Canonical Allele Identifier: CA645556781
Gene: BRAF HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140781632del , CM000669.2:g.140781632del GRCh38
NC_000007.13:g.140481432del , CM000669.1:g.140481432del GRCh37
NC_000007.12:g.140127901del NCBI36
NG_007873.3:g.148133del , LRG_299:g.148133del

Transcript Alleles

HGVS Amino-acid change
ENST00000646891.2:c.1376del MANE Select ENSP00000493543.1:p.Val459GlyfsTer24
ENST00000288602.11:c.1496del ENSP00000288602.7:p.Val499GlyfsTer24
ENST00000479537.6:c.46del
ENST00000496384.7:c.1376del ENSP00000419060.2:p.Val459GlyfsTer24
ENST00000497784.2:c.*826del ENSP00000420119.2:n.*826del
ENST00000642228.1:c.*454del ENSP00000493678.1:n.*454del
ENST00000642875.1:n.818del
ENST00000644120.1:n.1766del
ENST00000644650.1:c.472del
ENST00000644905.1:n.1465del
ENST00000644969.2:c.1496del MANE Plus Clinical ENSP00000496776.1:p.Val499GlyfsTer24
ENST00000646334.1:n.506del
ENST00000646730.1:c.1376del ENSP00000494784.1:p.Val459GlyfsTer24
ENST00000646891.1:c.1376del ENSP00000493543.1:p.Val459GlyfsTer24
ENST00000647434.1:c.419del ENSP00000495132.1:p.Val140GlyfsTer24
ENST00000288602.10:c.1376del ENSP00000288602.6:p.Val459GlyfsTer24
ENST00000496384.6:c.199del
ENST00000497784.1:c.1411del ENSP00000420119.1:n.1411del
NM_004333.4:c.1376del , LRG_299t1:c.1376del NP_004324.2:p.Val459GlyfsTer24
XM_005250045.1:c.1376del XP_005250102.1:p.Val459GlyfsTer24
XM_005250046.1:c.1376del XP_005250103.1:p.Val459GlyfsTer24
XM_011516529.1:c.1376del XP_011514831.1:p.Val459GlyfsTer24
XM_011516530.1:c.1376del XP_011514832.1:p.Val459GlyfsTer24
XR_242190.1:n.1384del
XR_927520.1:n.1384del
XR_927521.1:n.1384del
XR_927522.1:n.1384del
XR_927523.1:n.1384del
NM_001354609.1:c.1376del NP_001341538.1:p.Val459GlyfsTer24
NM_004333.5:c.1376del NP_004324.2:p.Val459GlyfsTer24
NR_148928.1:n.1681del
XM_017012558.1:c.1496del XP_016868047.1:p.Val499GlyfsTer24
XM_017012559.1:c.1496del XP_016868048.1:p.Val499GlyfsTer24
XR_001744857.1:n.1504del
XR_001744858.1:n.1504del
NM_001354609.2:c.1376del NP_001341538.1:p.Val459GlyfsTer24
NM_001374244.1:c.1496del NP_001361173.1:p.Val499GlyfsTer24
NM_001374258.1:c.1496del MANE Plus Clinical NP_001361187.1:p.Val499GlyfsTer24
NM_004333.6:c.1376del MANE Select NP_004324.2:p.Val459GlyfsTer24
NM_001378467.1:c.1385del NP_001365396.1:p.Val462GlyfsTer24
NM_001378468.1:c.1376del NP_001365397.1:p.Val459GlyfsTer24
NM_001378469.1:c.1310del NP_001365398.1:p.Val437GlyfsTer24
NM_001378470.1:c.1274del NP_001365399.1:p.Val425GlyfsTer24
NM_001378471.1:c.1265del NP_001365400.1:p.Val422GlyfsTer24
NM_001378472.1:c.1220del NP_001365401.1:p.Val407GlyfsTer24
NM_001378473.1:c.1220del NP_001365402.1:p.Val407GlyfsTer24
NM_001378474.1:c.1376del NP_001365403.1:p.Val459GlyfsTer24
NM_001378475.1:c.1112del NP_001365404.1:p.Val371GlyfsTer24