Canonical Allele Identifier: CA1747718417
Gene: BRAF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140781670C= , CM000669.2:g.140781670C= GRCh38
NC_000007.13:g.140481470C= , CM000669.1:g.140481470C= GRCh37
NC_000007.12:g.140127939C= NCBI36
NG_007873.3:g.148095G= , LRG_299:g.148095G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000646891.2:c.1338G= MANE Select ENSP00000493543.1:p.Ser446=
ENST00000288602.11:c.1458G= ENSP00000288602.7:p.Ser486=
ENST00000479537.6:c.8G=
ENST00000496384.7:c.1338G= ENSP00000419060.2:p.Ser446=
ENST00000497784.2:c.*788G= ENSP00000420119.2:n.*788G=
ENST00000642228.1:c.*416G= ENSP00000493678.1:n.*416G=
ENST00000642875.1:n.780G=
ENST00000644120.1:n.1728G=
ENST00000644650.1:c.434G=
ENST00000644905.1:n.1427G=
ENST00000644969.2:c.1458G= MANE Plus Clinical ENSP00000496776.1:p.Ser486=
ENST00000646334.1:n.468G=
ENST00000646730.1:c.1338G= ENSP00000494784.1:p.Ser446=
ENST00000646891.1:c.1338G= ENSP00000493543.1:p.Ser446=
ENST00000647434.1:c.381G= ENSP00000495132.1:p.Ser127=
ENST00000288602.10:c.1338G= ENSP00000288602.6:p.Ser446=
ENST00000496384.6:c.161G=
ENST00000497784.1:c.1373G= ENSP00000420119.1:n.1373G=
NM_004333.4:c.1338G= , LRG_299t1:c.1338G= NP_004324.2:p.Ser446=
XM_005250045.1:c.1338G= XP_005250102.1:p.Ser446=
XM_005250046.1:c.1338G= XP_005250103.1:p.Ser446=
XM_011516529.1:c.1338G= XP_011514831.1:p.Ser446=
XM_011516530.1:c.1338G= XP_011514832.1:p.Ser446=
XR_242190.1:n.1346G=
XR_927520.1:n.1346G=
XR_927521.1:n.1346G=
XR_927522.1:n.1346G=
XR_927523.1:n.1346G=
NM_001354609.1:c.1338G= NP_001341538.1:p.Ser446=
NM_004333.5:c.1338G= NP_004324.2:p.Ser446=
NR_148928.1:n.1643G=
XM_017012558.1:c.1458G= XP_016868047.1:p.Ser486=
XM_017012559.1:c.1458G= XP_016868048.1:p.Ser486=
XR_001744857.1:n.1466G=
XR_001744858.1:n.1466G=
NM_001354609.2:c.1338G= NP_001341538.1:p.Ser446=
NM_001374244.1:c.1458G= NP_001361173.1:p.Ser486=
NM_001374258.1:c.1458G= MANE Plus Clinical NP_001361187.1:p.Ser486=
NM_004333.6:c.1338G= MANE Select NP_004324.2:p.Ser446=
NM_001378467.1:c.1347G= NP_001365396.1:p.Ser449=
NM_001378468.1:c.1338G= NP_001365397.1:p.Ser446=
NM_001378469.1:c.1272G= NP_001365398.1:p.Ser424=
NM_001378470.1:c.1236G= NP_001365399.1:p.Ser412=
NM_001378471.1:c.1227G= NP_001365400.1:p.Ser409=
NM_001378472.1:c.1182G= NP_001365401.1:p.Ser394=
NM_001378473.1:c.1182G= NP_001365402.1:p.Ser394=
NM_001378474.1:c.1338G= NP_001365403.1:p.Ser446=
NM_001378475.1:c.1074G= NP_001365404.1:p.Ser358=