Canonical Allele Identifier: CA2967272943
Gene: BRAF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140753368_140753369insTACTACAC , CM000669.2:g.140753368_140753369insTACTACAC GRCh38
NC_000007.13:g.140453168_140453169insTACTACAC , CM000669.1:g.140453168_140453169insTACTACAC GRCh37
NC_000007.12:g.140099637_140099638insTACTACAC NCBI36
NG_007873.3:g.176396_176397insGTGTAGTA , LRG_299:g.176396_176397insGTGTAGTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000646891.2:c.1766_1767insGTGTAGTA MANE Select ENSP00000493543.1:p.Val590CysfsTer4
ENST00000288602.11:c.1886_1887insGTGTAGTA ENSP00000288602.7:p.Val630CysfsTer4
ENST00000479537.6:c.436_437insGTGTAGTA
ENST00000496384.7:c.1766_1767insGTGTAGTA ENSP00000419060.2:p.Val590CysfsTer4
ENST00000497784.2:c.*1216_*1217insGTGTAGTA ENSP00000420119.2:n.*1216_*1217insGTGTAGTA
ENST00000642228.1:c.*844_*845insGTGTAGTA ENSP00000493678.1:n.*844_*845insGTGTAGTA
ENST00000642875.1:n.1259-3951_1259-3950insGTGTAGTA
ENST00000644120.1:n.2156_2157insGTGTAGTA
ENST00000644650.1:c.862_863insGTGTAGTA
ENST00000644905.1:n.2648_2649insGTGTAGTA
ENST00000644969.2:c.1886_1887insGTGTAGTA MANE Plus Clinical ENSP00000496776.1:p.Val630CysfsTer4
ENST00000646730.1:c.*342_*343insGTGTAGTA ENSP00000494784.1:n.*342_*343insGTGTAGTA
ENST00000646891.1:c.1766_1767insGTGTAGTA ENSP00000493543.1:p.Val590CysfsTer4
ENST00000647434.1:c.738-3951_738-3950insGTGTAGTA ENSP00000495132.1:n.738-3951_738-3950insGTGTAGTA
ENST00000288602.10:c.1766_1767insGTGTAGTA ENSP00000288602.6:p.Val590CysfsTer4
ENST00000479537.5:c.50_51insGTGTAGTA ENSP00000418033.1:p.Val18CysfsTer4
ENST00000496384.6:c.589_590insGTGTAGTA
ENST00000497784.1:c.1801_1802insGTGTAGTA ENSP00000420119.1:n.1801_1802insGTGTAGTA
NM_004333.4:c.1766_1767insGTGTAGTA , LRG_299t1:c.1766_1767insGTGTAGTA NP_004324.2:p.Val590CysfsTer4
XM_005250045.1:c.1766_1767insGTGTAGTA XP_005250102.1:p.Val590CysfsTer4
XM_005250046.1:c.1766_1767insGTGTAGTA XP_005250103.1:p.Val590CysfsTer4
XM_011516529.1:c.1766_1767insGTGTAGTA XP_011514831.1:p.Val590CysfsTer4
XM_011516530.1:c.1695-3951_1695-3950insGTGTAGTA XP_011514832.1:n.1695-3951_1695-3950insGTGTAGTA
XR_242190.1:n.1774_1775insGTGTAGTA
XR_927520.1:n.1774_1775insGTGTAGTA
XR_927521.1:n.1774_1775insGTGTAGTA
XR_927522.1:n.1703-3951_1703-3950insGTGTAGTA
XR_927523.1:n.1703-3951_1703-3950insGTGTAGTA
NM_001354609.1:c.1766_1767insGTGTAGTA NP_001341538.1:p.Val590CysfsTer4
NM_004333.5:c.1766_1767insGTGTAGTA NP_004324.2:p.Val590CysfsTer4
NR_148928.1:n.2864_2865insGTGTAGTA
XM_017012558.1:c.1886_1887insGTGTAGTA XP_016868047.1:p.Val630CysfsTer4
XM_017012559.1:c.1886_1887insGTGTAGTA XP_016868048.1:p.Val630CysfsTer4
XR_001744857.1:n.1894_1895insGTGTAGTA
XR_001744858.1:n.1823-3951_1823-3950insGTGTAGTA
NM_001354609.2:c.1766_1767insGTGTAGTA NP_001341538.1:p.Val590CysfsTer4
NM_001374244.1:c.1886_1887insGTGTAGTA NP_001361173.1:p.Val630CysfsTer4
NM_001374258.1:c.1886_1887insGTGTAGTA MANE Plus Clinical NP_001361187.1:p.Val630CysfsTer4
NM_004333.6:c.1766_1767insGTGTAGTA MANE Select NP_004324.2:p.Val590CysfsTer4
NM_001378467.1:c.1775_1776insGTGTAGTA NP_001365396.1:p.Val593CysfsTer4
NM_001378468.1:c.1766_1767insGTGTAGTA NP_001365397.1:p.Val590CysfsTer4
NM_001378469.1:c.1700_1701insGTGTAGTA NP_001365398.1:p.Val568CysfsTer4
NM_001378470.1:c.1664_1665insGTGTAGTA NP_001365399.1:p.Val556CysfsTer4
NM_001378471.1:c.1655_1656insGTGTAGTA NP_001365400.1:p.Val553CysfsTer4
NM_001378472.1:c.1610_1611insGTGTAGTA NP_001365401.1:p.Val538CysfsTer4
NM_001378473.1:c.1610_1611insGTGTAGTA NP_001365402.1:p.Val538CysfsTer4
NM_001378474.1:c.1766_1767insGTGTAGTA NP_001365403.1:p.Val590CysfsTer4
NM_001378475.1:c.1502_1503insGTGTAGTA NP_001365404.1:p.Val502CysfsTer4