Canonical Allele Identifier: CA645556779

Gene: BRAF

Linked Data

• COSMIC: COSM5751172

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140781599dup , CM000669.2:g.140781599dup	GRCh38
NC_000007.13:g.140481399dup , CM000669.1:g.140481399dup	GRCh37
NC_000007.12:g.140127868dup	NCBI36
NG_007873.3:g.148166dup , LRG_299:g.148166dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000646891.2:c.1409dup MANE Select	ENSP00000493543.1:p.Val471SerfsTer9
ENST00000288602.11:c.1529dup	ENSP00000288602.7:p.Val511SerfsTer9
ENST00000479537.6:c.79dup
ENST00000496384.7:c.1409dup	ENSP00000419060.2:p.Val471SerfsTer9
ENST00000497784.2:c.*859dup	ENSP00000420119.2:n.*859dup
ENST00000642228.1:c.*487dup	ENSP00000493678.1:n.*487dup
ENST00000642875.1:n.851dup
ENST00000644120.1:n.1799dup
ENST00000644650.1:c.505dup
ENST00000644905.1:n.1498dup
ENST00000644969.2:c.1529dup MANE Plus Clinical	ENSP00000496776.1:p.Val511SerfsTer9
ENST00000646334.1:n.539dup
ENST00000646730.1:c.1409dup	ENSP00000494784.1:p.Val471SerfsTer9
ENST00000646891.1:c.1409dup	ENSP00000493543.1:p.Val471SerfsTer9
ENST00000647434.1:c.452dup	ENSP00000495132.1:p.Val152SerfsTer9
ENST00000288602.10:c.1409dup	ENSP00000288602.6:p.Val471SerfsTer9
ENST00000496384.6:c.232dup
ENST00000497784.1:c.1444dup	ENSP00000420119.1:n.1444dup
NM_004333.4:c.1409dup , LRG_299t1:c.1409dup	NP_004324.2:p.Val471SerfsTer9
XM_005250045.1:c.1409dup	XP_005250102.1:p.Val471SerfsTer9
XM_005250046.1:c.1409dup	XP_005250103.1:p.Val471SerfsTer9
XM_011516529.1:c.1409dup	XP_011514831.1:p.Val471SerfsTer9
XM_011516530.1:c.1409dup	XP_011514832.1:p.Val471SerfsTer9
XR_242190.1:n.1417dup
XR_927520.1:n.1417dup
XR_927521.1:n.1417dup
XR_927522.1:n.1417dup
XR_927523.1:n.1417dup
NM_001354609.1:c.1409dup	NP_001341538.1:p.Val471SerfsTer9
NM_004333.5:c.1409dup	NP_004324.2:p.Val471SerfsTer9
NR_148928.1:n.1714dup
XM_017012558.1:c.1529dup	XP_016868047.1:p.Val511SerfsTer9
XM_017012559.1:c.1529dup	XP_016868048.1:p.Val511SerfsTer9
XR_001744857.1:n.1537dup
XR_001744858.1:n.1537dup
NM_001354609.2:c.1409dup	NP_001341538.1:p.Val471SerfsTer9
NM_001374244.1:c.1529dup	NP_001361173.1:p.Val511SerfsTer9
NM_001374258.1:c.1529dup MANE Plus Clinical	NP_001361187.1:p.Val511SerfsTer9
NM_004333.6:c.1409dup MANE Select	NP_004324.2:p.Val471SerfsTer9
NM_001378467.1:c.1418dup	NP_001365396.1:p.Val474SerfsTer9
NM_001378468.1:c.1409dup	NP_001365397.1:p.Val471SerfsTer9
NM_001378469.1:c.1343dup	NP_001365398.1:p.Val449SerfsTer9
NM_001378470.1:c.1307dup	NP_001365399.1:p.Val437SerfsTer9
NM_001378471.1:c.1298dup	NP_001365400.1:p.Val434SerfsTer9
NM_001378472.1:c.1253dup	NP_001365401.1:p.Val419SerfsTer9
NM_001378473.1:c.1253dup	NP_001365402.1:p.Val419SerfsTer9
NM_001378474.1:c.1409dup	NP_001365403.1:p.Val471SerfsTer9
NM_001378475.1:c.1145dup	NP_001365404.1:p.Val383SerfsTer9