Canonical Allele Identifier: CA2846055290
Gene: BRAF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140749367_140749368insACTTCGAATCGTAGCCATTCCGCCTCTAGCTTGTTCCGGAGATAAATAATGAACAGATCCTAA , CM000669.2:g.140749367_140749368insACTTCGAATCGTAGCCATTCCGCCTCTAGCTTGTTCCGGAGATAAATAATGAACAGATCCTAA GRCh38
NC_000007.13:g.140449167_140449168insACTTCGAATCGTAGCCATTCCGCCTCTAGCTTGTTCCGGAGATAAATAATGAACAGATCCTAA , CM000669.1:g.140449167_140449168insACTTCGAATCGTAGCCATTCCGCCTCTAGCTTGTTCCGGAGATAAATAATGAACAGATCCTAA GRCh37
NC_000007.12:g.140095636_140095637insACTTCGAATCGTAGCCATTCCGCCTCTAGCTTGTTCCGGAGATAAATAATGAACAGATCCTAA NCBI36
NG_007873.3:g.180397_180398insTTAGGATCTGTTCATTATTTATCTCCGGAACAAGCTAGAGGCGGAATGGCTACGATTCGAAGT , LRG_299:g.180397_180398insTTAGGATCTGTTCATTATTTATCTCCGGAACAAGCTAGAGGCGGAATGGCTACGATTCGAAGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000646891.2:c.1911_1912insTTAGGATCTGTTCATTATTTATCTCCGGAACAAGCTAGAGGCGGAATGGCTACGATTCGAAGT MANE Select ENSP00000493543.1:p.Ser637_Asp638insLeuGlySerValHisTyrLeuSerP...
ENST00000288602.11:c.2031_2032insTTAGGATCTGTTCATTATTTATCTCCGGAACAAGCTAGAGGCGGAATGGCTACGATTCGAAGT ENSP00000288602.7:p.Ser677_Asp678insLeuGlySerValHisTyrLeuSerP...
ENST00000479537.6:c.581_582insTTAGGATCTGTTCATTATTTATCTCCGGAACAAGCTAGAGGCGGAATGGCTACGATTCGAAGT
ENST00000496384.7:c.1911_1912insTTAGGATCTGTTCATTATTTATCTCCGGAACAAGCTAGAGGCGGAATGGCTACGATTCGAAGT ENSP00000419060.2:p.Ser637_Asp638insLeuGlySerValHisTyrLeuSerP...
ENST00000497784.2:c.*1361_*1362insTTAGGATCTGTTCATTATTTATCTCCGGAACAAGCTAGAGGCGGAATGGCTACGATTCGAAGT ENSP00000420119.2:n.*1361_*1362insTTAGGATCTGTTCATTATTTATCTCCG...
ENST00000642228.1:c.*989_*990insTTAGGATCTGTTCATTATTTATCTCCGGAACAAGCTAGAGGCGGAATGGCTACGATTCGAAGT ENSP00000493678.1:n.*989_*990insTTAGGATCTGTTCATTATTTATCTCCGGA...
ENST00000642875.1:n.1309_1310insTTAGGATCTGTTCATTATTTATCTCCGGAACAAGCTAGAGGCGGAATGGCTACGATTCGAAGT
ENST00000644120.1:n.2301_2302insTTAGGATCTGTTCATTATTTATCTCCGGAACAAGCTAGAGGCGGAATGGCTACGATTCGAAGT
ENST00000644650.1:c.1007_1008insTTAGGATCTGTTCATTATTTATCTCCGGAACAAGCTAGAGGCGGAATGGCTACGATTCGAAGT
ENST00000644905.1:n.2793_2794insTTAGGATCTGTTCATTATTTATCTCCGGAACAAGCTAGAGGCGGAATGGCTACGATTCGAAGT
ENST00000644969.2:c.2031_2032insTTAGGATCTGTTCATTATTTATCTCCGGAACAAGCTAGAGGCGGAATGGCTACGATTCGAAGT MANE Plus Clinical ENSP00000496776.1:p.Ser677_Asp678insLeuGlySerValHisTyrLeuSerP...
ENST00000646730.1:c.*487_*488insTTAGGATCTGTTCATTATTTATCTCCGGAACAAGCTAGAGGCGGAATGGCTACGATTCGAAGT ENSP00000494784.1:n.*487_*488insTTAGGATCTGTTCATTATTTATCTCCGGA...
ENST00000646891.1:c.1911_1912insTTAGGATCTGTTCATTATTTATCTCCGGAACAAGCTAGAGGCGGAATGGCTACGATTCGAAGT ENSP00000493543.1:p.Ser637_Asp638insLeuGlySerValHisTyrLeuSerP...
