Canonical Allele Identifier: CA16618359
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 422080
ClinVar RCV Id: RCV000486116
dbSNP Id: rs1064795542

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140734633_140734634delinsAC , CM000669.2:g.140734633_140734634delinsAC GRCh38
NC_000007.13:g.140434433_140434434delinsAC , CM000669.1:g.140434433_140434434delinsAC GRCh37
NC_000007.12:g.140080902_140080903delinsAC NCBI36
NG_007873.3:g.195131_195132delinsGT , LRG_299:g.195131_195132delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000646891.2:c.2264_2265delinsGT MANE Select ENSP00000493543.1:p.Ile755Ser
ENST00000288602.11:c.2384_2385delinsGT ENSP00000288602.7:p.Ile795Ser
ENST00000479537.6:c.1016_1017delinsGT
ENST00000496384.7:c.2264_2265delinsGT ENSP00000419060.2:p.Ile755Ser
ENST00000497784.2:c.*1714_*1715delinsGT ENSP00000420119.2:n.*1714_*1715delinsGT
ENST00000642228.1:c.*1342_*1343delinsGT ENSP00000493678.1:n.*1342_*1343delinsGT
ENST00000642875.1:n.1662_1663delinsGT
ENST00000644120.1:n.2517+5178_2517+5179delinsGT
ENST00000644650.1:c.1563_1564delinsGT
ENST00000644905.1:n.3146_3147delinsGT
ENST00000644969.2:c.2384_2385delinsGT MANE Plus Clinical ENSP00000496776.1:p.Ile795Ser
ENST00000645443.1:n.2043_2044delinsGT
ENST00000646730.1:c.*922_*923delinsGT ENSP00000494784.1:n.*922_*923delinsGT
ENST00000646891.1:c.2264_2265delinsGT ENSP00000493543.1:p.Ile755Ser
ENST00000647434.1:c.1141_1142delinsGT ENSP00000495132.1:n.1141_1142delinsGT
ENST00000288602.10:c.2264_2265delinsGT ENSP00000288602.6:p.Ile755Ser
ENST00000479537.5:c.630_631delinsGT ENSP00000418033.1:n.630_631delinsGT
ENST00000496384.6:c.1087_1088delinsGT
ENST00000497784.1:c.2299_2300delinsGT ENSP00000420119.1:n.2299_2300delinsGT
NM_004333.4:c.2264_2265delinsGT , LRG_299t1:c.2264_2265delinsGT NP_004324.2:p.Ile755Ser
XM_005250045.1:c.2264_2265delinsGT XP_005250102.1:p.Ile755Ser
XM_005250046.1:c.2127+5178_2127+5179delinsGT XP_005250103.1:n.2127+5178_2127+5179delinsGT
XM_011516529.1:c.2127+5178_2127+5179delinsGT XP_011514831.1:n.2127+5178_2127+5179delinsGT
XR_242190.1:n.2354_2355delinsGT
XR_927520.1:n.2393_2394delinsGT
XR_927521.1:n.2475_2476delinsGT
XR_927522.1:n.2106_2107delinsGT
XR_927523.1:n.2188_2189delinsGT
NM_001354609.1:c.2264_2265delinsGT NP_001341538.1:p.Ile755Ser
NM_004333.5:c.2264_2265delinsGT NP_004324.2:p.Ile755Ser
NR_148928.1:n.3362_3363delinsGT
XM_017012558.1:c.2384_2385delinsGT XP_016868047.1:p.Ile795Ser
XM_017012559.1:c.2247+5178_2247+5179delinsGT XP_016868048.1:n.2247+5178_2247+5179delinsGT
XR_001744857.1:n.2474_2475delinsGT
XR_001744858.1:n.2226_2227delinsGT
NM_001354609.2:c.2264_2265delinsGT NP_001341538.1:p.Ile755Ser
NM_001374244.1:c.2384_2385delinsGT NP_001361173.1:p.Ile795Ser
NM_001374258.1:c.2384_2385delinsGT MANE Plus Clinical NP_001361187.1:p.Ile795Ser
NM_004333.6:c.2264_2265delinsGT MANE Select NP_004324.2:p.Ile755Ser
NM_001378467.1:c.2273_2274delinsGT NP_001365396.1:p.Ile758Ser
NM_001378468.1:c.2127+5178_2127+5179delinsGT NP_001365397.1:n.2127+5178_2127+5179delinsGT
NM_001378469.1:c.2198_2199delinsGT NP_001365398.1:p.Ile733Ser
NM_001378470.1:c.2162_2163delinsGT NP_001365399.1:p.Ile721Ser
NM_001378471.1:c.2153_2154delinsGT NP_001365400.1:p.Ile718Ser
NM_001378472.1:c.2108_2109delinsGT NP_001365401.1:p.Ile703Ser
NM_001378473.1:c.2108_2109delinsGT NP_001365402.1:p.Ile703Ser
NM_001378474.1:c.2127+5178_2127+5179delinsGT NP_001365403.1:n.2127+5178_2127+5179delinsGT
NM_001378475.1:c.2000_2001delinsGT NP_001365404.1:p.Ile667Ser