Canonical Allele Identifier: CA279970
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 13974
dbSNP Id: rs121913355
COSMIC: COSM461
CIViC: CA279970

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140781602C>T , CM000669.2:g.140781602C>T GRCh38
NC_000007.13:g.140481402C>T , CM000669.1:g.140481402C>T GRCh37
NC_000007.12:g.140127871C>T NCBI36
NG_007873.3:g.148163G>A , LRG_299:g.148163G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000646891.2:c.1406G>A MANE Select ENSP00000493543.1:p.Gly469Glu
ENST00000288602.11:c.1526G>A ENSP00000288602.7:p.Gly509Glu
ENST00000479537.6:c.76G>A
ENST00000496384.7:c.1406G>A ENSP00000419060.2:p.Gly469Glu
ENST00000497784.2:c.*856G>A ENSP00000420119.2:n.*856G>A
ENST00000642228.1:c.*484G>A ENSP00000493678.1:n.*484G>A
ENST00000642875.1:n.848G>A
ENST00000644120.1:n.1796G>A
ENST00000644650.1:c.502G>A
ENST00000644905.1:n.1495G>A
ENST00000644969.2:c.1526G>A MANE Plus Clinical ENSP00000496776.1:p.Gly509Glu
ENST00000646334.1:n.536G>A
ENST00000646730.1:c.1406G>A ENSP00000494784.1:p.Gly469Glu
ENST00000646891.1:c.1406G>A ENSP00000493543.1:p.Gly469Glu
ENST00000647434.1:c.449G>A ENSP00000495132.1:p.Gly150Glu
ENST00000288602.10:c.1406G>A ENSP00000288602.6:p.Gly469Glu
ENST00000496384.6:c.229G>A
ENST00000497784.1:c.1441G>A ENSP00000420119.1:n.1441G>A
NM_004333.4:c.1406G>A , LRG_299t1:c.1406G>A NP_004324.2:p.Gly469Glu
XM_005250045.1:c.1406G>A XP_005250102.1:p.Gly469Glu
XM_005250046.1:c.1406G>A XP_005250103.1:p.Gly469Glu
XM_011516529.1:c.1406G>A XP_011514831.1:p.Gly469Glu
XM_011516530.1:c.1406G>A XP_011514832.1:p.Gly469Glu
XR_242190.1:n.1414G>A
XR_927520.1:n.1414G>A
XR_927521.1:n.1414G>A
XR_927522.1:n.1414G>A
XR_927523.1:n.1414G>A
NM_001354609.1:c.1406G>A NP_001341538.1:p.Gly469Glu
NM_004333.5:c.1406G>A NP_004324.2:p.Gly469Glu
NR_148928.1:n.1711G>A
XM_017012558.1:c.1526G>A XP_016868047.1:p.Gly509Glu
XM_017012559.1:c.1526G>A XP_016868048.1:p.Gly509Glu
XR_001744857.1:n.1534G>A
XR_001744858.1:n.1534G>A
NM_001354609.2:c.1406G>A NP_001341538.1:p.Gly469Glu
NM_001374244.1:c.1526G>A NP_001361173.1:p.Gly509Glu
NM_001374258.1:c.1526G>A MANE Plus Clinical NP_001361187.1:p.Gly509Glu
NM_004333.6:c.1406G>A MANE Select NP_004324.2:p.Gly469Glu
NM_001378467.1:c.1415G>A NP_001365396.1:p.Gly472Glu
NM_001378468.1:c.1406G>A NP_001365397.1:p.Gly469Glu
NM_001378469.1:c.1340G>A NP_001365398.1:p.Gly447Glu
NM_001378470.1:c.1304G>A NP_001365399.1:p.Gly435Glu
NM_001378471.1:c.1295G>A NP_001365400.1:p.Gly432Glu
NM_001378472.1:c.1250G>A NP_001365401.1:p.Gly417Glu
NM_001378473.1:c.1250G>A NP_001365402.1:p.Gly417Glu
NM_001378474.1:c.1406G>A NP_001365403.1:p.Gly469Glu
NM_001378475.1:c.1142G>A NP_001365404.1:p.Gly381Glu