Canonical Allele Identifier: CA1747710399
Gene: BRAF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140754208G= , CM000669.2:g.140754208G= GRCh38
NC_000007.13:g.140454008G= , CM000669.1:g.140454008G= GRCh37
NC_000007.12:g.140100477G= NCBI36
NG_007873.3:g.175557C= , LRG_299:g.175557C=

Transcript Alleles

HGVS Amino-acid change
ENST00000646891.2:c.1720C= MANE Select ENSP00000493543.1:p.His574=
ENST00000288602.11:c.1840C= ENSP00000288602.7:p.His614=
ENST00000479537.6:c.390C=
ENST00000496384.7:c.1720C= ENSP00000419060.2:p.His574=
ENST00000497784.2:c.*1170C= ENSP00000420119.2:n.*1170C=
ENST00000642228.1:c.*798C= ENSP00000493678.1:n.*798C=
ENST00000642875.1:n.1259-4790C=
ENST00000644120.1:n.2110C=
ENST00000644650.1:c.816C=
ENST00000644905.1:n.1809C=
ENST00000644969.2:c.1840C= MANE Plus Clinical ENSP00000496776.1:p.His614=
ENST00000646730.1:c.*296C= ENSP00000494784.1:n.*296C=
ENST00000646891.1:c.1720C= ENSP00000493543.1:p.His574=
ENST00000647434.1:c.738-4790C= ENSP00000495132.1:n.738-4790C=
ENST00000288602.10:c.1720C= ENSP00000288602.6:p.His574=
ENST00000479537.5:c.4C= ENSP00000418033.1:p.His2=
ENST00000496384.6:c.543C=
ENST00000497784.1:c.1755C= ENSP00000420119.1:n.1755C=
NM_004333.4:c.1720C= , LRG_299t1:c.1720C= NP_004324.2:p.His574=
XM_005250045.1:c.1720C= XP_005250102.1:p.His574=
XM_005250046.1:c.1720C= XP_005250103.1:p.His574=
XM_011516529.1:c.1720C= XP_011514831.1:p.His574=
XM_011516530.1:c.1695-4790C= XP_011514832.1:n.1695-4790C=
XR_242190.1:n.1728C=
XR_927520.1:n.1728C=
XR_927521.1:n.1728C=
XR_927522.1:n.1703-4790C=
XR_927523.1:n.1703-4790C=
NM_001354609.1:c.1720C= NP_001341538.1:p.His574=
NM_004333.5:c.1720C= NP_004324.2:p.His574=
NR_148928.1:n.2025C=
XM_017012558.1:c.1840C= XP_016868047.1:p.His614=
XM_017012559.1:c.1840C= XP_016868048.1:p.His614=
XR_001744857.1:n.1848C=
XR_001744858.1:n.1823-4790C=
NM_001354609.2:c.1720C= NP_001341538.1:p.His574=
NM_001374244.1:c.1840C= NP_001361173.1:p.His614=
NM_001374258.1:c.1840C= MANE Plus Clinical NP_001361187.1:p.His614=
NM_004333.6:c.1720C= MANE Select NP_004324.2:p.His574=
NM_001378467.1:c.1729C= NP_001365396.1:p.His577=
NM_001378468.1:c.1720C= NP_001365397.1:p.His574=
NM_001378469.1:c.1654C= NP_001365398.1:p.His552=
NM_001378470.1:c.1618C= NP_001365399.1:p.His540=
NM_001378471.1:c.1609C= NP_001365400.1:p.His537=
NM_001378472.1:c.1564C= NP_001365401.1:p.His522=
NM_001378473.1:c.1564C= NP_001365402.1:p.His522=
NM_001378474.1:c.1720C= NP_001365403.1:p.His574=
NM_001378475.1:c.1456C= NP_001365404.1:p.His486=