Canonical Allele Identifier: CA2695208552
Gene: BRAF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140781602_140781625del , CM000669.2:g.140781602_140781625del GRCh38
NC_000007.13:g.140481402_140481425del , CM000669.1:g.140481402_140481425del GRCh37
NC_000007.12:g.140127871_140127894del NCBI36
NG_007873.3:g.148142_148165del , LRG_299:g.148142_148165del

Transcript Alleles

HGVS Amino-acid change
ENST00000646891.2:c.1385_1408del MANE Select ENSP00000493543.1:p.Arg462_Gly469del
ENST00000288602.11:c.1505_1528del ENSP00000288602.7:p.Arg502_Gly509del
ENST00000479537.6:c.55_78del
ENST00000496384.7:c.1385_1408del ENSP00000419060.2:p.Arg462_Gly469del
ENST00000497784.2:c.*835_*858del ENSP00000420119.2:n.*835_*858del
ENST00000642228.1:c.*463_*486del ENSP00000493678.1:n.*463_*486del
ENST00000642875.1:n.827_850del
ENST00000644120.1:n.1775_1798del
ENST00000644650.1:c.481_504del
ENST00000644905.1:n.1474_1497del
ENST00000644969.2:c.1505_1528del MANE Plus Clinical ENSP00000496776.1:p.Arg502_Gly509del
ENST00000646334.1:n.515_538del
ENST00000646730.1:c.1385_1408del ENSP00000494784.1:p.Arg462_Gly469del
ENST00000646891.1:c.1385_1408del ENSP00000493543.1:p.Arg462_Gly469del
ENST00000647434.1:c.428_451del ENSP00000495132.1:p.Arg143_Gly150del
ENST00000288602.10:c.1385_1408del ENSP00000288602.6:p.Arg462_Gly469del
ENST00000496384.6:c.208_231del
ENST00000497784.1:c.1420_1443del ENSP00000420119.1:n.1420_1443del
NM_004333.4:c.1385_1408del , LRG_299t1:c.1385_1408del NP_004324.2:p.Arg462_Gly469del
XM_005250045.1:c.1385_1408del XP_005250102.1:p.Arg462_Gly469del
XM_005250046.1:c.1385_1408del XP_005250103.1:p.Arg462_Gly469del
XM_011516529.1:c.1385_1408del XP_011514831.1:p.Arg462_Gly469del
XM_011516530.1:c.1385_1408del XP_011514832.1:p.Arg462_Gly469del
XR_242190.1:n.1393_1416del
XR_927520.1:n.1393_1416del
XR_927521.1:n.1393_1416del
XR_927522.1:n.1393_1416del
XR_927523.1:n.1393_1416del
NM_001354609.1:c.1385_1408del NP_001341538.1:p.Arg462_Gly469del
NM_004333.5:c.1385_1408del NP_004324.2:p.Arg462_Gly469del
NR_148928.1:n.1690_1713del
XM_017012558.1:c.1505_1528del XP_016868047.1:p.Arg502_Gly509del
XM_017012559.1:c.1505_1528del XP_016868048.1:p.Arg502_Gly509del
XR_001744857.1:n.1513_1536del
XR_001744858.1:n.1513_1536del
NM_001354609.2:c.1385_1408del NP_001341538.1:p.Arg462_Gly469del
NM_001374244.1:c.1505_1528del NP_001361173.1:p.Arg502_Gly509del
NM_001374258.1:c.1505_1528del MANE Plus Clinical NP_001361187.1:p.Arg502_Gly509del
NM_004333.6:c.1385_1408del MANE Select NP_004324.2:p.Arg462_Gly469del
NM_001378467.1:c.1394_1417del NP_001365396.1:p.Arg465_Gly472del
NM_001378468.1:c.1385_1408del NP_001365397.1:p.Arg462_Gly469del
NM_001378469.1:c.1319_1342del NP_001365398.1:p.Arg440_Gly447del
NM_001378470.1:c.1283_1306del NP_001365399.1:p.Arg428_Gly435del
NM_001378471.1:c.1274_1297del NP_001365400.1:p.Arg425_Gly432del
NM_001378472.1:c.1229_1252del NP_001365401.1:p.Arg410_Gly417del
NM_001378473.1:c.1229_1252del NP_001365402.1:p.Arg410_Gly417del
NM_001378474.1:c.1385_1408del NP_001365403.1:p.Arg462_Gly469del
NM_001378475.1:c.1121_1144del NP_001365404.1:p.Arg374_Gly381del