Canonical Allele Identifier: CA1747709984
Gene: BRAF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140753287G= , CM000669.2:g.140753287G= GRCh38
NC_000007.13:g.140453087G= , CM000669.1:g.140453087G= GRCh37
NC_000007.12:g.140099556G= NCBI36
NG_007873.3:g.176478C= , LRG_299:g.176478C=

Transcript Alleles

HGVS Amino-acid change
ENST00000646891.2:c.1848C= MANE Select ENSP00000493543.1:p.Ser616=
ENST00000288602.11:c.1968C= ENSP00000288602.7:p.Ser656=
ENST00000479537.6:c.518C=
ENST00000496384.7:c.1848C= ENSP00000419060.2:p.Ser616=
ENST00000497784.2:c.*1298C= ENSP00000420119.2:n.*1298C=
ENST00000642228.1:c.*926C= ENSP00000493678.1:n.*926C=
ENST00000642875.1:n.1259-3869C=
ENST00000644120.1:n.2238C=
ENST00000644650.1:c.944C=
ENST00000644905.1:n.2730C=
ENST00000644969.2:c.1968C= MANE Plus Clinical ENSP00000496776.1:p.Ser656=
ENST00000646730.1:c.*424C= ENSP00000494784.1:n.*424C=
ENST00000646891.1:c.1848C= ENSP00000493543.1:p.Ser616=
ENST00000647434.1:c.738-3869C= ENSP00000495132.1:n.738-3869C=
ENST00000288602.10:c.1848C= ENSP00000288602.6:p.Ser616=
ENST00000479537.5:c.132C= ENSP00000418033.1:p.Ser44=
ENST00000496384.6:c.671C=
ENST00000497784.1:c.1883C= ENSP00000420119.1:n.1883C=
NM_004333.4:c.1848C= , LRG_299t1:c.1848C= NP_004324.2:p.Ser616=
XM_005250045.1:c.1848C= XP_005250102.1:p.Ser616=
XM_005250046.1:c.1848C= XP_005250103.1:p.Ser616=
XM_011516529.1:c.1848C= XP_011514831.1:p.Ser616=
XM_011516530.1:c.1695-3869C= XP_011514832.1:n.1695-3869C=
XR_242190.1:n.1856C=
XR_927520.1:n.1856C=
XR_927521.1:n.1856C=
XR_927522.1:n.1703-3869C=
XR_927523.1:n.1703-3869C=
NM_001354609.1:c.1848C= NP_001341538.1:p.Ser616=
NM_004333.5:c.1848C= NP_004324.2:p.Ser616=
NR_148928.1:n.2946C=
XM_017012558.1:c.1968C= XP_016868047.1:p.Ser656=
XM_017012559.1:c.1968C= XP_016868048.1:p.Ser656=
XR_001744857.1:n.1976C=
XR_001744858.1:n.1823-3869C=
NM_001354609.2:c.1848C= NP_001341538.1:p.Ser616=
NM_001374244.1:c.1968C= NP_001361173.1:p.Ser656=
NM_001374258.1:c.1968C= MANE Plus Clinical NP_001361187.1:p.Ser656=
NM_004333.6:c.1848C= MANE Select NP_004324.2:p.Ser616=
NM_001378467.1:c.1857C= NP_001365396.1:p.Ser619=
NM_001378468.1:c.1848C= NP_001365397.1:p.Ser616=
NM_001378469.1:c.1782C= NP_001365398.1:p.Ser594=
NM_001378470.1:c.1746C= NP_001365399.1:p.Ser582=
NM_001378471.1:c.1737C= NP_001365400.1:p.Ser579=
NM_001378472.1:c.1692C= NP_001365401.1:p.Ser564=
NM_001378473.1:c.1692C= NP_001365402.1:p.Ser564=
NM_001378474.1:c.1848C= NP_001365403.1:p.Ser616=
NM_001378475.1:c.1584C= NP_001365404.1:p.Ser528=