Canonical Allele Identifier: CA369589016
Gene: BRAF HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140781669T>G , CM000669.2:g.140781669T>G GRCh38
NC_000007.13:g.140481469T>G , CM000669.1:g.140481469T>G GRCh37
NC_000007.12:g.140127938T>G NCBI36
NG_007873.3:g.148096A>C , LRG_299:g.148096A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000646891.2:c.1339A>C MANE Select ENSP00000493543.1:p.Ser447Arg
ENST00000288602.11:c.1459A>C ENSP00000288602.7:p.Ser487Arg
ENST00000479537.6:c.9A>C
ENST00000496384.7:c.1339A>C ENSP00000419060.2:p.Ser447Arg
ENST00000497784.2:c.*789A>C ENSP00000420119.2:n.*789A>C
ENST00000642228.1:c.*417A>C ENSP00000493678.1:n.*417A>C
ENST00000642875.1:n.781A>C
ENST00000644120.1:n.1729A>C
ENST00000644650.1:c.435A>C
ENST00000644905.1:n.1428A>C
ENST00000644969.2:c.1459A>C MANE Plus Clinical ENSP00000496776.1:p.Ser487Arg
ENST00000646334.1:n.469A>C
ENST00000646730.1:c.1339A>C ENSP00000494784.1:p.Ser447Arg
ENST00000646891.1:c.1339A>C ENSP00000493543.1:p.Ser447Arg
ENST00000647434.1:c.382A>C ENSP00000495132.1:p.Ser128Arg
ENST00000288602.10:c.1339A>C ENSP00000288602.6:p.Ser447Arg
ENST00000496384.6:c.162A>C
ENST00000497784.1:c.1374A>C ENSP00000420119.1:n.1374A>C
NM_004333.4:c.1339A>C , LRG_299t1:c.1339A>C NP_004324.2:p.Ser447Arg
XM_005250045.1:c.1339A>C XP_005250102.1:p.Ser447Arg
XM_005250046.1:c.1339A>C XP_005250103.1:p.Ser447Arg
XM_011516529.1:c.1339A>C XP_011514831.1:p.Ser447Arg
XM_011516530.1:c.1339A>C XP_011514832.1:p.Ser447Arg
XR_242190.1:n.1347A>C
XR_927520.1:n.1347A>C
XR_927521.1:n.1347A>C
XR_927522.1:n.1347A>C
XR_927523.1:n.1347A>C
NM_001354609.1:c.1339A>C NP_001341538.1:p.Ser447Arg
NM_004333.5:c.1339A>C NP_004324.2:p.Ser447Arg
NR_148928.1:n.1644A>C
XM_017012558.1:c.1459A>C XP_016868047.1:p.Ser487Arg
XM_017012559.1:c.1459A>C XP_016868048.1:p.Ser487Arg
XR_001744857.1:n.1467A>C
XR_001744858.1:n.1467A>C
NM_001354609.2:c.1339A>C NP_001341538.1:p.Ser447Arg
NM_001374244.1:c.1459A>C NP_001361173.1:p.Ser487Arg
NM_001374258.1:c.1459A>C MANE Plus Clinical NP_001361187.1:p.Ser487Arg
NM_004333.6:c.1339A>C MANE Select NP_004324.2:p.Ser447Arg
NM_001378467.1:c.1348A>C NP_001365396.1:p.Ser450Arg
NM_001378468.1:c.1339A>C NP_001365397.1:p.Ser447Arg
NM_001378469.1:c.1273A>C NP_001365398.1:p.Ser425Arg
NM_001378470.1:c.1237A>C NP_001365399.1:p.Ser413Arg
NM_001378471.1:c.1228A>C NP_001365400.1:p.Ser410Arg
NM_001378472.1:c.1183A>C NP_001365401.1:p.Ser395Arg
NM_001378473.1:c.1183A>C NP_001365402.1:p.Ser395Arg
NM_001378474.1:c.1339A>C NP_001365403.1:p.Ser447Arg
NM_001378475.1:c.1075A>C NP_001365404.1:p.Ser359Arg