Canonical Allele Identifier: CA168090855
Gene: BRAF HGNC NCBI

Linked Data

dbSNP Id: rs771444844

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140781921_140781925del , CM000669.2:g.140781921_140781925del GRCh38
NC_000007.13:g.140481721_140481725del , CM000669.1:g.140481721_140481725del GRCh37
NC_000007.12:g.140128190_140128194del NCBI36
NG_007873.3:g.147847_147851del , LRG_299:g.147847_147851del

Transcript Alleles

HGVS Amino-acid Change
ENST00000646891.2:c.1315-225_1315-221del MANE Select ENSP00000493543.1:n.1315-225_1315-221del
ENST00000288602.11:c.1435-225_1435-221del ENSP00000288602.7:n.1435-225_1435-221del
ENST00000496384.7:c.1315-225_1315-221del ENSP00000419060.2:n.1315-225_1315-221del
ENST00000497784.2:c.*765-225_*765-221del ENSP00000420119.2:n.*765-225_*765-221del
ENST00000642228.1:c.*393-225_*393-221del ENSP00000493678.1:n.*393-225_*393-221del
ENST00000642875.1:n.757-225_757-221del
ENST00000644120.1:n.1705-225_1705-221del
ENST00000644650.1:c.411-225_411-221del
ENST00000644905.1:n.1404-225_1404-221del
ENST00000644969.2:c.1435-225_1435-221del MANE Plus Clinical ENSP00000496776.1:n.1435-225_1435-221del
ENST00000646334.1:n.445-225_445-221del
ENST00000646730.1:c.1315-225_1315-221del ENSP00000494784.1:n.1315-225_1315-221del
ENST00000646891.1:c.1315-225_1315-221del ENSP00000493543.1:n.1315-225_1315-221del
ENST00000647434.1:c.358-225_358-221del ENSP00000495132.1:n.358-225_358-221del
ENST00000288602.10:c.1315-225_1315-221del ENSP00000288602.6:n.1315-225_1315-221del
ENST00000496384.6:c.138-225_138-221del
ENST00000497784.1:c.1350-225_1350-221del ENSP00000420119.1:n.1350-225_1350-221del
NM_004333.4:c.1315-225_1315-221del , LRG_299t1:c.1315-225_1315-221del NP_004324.2:n.1315-225_1315-221del
XM_005250045.1:c.1315-225_1315-221del XP_005250102.1:n.1315-225_1315-221del
XM_005250046.1:c.1315-225_1315-221del XP_005250103.1:n.1315-225_1315-221del
XM_011516529.1:c.1315-225_1315-221del XP_011514831.1:n.1315-225_1315-221del
XM_011516530.1:c.1315-225_1315-221del XP_011514832.1:n.1315-225_1315-221del
XR_242190.1:n.1323-225_1323-221del
XR_927520.1:n.1323-225_1323-221del
XR_927521.1:n.1323-225_1323-221del
XR_927522.1:n.1323-225_1323-221del
XR_927523.1:n.1323-225_1323-221del
NM_001354609.1:c.1315-225_1315-221del NP_001341538.1:n.1315-225_1315-221del
NM_004333.5:c.1315-225_1315-221del NP_004324.2:n.1315-225_1315-221del
NR_148928.1:n.1620-225_1620-221del
XM_017012558.1:c.1435-225_1435-221del XP_016868047.1:n.1435-225_1435-221del
XM_017012559.1:c.1435-225_1435-221del XP_016868048.1:n.1435-225_1435-221del
XR_001744857.1:n.1443-225_1443-221del
XR_001744858.1:n.1443-225_1443-221del
NM_001354609.2:c.1315-225_1315-221del NP_001341538.1:n.1315-225_1315-221del
NM_001374244.1:c.1435-225_1435-221del NP_001361173.1:n.1435-225_1435-221del
NM_001374258.1:c.1435-225_1435-221del MANE Plus Clinical NP_001361187.1:n.1435-225_1435-221del
NM_004333.6:c.1315-225_1315-221del MANE Select NP_004324.2:n.1315-225_1315-221del
NM_001378467.1:c.1324-225_1324-221del NP_001365396.1:n.1324-225_1324-221del
NM_001378468.1:c.1315-225_1315-221del NP_001365397.1:n.1315-225_1315-221del
NM_001378469.1:c.1249-225_1249-221del NP_001365398.1:n.1249-225_1249-221del
NM_001378470.1:c.1213-225_1213-221del NP_001365399.1:n.1213-225_1213-221del
NM_001378471.1:c.1204-225_1204-221del NP_001365400.1:n.1204-225_1204-221del
NM_001378472.1:c.1159-225_1159-221del NP_001365401.1:n.1159-225_1159-221del
NM_001378473.1:c.1159-225_1159-221del NP_001365402.1:n.1159-225_1159-221del
NM_001378474.1:c.1315-225_1315-221del NP_001365403.1:n.1315-225_1315-221del
NM_001378475.1:c.1051-225_1051-221del NP_001365404.1:n.1051-225_1051-221del