Canonical Allele Identifier: CA351501612
Gene: RAF1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12590798T>A , CM000665.2:g.12590798T>A GRCh38
NC_000003.11:g.12632297T>A , CM000665.1:g.12632297T>A GRCh37
NC_000003.10:g.12607297T>A NCBI36
NG_007467.1:g.78382A>T , LRG_413:g.78382A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000251849.9:c.1370A>T ENSP00000251849.4:p.Asp457Val
ENST00000442415.7:c.1430A>T MANE Select ENSP00000401888.2:p.Asp477Val
ENST00000251849.8:c.1370A>T ENSP00000251849.4:p.Asp457Val
ENST00000423275.5:c.*1047A>T ENSP00000401088.1:p.=
ENST00000432427.2:n.1007A>T ENSP00000398591.2:p.Asp336Val
ENST00000442415.6:c.1430A>T ENSP00000401888.2:p.Asp477Val
ENST00000460610.1:n.327A>T
ENST00000465826.5:n.727A>T
ENST00000475353.1:n.538A>T
ENST00000494557.1:n.386A>T
NM_002880.3:c.1370A>T , LRG_413t1:c.1370A>T NP_002871.1:p.Asp457Val
XM_005265355.1:c.1370A>T XP_005265412.1:p.Asp457Val
XM_005265357.1:c.1271A>T XP_005265414.1:p.Asp424Val
XM_005265358.3:c.1127A>T XP_005265415.1:p.Asp376Val
XM_005265359.3:c.1028A>T XP_005265416.1:p.Asp343Val
XM_005265360.1:c.1370A>T XP_005265417.1:p.Asp457Val
XM_011533974.1:c.1370A>T XP_011532276.1:p.Asp457Val
XM_011533975.1:c.1127A>T XP_011532277.1:p.Asp376Val
NM_001354689.1:c.1430A>T NP_001341618.1:p.Asp477Val
NM_001354690.1:c.1370A>T NP_001341619.1:p.Asp457Val
NM_001354691.1:c.1127A>T NP_001341620.1:p.Asp376Val
NM_001354692.1:c.1127A>T NP_001341621.1:p.Asp376Val
NM_001354693.1:c.1271A>T NP_001341622.1:p.Asp424Val
NM_001354694.1:c.1187A>T NP_001341623.1:p.Asp396Val
NM_001354695.1:c.1028A>T NP_001341624.1:p.Asp343Val
NR_148940.1:n.1898A>T
NR_148941.1:n.1844A>T
NR_148942.1:n.1783A>T
XM_011533974.3:c.1370A>T XP_011532276.1:p.Asp457Val
XM_017006966.1:c.1271A>T XP_016862455.1:p.Asp424Val
NM_001354689.3:c.1430A>T MANE Select NP_001341618.1:p.Asp477Val
NM_001354690.2:c.1370A>T NP_001341619.1:p.Asp457Val
NM_001354691.2:c.1127A>T NP_001341620.1:p.Asp376Val
NM_001354692.2:c.1127A>T NP_001341621.1:p.Asp376Val
NM_001354693.2:c.1271A>T NP_001341622.1:p.Asp424Val
NM_001354694.2:c.1187A>T NP_001341623.1:p.Asp396Val
NM_001354695.2:c.1028A>T NP_001341624.1:p.Asp343Val
NR_148940.2:n.1814A>T
NR_148941.2:n.1760A>T
NR_148942.2:n.1699A>T
NM_001354690.3:c.1370A>T NP_001341619.1:p.Asp457Val
NM_001354691.3:c.1127A>T NP_001341620.1:p.Asp376Val
NM_001354692.3:c.1127A>T NP_001341621.1:p.Asp376Val
NM_001354693.3:c.1271A>T NP_001341622.1:p.Asp424Val
NM_001354694.3:c.1187A>T NP_001341623.1:p.Asp396Val
NM_001354695.3:c.1028A>T NP_001341624.1:p.Asp343Val
NM_002880.4:c.1370A>T NP_002871.1:p.Asp457Val
NR_148940.3:n.1814A>T
NR_148941.3:n.1760A>T
NR_148942.3:n.1699A>T