Canonical Allele Identifier: CA1747718365
Gene: BRAF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140781625T= , CM000669.2:g.140781625T= GRCh38
NC_000007.13:g.140481425T= , CM000669.1:g.140481425T= GRCh37
NC_000007.12:g.140127894T= NCBI36
NG_007873.3:g.148140A= , LRG_299:g.148140A=

Transcript Alleles

HGVS Amino-acid change
ENST00000646891.2:c.1383A= MANE Select ENSP00000493543.1:p.Gln461=
ENST00000288602.11:c.1503A= ENSP00000288602.7:p.Gln501=
ENST00000479537.6:c.53A=
ENST00000496384.7:c.1383A= ENSP00000419060.2:p.Gln461=
ENST00000497784.2:c.*833A= ENSP00000420119.2:n.*833A=
ENST00000642228.1:c.*461A= ENSP00000493678.1:n.*461A=
ENST00000642875.1:n.825A=
ENST00000644120.1:n.1773A=
ENST00000644650.1:c.479A=
ENST00000644905.1:n.1472A=
ENST00000644969.2:c.1503A= MANE Plus Clinical ENSP00000496776.1:p.Gln501=
ENST00000646334.1:n.513A=
ENST00000646730.1:c.1383A= ENSP00000494784.1:p.Gln461=
ENST00000646891.1:c.1383A= ENSP00000493543.1:p.Gln461=
ENST00000647434.1:c.426A= ENSP00000495132.1:p.Gln142=
ENST00000288602.10:c.1383A= ENSP00000288602.6:p.Gln461=
ENST00000496384.6:c.206A=
ENST00000497784.1:c.1418A= ENSP00000420119.1:n.1418A=
NM_004333.4:c.1383A= , LRG_299t1:c.1383A= NP_004324.2:p.Gln461=
XM_005250045.1:c.1383A= XP_005250102.1:p.Gln461=
XM_005250046.1:c.1383A= XP_005250103.1:p.Gln461=
XM_011516529.1:c.1383A= XP_011514831.1:p.Gln461=
XM_011516530.1:c.1383A= XP_011514832.1:p.Gln461=
XR_242190.1:n.1391A=
XR_927520.1:n.1391A=
XR_927521.1:n.1391A=
XR_927522.1:n.1391A=
XR_927523.1:n.1391A=
NM_001354609.1:c.1383A= NP_001341538.1:p.Gln461=
NM_004333.5:c.1383A= NP_004324.2:p.Gln461=
NR_148928.1:n.1688A=
XM_017012558.1:c.1503A= XP_016868047.1:p.Gln501=
XM_017012559.1:c.1503A= XP_016868048.1:p.Gln501=
XR_001744857.1:n.1511A=
XR_001744858.1:n.1511A=
NM_001354609.2:c.1383A= NP_001341538.1:p.Gln461=
NM_001374244.1:c.1503A= NP_001361173.1:p.Gln501=
NM_001374258.1:c.1503A= MANE Plus Clinical NP_001361187.1:p.Gln501=
NM_004333.6:c.1383A= MANE Select NP_004324.2:p.Gln461=
NM_001378467.1:c.1392A= NP_001365396.1:p.Gln464=
NM_001378468.1:c.1383A= NP_001365397.1:p.Gln461=
NM_001378469.1:c.1317A= NP_001365398.1:p.Gln439=
NM_001378470.1:c.1281A= NP_001365399.1:p.Gln427=
NM_001378471.1:c.1272A= NP_001365400.1:p.Gln424=
NM_001378472.1:c.1227A= NP_001365401.1:p.Gln409=
NM_001378473.1:c.1227A= NP_001365402.1:p.Gln409=
NM_001378474.1:c.1383A= NP_001365403.1:p.Gln461=
NM_001378475.1:c.1119A= NP_001365404.1:p.Gln373=