000251849.8:c.768G>C ENSP00000251849.4:p.Arg256Ser
ENST00000416093.1:c.*346G>C ENSP00000391265.1:p.=
ENST00000423275.5:c.*445G>C ENSP00000401088.1:p.=
ENST00000432427.2:n.405G>C ENSP00000398591.2:p.Arg135Ser
ENST00000442415.6:c.768G>C ENSP00000401888.2:p.Arg256Ser
ENST00000465826.5:n.12G>C
ENST00000491290.1:n.289G>C
NM_002880.3:c.768G>C , LRG_413t1:c.768G>C NP_002871.1:p.Arg256Ser
XM_005265355.1:c.768G>C XP_005265412.1:p.Arg256Ser
XM_005265357.1:c.669G>C XP_005265414.1:p.Arg223Ser
XM_005265358.3:c.525G>C XP_005265415.1:p.Arg175Ser
XM_005265359.3:c.426G>C XP_005265416.1:p.Arg142Ser
XM_005265360.1:c.768G>C XP_005265417.1:p.Arg256Ser
XM_011533974.1:c.768G>C XP_011532276.1:p.Arg256Ser
XM_011533975.1:c.525G>C XP_011532277.1:p.Arg175Ser
NM_001354689.1:c.768G>C NP_001341618.1:p.Arg256Ser
NM_001354690.1:c.768G>C NP_001341619.1:p.Arg256Ser
NM_001354691.1:c.525G>C NP_001341620.1:p.Arg175Ser
NM_001354692.1:c.525G>C NP_001341621.1:p.Arg175Ser
NM_001354693.1:c.669G>C NP_001341622.1:p.Arg223Ser
NM_001354694.1:c.525G>C NP_001341623.1:p.Arg175Ser
NM_001354695.1:c.426G>C NP_001341624.1:p.Arg142Ser
NR_148940.1:n.1183G>C
NR_148941.1:n.1183G>C
NR_148942.1:n.1183G>C
XM_011533974.3:c.768G>C XP_011532276.1:p.Arg256Ser
XM_017006966.1:c.669G>C XP_016862455.1:p.Arg223Ser
XR_001740227.1:n.1000G>C
NM_001354689.3:c.768G>C MANE Select NP_001341618.1:p.Arg256Ser
NM_001354690.2:c.768G>C NP_001341619.1:p.Arg256Ser
NM_001354691.2:c.525G>C NP_001341620.1:p.Arg175Ser
NM_001354692.2:c.525G>C NP_001341621.1:p.Arg175Ser
NM_001354693.2:c.669G>C NP_001341622.1:p.Arg223Ser
NM_001354694.2:c.525G>C NP_001341623.1:p.Arg175Ser
NM_001354695.2:c.426G>C NP_001341624.1:p.Arg142Ser
NR_148940.2:n.1099G>C
NR_148941.2:n.1099G>C
NR_148942.2:n.1099G>C
NM_001354690.3:c.768G>C NP_001341619.1:p.Arg256Ser
NM_001354691.3:c.525G>C NP_001341620.1:p.Arg175Ser
NM_001354692.3:c.525G>C NP_001341621.1:p.Arg175Ser
NM_001354693.3:c.669G>C NP_001341622.1:p.Arg223Ser
NM_001354694.3:c.525G>C NP_001341623.1:p.Arg175Ser
NM_001354695.3:c.426G>C NP_001341624.1:p.Arg142Ser
NM_002880.4:c.768G>C NP_002871.1:p.Arg256Ser
NR_148940.3:n.1099G>C
NR_148941.3:n.1099G>C
NR_148942.3:n.1099G>C