Canonical Allele Identifier: CA2580077573
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 1711058
ClinVar RCV Id: RCV002292345

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140781603_140781604del , CM000669.2:g.140781603_140781604del GRCh38
NC_000007.13:g.140481403_140481404del , CM000669.1:g.140481403_140481404del GRCh37
NC_000007.12:g.140127872_140127873del NCBI36
NG_007873.3:g.148161_148162del , LRG_299:g.148161_148162del

Transcript Alleles

HGVS Amino-acid Change
ENST00000646891.2:c.1404_1405del MANE Select ENSP00000493543.1:p.Phe468LeufsTer11
ENST00000288602.11:c.1524_1525del ENSP00000288602.7:p.Phe508LeufsTer11
ENST00000479537.6:c.74_75del
ENST00000496384.7:c.1404_1405del ENSP00000419060.2:p.Phe468LeufsTer11
ENST00000497784.2:c.*854_*855del ENSP00000420119.2:n.*854_*855del
ENST00000642228.1:c.*482_*483del ENSP00000493678.1:n.*482_*483del
ENST00000642875.1:n.846_847del
ENST00000644120.1:n.1794_1795del
ENST00000644650.1:c.500_501del
ENST00000644905.1:n.1493_1494del
ENST00000644969.2:c.1524_1525del MANE Plus Clinical ENSP00000496776.1:p.Phe508LeufsTer11
ENST00000646334.1:n.534_535del
ENST00000646730.1:c.1404_1405del ENSP00000494784.1:p.Phe468LeufsTer11
ENST00000646891.1:c.1404_1405del ENSP00000493543.1:p.Phe468LeufsTer11
ENST00000647434.1:c.447_448del ENSP00000495132.1:p.Phe149LeufsTer11
ENST00000288602.10:c.1404_1405del ENSP00000288602.6:p.Phe468LeufsTer11
ENST00000496384.6:c.227_228del
ENST00000497784.1:c.1439_1440del ENSP00000420119.1:n.1439_1440del
NM_004333.4:c.1404_1405del , LRG_299t1:c.1404_1405del NP_004324.2:p.Phe468LeufsTer11
XM_005250045.1:c.1404_1405del XP_005250102.1:p.Phe468LeufsTer11
XM_005250046.1:c.1404_1405del XP_005250103.1:p.Phe468LeufsTer11
XM_011516529.1:c.1404_1405del XP_011514831.1:p.Phe468LeufsTer11
XM_011516530.1:c.1404_1405del XP_011514832.1:p.Phe468LeufsTer11
XR_242190.1:n.1412_1413del
XR_927520.1:n.1412_1413del
XR_927521.1:n.1412_1413del
XR_927522.1:n.1412_1413del
XR_927523.1:n.1412_1413del
NM_001354609.1:c.1404_1405del NP_001341538.1:p.Phe468LeufsTer11
NM_004333.5:c.1404_1405del NP_004324.2:p.Phe468LeufsTer11
NR_148928.1:n.1709_1710del
XM_017012558.1:c.1524_1525del XP_016868047.1:p.Phe508LeufsTer11
XM_017012559.1:c.1524_1525del XP_016868048.1:p.Phe508LeufsTer11
XR_001744857.1:n.1532_1533del
XR_001744858.1:n.1532_1533del
NM_001354609.2:c.1404_1405del NP_001341538.1:p.Phe468LeufsTer11
NM_001374244.1:c.1524_1525del NP_001361173.1:p.Phe508LeufsTer11
NM_001374258.1:c.1524_1525del MANE Plus Clinical NP_001361187.1:p.Phe508LeufsTer11
NM_004333.6:c.1404_1405del MANE Select NP_004324.2:p.Phe468LeufsTer11
NM_001378467.1:c.1413_1414del NP_001365396.1:p.Phe471LeufsTer11
NM_001378468.1:c.1404_1405del NP_001365397.1:p.Phe468LeufsTer11
NM_001378469.1:c.1338_1339del NP_001365398.1:p.Phe446LeufsTer11
NM_001378470.1:c.1302_1303del NP_001365399.1:p.Phe434LeufsTer11
NM_001378471.1:c.1293_1294del NP_001365400.1:p.Phe431LeufsTer11
NM_001378472.1:c.1248_1249del NP_001365401.1:p.Phe416LeufsTer11
NM_001378473.1:c.1248_1249del NP_001365402.1:p.Phe416LeufsTer11
NM_001378474.1:c.1404_1405del NP_001365403.1:p.Phe468LeufsTer11
NM_001378475.1:c.1140_1141del NP_001365404.1:p.Phe380LeufsTer11