Canonical Allele Identifier: CA2838946451

Gene: BRAF

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140754301_140754303del , CM000669.2:g.140754301_140754303del	GRCh38
NC_000007.13:g.140454101_140454103del , CM000669.1:g.140454101_140454103del	GRCh37
NC_000007.12:g.140100570_140100572del	NCBI36
NG_007873.3:g.175462_175464del , LRG_299:g.175462_175464del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646891.2:c.1695-70_1695-68del MANE Select	ENSP00000493543.1:n.1695-70_1695-68del
ENST00000288602.11:c.1815-70_1815-68del	ENSP00000288602.7:n.1815-70_1815-68del
ENST00000479537.6:c.365-70_365-68del
ENST00000496384.7:c.1695-70_1695-68del	ENSP00000419060.2:n.1695-70_1695-68del
ENST00000497784.2:c.*1145-70_*1145-68del	ENSP00000420119.2:n.*1145-70_*1145-68del
ENST00000642228.1:c.*773-70_*773-68del	ENSP00000493678.1:n.*773-70_*773-68del
ENST00000642875.1:n.1259-4885_1259-4883del
ENST00000644120.1:n.2085-70_2085-68del
ENST00000644650.1:c.791-70_791-68del
ENST00000644905.1:n.1784-70_1784-68del
ENST00000644969.2:c.1815-70_1815-68del MANE Plus Clinical	ENSP00000496776.1:n.1815-70_1815-68del
ENST00000646730.1:c.*271-70_*271-68del	ENSP00000494784.1:n.*271-70_*271-68del
ENST00000646891.1:c.1695-70_1695-68del	ENSP00000493543.1:n.1695-70_1695-68del
ENST00000647434.1:c.738-4885_738-4883del	ENSP00000495132.1:n.738-4885_738-4883del
ENST00000288602.10:c.1695-70_1695-68del	ENSP00000288602.6:n.1695-70_1695-68del
ENST00000496384.6:c.518-70_518-68del
ENST00000497784.1:c.1730-70_1730-68del	ENSP00000420119.1:n.1730-70_1730-68del
NM_004333.4:c.1695-70_1695-68del , LRG_299t1:c.1695-70_1695-68del	NP_004324.2:n.1695-70_1695-68del
XM_005250045.1:c.1695-70_1695-68del	XP_005250102.1:n.1695-70_1695-68del
XM_005250046.1:c.1695-70_1695-68del	XP_005250103.1:n.1695-70_1695-68del
XM_011516529.1:c.1695-70_1695-68del	XP_011514831.1:n.1695-70_1695-68del
XM_011516530.1:c.1695-4885_1695-4883del	XP_011514832.1:n.1695-4885_1695-4883del
XR_242190.1:n.1703-70_1703-68del
XR_927520.1:n.1703-70_1703-68del
XR_927521.1:n.1703-70_1703-68del
XR_927522.1:n.1703-4885_1703-4883del
XR_927523.1:n.1703-4885_1703-4883del
NM_001354609.1:c.1695-70_1695-68del	NP_001341538.1:n.1695-70_1695-68del
NM_004333.5:c.1695-70_1695-68del	NP_004324.2:n.1695-70_1695-68del
NR_148928.1:n.2000-70_2000-68del
XM_017012558.1:c.1815-70_1815-68del	XP_016868047.1:n.1815-70_1815-68del
XM_017012559.1:c.1815-70_1815-68del	XP_016868048.1:n.1815-70_1815-68del
XR_001744857.1:n.1823-70_1823-68del
XR_001744858.1:n.1823-4885_1823-4883del
NM_001354609.2:c.1695-70_1695-68del	NP_001341538.1:n.1695-70_1695-68del
NM_001374244.1:c.1815-70_1815-68del	NP_001361173.1:n.1815-70_1815-68del
NM_001374258.1:c.1815-70_1815-68del MANE Plus Clinical	NP_001361187.1:n.1815-70_1815-68del
NM_004333.6:c.1695-70_1695-68del MANE Select	NP_004324.2:n.1695-70_1695-68del
NM_001378467.1:c.1704-70_1704-68del	NP_001365396.1:n.1704-70_1704-68del
NM_001378468.1:c.1695-70_1695-68del	NP_001365397.1:n.1695-70_1695-68del
NM_001378469.1:c.1629-70_1629-68del	NP_001365398.1:n.1629-70_1629-68del
NM_001378470.1:c.1593-70_1593-68del	NP_001365399.1:n.1593-70_1593-68del
NM_001378471.1:c.1584-70_1584-68del	NP_001365400.1:n.1584-70_1584-68del
NM_001378472.1:c.1539-70_1539-68del	NP_001365401.1:n.1539-70_1539-68del
NM_001378473.1:c.1539-70_1539-68del	NP_001365402.1:n.1539-70_1539-68del
NM_001378474.1:c.1695-70_1695-68del	NP_001365403.1:n.1695-70_1695-68del
NM_001378475.1:c.1431-70_1431-68del	NP_001365404.1:n.1431-70_1431-68del