Canonical Allele Identifier: CA645544102
Gene: BRAF HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140753337delinsTGTA , CM000669.2:g.140753337delinsTGTA GRCh38
NC_000007.13:g.140453137delinsTGTA , CM000669.1:g.140453137delinsTGTA GRCh37
NC_000007.12:g.140099606delinsTGTA NCBI36
NG_007873.3:g.176428delinsTACA , LRG_299:g.176428delinsTACA

Transcript Alleles

HGVS Amino-acid Change
ENST00000646891.2:c.1798delinsTACA MANE Select ENSP00000493543.1:p.Val600delinsTyrMet
ENST00000288602.11:c.1918delinsTACA ENSP00000288602.7:p.Val640delinsTyrMet
ENST00000479537.6:c.468delinsTACA
ENST00000496384.7:c.1798delinsTACA ENSP00000419060.2:p.Val600delinsTyrMet
ENST00000497784.2:c.*1248delinsTACA ENSP00000420119.2:n.*1248delinsTACA
ENST00000642228.1:c.*876delinsTACA ENSP00000493678.1:n.*876delinsTACA
ENST00000642875.1:n.1259-3919delinsTACA
ENST00000644120.1:n.2188delinsTACA
ENST00000644650.1:c.894delinsTACA
ENST00000644905.1:n.2680delinsTACA
ENST00000644969.2:c.1918delinsTACA MANE Plus Clinical ENSP00000496776.1:p.Val640delinsTyrMet
ENST00000646730.1:c.*374delinsTACA ENSP00000494784.1:n.*374delinsTACA
ENST00000646891.1:c.1798delinsTACA ENSP00000493543.1:p.Val600delinsTyrMet
ENST00000647434.1:c.738-3919delinsTACA ENSP00000495132.1:n.738-3919delinsTACA
ENST00000288602.10:c.1798delinsTACA ENSP00000288602.6:p.Val600delinsTyrMet
ENST00000479537.5:c.82delinsTACA ENSP00000418033.1:p.Val28delinsTyrMet
ENST00000496384.6:c.621delinsTACA
ENST00000497784.1:c.1833delinsTACA ENSP00000420119.1:n.1833delinsTACA
NM_004333.4:c.1798delinsTACA , LRG_299t1:c.1798delinsTACA NP_004324.2:p.Val600delinsTyrMet
XM_005250045.1:c.1798delinsTACA XP_005250102.1:p.Val600delinsTyrMet
XM_005250046.1:c.1798delinsTACA XP_005250103.1:p.Val600delinsTyrMet
XM_011516529.1:c.1798delinsTACA XP_011514831.1:p.Val600delinsTyrMet
XM_011516530.1:c.1695-3919delinsTACA XP_011514832.1:n.1695-3919delinsTACA
XR_242190.1:n.1806delinsTACA
XR_927520.1:n.1806delinsTACA
XR_927521.1:n.1806delinsTACA
XR_927522.1:n.1703-3919delinsTACA
XR_927523.1:n.1703-3919delinsTACA
NM_001354609.1:c.1798delinsTACA NP_001341538.1:p.Val600delinsTyrMet
NM_004333.5:c.1798delinsTACA NP_004324.2:p.Val600delinsTyrMet
NR_148928.1:n.2896delinsTACA
XM_017012558.1:c.1918delinsTACA XP_016868047.1:p.Val640delinsTyrMet
XM_017012559.1:c.1918delinsTACA XP_016868048.1:p.Val640delinsTyrMet
XR_001744857.1:n.1926delinsTACA
XR_001744858.1:n.1823-3919delinsTACA
NM_001354609.2:c.1798delinsTACA NP_001341538.1:p.Val600delinsTyrMet
NM_001374244.1:c.1918delinsTACA NP_001361173.1:p.Val640delinsTyrMet
NM_001374258.1:c.1918delinsTACA MANE Plus Clinical NP_001361187.1:p.Val640delinsTyrMet
NM_004333.6:c.1798delinsTACA MANE Select NP_004324.2:p.Val600delinsTyrMet
NM_001378467.1:c.1807delinsTACA NP_001365396.1:p.Val603delinsTyrMet
NM_001378468.1:c.1798delinsTACA NP_001365397.1:p.Val600delinsTyrMet
NM_001378469.1:c.1732delinsTACA NP_001365398.1:p.Val578delinsTyrMet
NM_001378470.1:c.1696delinsTACA NP_001365399.1:p.Val566delinsTyrMet
NM_001378471.1:c.1687delinsTACA NP_001365400.1:p.Val563delinsTyrMet
NM_001378472.1:c.1642delinsTACA NP_001365401.1:p.Val548delinsTyrMet
NM_001378473.1:c.1642delinsTACA NP_001365402.1:p.Val548delinsTyrMet
NM_001378474.1:c.1798delinsTACA NP_001365403.1:p.Val600delinsTyrMet
NM_001378475.1:c.1534delinsTACA NP_001365404.1:p.Val512delinsTyrMet