Canonical Allele Identifier: CA2580077581
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 1711060
ClinVar RCV Id: RCV002292347

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140781631del , CM000669.2:g.140781631del GRCh38
NC_000007.13:g.140481431del , CM000669.1:g.140481431del GRCh37
NC_000007.12:g.140127900del NCBI36
NG_007873.3:g.148136del , LRG_299:g.148136del

Transcript Alleles

HGVS Amino-acid change
ENST00000646891.2:c.1379del MANE Select ENSP00000493543.1:p.Gly460AspfsTer23
ENST00000288602.11:c.1499del ENSP00000288602.7:p.Gly500AspfsTer23
ENST00000479537.6:c.49del
ENST00000496384.7:c.1379del ENSP00000419060.2:p.Gly460AspfsTer23
ENST00000497784.2:c.*829del ENSP00000420119.2:n.*829del
ENST00000642228.1:c.*457del ENSP00000493678.1:n.*457del
ENST00000642875.1:n.821del
ENST00000644120.1:n.1769del
ENST00000644650.1:c.475del
ENST00000644905.1:n.1468del
ENST00000644969.2:c.1499del MANE Plus Clinical ENSP00000496776.1:p.Gly500AspfsTer23
ENST00000646334.1:n.509del
ENST00000646730.1:c.1379del ENSP00000494784.1:p.Gly460AspfsTer23
ENST00000646891.1:c.1379del ENSP00000493543.1:p.Gly460AspfsTer23
ENST00000647434.1:c.422del ENSP00000495132.1:p.Gly141AspfsTer23
ENST00000288602.10:c.1379del ENSP00000288602.6:p.Gly460AspfsTer23
ENST00000496384.6:c.202del
ENST00000497784.1:c.1414del ENSP00000420119.1:n.1414del
NM_004333.4:c.1379del , LRG_299t1:c.1379del NP_004324.2:p.Gly460AspfsTer23
XM_005250045.1:c.1379del XP_005250102.1:p.Gly460AspfsTer23
XM_005250046.1:c.1379del XP_005250103.1:p.Gly460AspfsTer23
XM_011516529.1:c.1379del XP_011514831.1:p.Gly460AspfsTer23
XM_011516530.1:c.1379del XP_011514832.1:p.Gly460AspfsTer23
XR_242190.1:n.1387del
XR_927520.1:n.1387del
XR_927521.1:n.1387del
XR_927522.1:n.1387del
XR_927523.1:n.1387del
NM_001354609.1:c.1379del NP_001341538.1:p.Gly460AspfsTer23
NM_004333.5:c.1379del NP_004324.2:p.Gly460AspfsTer23
NR_148928.1:n.1684del
XM_017012558.1:c.1499del XP_016868047.1:p.Gly500AspfsTer23
XM_017012559.1:c.1499del XP_016868048.1:p.Gly500AspfsTer23
XR_001744857.1:n.1507del
XR_001744858.1:n.1507del
NM_001354609.2:c.1379del NP_001341538.1:p.Gly460AspfsTer23
NM_001374244.1:c.1499del NP_001361173.1:p.Gly500AspfsTer23
NM_001374258.1:c.1499del MANE Plus Clinical NP_001361187.1:p.Gly500AspfsTer23
NM_004333.6:c.1379del MANE Select NP_004324.2:p.Gly460AspfsTer23
NM_001378467.1:c.1388del NP_001365396.1:p.Gly463AspfsTer23
NM_001378468.1:c.1379del NP_001365397.1:p.Gly460AspfsTer23
NM_001378469.1:c.1313del NP_001365398.1:p.Gly438AspfsTer23
NM_001378470.1:c.1277del NP_001365399.1:p.Gly426AspfsTer23
NM_001378471.1:c.1268del NP_001365400.1:p.Gly423AspfsTer23
NM_001378472.1:c.1223del NP_001365401.1:p.Gly408AspfsTer23
NM_001378473.1:c.1223del NP_001365402.1:p.Gly408AspfsTer23
NM_001378474.1:c.1379del NP_001365403.1:p.Gly460AspfsTer23
NM_001378475.1:c.1115del NP_001365404.1:p.Gly372AspfsTer23