Canonical Allele Identifier: CA2580077584
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 1711809
ClinVar RCV Id: RCV002293354

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140781633dup , CM000669.2:g.140781633dup GRCh38
NC_000007.13:g.140481433dup , CM000669.1:g.140481433dup GRCh37
NC_000007.12:g.140127902dup NCBI36
NG_007873.3:g.148132dup , LRG_299:g.148132dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000646891.2:c.1375dup MANE Select ENSP00000493543.1:p.Val459GlyfsTer21
ENST00000288602.11:c.1495dup ENSP00000288602.7:p.Val499GlyfsTer21
ENST00000479537.6:c.45dup
ENST00000496384.7:c.1375dup ENSP00000419060.2:p.Val459GlyfsTer21
ENST00000497784.2:c.*825dup ENSP00000420119.2:n.*825dup
ENST00000642228.1:c.*453dup ENSP00000493678.1:n.*453dup
ENST00000642875.1:n.817dup
ENST00000644120.1:n.1765dup
ENST00000644650.1:c.471dup
ENST00000644905.1:n.1464dup
ENST00000644969.2:c.1495dup MANE Plus Clinical ENSP00000496776.1:p.Val499GlyfsTer21
ENST00000646334.1:n.505dup
ENST00000646730.1:c.1375dup ENSP00000494784.1:p.Val459GlyfsTer21
ENST00000646891.1:c.1375dup ENSP00000493543.1:p.Val459GlyfsTer21
ENST00000647434.1:c.418dup ENSP00000495132.1:p.Val140GlyfsTer21
ENST00000288602.10:c.1375dup ENSP00000288602.6:p.Val459GlyfsTer21
ENST00000496384.6:c.198dup
ENST00000497784.1:c.1410dup ENSP00000420119.1:n.1410dup
NM_004333.4:c.1375dup , LRG_299t1:c.1375dup NP_004324.2:p.Val459GlyfsTer21
XM_005250045.1:c.1375dup XP_005250102.1:p.Val459GlyfsTer21
XM_005250046.1:c.1375dup XP_005250103.1:p.Val459GlyfsTer21
XM_011516529.1:c.1375dup XP_011514831.1:p.Val459GlyfsTer21
XM_011516530.1:c.1375dup XP_011514832.1:p.Val459GlyfsTer21
XR_242190.1:n.1383dup
XR_927520.1:n.1383dup
XR_927521.1:n.1383dup
XR_927522.1:n.1383dup
XR_927523.1:n.1383dup
NM_001354609.1:c.1375dup NP_001341538.1:p.Val459GlyfsTer21
NM_004333.5:c.1375dup NP_004324.2:p.Val459GlyfsTer21
NR_148928.1:n.1680dup
XM_017012558.1:c.1495dup XP_016868047.1:p.Val499GlyfsTer21
XM_017012559.1:c.1495dup XP_016868048.1:p.Val499GlyfsTer21
XR_001744857.1:n.1503dup
XR_001744858.1:n.1503dup
NM_001354609.2:c.1375dup NP_001341538.1:p.Val459GlyfsTer21
NM_001374244.1:c.1495dup NP_001361173.1:p.Val499GlyfsTer21
NM_001374258.1:c.1495dup MANE Plus Clinical NP_001361187.1:p.Val499GlyfsTer21
NM_004333.6:c.1375dup MANE Select NP_004324.2:p.Val459GlyfsTer21
NM_001378467.1:c.1384dup NP_001365396.1:p.Val462GlyfsTer21
NM_001378468.1:c.1375dup NP_001365397.1:p.Val459GlyfsTer21
NM_001378469.1:c.1309dup NP_001365398.1:p.Val437GlyfsTer21
NM_001378470.1:c.1273dup NP_001365399.1:p.Val425GlyfsTer21
NM_001378471.1:c.1264dup NP_001365400.1:p.Val422GlyfsTer21
NM_001378472.1:c.1219dup NP_001365401.1:p.Val407GlyfsTer21
NM_001378473.1:c.1219dup NP_001365402.1:p.Val407GlyfsTer21
NM_001378474.1:c.1375dup NP_001365403.1:p.Val459GlyfsTer21
NM_001378475.1:c.1111dup NP_001365404.1:p.Val371GlyfsTer21