Canonical Allele Identifier: CA1747718278
Gene: BRAF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140781605A= , CM000669.2:g.140781605A= GRCh38
NC_000007.13:g.140481405A= , CM000669.1:g.140481405A= GRCh37
NC_000007.12:g.140127874A= NCBI36
NG_007873.3:g.148160T= , LRG_299:g.148160T=

Transcript Alleles

HGVS Amino-acid change
ENST00000646891.2:c.1403T= MANE Select ENSP00000493543.1:p.Phe468=
ENST00000288602.11:c.1523T= ENSP00000288602.7:p.Phe508=
ENST00000479537.6:c.73T=
ENST00000496384.7:c.1403T= ENSP00000419060.2:p.Phe468=
ENST00000497784.2:c.*853T= ENSP00000420119.2:n.*853T=
ENST00000642228.1:c.*481T= ENSP00000493678.1:n.*481T=
ENST00000642875.1:n.845T=
ENST00000644120.1:n.1793T=
ENST00000644650.1:c.499T=
ENST00000644905.1:n.1492T=
ENST00000644969.2:c.1523T= MANE Plus Clinical ENSP00000496776.1:p.Phe508=
ENST00000646334.1:n.533T=
ENST00000646730.1:c.1403T= ENSP00000494784.1:p.Phe468=
ENST00000646891.1:c.1403T= ENSP00000493543.1:p.Phe468=
ENST00000647434.1:c.446T= ENSP00000495132.1:p.Phe149=
ENST00000288602.10:c.1403T= ENSP00000288602.6:p.Phe468=
ENST00000496384.6:c.226T=
ENST00000497784.1:c.1438T= ENSP00000420119.1:n.1438T=
NM_004333.4:c.1403T= , LRG_299t1:c.1403T= NP_004324.2:p.Phe468=
XM_005250045.1:c.1403T= XP_005250102.1:p.Phe468=
XM_005250046.1:c.1403T= XP_005250103.1:p.Phe468=
XM_011516529.1:c.1403T= XP_011514831.1:p.Phe468=
XM_011516530.1:c.1403T= XP_011514832.1:p.Phe468=
XR_242190.1:n.1411T=
XR_927520.1:n.1411T=
XR_927521.1:n.1411T=
XR_927522.1:n.1411T=
XR_927523.1:n.1411T=
NM_001354609.1:c.1403T= NP_001341538.1:p.Phe468=
NM_004333.5:c.1403T= NP_004324.2:p.Phe468=
NR_148928.1:n.1708T=
XM_017012558.1:c.1523T= XP_016868047.1:p.Phe508=
XM_017012559.1:c.1523T= XP_016868048.1:p.Phe508=
XR_001744857.1:n.1531T=
XR_001744858.1:n.1531T=
NM_001354609.2:c.1403T= NP_001341538.1:p.Phe468=
NM_001374244.1:c.1523T= NP_001361173.1:p.Phe508=
NM_001374258.1:c.1523T= MANE Plus Clinical NP_001361187.1:p.Phe508=
NM_004333.6:c.1403T= MANE Select NP_004324.2:p.Phe468=
NM_001378467.1:c.1412T= NP_001365396.1:p.Phe471=
NM_001378468.1:c.1403T= NP_001365397.1:p.Phe468=
NM_001378469.1:c.1337T= NP_001365398.1:p.Phe446=
NM_001378470.1:c.1301T= NP_001365399.1:p.Phe434=
NM_001378471.1:c.1292T= NP_001365400.1:p.Phe431=
NM_001378472.1:c.1247T= NP_001365401.1:p.Phe416=
NM_001378473.1:c.1247T= NP_001365402.1:p.Phe416=
NM_001378474.1:c.1403T= NP_001365403.1:p.Phe468=
NM_001378475.1:c.1139T= NP_001365404.1:p.Phe380=