Canonical Allele Identifier: CA1747732049

Gene: BRAF

Linked Data

• dbSNP Id: rs1802967426

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140800373_140800374insACAGGAA , CM000669.2:g.140800373_140800374insACAGGAA	GRCh38
NC_000007.13:g.140500173_140500174insACAGGAA , CM000669.1:g.140500173_140500174insACAGGAA	GRCh37
NC_000007.12:g.140146642_140146643insACAGGAA	NCBI36
NG_007873.3:g.129391_129392insTTCCTGT , LRG_299:g.129391_129392insTTCCTGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000646891.2:c.968_969insTTCCTGT MANE Select	ENSP00000493543.1:p.Asp324SerfsTer30
ENST00000288602.11:c.968_969insTTCCTGT	ENSP00000288602.7:p.Asp324SerfsTer30
ENST00000496384.7:c.968_969insTTCCTGT	ENSP00000419060.2:p.Asp324SerfsTer30
ENST00000497784.2:c.*418_*419insTTCCTGT	ENSP00000420119.2:n.*418_*419insTTCCTGT
ENST00000642228.1:c.*46_*47insTTCCTGT	ENSP00000493678.1:n.*46_*47insTTCCTGT
ENST00000642272.1:n.1000_1001insTTCCTGT
ENST00000642875.1:n.462_463insTTCCTGT
ENST00000644120.1:n.1410_1411insTTCCTGT
ENST00000644650.1:c.64_65insTTCCTGT
ENST00000644905.1:n.1057_1058insTTCCTGT
ENST00000644969.2:c.968_969insTTCCTGT MANE Plus Clinical	ENSP00000496776.1:p.Asp324SerfsTer30
ENST00000646730.1:c.968_969insTTCCTGT	ENSP00000494784.1:p.Asp324SerfsTer30
ENST00000646891.1:c.968_969insTTCCTGT	ENSP00000493543.1:p.Asp324SerfsTer30
ENST00000647434.1:c.11_12insTTCCTGT	ENSP00000495132.1:p.Asp5SerfsTer30
ENST00000288602.10:c.968_969insTTCCTGT	ENSP00000288602.6:p.Asp324SerfsTer30
ENST00000497784.1:c.1003_1004insTTCCTGT	ENSP00000420119.1:n.1003_1004insTTCCTGT
NM_004333.4:c.968_969insTTCCTGT , LRG_299t1:c.968_969insTTCCTGT	NP_004324.2:p.Asp324SerfsTer30
XM_005250045.1:c.968_969insTTCCTGT	XP_005250102.1:p.Asp324SerfsTer30
XM_005250046.1:c.968_969insTTCCTGT	XP_005250103.1:p.Asp324SerfsTer30
XM_011516529.1:c.968_969insTTCCTGT	XP_011514831.1:p.Asp324SerfsTer30
XM_011516530.1:c.968_969insTTCCTGT	XP_011514832.1:p.Asp324SerfsTer30
XR_242190.1:n.976_977insTTCCTGT
XR_927520.1:n.976_977insTTCCTGT
XR_927521.1:n.976_977insTTCCTGT
XR_927522.1:n.976_977insTTCCTGT
XR_927523.1:n.976_977insTTCCTGT
NM_001354609.1:c.968_969insTTCCTGT	NP_001341538.1:p.Asp324SerfsTer30
NM_004333.5:c.968_969insTTCCTGT	NP_004324.2:p.Asp324SerfsTer30
NR_148928.1:n.1273_1274insTTCCTGT
XM_017012558.1:c.968_969insTTCCTGT	XP_016868047.1:p.Asp324SerfsTer30
XM_017012559.1:c.968_969insTTCCTGT	XP_016868048.1:p.Asp324SerfsTer30
XR_001744857.1:n.976_977insTTCCTGT
XR_001744858.1:n.976_977insTTCCTGT
NM_001354609.2:c.968_969insTTCCTGT	NP_001341538.1:p.Asp324SerfsTer30
NM_001374244.1:c.968_969insTTCCTGT	NP_001361173.1:p.Asp324SerfsTer30
NM_001374258.1:c.968_969insTTCCTGT MANE Plus Clinical	NP_001361187.1:p.Asp324SerfsTer30
NM_004333.6:c.968_969insTTCCTGT MANE Select	NP_004324.2:p.Asp324SerfsTer30
NM_001378467.1:c.977_978insTTCCTGT	NP_001365396.1:p.Asp327SerfsTer30
NM_001378468.1:c.968_969insTTCCTGT	NP_001365397.1:p.Asp324SerfsTer30
NM_001378469.1:c.968_969insTTCCTGT	NP_001365398.1:p.Asp324SerfsTer30
NM_001378470.1:c.866_867insTTCCTGT	NP_001365399.1:p.Asp290SerfsTer30
NM_001378471.1:c.968_969insTTCCTGT	NP_001365400.1:p.Asp324SerfsTer30
NM_001378472.1:c.812_813insTTCCTGT	NP_001365401.1:p.Asp272SerfsTer30
NM_001378473.1:c.812_813insTTCCTGT	NP_001365402.1:p.Asp272SerfsTer30
NM_001378474.1:c.968_969insTTCCTGT	NP_001365403.1:p.Asp324SerfsTer30
NM_001378475.1:c.704_705insTTCCTGT	NP_001365404.1:p.Asp236SerfsTer30