Canonical Allele Identifier: CA1747710022
Gene: BRAF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140753355C= , CM000669.2:g.140753355C= GRCh38
NC_000007.13:g.140453155C= , CM000669.1:g.140453155C= GRCh37
NC_000007.12:g.140099624C= NCBI36
NG_007873.3:g.176410G= , LRG_299:g.176410G=

Transcript Alleles

HGVS Amino-acid change
ENST00000646891.2:c.1780G= MANE Select ENSP00000493543.1:p.Asp594=
ENST00000288602.11:c.1900G= ENSP00000288602.7:p.Asp634=
ENST00000479537.6:c.450G=
ENST00000496384.7:c.1780G= ENSP00000419060.2:p.Asp594=
ENST00000497784.2:c.*1230G= ENSP00000420119.2:n.*1230G=
ENST00000642228.1:c.*858G= ENSP00000493678.1:n.*858G=
ENST00000642875.1:n.1259-3937G=
ENST00000644120.1:n.2170G=
ENST00000644650.1:c.876G=
ENST00000644905.1:n.2662G=
ENST00000644969.2:c.1900G= MANE Plus Clinical ENSP00000496776.1:p.Asp634=
ENST00000646730.1:c.*356G= ENSP00000494784.1:n.*356G=
ENST00000646891.1:c.1780G= ENSP00000493543.1:p.Asp594=
ENST00000647434.1:c.738-3937G= ENSP00000495132.1:n.738-3937G=
ENST00000288602.10:c.1780G= ENSP00000288602.6:p.Asp594=
ENST00000479537.5:c.64G= ENSP00000418033.1:p.Asp22=
ENST00000496384.6:c.603G=
ENST00000497784.1:c.1815G= ENSP00000420119.1:n.1815G=
NM_004333.4:c.1780G= , LRG_299t1:c.1780G= NP_004324.2:p.Asp594=
XM_005250045.1:c.1780G= XP_005250102.1:p.Asp594=
XM_005250046.1:c.1780G= XP_005250103.1:p.Asp594=
XM_011516529.1:c.1780G= XP_011514831.1:p.Asp594=
XM_011516530.1:c.1695-3937G= XP_011514832.1:n.1695-3937G=
XR_242190.1:n.1788G=
XR_927520.1:n.1788G=
XR_927521.1:n.1788G=
XR_927522.1:n.1703-3937G=
XR_927523.1:n.1703-3937G=
NM_001354609.1:c.1780G= NP_001341538.1:p.Asp594=
NM_004333.5:c.1780G= NP_004324.2:p.Asp594=
NR_148928.1:n.2878G=
XM_017012558.1:c.1900G= XP_016868047.1:p.Asp634=
XM_017012559.1:c.1900G= XP_016868048.1:p.Asp634=
XR_001744857.1:n.1908G=
XR_001744858.1:n.1823-3937G=
NM_001354609.2:c.1780G= NP_001341538.1:p.Asp594=
NM_001374244.1:c.1900G= NP_001361173.1:p.Asp634=
NM_001374258.1:c.1900G= MANE Plus Clinical NP_001361187.1:p.Asp634=
NM_004333.6:c.1780G= MANE Select NP_004324.2:p.Asp594=
NM_001378467.1:c.1789G= NP_001365396.1:p.Asp597=
NM_001378468.1:c.1780G= NP_001365397.1:p.Asp594=
NM_001378469.1:c.1714G= NP_001365398.1:p.Asp572=
NM_001378470.1:c.1678G= NP_001365399.1:p.Asp560=
NM_001378471.1:c.1669G= NP_001365400.1:p.Asp557=
NM_001378472.1:c.1624G= NP_001365401.1:p.Asp542=
NM_001378473.1:c.1624G= NP_001365402.1:p.Asp542=
NM_001378474.1:c.1780G= NP_001365403.1:p.Asp594=
NM_001378475.1:c.1516G= NP_001365404.1:p.Asp506=