Canonical Allele Identifier: CA261626
Gene: RAF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 40605
dbSNP Id: rs121434594

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12604189G>C , CM000665.2:g.12604189G>C GRCh38
NC_000003.11:g.12645688G>C , CM000665.1:g.12645688G>C GRCh37
NC_000003.10:g.12620688G>C NCBI36
NG_007467.1:g.64991C>G , LRG_413:g.64991C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000251849.9:c.781C>G ENSP00000251849.4:p.Pro261Ala
ENST00000442415.7:c.781C>G MANE Select ENSP00000401888.2:p.Pro261Ala
ENST00000251849.8:c.781C>G ENSP00000251849.4:p.Pro261Ala
ENST00000416093.1:c.*359C>G ENSP00000391265.1:p.=
ENST00000423275.5:c.*458C>G ENSP00000401088.1:p.=
ENST00000432427.2:n.418C>G ENSP00000398591.2:p.Pro140Ala
ENST00000442415.6:c.781C>G ENSP00000401888.2:p.Pro261Ala
ENST00000465826.5:n.25C>G
ENST00000491290.1:n.302C>G
NM_002880.3:c.781C>G , LRG_413t1:c.781C>G NP_002871.1:p.Pro261Ala
XM_005265355.1:c.781C>G XP_005265412.1:p.Pro261Ala
XM_005265357.1:c.682C>G XP_005265414.1:p.Pro228Ala
XM_005265358.3:c.538C>G XP_005265415.1:p.Pro180Ala
XM_005265359.3:c.439C>G XP_005265416.1:p.Pro147Ala
XM_005265360.1:c.781C>G XP_005265417.1:p.Pro261Ala
XM_011533974.1:c.781C>G XP_011532276.1:p.Pro261Ala
XM_011533975.1:c.538C>G XP_011532277.1:p.Pro180Ala
NM_001354689.1:c.781C>G NP_001341618.1:p.Pro261Ala
NM_001354690.1:c.781C>G NP_001341619.1:p.Pro261Ala
NM_001354691.1:c.538C>G NP_001341620.1:p.Pro180Ala
NM_001354692.1:c.538C>G NP_001341621.1:p.Pro180Ala
NM_001354693.1:c.682C>G NP_001341622.1:p.Pro228Ala
NM_001354694.1:c.538C>G NP_001341623.1:p.Pro180Ala
NM_001354695.1:c.439C>G NP_001341624.1:p.Pro147Ala
NR_148940.1:n.1196C>G
NR_148941.1:n.1196C>G
NR_148942.1:n.1196C>G
XM_011533974.3:c.781C>G XP_011532276.1:p.Pro261Ala
XM_017006966.1:c.682C>G XP_016862455.1:p.Pro228Ala
XR_001740227.1:n.1013C>G
NM_001354689.3:c.781C>G MANE Select NP_001341618.1:p.Pro261Ala
NM_001354690.2:c.781C>G NP_001341619.1:p.Pro261Ala
NM_001354691.2:c.538C>G NP_001341620.1:p.Pro180Ala
NM_001354692.2:c.538C>G NP_001341621.1:p.Pro180Ala
NM_001354693.2:c.682C>G NP_001341622.1:p.Pro228Ala
NM_001354694.2:c.538C>G NP_001341623.1:p.Pro180Ala
NM_001354695.2:c.439C>G NP_001341624.1:p.Pro147Ala
NR_148940.2:n.1112C>G
NR_148941.2:n.1112C>G
NR_148942.2:n.1112C>G
NM_001354690.3:c.781C>G NP_001341619.1:p.Pro261Ala
NM_001354691.3:c.538C>G NP_001341620.1:p.Pro180Ala
NM_001354692.3:c.538C>G NP_001341621.1:p.Pro180Ala
NM_001354693.3:c.682C>G NP_001341622.1:p.Pro228Ala
NM_001354694.3:c.538C>G NP_001341623.1:p.Pro180Ala
NM_001354695.3:c.439C>G NP_001341624.1:p.Pro147Ala
NM_002880.4:c.781C>G NP_002871.1:p.Pro261Ala
NR_148940.3:n.1112C>G
NR_148941.3:n.1112C>G
NR_148942.3:n.1112C>G