Canonical Allele Identifier: CA891842039
Gene: BRAF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140781589_140781597dup , CM000669.2:g.140781589_140781597dup GRCh38
NC_000007.13:g.140481389_140481397dup , CM000669.1:g.140481389_140481397dup GRCh37
NC_000007.12:g.140127858_140127866dup NCBI36
NG_007873.3:g.148169_148177dup , LRG_299:g.148169_148177dup

Transcript Alleles

HGVS Amino-acid change
ENST00000646891.2:c.1412_1420dup MANE Select ENSP00000493543.1:p.Lys473_Gly474insValTy...
ENST00000288602.11:c.1532_1540dup ENSP00000288602.7:p.Lys513_Gly514insValTy...
ENST00000479537.6:c.82_90dup
ENST00000496384.7:c.1412_1420dup ENSP00000419060.2:p.Lys473_Gly474insValTy...
ENST00000497784.2:c.*862_*870dup ENSP00000420119.2:n.*862_*870dup
ENST00000642228.1:c.*490_*498dup ENSP00000493678.1:n.*490_*498dup
ENST00000642875.1:n.854_862dup
ENST00000644120.1:n.1802_1810dup
ENST00000644650.1:c.508_516dup
ENST00000644905.1:n.1501_1509dup
ENST00000644969.2:c.1532_1540dup MANE Plus Clinical ENSP00000496776.1:p.Lys513_Gly514insValTy...
ENST00000646334.1:n.542_550dup
ENST00000646730.1:c.1412_1420dup ENSP00000494784.1:p.Lys473_Gly474insValTy...
ENST00000646891.1:c.1412_1420dup ENSP00000493543.1:p.Lys473_Gly474insValTy...
ENST00000647434.1:c.455_463dup ENSP00000495132.1:p.Lys154_Gly155insValTy...
ENST00000288602.10:c.1412_1420dup ENSP00000288602.6:p.Lys473_Gly474insValTy...
ENST00000496384.6:c.235_243dup
ENST00000497784.1:c.1447_1455dup ENSP00000420119.1:n.1447_1455dup
NM_004333.4:c.1412_1420dup , LRG_299t1:c.1412_1420dup NP_004324.2:p.Lys473_Gly474insValTyrLys
XM_005250045.1:c.1412_1420dup XP_005250102.1:p.Lys473_Gly474insValTyrLy...
XM_005250046.1:c.1412_1420dup XP_005250103.1:p.Lys473_Gly474insValTyrLy...
XM_011516529.1:c.1412_1420dup XP_011514831.1:p.Lys473_Gly474insValTyrLy...
XM_011516530.1:c.1412_1420dup XP_011514832.1:p.Lys473_Gly474insValTyrLy...
XR_242190.1:n.1420_1428dup
XR_927520.1:n.1420_1428dup
XR_927521.1:n.1420_1428dup
XR_927522.1:n.1420_1428dup
XR_927523.1:n.1420_1428dup
NM_001354609.1:c.1412_1420dup NP_001341538.1:p.Lys473_Gly474insValTyrLy...
NM_004333.5:c.1412_1420dup NP_004324.2:p.Lys473_Gly474insValTyrLys
NR_148928.1:n.1717_1725dup
XM_017012558.1:c.1532_1540dup XP_016868047.1:p.Lys513_Gly514insValTyrLy...
XM_017012559.1:c.1532_1540dup XP_016868048.1:p.Lys513_Gly514insValTyrLy...
XR_001744857.1:n.1540_1548dup
XR_001744858.1:n.1540_1548dup
NM_001354609.2:c.1412_1420dup NP_001341538.1:p.Lys473_Gly474insValTyrLy...
NM_001374244.1:c.1532_1540dup NP_001361173.1:p.Lys513_Gly514insValTyrLy...
NM_001374258.1:c.1532_1540dup MANE Plus Clinical NP_001361187.1:p.Lys513_Gly514insValTyrLy...
NM_004333.6:c.1412_1420dup MANE Select NP_004324.2:p.Lys473_Gly474insValTyrLys
NM_001378467.1:c.1421_1429dup NP_001365396.1:p.Lys476_Gly477insValTyrLy...
NM_001378468.1:c.1412_1420dup NP_001365397.1:p.Lys473_Gly474insValTyrLy...
NM_001378469.1:c.1346_1354dup NP_001365398.1:p.Lys451_Gly452insValTyrLy...
NM_001378470.1:c.1310_1318dup NP_001365399.1:p.Lys439_Gly440insValTyrLy...
NM_001378471.1:c.1301_1309dup NP_001365400.1:p.Lys436_Gly437insValTyrLy...
NM_001378472.1:c.1256_1264dup NP_001365401.1:p.Lys421_Gly422insValTyrLy...
NM_001378473.1:c.1256_1264dup NP_001365402.1:p.Lys421_Gly422insValTyrLy...
NM_001378474.1:c.1412_1420dup NP_001365403.1:p.Lys473_Gly474insValTyrLy...
NM_001378475.1:c.1148_1156dup NP_001365404.1:p.Lys385_Gly386insValTyrLy...