Canonical Allele Identifier: CA1747715048

Gene: BRAF

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140778036_140778051delinsGTAGGTGCTGTCACAT , CM000669.2:g.140778036_140778051delinsGTAGGTGCTGTCACAT	GRCh38
NC_000007.13:g.140477836_140477851delinsGTAGGTGCTGTCACAT , CM000669.1:g.140477836_140477851delinsGTAGGTGCTGTCACAT	GRCh37
NC_000007.12:g.140124305_140124320delinsGTAGGTGCTGTCACAT	NCBI36
NG_007873.3:g.151714_151729delinsATGTGACAGCACCTAC , LRG_299:g.151714_151729delinsATGTGACAGCACCTAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646891.2:c.1457_1472delinsATGTGACAGCACCTAC MANE Select	ENSP00000493543.1:p.Asn486=
ENST00000288602.11:c.1577_1592delinsATGTGACAGCACCTAC	ENSP00000288602.7:p.Asn526=
ENST00000479537.6:c.127_142delinsATGTGACAGCACCTAC
ENST00000496384.7:c.1457_1472delinsATGTGACAGCACCTAC	ENSP00000419060.2:p.Asn486=
ENST00000497784.2:c.*907_*922delinsATGTGACAGCACCTAC	ENSP00000420119.2:n.*907_*922delinsATGTGACAGCACCTAC
ENST00000642228.1:c.*535_*550delinsATGTGACAGCACCTAC	ENSP00000493678.1:n.*535_*550delinsATGTGACAGCACCTAC
ENST00000642875.1:n.1021_1036delinsATGTGACAGCACCTAC
ENST00000644120.1:n.1847_1862delinsATGTGACAGCACCTAC
ENST00000644650.1:c.553_568delinsATGTGACAGCACCTAC
ENST00000644905.1:n.1546_1561delinsATGTGACAGCACCTAC
ENST00000644969.2:c.1577_1592delinsATGTGACAGCACCTAC MANE Plus Clinical	ENSP00000496776.1:p.Asn526=
ENST00000646730.1:c.1457_1472delinsATGTGACAGCACCTAC	ENSP00000494784.1:p.Asn486=
ENST00000646891.1:c.1457_1472delinsATGTGACAGCACCTAC	ENSP00000493543.1:p.Asn486=
ENST00000647434.1:c.500_515delinsATGTGACAGCACCTAC	ENSP00000495132.1:p.Asn167=
ENST00000288602.10:c.1457_1472delinsATGTGACAGCACCTAC	ENSP00000288602.6:p.Asn486=
ENST00000496384.6:c.280_295delinsATGTGACAGCACCTAC
ENST00000497784.1:c.1492_1507delinsATGTGACAGCACCTAC	ENSP00000420119.1:n.1492_1507delinsATGTGACAGCACCTAC
NM_004333.4:c.1457_1472delinsATGTGACAGCACCTAC , LRG_299t1:c.1457_1472delinsATGTGACAGCACCTAC	NP_004324.2:p.Asn486=
XM_005250045.1:c.1457_1472delinsATGTGACAGCACCTAC	XP_005250102.1:p.Asn486=
XM_005250046.1:c.1457_1472delinsATGTGACAGCACCTAC	XP_005250103.1:p.Asn486=
XM_011516529.1:c.1457_1472delinsATGTGACAGCACCTAC	XP_011514831.1:p.Asn486=
XM_011516530.1:c.1457_1472delinsATGTGACAGCACCTAC	XP_011514832.1:p.Asn486=
XR_242190.1:n.1465_1480delinsATGTGACAGCACCTAC
XR_927520.1:n.1465_1480delinsATGTGACAGCACCTAC
XR_927521.1:n.1465_1480delinsATGTGACAGCACCTAC
XR_927522.1:n.1465_1480delinsATGTGACAGCACCTAC
XR_927523.1:n.1465_1480delinsATGTGACAGCACCTAC
NM_001354609.1:c.1457_1472delinsATGTGACAGCACCTAC	NP_001341538.1:p.Asn486=
NM_004333.5:c.1457_1472delinsATGTGACAGCACCTAC	NP_004324.2:p.Asn486=
NR_148928.1:n.1762_1777delinsATGTGACAGCACCTAC
XM_017012558.1:c.1577_1592delinsATGTGACAGCACCTAC	XP_016868047.1:p.Asn526=
XM_017012559.1:c.1577_1592delinsATGTGACAGCACCTAC	XP_016868048.1:p.Asn526=
XR_001744857.1:n.1585_1600delinsATGTGACAGCACCTAC
XR_001744858.1:n.1585_1600delinsATGTGACAGCACCTAC
NM_001354609.2:c.1457_1472delinsATGTGACAGCACCTAC	NP_001341538.1:p.Asn486=
NM_001374244.1:c.1577_1592delinsATGTGACAGCACCTAC	NP_001361173.1:p.Asn526=
NM_001374258.1:c.1577_1592delinsATGTGACAGCACCTAC MANE Plus Clinical	NP_001361187.1:p.Asn526=
NM_004333.6:c.1457_1472delinsATGTGACAGCACCTAC MANE Select	NP_004324.2:p.Asn486=
NM_001378467.1:c.1466_1481delinsATGTGACAGCACCTAC	NP_001365396.1:p.Asn489=
NM_001378468.1:c.1457_1472delinsATGTGACAGCACCTAC	NP_001365397.1:p.Asn486=
NM_001378469.1:c.1391_1406delinsATGTGACAGCACCTAC	NP_001365398.1:p.Asn464=
NM_001378470.1:c.1355_1370delinsATGTGACAGCACCTAC	NP_001365399.1:p.Asn452=
NM_001378471.1:c.1346_1361delinsATGTGACAGCACCTAC	NP_001365400.1:p.Asn449=
NM_001378472.1:c.1301_1316delinsATGTGACAGCACCTAC	NP_001365401.1:p.Asn434=
NM_001378473.1:c.1301_1316delinsATGTGACAGCACCTAC	NP_001365402.1:p.Asn434=
NM_001378474.1:c.1457_1472delinsATGTGACAGCACCTAC	NP_001365403.1:p.Asn486=
NM_001378475.1:c.1193_1208delinsATGTGACAGCACCTAC	NP_001365404.1:p.Asn398=