Canonical Allele Identifier: CA1747710844
Gene: BRAF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140755224C= , CM000669.2:g.140755224C= GRCh38
NC_000007.13:g.140455024C= , CM000669.1:g.140455024C= GRCh37
NC_000007.12:g.140101493C= NCBI36
NG_007873.3:g.174541G= , LRG_299:g.174541G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000646891.2:c.1695-991G= MANE Select ENSP00000493543.1:n.1695-991G=
ENST00000288602.11:c.1815-991G= ENSP00000288602.7:n.1815-991G=
ENST00000479537.6:c.365-991G=
ENST00000496384.7:c.1695-991G= ENSP00000419060.2:n.1695-991G=
ENST00000497784.2:c.*1145-991G= ENSP00000420119.2:n.*1145-991G=
ENST00000642228.1:c.*773-991G= ENSP00000493678.1:n.*773-991G=
ENST00000642875.1:n.1259-5806G=
ENST00000644120.1:n.2085-991G=
ENST00000644650.1:c.791-991G=
ENST00000644905.1:n.1784-991G=
ENST00000644969.2:c.1815-991G= MANE Plus Clinical ENSP00000496776.1:n.1815-991G=
ENST00000646730.1:c.*271-991G= ENSP00000494784.1:n.*271-991G=
ENST00000646891.1:c.1695-991G= ENSP00000493543.1:n.1695-991G=
ENST00000647434.1:c.738-5806G= ENSP00000495132.1:n.738-5806G=
ENST00000288602.10:c.1695-991G= ENSP00000288602.6:n.1695-991G=
ENST00000496384.6:c.518-991G=
ENST00000497784.1:c.1730-991G= ENSP00000420119.1:n.1730-991G=
NM_004333.4:c.1695-991G= , LRG_299t1:c.1695-991G= NP_004324.2:n.1695-991G=
XM_005250045.1:c.1695-991G= XP_005250102.1:n.1695-991G=
XM_005250046.1:c.1695-991G= XP_005250103.1:n.1695-991G=
XM_011516529.1:c.1695-991G= XP_011514831.1:n.1695-991G=
XM_011516530.1:c.1695-5806G= XP_011514832.1:n.1695-5806G=
XR_242190.1:n.1703-991G=
XR_927520.1:n.1703-991G=
XR_927521.1:n.1703-991G=
XR_927522.1:n.1703-5806G=
XR_927523.1:n.1703-5806G=
NM_001354609.1:c.1695-991G= NP_001341538.1:n.1695-991G=
NM_004333.5:c.1695-991G= NP_004324.2:n.1695-991G=
NR_148928.1:n.2000-991G=
XM_017012558.1:c.1815-991G= XP_016868047.1:n.1815-991G=
XM_017012559.1:c.1815-991G= XP_016868048.1:n.1815-991G=
XR_001744857.1:n.1823-991G=
XR_001744858.1:n.1823-5806G=
NM_001354609.2:c.1695-991G= NP_001341538.1:n.1695-991G=
NM_001374244.1:c.1815-991G= NP_001361173.1:n.1815-991G=
NM_001374258.1:c.1815-991G= MANE Plus Clinical NP_001361187.1:n.1815-991G=
NM_004333.6:c.1695-991G= MANE Select NP_004324.2:n.1695-991G=
NM_001378467.1:c.1704-991G= NP_001365396.1:n.1704-991G=
NM_001378468.1:c.1695-991G= NP_001365397.1:n.1695-991G=
NM_001378469.1:c.1629-991G= NP_001365398.1:n.1629-991G=
NM_001378470.1:c.1593-991G= NP_001365399.1:n.1593-991G=
NM_001378471.1:c.1584-991G= NP_001365400.1:n.1584-991G=
NM_001378472.1:c.1539-991G= NP_001365401.1:n.1539-991G=
NM_001378473.1:c.1539-991G= NP_001365402.1:n.1539-991G=
NM_001378474.1:c.1695-991G= NP_001365403.1:n.1695-991G=
NM_001378475.1:c.1431-991G= NP_001365404.1:n.1431-991G=