Canonical Allele Identifier: CA1747718125
Gene: BRAF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140781529_140781531delinsCAT , CM000669.2:g.140781529_140781531delinsCAT GRCh38
NC_000007.13:g.140481329_140481331delinsCAT , CM000669.1:g.140481329_140481331delinsCAT GRCh37
NC_000007.12:g.140127798_140127800delinsCAT NCBI36
NG_007873.3:g.148234_148236delinsATG , LRG_299:g.148234_148236delinsATG

Transcript Alleles

HGVS Amino-acid change
ENST00000646891.2:c.1432+45_1432+47delinsATG MANE Select ENSP00000493543.1:n.1432+45_1432+47delins...
ENST00000288602.11:c.1552+45_1552+47delinsATG ENSP00000288602.7:n.1552+45_1552+47delins...
ENST00000479537.6:c.102+45_102+47delinsATG
ENST00000496384.7:c.1432+45_1432+47delinsATG ENSP00000419060.2:n.1432+45_1432+47delins...
ENST00000497784.2:c.*882+45_*882+47delinsATG ENSP00000420119.2:n.*882+45_*882+47delins...
ENST00000642228.1:c.*510+45_*510+47delinsATG ENSP00000493678.1:n.*510+45_*510+47delins...
ENST00000642875.1:n.874+45_874+47delinsATG
ENST00000644120.1:n.1822+45_1822+47delinsATG
ENST00000644650.1:c.528+45_528+47delinsATG
ENST00000644905.1:n.1521+45_1521+47delinsATG
ENST00000644969.2:c.1552+45_1552+47delinsATG MANE Plus Clinical ENSP00000496776.1:n.1552+45_1552+47delins...
ENST00000646334.1:n.607_609delinsATG
ENST00000646730.1:c.1432+45_1432+47delinsATG ENSP00000494784.1:n.1432+45_1432+47delins...
ENST00000646891.1:c.1432+45_1432+47delinsATG ENSP00000493543.1:n.1432+45_1432+47delins...
ENST00000647434.1:c.475+45_475+47delinsATG ENSP00000495132.1:n.475+45_475+47delinsAT...
ENST00000288602.10:c.1432+45_1432+47delinsATG ENSP00000288602.6:n.1432+45_1432+47delins...
ENST00000496384.6:c.255+45_255+47delinsATG
ENST00000497784.1:c.1467+45_1467+47delinsATG ENSP00000420119.1:n.1467+45_1467+47delins...
NM_004333.4:c.1432+45_1432+47delinsATG , LRG_299t1:c.1432+45_1432+47delinsATG NP_004324.2:n.1432+45_1432+47delinsATG
XM_005250045.1:c.1432+45_1432+47delinsATG XP_005250102.1:n.1432+45_1432+47delinsATG...
XM_005250046.1:c.1432+45_1432+47delinsATG XP_005250103.1:n.1432+45_1432+47delinsATG...
XM_011516529.1:c.1432+45_1432+47delinsATG XP_011514831.1:n.1432+45_1432+47delinsATG...
XM_011516530.1:c.1432+45_1432+47delinsATG XP_011514832.1:n.1432+45_1432+47delinsATG...
XR_242190.1:n.1440+45_1440+47delinsATG
XR_927520.1:n.1440+45_1440+47delinsATG
XR_927521.1:n.1440+45_1440+47delinsATG
XR_927522.1:n.1440+45_1440+47delinsATG
XR_927523.1:n.1440+45_1440+47delinsATG
NM_001354609.1:c.1432+45_1432+47delinsATG NP_001341538.1:n.1432+45_1432+47delinsATG...
NM_004333.5:c.1432+45_1432+47delinsATG NP_004324.2:n.1432+45_1432+47delinsATG
NR_148928.1:n.1737+45_1737+47delinsATG
XM_017012558.1:c.1552+45_1552+47delinsATG XP_016868047.1:n.1552+45_1552+47delinsATG...
XM_017012559.1:c.1552+45_1552+47delinsATG XP_016868048.1:n.1552+45_1552+47delinsATG...
XR_001744857.1:n.1560+45_1560+47delinsATG
XR_001744858.1:n.1560+45_1560+47delinsATG
NM_001354609.2:c.1432+45_1432+47delinsATG NP_001341538.1:n.1432+45_1432+47delinsATG...
NM_001374244.1:c.1552+45_1552+47delinsATG NP_001361173.1:n.1552+45_1552+47delinsATG...
NM_001374258.1:c.1552+45_1552+47delinsATG MANE Plus Clinical NP_001361187.1:n.1552+45_1552+47delinsATG...
NM_004333.6:c.1432+45_1432+47delinsATG MANE Select NP_004324.2:n.1432+45_1432+47delinsATG
NM_001378467.1:c.1441+45_1441+47delinsATG NP_001365396.1:n.1441+45_1441+47delinsATG...
NM_001378468.1:c.1432+45_1432+47delinsATG NP_001365397.1:n.1432+45_1432+47delinsATG...
NM_001378469.1:c.1366+45_1366+47delinsATG NP_001365398.1:n.1366+45_1366+47delinsATG...
NM_001378470.1:c.1330+45_1330+47delinsATG NP_001365399.1:n.1330+45_1330+47delinsATG...
NM_001378471.1:c.1321+45_1321+47delinsATG NP_001365400.1:n.1321+45_1321+47delinsATG...
NM_001378472.1:c.1276+45_1276+47delinsATG NP_001365401.1:n.1276+45_1276+47delinsATG...
NM_001378473.1:c.1276+45_1276+47delinsATG NP_001365402.1:n.1276+45_1276+47delinsATG...
NM_001378474.1:c.1432+45_1432+47delinsATG NP_001365403.1:n.1432+45_1432+47delinsATG...
NM_001378475.1:c.1168+45_1168+47delinsATG NP_001365404.1:n.1168+45_1168+47delinsATG...