Canonical Allele Identifier: CA1747718116
Gene: BRAF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140781501_140781502delinsTA , CM000669.2:g.140781501_140781502delinsTA GRCh38
NC_000007.13:g.140481301_140481302delinsTA , CM000669.1:g.140481301_140481302delinsTA GRCh37
NC_000007.12:g.140127770_140127771delinsTA NCBI36
NG_007873.3:g.148263_148264delinsTA , LRG_299:g.148263_148264delinsTA

Transcript Alleles

HGVS Amino-acid change
ENST00000646891.2:c.1432+74_1432+75delinsTA MANE Select ENSP00000493543.1:n.1432+74_1432+75delins...
ENST00000288602.11:c.1552+74_1552+75delinsTA ENSP00000288602.7:n.1552+74_1552+75delins...
ENST00000479537.6:c.102+74_102+75delinsTA
ENST00000496384.7:c.1432+74_1432+75delinsTA ENSP00000419060.2:n.1432+74_1432+75delins...
ENST00000497784.2:c.*882+74_*882+75delinsTA ENSP00000420119.2:n.*882+74_*882+75delins...
ENST00000642228.1:c.*510+74_*510+75delinsTA ENSP00000493678.1:n.*510+74_*510+75delins...
ENST00000642875.1:n.874+74_874+75delinsTA
ENST00000644120.1:n.1822+74_1822+75delinsTA
ENST00000644650.1:c.528+74_528+75delinsTA
ENST00000644905.1:n.1521+74_1521+75delinsTA
ENST00000644969.2:c.1552+74_1552+75delinsTA MANE Plus Clinical ENSP00000496776.1:n.1552+74_1552+75delins...
ENST00000646334.1:n.636_637delinsTA
ENST00000646730.1:c.1432+74_1432+75delinsTA ENSP00000494784.1:n.1432+74_1432+75delins...
ENST00000646891.1:c.1432+74_1432+75delinsTA ENSP00000493543.1:n.1432+74_1432+75delins...
ENST00000647434.1:c.475+74_475+75delinsTA ENSP00000495132.1:n.475+74_475+75delinsTA...
ENST00000288602.10:c.1432+74_1432+75delinsTA ENSP00000288602.6:n.1432+74_1432+75delins...
ENST00000496384.6:c.255+74_255+75delinsTA
ENST00000497784.1:c.1467+74_1467+75delinsTA ENSP00000420119.1:n.1467+74_1467+75delins...
NM_004333.4:c.1432+74_1432+75delinsTA , LRG_299t1:c.1432+74_1432+75delinsTA NP_004324.2:n.1432+74_1432+75delinsTA
XM_005250045.1:c.1432+74_1432+75delinsTA XP_005250102.1:n.1432+74_1432+75delinsTA
XM_005250046.1:c.1432+74_1432+75delinsTA XP_005250103.1:n.1432+74_1432+75delinsTA
XM_011516529.1:c.1432+74_1432+75delinsTA XP_011514831.1:n.1432+74_1432+75delinsTA
XM_011516530.1:c.1432+74_1432+75delinsTA XP_011514832.1:n.1432+74_1432+75delinsTA
XR_242190.1:n.1440+74_1440+75delinsTA
XR_927520.1:n.1440+74_1440+75delinsTA
XR_927521.1:n.1440+74_1440+75delinsTA
XR_927522.1:n.1440+74_1440+75delinsTA
XR_927523.1:n.1440+74_1440+75delinsTA
NM_001354609.1:c.1432+74_1432+75delinsTA NP_001341538.1:n.1432+74_1432+75delinsTA
NM_004333.5:c.1432+74_1432+75delinsTA NP_004324.2:n.1432+74_1432+75delinsTA
NR_148928.1:n.1737+74_1737+75delinsTA
XM_017012558.1:c.1552+74_1552+75delinsTA XP_016868047.1:n.1552+74_1552+75delinsTA
XM_017012559.1:c.1552+74_1552+75delinsTA XP_016868048.1:n.1552+74_1552+75delinsTA
XR_001744857.1:n.1560+74_1560+75delinsTA
XR_001744858.1:n.1560+74_1560+75delinsTA
NM_001354609.2:c.1432+74_1432+75delinsTA NP_001341538.1:n.1432+74_1432+75delinsTA
NM_001374244.1:c.1552+74_1552+75delinsTA NP_001361173.1:n.1552+74_1552+75delinsTA
NM_001374258.1:c.1552+74_1552+75delinsTA MANE Plus Clinical NP_001361187.1:n.1552+74_1552+75delinsTA
NM_004333.6:c.1432+74_1432+75delinsTA MANE Select NP_004324.2:n.1432+74_1432+75delinsTA
NM_001378467.1:c.1441+74_1441+75delinsTA NP_001365396.1:n.1441+74_1441+75delinsTA
NM_001378468.1:c.1432+74_1432+75delinsTA NP_001365397.1:n.1432+74_1432+75delinsTA
NM_001378469.1:c.1366+74_1366+75delinsTA NP_001365398.1:n.1366+74_1366+75delinsTA
NM_001378470.1:c.1330+74_1330+75delinsTA NP_001365399.1:n.1330+74_1330+75delinsTA
NM_001378471.1:c.1321+74_1321+75delinsTA NP_001365400.1:n.1321+74_1321+75delinsTA
NM_001378472.1:c.1276+74_1276+75delinsTA NP_001365401.1:n.1276+74_1276+75delinsTA
NM_001378473.1:c.1276+74_1276+75delinsTA NP_001365402.1:n.1276+74_1276+75delinsTA
NM_001378474.1:c.1432+74_1432+75delinsTA NP_001365403.1:n.1432+74_1432+75delinsTA
NM_001378475.1:c.1168+74_1168+75delinsTA NP_001365404.1:n.1168+74_1168+75delinsTA