Canonical Allele Identifier: CA645544106

Gene: BRAF

Linked Data

• COSMIC: COSM1169497

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140753340_140753342del , CM000669.2:g.140753340_140753342del	GRCh38
NC_000007.13:g.140453140_140453142del , CM000669.1:g.140453140_140453142del	GRCh37
NC_000007.12:g.140099609_140099611del	NCBI36
NG_007873.3:g.176424_176426del , LRG_299:g.176424_176426del

Transcript Alleles

HGVS	Amino-acid change
ENST00000646891.2:c.1794_1796del MANE Select	ENSP00000493543.1:p.Thr599del
ENST00000288602.11:c.1914_1916del	ENSP00000288602.7:p.Thr639del
ENST00000479537.6:c.464_466del
ENST00000496384.7:c.1794_1796del	ENSP00000419060.2:p.Thr599del
ENST00000497784.2:c.*1244_*1246del	ENSP00000420119.2:n.*1244_*1246del
ENST00000642228.1:c.*872_*874del	ENSP00000493678.1:n.*872_*874del
ENST00000642875.1:n.1259-3923_1259-3921del
ENST00000644120.1:n.2184_2186del
ENST00000644650.1:c.890_892del
ENST00000644905.1:n.2676_2678del
ENST00000644969.2:c.1914_1916del MANE Plus Clinical	ENSP00000496776.1:p.Thr639del
ENST00000646730.1:c.*370_*372del	ENSP00000494784.1:n.*370_*372del
ENST00000646891.1:c.1794_1796del	ENSP00000493543.1:p.Thr599del
ENST00000647434.1:c.738-3923_738-3921del	ENSP00000495132.1:n.738-3923_738-3921del
ENST00000288602.10:c.1794_1796del	ENSP00000288602.6:p.Thr599del
ENST00000479537.5:c.78_80del	ENSP00000418033.1:p.Thr27del
ENST00000496384.6:c.617_619del
ENST00000497784.1:c.1829_1831del	ENSP00000420119.1:n.1829_1831del
NM_004333.4:c.1794_1796del , LRG_299t1:c.1794_1796del	NP_004324.2:p.Thr599del
XM_005250045.1:c.1794_1796del	XP_005250102.1:p.Thr599del
XM_005250046.1:c.1794_1796del	XP_005250103.1:p.Thr599del
XM_011516529.1:c.1794_1796del	XP_011514831.1:p.Thr599del
XM_011516530.1:c.1695-3923_1695-3921del	XP_011514832.1:n.1695-3923_1695-3921del
XR_242190.1:n.1802_1804del
XR_927520.1:n.1802_1804del
XR_927521.1:n.1802_1804del
XR_927522.1:n.1703-3923_1703-3921del
XR_927523.1:n.1703-3923_1703-3921del
NM_001354609.1:c.1794_1796del	NP_001341538.1:p.Thr599del
NM_004333.5:c.1794_1796del	NP_004324.2:p.Thr599del
NR_148928.1:n.2892_2894del
XM_017012558.1:c.1914_1916del	XP_016868047.1:p.Thr639del
XM_017012559.1:c.1914_1916del	XP_016868048.1:p.Thr639del
XR_001744857.1:n.1922_1924del
XR_001744858.1:n.1823-3923_1823-3921del
NM_001354609.2:c.1794_1796del	NP_001341538.1:p.Thr599del
NM_001374244.1:c.1914_1916del	NP_001361173.1:p.Thr639del
NM_001374258.1:c.1914_1916del MANE Plus Clinical	NP_001361187.1:p.Thr639del
NM_004333.6:c.1794_1796del MANE Select	NP_004324.2:p.Thr599del
NM_001378467.1:c.1803_1805del	NP_001365396.1:p.Thr602del
NM_001378468.1:c.1794_1796del	NP_001365397.1:p.Thr599del
NM_001378469.1:c.1728_1730del	NP_001365398.1:p.Thr577del
NM_001378470.1:c.1692_1694del	NP_001365399.1:p.Thr565del
NM_001378471.1:c.1683_1685del	NP_001365400.1:p.Thr562del
NM_001378472.1:c.1638_1640del	NP_001365401.1:p.Thr547del
NM_001378473.1:c.1638_1640del	NP_001365402.1:p.Thr547del
NM_001378474.1:c.1794_1796del	NP_001365403.1:p.Thr599del
NM_001378475.1:c.1530_1532del	NP_001365404.1:p.Thr511del