Canonical Allele Identifier: CA261628
Gene: RAF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 44634
dbSNP Id: rs397516829

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12604184A>T , CM000665.2:g.12604184A>T GRCh38
NC_000003.11:g.12645683A>T , CM000665.1:g.12645683A>T GRCh37
NC_000003.10:g.12620683A>T NCBI36
NG_007467.1:g.64996T>A , LRG_413:g.64996T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000251849.9:c.786T>A ENSP00000251849.4:p.Asn262Lys
ENST00000442415.7:c.786T>A MANE Select ENSP00000401888.2:p.Asn262Lys
ENST00000251849.8:c.786T>A ENSP00000251849.4:p.Asn262Lys
ENST00000416093.1:c.*364T>A ENSP00000391265.1:p.=
ENST00000423275.5:c.*463T>A ENSP00000401088.1:p.=
ENST00000432427.2:n.423T>A ENSP00000398591.2:p.Asn141Lys
ENST00000442415.6:c.786T>A ENSP00000401888.2:p.Asn262Lys
ENST00000465826.5:n.30T>A
ENST00000491290.1:n.307T>A
NM_002880.3:c.786T>A , LRG_413t1:c.786T>A NP_002871.1:p.Asn262Lys
XM_005265355.1:c.786T>A XP_005265412.1:p.Asn262Lys
XM_005265357.1:c.687T>A XP_005265414.1:p.Asn229Lys
XM_005265358.3:c.543T>A XP_005265415.1:p.Asn181Lys
XM_005265359.3:c.444T>A XP_005265416.1:p.Asn148Lys
XM_005265360.1:c.786T>A XP_005265417.1:p.Asn262Lys
XM_011533974.1:c.786T>A XP_011532276.1:p.Asn262Lys
XM_011533975.1:c.543T>A XP_011532277.1:p.Asn181Lys
NM_001354689.1:c.786T>A NP_001341618.1:p.Asn262Lys
NM_001354690.1:c.786T>A NP_001341619.1:p.Asn262Lys
NM_001354691.1:c.543T>A NP_001341620.1:p.Asn181Lys
NM_001354692.1:c.543T>A NP_001341621.1:p.Asn181Lys
NM_001354693.1:c.687T>A NP_001341622.1:p.Asn229Lys
NM_001354694.1:c.543T>A NP_001341623.1:p.Asn181Lys
NM_001354695.1:c.444T>A NP_001341624.1:p.Asn148Lys
NR_148940.1:n.1201T>A
NR_148941.1:n.1201T>A
NR_148942.1:n.1201T>A
XM_011533974.3:c.786T>A XP_011532276.1:p.Asn262Lys
XM_017006966.1:c.687T>A XP_016862455.1:p.Asn229Lys
XR_001740227.1:n.1018T>A
NM_001354689.3:c.786T>A MANE Select NP_001341618.1:p.Asn262Lys
NM_001354690.2:c.786T>A NP_001341619.1:p.Asn262Lys
NM_001354691.2:c.543T>A NP_001341620.1:p.Asn181Lys
NM_001354692.2:c.543T>A NP_001341621.1:p.Asn181Lys
NM_001354693.2:c.687T>A NP_001341622.1:p.Asn229Lys
NM_001354694.2:c.543T>A NP_001341623.1:p.Asn181Lys
NM_001354695.2:c.444T>A NP_001341624.1:p.Asn148Lys
NR_148940.2:n.1117T>A
NR_148941.2:n.1117T>A
NR_148942.2:n.1117T>A
NM_001354690.3:c.786T>A NP_001341619.1:p.Asn262Lys
NM_001354691.3:c.543T>A NP_001341620.1:p.Asn181Lys
NM_001354692.3:c.543T>A NP_001341621.1:p.Asn181Lys
NM_001354693.3:c.687T>A NP_001341622.1:p.Asn229Lys
NM_001354694.3:c.543T>A NP_001341623.1:p.Asn181Lys
NM_001354695.3:c.444T>A NP_001341624.1:p.Asn148Lys
NM_002880.4:c.786T>A NP_002871.1:p.Asn262Lys
NR_148940.3:n.1117T>A
NR_148941.3:n.1117T>A
NR_148942.3:n.1117T>A