ENST00000647434.1:c.788_789insTTAGGATCTGTTCATTATTTATCTCCGGAACAAGCTAGAGGCGGAATGGCTACGATTCGAAGT ENSP00000495132.1:p.Gln263HisfsTer2
ENST00000288602.10:c.1911_1912insTTAGGATCTGTTCATTATTTATCTCCGGAACAAGCTAGAGGCGGAATGGCTACGATTCGAAGT ENSP00000288602.6:p.Ser637_Asp638insLeuGlySerValHisTyrLeuSerP...
ENST00000479537.5:c.195_196insTTAGGATCTGTTCATTATTTATCTCCGGAACAAGCTAGAGGCGGAATGGCTACGATTCGAAGT ENSP00000418033.1:p.Ser65_Asp66insLeuGlySerValHisTyrLeuSerPro...
ENST00000496384.6:c.734_735insTTAGGATCTGTTCATTATTTATCTCCGGAACAAGCTAGAGGCGGAATGGCTACGATTCGAAGT
ENST00000497784.1:c.1946_1947insTTAGGATCTGTTCATTATTTATCTCCGGAACAAGCTAGAGGCGGAATGGCTACGATTCGAAGT ENSP00000420119.1:n.1946_1947insTTAGGATCTGTTCATTATTTATCTCCGGA...
NM_004333.4:c.1911_1912insTTAGGATCTGTTCATTATTTATCTCCGGAACAAGCTAGAGGCGGAATGGCTACGATTCGAAGT , LRG_299t1:c.1911_1912insTTAGGATCTGTTCATTATTTATCTCCGGAACAAGCTAGAGGCGGAATGGCTACGATTCGAAGT NP_004324.2:p.Ser637_Asp638insLeuGlySerValHisTyrLeuSerProGluG...
XM_005250045.1:c.1911_1912insTTAGGATCTGTTCATTATTTATCTCCGGAACAAGCTAGAGGCGGAATGGCTACGATTCGAAGT XP_005250102.1:p.Ser637_Asp638insLeuGlySerValHisTyrLeuSerProG...
XM_005250046.1:c.1911_1912insTTAGGATCTGTTCATTATTTATCTCCGGAACAAGCTAGAGGCGGAATGGCTACGATTCGAAGT XP_005250103.1:p.Ser637_Asp638insLeuGlySerValHisTyrLeuSerProG...
XM_011516529.1:c.1911_1912insTTAGGATCTGTTCATTATTTATCTCCGGAACAAGCTAGAGGCGGAATGGCTACGATTCGAAGT XP_011514831.1:p.Ser637_Asp638insLeuGlySerValHisTyrLeuSerProG...
XM_011516530.1:c.1745_1746insTTAGGATCTGTTCATTATTTATCTCCGGAACAAGCTAGAGGCGGAATGGCTACGATTCGAAGT XP_011514832.1:p.Gln582HisfsTer2
XR_242190.1:n.1919_1920insTTAGGATCTGTTCATTATTTATCTCCGGAACAAGCTAGAGGCGGAATGGCTACGATTCGAAGT
XR_927520.1:n.1919_1920insTTAGGATCTGTTCATTATTTATCTCCGGAACAAGCTAGAGGCGGAATGGCTACGATTCGAAGT
XR_927521.1:n.1919_1920insTTAGGATCTGTTCATTATTTATCTCCGGAACAAGCTAGAGGCGGAATGGCTACGATTCGAAGT
XR_927522.1:n.1753_1754insTTAGGATCTGTTCATTATTTATCTCCGGAACAAGCTAGAGGCGGAATGGCTACGATTCGAAGT
XR_927523.1:n.1753_1754insTTAGGATCTGTTCATTATTTATCTCCGGAACAAGCTAGAGGCGGAATGGCTACGATTCGAAGT
NM_001354609.1:c.1911_1912insTTAGGATCTGTTCATTATTTATCTCCGGAACAAGCTAGAGGCGGAATGGCTACGATTCGAAGT NP_001341538.1:p.Ser637_Asp638insLeuGlySerValHisTyrLeuSerProG...
NM_004333.5:c.1911_1912insTTAGGATCTGTTCATTATTTATCTCCGGAACAAGCTAGAGGCGGAATGGCTACGATTCGAAGT NP_004324.2:p.Ser637_Asp638insLeuGlySerValHisTyrLeuSerProGluG...
NR_148928.1:n.3009_3010insTTAGGATCTGTTCATTATTTATCTCCGGAACAAGCTAGAGGCGGAATGGCTACGATTCGAAGT
XM_017012558.1:c.2031_2032insTTAGGATCTGTTCATTATTTATCTCCGGAACAAGCTAGAGGCGGAATGGCTACGATTCGAAGT XP_016868047.1:p.Ser677_Asp678insLeuGlySerValHisTyrLeuSerProG...
