Canonical Allele Identifier: CA1747709992
Gene: BRAF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140753319C= , CM000669.2:g.140753319C= GRCh38
NC_000007.13:g.140453119C= , CM000669.1:g.140453119C= GRCh37
NC_000007.12:g.140099588C= NCBI36
NG_007873.3:g.176446G= , LRG_299:g.176446G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000646891.2:c.1816G= MANE Select ENSP00000493543.1:p.Gly606=
ENST00000288602.11:c.1936G= ENSP00000288602.7:p.Gly646=
ENST00000479537.6:c.486G=
ENST00000496384.7:c.1816G= ENSP00000419060.2:p.Gly606=
ENST00000497784.2:c.*1266G= ENSP00000420119.2:n.*1266G=
ENST00000642228.1:c.*894G= ENSP00000493678.1:n.*894G=
ENST00000642875.1:n.1259-3901G=
ENST00000644120.1:n.2206G=
ENST00000644650.1:c.912G=
ENST00000644905.1:n.2698G=
ENST00000644969.2:c.1936G= MANE Plus Clinical ENSP00000496776.1:p.Gly646=
ENST00000646730.1:c.*392G= ENSP00000494784.1:n.*392G=
ENST00000646891.1:c.1816G= ENSP00000493543.1:p.Gly606=
ENST00000647434.1:c.738-3901G= ENSP00000495132.1:n.738-3901G=
ENST00000288602.10:c.1816G= ENSP00000288602.6:p.Gly606=
ENST00000479537.5:c.100G= ENSP00000418033.1:p.Gly34=
ENST00000496384.6:c.639G=
ENST00000497784.1:c.1851G= ENSP00000420119.1:n.1851G=
NM_004333.4:c.1816G= , LRG_299t1:c.1816G= NP_004324.2:p.Gly606=
XM_005250045.1:c.1816G= XP_005250102.1:p.Gly606=
XM_005250046.1:c.1816G= XP_005250103.1:p.Gly606=
XM_011516529.1:c.1816G= XP_011514831.1:p.Gly606=
XM_011516530.1:c.1695-3901G= XP_011514832.1:n.1695-3901G=
XR_242190.1:n.1824G=
XR_927520.1:n.1824G=
XR_927521.1:n.1824G=
XR_927522.1:n.1703-3901G=
XR_927523.1:n.1703-3901G=
NM_001354609.1:c.1816G= NP_001341538.1:p.Gly606=
NM_004333.5:c.1816G= NP_004324.2:p.Gly606=
NR_148928.1:n.2914G=
XM_017012558.1:c.1936G= XP_016868047.1:p.Gly646=
XM_017012559.1:c.1936G= XP_016868048.1:p.Gly646=
XR_001744857.1:n.1944G=
XR_001744858.1:n.1823-3901G=
NM_001354609.2:c.1816G= NP_001341538.1:p.Gly606=
NM_001374244.1:c.1936G= NP_001361173.1:p.Gly646=
NM_001374258.1:c.1936G= MANE Plus Clinical NP_001361187.1:p.Gly646=
NM_004333.6:c.1816G= MANE Select NP_004324.2:p.Gly606=
NM_001378467.1:c.1825G= NP_001365396.1:p.Gly609=
NM_001378468.1:c.1816G= NP_001365397.1:p.Gly606=
NM_001378469.1:c.1750G= NP_001365398.1:p.Gly584=
NM_001378470.1:c.1714G= NP_001365399.1:p.Gly572=
NM_001378471.1:c.1705G= NP_001365400.1:p.Gly569=
NM_001378472.1:c.1660G= NP_001365401.1:p.Gly554=
NM_001378473.1:c.1660G= NP_001365402.1:p.Gly554=
NM_001378474.1:c.1816G= NP_001365403.1:p.Gly606=
NM_001378475.1:c.1552G= NP_001365404.1:p.Gly518=