Canonical Allele Identifier: CA2839977655

Gene: BRAF

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140754298_140754299del , CM000669.2:g.140754298_140754299del	GRCh38
NC_000007.13:g.140454098_140454099del , CM000669.1:g.140454098_140454099del	GRCh37
NC_000007.12:g.140100567_140100568del	NCBI36
NG_007873.3:g.175466_175467del , LRG_299:g.175466_175467del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646891.2:c.1695-66_1695-65del MANE Select	ENSP00000493543.1:n.1695-66_1695-65del
ENST00000288602.11:c.1815-66_1815-65del	ENSP00000288602.7:n.1815-66_1815-65del
ENST00000479537.6:c.365-66_365-65del
ENST00000496384.7:c.1695-66_1695-65del	ENSP00000419060.2:n.1695-66_1695-65del
ENST00000497784.2:c.*1145-66_*1145-65del	ENSP00000420119.2:n.*1145-66_*1145-65del
ENST00000642228.1:c.*773-66_*773-65del	ENSP00000493678.1:n.*773-66_*773-65del
ENST00000642875.1:n.1259-4881_1259-4880del
ENST00000644120.1:n.2085-66_2085-65del
ENST00000644650.1:c.791-66_791-65del
ENST00000644905.1:n.1784-66_1784-65del
ENST00000644969.2:c.1815-66_1815-65del MANE Plus Clinical	ENSP00000496776.1:n.1815-66_1815-65del
ENST00000646730.1:c.*271-66_*271-65del	ENSP00000494784.1:n.*271-66_*271-65del
ENST00000646891.1:c.1695-66_1695-65del	ENSP00000493543.1:n.1695-66_1695-65del
ENST00000647434.1:c.738-4881_738-4880del	ENSP00000495132.1:n.738-4881_738-4880del
ENST00000288602.10:c.1695-66_1695-65del	ENSP00000288602.6:n.1695-66_1695-65del
ENST00000496384.6:c.518-66_518-65del
ENST00000497784.1:c.1730-66_1730-65del	ENSP00000420119.1:n.1730-66_1730-65del
NM_004333.4:c.1695-66_1695-65del , LRG_299t1:c.1695-66_1695-65del	NP_004324.2:n.1695-66_1695-65del
XM_005250045.1:c.1695-66_1695-65del	XP_005250102.1:n.1695-66_1695-65del
XM_005250046.1:c.1695-66_1695-65del	XP_005250103.1:n.1695-66_1695-65del
XM_011516529.1:c.1695-66_1695-65del	XP_011514831.1:n.1695-66_1695-65del
XM_011516530.1:c.1695-4881_1695-4880del	XP_011514832.1:n.1695-4881_1695-4880del
XR_242190.1:n.1703-66_1703-65del
XR_927520.1:n.1703-66_1703-65del
XR_927521.1:n.1703-66_1703-65del
XR_927522.1:n.1703-4881_1703-4880del
XR_927523.1:n.1703-4881_1703-4880del
NM_001354609.1:c.1695-66_1695-65del	NP_001341538.1:n.1695-66_1695-65del
NM_004333.5:c.1695-66_1695-65del	NP_004324.2:n.1695-66_1695-65del
NR_148928.1:n.2000-66_2000-65del
XM_017012558.1:c.1815-66_1815-65del	XP_016868047.1:n.1815-66_1815-65del
XM_017012559.1:c.1815-66_1815-65del	XP_016868048.1:n.1815-66_1815-65del
XR_001744857.1:n.1823-66_1823-65del
XR_001744858.1:n.1823-4881_1823-4880del
NM_001354609.2:c.1695-66_1695-65del	NP_001341538.1:n.1695-66_1695-65del
NM_001374244.1:c.1815-66_1815-65del	NP_001361173.1:n.1815-66_1815-65del
NM_001374258.1:c.1815-66_1815-65del MANE Plus Clinical	NP_001361187.1:n.1815-66_1815-65del
NM_004333.6:c.1695-66_1695-65del MANE Select	NP_004324.2:n.1695-66_1695-65del
NM_001378467.1:c.1704-66_1704-65del	NP_001365396.1:n.1704-66_1704-65del
NM_001378468.1:c.1695-66_1695-65del	NP_001365397.1:n.1695-66_1695-65del
NM_001378469.1:c.1629-66_1629-65del	NP_001365398.1:n.1629-66_1629-65del
NM_001378470.1:c.1593-66_1593-65del	NP_001365399.1:n.1593-66_1593-65del
NM_001378471.1:c.1584-66_1584-65del	NP_001365400.1:n.1584-66_1584-65del
NM_001378472.1:c.1539-66_1539-65del	NP_001365401.1:n.1539-66_1539-65del
NM_001378473.1:c.1539-66_1539-65del	NP_001365402.1:n.1539-66_1539-65del
NM_001378474.1:c.1695-66_1695-65del	NP_001365403.1:n.1695-66_1695-65del
NM_001378475.1:c.1431-66_1431-65del	NP_001365404.1:n.1431-66_1431-65del