Canonical Allele Identifier: CA168090758
Gene: BRAF HGNC NCBI

Linked Data

dbSNP Id: rs915762408

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140781868_140781872del , CM000669.2:g.140781868_140781872del GRCh38
NC_000007.13:g.140481668_140481672del , CM000669.1:g.140481668_140481672del GRCh37
NC_000007.12:g.140128137_140128141del NCBI36
NG_007873.3:g.147895_147899del , LRG_299:g.147895_147899del

Transcript Alleles

HGVS Amino-acid Change
ENST00000646891.2:c.1315-177_1315-173del MANE Select ENSP00000493543.1:n.1315-177_1315-173del
ENST00000288602.11:c.1435-177_1435-173del ENSP00000288602.7:n.1435-177_1435-173del
ENST00000496384.7:c.1315-177_1315-173del ENSP00000419060.2:n.1315-177_1315-173del
ENST00000497784.2:c.*765-177_*765-173del ENSP00000420119.2:n.*765-177_*765-173del
ENST00000642228.1:c.*393-177_*393-173del ENSP00000493678.1:n.*393-177_*393-173del
ENST00000642875.1:n.757-177_757-173del
ENST00000644120.1:n.1705-177_1705-173del
ENST00000644650.1:c.411-177_411-173del
ENST00000644905.1:n.1404-177_1404-173del
ENST00000644969.2:c.1435-177_1435-173del MANE Plus Clinical ENSP00000496776.1:n.1435-177_1435-173del
ENST00000646334.1:n.445-177_445-173del
ENST00000646730.1:c.1315-177_1315-173del ENSP00000494784.1:n.1315-177_1315-173del
ENST00000646891.1:c.1315-177_1315-173del ENSP00000493543.1:n.1315-177_1315-173del
ENST00000647434.1:c.358-177_358-173del ENSP00000495132.1:n.358-177_358-173del
ENST00000288602.10:c.1315-177_1315-173del ENSP00000288602.6:n.1315-177_1315-173del
ENST00000496384.6:c.138-177_138-173del
ENST00000497784.1:c.1350-177_1350-173del ENSP00000420119.1:n.1350-177_1350-173del
NM_004333.4:c.1315-177_1315-173del , LRG_299t1:c.1315-177_1315-173del NP_004324.2:n.1315-177_1315-173del
XM_005250045.1:c.1315-177_1315-173del XP_005250102.1:n.1315-177_1315-173del
XM_005250046.1:c.1315-177_1315-173del XP_005250103.1:n.1315-177_1315-173del
XM_011516529.1:c.1315-177_1315-173del XP_011514831.1:n.1315-177_1315-173del
XM_011516530.1:c.1315-177_1315-173del XP_011514832.1:n.1315-177_1315-173del
XR_242190.1:n.1323-177_1323-173del
XR_927520.1:n.1323-177_1323-173del
XR_927521.1:n.1323-177_1323-173del
XR_927522.1:n.1323-177_1323-173del
XR_927523.1:n.1323-177_1323-173del
NM_001354609.1:c.1315-177_1315-173del NP_001341538.1:n.1315-177_1315-173del
NM_004333.5:c.1315-177_1315-173del NP_004324.2:n.1315-177_1315-173del
NR_148928.1:n.1620-177_1620-173del
XM_017012558.1:c.1435-177_1435-173del XP_016868047.1:n.1435-177_1435-173del
XM_017012559.1:c.1435-177_1435-173del XP_016868048.1:n.1435-177_1435-173del
XR_001744857.1:n.1443-177_1443-173del
XR_001744858.1:n.1443-177_1443-173del
NM_001354609.2:c.1315-177_1315-173del NP_001341538.1:n.1315-177_1315-173del
NM_001374244.1:c.1435-177_1435-173del NP_001361173.1:n.1435-177_1435-173del
NM_001374258.1:c.1435-177_1435-173del MANE Plus Clinical NP_001361187.1:n.1435-177_1435-173del
NM_004333.6:c.1315-177_1315-173del MANE Select NP_004324.2:n.1315-177_1315-173del
NM_001378467.1:c.1324-177_1324-173del NP_001365396.1:n.1324-177_1324-173del
NM_001378468.1:c.1315-177_1315-173del NP_001365397.1:n.1315-177_1315-173del
NM_001378469.1:c.1249-177_1249-173del NP_001365398.1:n.1249-177_1249-173del
NM_001378470.1:c.1213-177_1213-173del NP_001365399.1:n.1213-177_1213-173del
NM_001378471.1:c.1204-177_1204-173del NP_001365400.1:n.1204-177_1204-173del
NM_001378472.1:c.1159-177_1159-173del NP_001365401.1:n.1159-177_1159-173del
NM_001378473.1:c.1159-177_1159-173del NP_001365402.1:n.1159-177_1159-173del
NM_001378474.1:c.1315-177_1315-173del NP_001365403.1:n.1315-177_1315-173del
NM_001378475.1:c.1051-177_1051-173del NP_001365404.1:n.1051-177_1051-173del