Canonical Allele Identifier: CA261612
Gene: RAF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 21342
dbSNP Id: rs80338799

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000251849.9:c.1472C>T ENSP00000251849.4:p.Thr491Ile
ENST00000442415.7:c.1532C>T MANE Select ENSP00000401888.2:p.Thr511Ile
ENST00000676541.1:c.*3492G>A ENSP00000503730.1:p.=
ENST00000677142.1:c.*3492G>A ENSP00000504455.1:p.=
ENST00000677816.1:c.*2047G>A ENSP00000502893.1:p.=
ENST00000677941.1:n.3555G>A
ENST00000251849.8:c.1472C>T ENSP00000251849.4:p.Thr491Ile
ENST00000423275.5:c.*1149C>T ENSP00000401088.1:p.=
ENST00000432427.2:n.1109C>T ENSP00000398591.2:p.Thr370Ile
ENST00000442415.6:c.1532C>T ENSP00000401888.2:p.Thr511Ile
ENST00000471449.1:n.161C>T
NM_002880.3:c.1472C>T , LRG_413t1:c.1472C>T NP_002871.1:p.Thr491Ile
XM_005265355.1:c.1472C>T XP_005265412.1:p.Thr491Ile
XM_005265357.1:c.1373C>T XP_005265414.1:p.Thr458Ile
XM_005265358.3:c.1229C>T XP_005265415.1:p.Thr410Ile
XM_005265359.3:c.1130C>T XP_005265416.1:p.Thr377Ile
XM_005265360.1:c.1418-339C>T XP_005265417.1:p.=
XM_011533974.1:c.1472C>T XP_011532276.1:p.Thr491Ile
XM_011533975.1:c.1229C>T XP_011532277.1:p.Thr410Ile
NM_001354689.1:c.1532C>T NP_001341618.1:p.Thr511Ile
NM_001354690.1:c.1472C>T NP_001341619.1:p.Thr491Ile
NM_001354691.1:c.1229C>T NP_001341620.1:p.Thr410Ile
NM_001354692.1:c.1229C>T NP_001341621.1:p.Thr410Ile
NM_001354693.1:c.1373C>T NP_001341622.1:p.Thr458Ile
NM_001354694.1:c.1289C>T NP_001341623.1:p.Thr430Ile
NM_001354695.1:c.1130C>T NP_001341624.1:p.Thr377Ile
NR_148940.1:n.2000C>T
NR_148941.1:n.1946C>T
NR_148942.1:n.1885C>T
XM_011533974.3:c.1472C>T XP_011532276.1:p.Thr491Ile
XM_017006966.1:c.1373C>T XP_016862455.1:p.Thr458Ile
NM_001354689.3:c.1532C>T MANE Select NP_001341618.1:p.Thr511Ile
NM_001354690.2:c.1472C>T NP_001341619.1:p.Thr491Ile
NM_001354691.2:c.1229C>T NP_001341620.1:p.Thr410Ile
NM_001354692.2:c.1229C>T NP_001341621.1:p.Thr410Ile
NM_001354693.2:c.1373C>T NP_001341622.1:p.Thr458Ile
NM_001354694.2:c.1289C>T NP_001341623.1:p.Thr430Ile
NM_001354695.2:c.1130C>T NP_001341624.1:p.Thr377Ile
NR_148940.2:n.1916C>T
NR_148941.2:n.1862C>T
NR_148942.2:n.1801C>T
NM_001354690.3:c.1472C>T NP_001341619.1:p.Thr491Ile
NM_001354691.3:c.1229C>T NP_001341620.1:p.Thr410Ile
NM_001354692.3:c.1229C>T NP_001341621.1:p.Thr410Ile
NM_001354693.3:c.1373C>T NP_001341622.1:p.Thr458Ile
NM_001354694.3:c.1289C>T NP_001341623.1:p.Thr430Ile
NM_001354695.3:c.1130C>T NP_001341624.1:p.Thr377Ile
NM_002880.4:c.1472C>T NP_002871.1:p.Thr491Ile
NR_148940.3:n.1916C>T
NR_148941.3:n.1862C>T
NR_148942.3:n.1801C>T