XM_017012559.1:c.2031_2032insTTAGGATCTGTTCATTATTTATCTCCGGAACAAGCTAGAGGCGGAATGGCTACGATTCGAAGT XP_016868048.1:p.Ser677_Asp678insLeuGlySerValHisTyrLeuSerProG...
XR_001744857.1:n.2039_2040insTTAGGATCTGTTCATTATTTATCTCCGGAACAAGCTAGAGGCGGAATGGCTACGATTCGAAGT
XR_001744858.1:n.1873_1874insTTAGGATCTGTTCATTATTTATCTCCGGAACAAGCTAGAGGCGGAATGGCTACGATTCGAAGT
NM_001354609.2:c.1911_1912insTTAGGATCTGTTCATTATTTATCTCCGGAACAAGCTAGAGGCGGAATGGCTACGATTCGAAGT NP_001341538.1:p.Ser637_Asp638insLeuGlySerValHisTyrLeuSerProG...
NM_001374244.1:c.2031_2032insTTAGGATCTGTTCATTATTTATCTCCGGAACAAGCTAGAGGCGGAATGGCTACGATTCGAAGT NP_001361173.1:p.Ser677_Asp678insLeuGlySerValHisTyrLeuSerProG...
NM_001374258.1:c.2031_2032insTTAGGATCTGTTCATTATTTATCTCCGGAACAAGCTAGAGGCGGAATGGCTACGATTCGAAGT MANE Plus Clinical NP_001361187.1:p.Ser677_Asp678insLeuGlySerValHisTyrLeuSerProG...
NM_004333.6:c.1911_1912insTTAGGATCTGTTCATTATTTATCTCCGGAACAAGCTAGAGGCGGAATGGCTACGATTCGAAGT MANE Select NP_004324.2:p.Ser637_Asp638insLeuGlySerValHisTyrLeuSerProGluG...
NM_001378467.1:c.1920_1921insTTAGGATCTGTTCATTATTTATCTCCGGAACAAGCTAGAGGCGGAATGGCTACGATTCGAAGT NP_001365396.1:p.Ser640_Asp641insLeuGlySerValHisTyrLeuSerProG...
NM_001378468.1:c.1911_1912insTTAGGATCTGTTCATTATTTATCTCCGGAACAAGCTAGAGGCGGAATGGCTACGATTCGAAGT NP_001365397.1:p.Ser637_Asp638insLeuGlySerValHisTyrLeuSerProG...
NM_001378469.1:c.1845_1846insTTAGGATCTGTTCATTATTTATCTCCGGAACAAGCTAGAGGCGGAATGGCTACGATTCGAAGT NP_001365398.1:p.Ser615_Asp616insLeuGlySerValHisTyrLeuSerProG...
NM_001378470.1:c.1809_1810insTTAGGATCTGTTCATTATTTATCTCCGGAACAAGCTAGAGGCGGAATGGCTACGATTCGAAGT NP_001365399.1:p.Ser603_Asp604insLeuGlySerValHisTyrLeuSerProG...
NM_001378471.1:c.1800_1801insTTAGGATCTGTTCATTATTTATCTCCGGAACAAGCTAGAGGCGGAATGGCTACGATTCGAAGT NP_001365400.1:p.Ser600_Asp601insLeuGlySerValHisTyrLeuSerProG...
NM_001378472.1:c.1755_1756insTTAGGATCTGTTCATTATTTATCTCCGGAACAAGCTAGAGGCGGAATGGCTACGATTCGAAGT NP_001365401.1:p.Ser585_Asp586insLeuGlySerValHisTyrLeuSerProG...
NM_001378473.1:c.1755_1756insTTAGGATCTGTTCATTATTTATCTCCGGAACAAGCTAGAGGCGGAATGGCTACGATTCGAAGT NP_001365402.1:p.Ser585_Asp586insLeuGlySerValHisTyrLeuSerProG...
NM_001378474.1:c.1911_1912insTTAGGATCTGTTCATTATTTATCTCCGGAACAAGCTAGAGGCGGAATGGCTACGATTCGAAGT NP_001365403.1:p.Ser637_Asp638insLeuGlySerValHisTyrLeuSerProG...
NM_001378475.1:c.1647_1648insTTAGGATCTGTTCATTATTTATCTCCGGAACAAGCTAGAGGCGGAATGGCTACGATTCGAAGT NP_001365404.1:p.Ser549_Asp550insLeuGlySerValHisTyrLeuSerProG...