Canonical Allele Identifier: CA135095
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 44813
dbSNP Id: rs397516896
COSMIC: COSM27639
CIViC: CA135095

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000288602.11:c.1900G>A ENSP00000288602.7:p.Asp634Asn
ENST00000479537.6:n.450G>A
ENST00000496384.7:c.1780G>A ENSP00000419060.2:p.Asp594Asn
ENST00000497784.2:c.*1230G>A ENSP00000420119.2:p.=
ENST00000642228.1:c.*858G>A ENSP00000493678.1:p.=
ENST00000642875.1:n.1259-3937G>A
ENST00000644120.1:n.2170G>A
ENST00000644650.1:n.876G>A
ENST00000644905.1:n.2662G>A
ENST00000644969.2:c.1900G>A MANE Select ENSP00000496776.1:p.Asp634Asn
ENST00000646730.1:c.*356G>A ENSP00000494784.1:p.=
ENST00000646891.1:c.1780G>A ENSP00000493543.1:p.Asp594Asn
ENST00000647434.1:n.738-3937G>A ENSP00000495132.1:p.=
ENST00000288602.10:c.1780G>A ENSP00000288602.6:p.Asp594Asn
ENST00000479537.5:n.64G>A ENSP00000418033.1:p.Asp22Asn
ENST00000496384.6:n.603G>A
ENST00000497784.1:n.1815G>A ENSP00000420119.1:p.=
NM_004333.4:c.1780G>A , LRG_299t1:c.1780G>A NP_004324.2:p.Asp594Asn
XM_005250045.1:c.1780G>A XP_005250102.1:p.Asp594Asn
XM_005250046.1:c.1780G>A XP_005250103.1:p.Asp594Asn
XM_011516529.1:c.1780G>A XP_011514831.1:p.Asp594Asn
XM_011516530.1:c.1695-3937G>A XP_011514832.1:p.=
XR_242190.1:n.1788G>A
XR_927520.1:n.1788G>A
XR_927521.1:n.1788G>A
XR_927522.1:n.1703-3937G>A
XR_927523.1:n.1703-3937G>A
NM_001354609.1:c.1780G>A NP_001341538.1:p.Asp594Asn
NM_004333.5:c.1780G>A NP_004324.2:p.Asp594Asn
NR_148928.1:n.2878G>A
XM_017012558.1:c.1900G>A XP_016868047.1:p.Asp634Asn
XM_017012559.1:c.1900G>A XP_016868048.1:p.Asp634Asn
XR_001744857.1:n.1908G>A
XR_001744858.1:n.1823-3937G>A
NM_001354609.2:c.1780G>A NP_001341538.1:p.Asp594Asn
NM_001374244.1:c.1900G>A NP_001361173.1:p.Asp634Asn
NM_001374258.1:c.1900G>A MANE Select NP_001361187.1:p.Asp634Asn
NM_004333.6:c.1780G>A NP_004324.2:p.Asp594Asn
NM_001378467.1:c.1789G>A NP_001365396.1:p.Asp597Asn
NM_001378468.1:c.1780G>A NP_001365397.1:p.Asp594Asn
NM_001378469.1:c.1714G>A NP_001365398.1:p.Asp572Asn
NM_001378470.1:c.1678G>A NP_001365399.1:p.Asp560Asn
NM_001378471.1:c.1669G>A NP_001365400.1:p.Asp557Asn
NM_001378472.1:c.1624G>A NP_001365401.1:p.Asp542Asn
NM_001378473.1:c.1624G>A NP_001365402.1:p.Asp542Asn
NM_001378474.1:c.1780G>A NP_001365403.1:p.Asp594Asn
NM_001378475.1:c.1516G>A NP_001365404.1:p.Asp506Asn