Canonical Allele Identifier: CA913189399
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 599445
dbSNP Id: rs1562956929

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140781603_140781623dup , CM000669.2:g.140781603_140781623dup GRCh38
NC_000007.13:g.140481403_140481423dup , CM000669.1:g.140481403_140481423dup GRCh37
NC_000007.12:g.140127872_140127892dup NCBI36
NG_007873.3:g.148145_148165dup , LRG_299:g.148145_148165dup

Transcript Alleles

HGVS Amino-acid change
ENST00000646891.2:c.1388_1408dup MANE Select ENSP00000493543.1:p.Gly469_Thr470insIleGl...
ENST00000288602.11:c.1508_1528dup ENSP00000288602.7:p.Gly509_Thr510insIleGl...
ENST00000479537.6:c.58_78dup
ENST00000496384.7:c.1388_1408dup ENSP00000419060.2:p.Gly469_Thr470insIleGl...
ENST00000497784.2:c.*838_*858dup ENSP00000420119.2:n.*838_*858dup
ENST00000642228.1:c.*466_*486dup ENSP00000493678.1:n.*466_*486dup
ENST00000642875.1:n.830_850dup
ENST00000644120.1:n.1778_1798dup
ENST00000644650.1:c.484_504dup
ENST00000644905.1:n.1477_1497dup
ENST00000644969.2:c.1508_1528dup MANE Plus Clinical ENSP00000496776.1:p.Gly509_Thr510insIleGl...
ENST00000646334.1:n.518_538dup
ENST00000646730.1:c.1388_1408dup ENSP00000494784.1:p.Gly469_Thr470insIleGl...
ENST00000646891.1:c.1388_1408dup ENSP00000493543.1:p.Gly469_Thr470insIleGl...
ENST00000647434.1:c.431_451dup ENSP00000495132.1:p.Gly150_Thr151insIleGl...
ENST00000288602.10:c.1388_1408dup ENSP00000288602.6:p.Gly469_Thr470insIleGl...
ENST00000496384.6:c.211_231dup
ENST00000497784.1:c.1423_1443dup ENSP00000420119.1:n.1423_1443dup
NM_004333.4:c.1388_1408dup , LRG_299t1:c.1388_1408dup NP_004324.2:p.Gly469_Thr470insIleGlySerGl...
XM_005250045.1:c.1388_1408dup XP_005250102.1:p.Gly469_Thr470insIleGlySe...
XM_005250046.1:c.1388_1408dup XP_005250103.1:p.Gly469_Thr470insIleGlySe...
XM_011516529.1:c.1388_1408dup XP_011514831.1:p.Gly469_Thr470insIleGlySe...
XM_011516530.1:c.1388_1408dup XP_011514832.1:p.Gly469_Thr470insIleGlySe...
XR_242190.1:n.1396_1416dup
XR_927520.1:n.1396_1416dup
XR_927521.1:n.1396_1416dup
XR_927522.1:n.1396_1416dup
XR_927523.1:n.1396_1416dup
NM_001354609.1:c.1388_1408dup NP_001341538.1:p.Gly469_Thr470insIleGlySe...
NM_004333.5:c.1388_1408dup NP_004324.2:p.Gly469_Thr470insIleGlySerGl...
NR_148928.1:n.1693_1713dup
XM_017012558.1:c.1508_1528dup XP_016868047.1:p.Gly509_Thr510insIleGlySe...
XM_017012559.1:c.1508_1528dup XP_016868048.1:p.Gly509_Thr510insIleGlySe...
XR_001744857.1:n.1516_1536dup
XR_001744858.1:n.1516_1536dup
NM_001354609.2:c.1388_1408dup NP_001341538.1:p.Gly469_Thr470insIleGlySe...
NM_001374244.1:c.1508_1528dup NP_001361173.1:p.Gly509_Thr510insIleGlySe...
NM_001374258.1:c.1508_1528dup MANE Plus Clinical NP_001361187.1:p.Gly509_Thr510insIleGlySe...
NM_004333.6:c.1388_1408dup MANE Select NP_004324.2:p.Gly469_Thr470insIleGlySerGl...
NM_001378467.1:c.1397_1417dup NP_001365396.1:p.Gly472_Thr473insIleGlySe...
NM_001378468.1:c.1388_1408dup NP_001365397.1:p.Gly469_Thr470insIleGlySe...
NM_001378469.1:c.1322_1342dup NP_001365398.1:p.Gly447_Thr448insIleGlySe...
NM_001378470.1:c.1286_1306dup NP_001365399.1:p.Gly435_Thr436insIleGlySe...
NM_001378471.1:c.1277_1297dup NP_001365400.1:p.Gly432_Thr433insIleGlySe...
NM_001378472.1:c.1232_1252dup NP_001365401.1:p.Gly417_Thr418insIleGlySe...
NM_001378473.1:c.1232_1252dup NP_001365402.1:p.Gly417_Thr418insIleGlySe...
NM_001378474.1:c.1388_1408dup NP_001365403.1:p.Gly469_Thr470insIleGlySe...
NM_001378475.1:c.1124_1144dup NP_001365404.1:p.Gly381_Thr382insIleGlySe...