Canonical Allele Identifier: CA257064
Gene: RAF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 13959
dbSNP Id: rs80338799

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12585745G>C , CM000665.2:g.12585745G>C GRCh38
NC_000003.11:g.12627244G>C , CM000665.1:g.12627244G>C GRCh37
NC_000003.10:g.12602244G>C NCBI36
NG_007467.1:g.83435C>G , LRG_413:g.83435C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000251849.9:c.1472C>G ENSP00000251849.4:p.Thr491Arg
ENST00000442415.7:c.1532C>G MANE Select ENSP00000401888.2:p.Thr511Arg
ENST00000676541.1:c.*3492G>C ENSP00000503730.1:p.=
ENST00000677142.1:c.*3492G>C ENSP00000504455.1:p.=
ENST00000677816.1:c.*2047G>C ENSP00000502893.1:p.=
ENST00000677941.1:n.3555G>C
ENST00000251849.8:c.1472C>G ENSP00000251849.4:p.Thr491Arg
ENST00000423275.5:c.*1149C>G ENSP00000401088.1:p.=
ENST00000432427.2:n.1109C>G ENSP00000398591.2:p.Thr370Arg
ENST00000442415.6:c.1532C>G ENSP00000401888.2:p.Thr511Arg
ENST00000471449.1:n.161C>G
NM_002880.3:c.1472C>G , LRG_413t1:c.1472C>G NP_002871.1:p.Thr491Arg
XM_005265355.1:c.1472C>G XP_005265412.1:p.Thr491Arg
XM_005265357.1:c.1373C>G XP_005265414.1:p.Thr458Arg
XM_005265358.3:c.1229C>G XP_005265415.1:p.Thr410Arg
XM_005265359.3:c.1130C>G XP_005265416.1:p.Thr377Arg
XM_005265360.1:c.1418-339C>G XP_005265417.1:p.=
XM_011533974.1:c.1472C>G XP_011532276.1:p.Thr491Arg
XM_011533975.1:c.1229C>G XP_011532277.1:p.Thr410Arg
NM_001354689.1:c.1532C>G NP_001341618.1:p.Thr511Arg
NM_001354690.1:c.1472C>G NP_001341619.1:p.Thr491Arg
NM_001354691.1:c.1229C>G NP_001341620.1:p.Thr410Arg
NM_001354692.1:c.1229C>G NP_001341621.1:p.Thr410Arg
NM_001354693.1:c.1373C>G NP_001341622.1:p.Thr458Arg
NM_001354694.1:c.1289C>G NP_001341623.1:p.Thr430Arg
NM_001354695.1:c.1130C>G NP_001341624.1:p.Thr377Arg
NR_148940.1:n.2000C>G
NR_148941.1:n.1946C>G
NR_148942.1:n.1885C>G
XM_011533974.3:c.1472C>G XP_011532276.1:p.Thr491Arg
XM_017006966.1:c.1373C>G XP_016862455.1:p.Thr458Arg
NM_001354689.3:c.1532C>G MANE Select NP_001341618.1:p.Thr511Arg
NM_001354690.2:c.1472C>G NP_001341619.1:p.Thr491Arg
NM_001354691.2:c.1229C>G NP_001341620.1:p.Thr410Arg
NM_001354692.2:c.1229C>G NP_001341621.1:p.Thr410Arg
NM_001354693.2:c.1373C>G NP_001341622.1:p.Thr458Arg
NM_001354694.2:c.1289C>G NP_001341623.1:p.Thr430Arg
NM_001354695.2:c.1130C>G NP_001341624.1:p.Thr377Arg
NR_148940.2:n.1916C>G
NR_148941.2:n.1862C>G
NR_148942.2:n.1801C>G
NM_001354690.3:c.1472C>G NP_001341619.1:p.Thr491Arg
NM_001354691.3:c.1229C>G NP_001341620.1:p.Thr410Arg
NM_001354692.3:c.1229C>G NP_001341621.1:p.Thr410Arg
NM_001354693.3:c.1373C>G NP_001341622.1:p.Thr458Arg
NM_001354694.3:c.1289C>G NP_001341623.1:p.Thr430Arg
NM_001354695.3:c.1130C>G NP_001341624.1:p.Thr377Arg
NM_002880.4:c.1472C>G NP_002871.1:p.Thr491Arg
NR_148940.3:n.1916C>G
NR_148941.3:n.1862C>G
NR_148942.3:n.1801C>G