Canonical Allele Identifier: CA2715966939
Gene: BRAF HGNC NCBI

Linked Data

dbSNP Id: rs2129024031

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140781721_140781725del , CM000669.2:g.140781721_140781725del GRCh38
NC_000007.13:g.140481521_140481525del , CM000669.1:g.140481521_140481525del GRCh37
NC_000007.12:g.140127990_140127994del NCBI36
NG_007873.3:g.148048_148052del , LRG_299:g.148048_148052del

Transcript Alleles

HGVS Amino-acid change
ENST00000646891.2:c.1315-24_1315-20del MANE Select ENSP00000493543.1:n.1315-24_1315-20del
ENST00000288602.11:c.1435-24_1435-20del ENSP00000288602.7:n.1435-24_1435-20del
ENST00000496384.7:c.1315-24_1315-20del ENSP00000419060.2:n.1315-24_1315-20del
ENST00000497784.2:c.*765-24_*765-20del ENSP00000420119.2:n.*765-24_*765-20del
ENST00000642228.1:c.*393-24_*393-20del ENSP00000493678.1:n.*393-24_*393-20del
ENST00000642875.1:n.757-24_757-20del
ENST00000644120.1:n.1705-24_1705-20del
ENST00000644650.1:c.411-24_411-20del
ENST00000644905.1:n.1404-24_1404-20del
ENST00000644969.2:c.1435-24_1435-20del MANE Plus Clinical ENSP00000496776.1:n.1435-24_1435-20del
ENST00000646334.1:n.445-24_445-20del
ENST00000646730.1:c.1315-24_1315-20del ENSP00000494784.1:n.1315-24_1315-20del
ENST00000646891.1:c.1315-24_1315-20del ENSP00000493543.1:n.1315-24_1315-20del
ENST00000647434.1:c.358-24_358-20del ENSP00000495132.1:n.358-24_358-20del
ENST00000288602.10:c.1315-24_1315-20del ENSP00000288602.6:n.1315-24_1315-20del
ENST00000496384.6:c.138-24_138-20del
ENST00000497784.1:c.1350-24_1350-20del ENSP00000420119.1:n.1350-24_1350-20del
NM_004333.4:c.1315-24_1315-20del , LRG_299t1:c.1315-24_1315-20del NP_004324.2:n.1315-24_1315-20del
XM_005250045.1:c.1315-24_1315-20del XP_005250102.1:n.1315-24_1315-20del
XM_005250046.1:c.1315-24_1315-20del XP_005250103.1:n.1315-24_1315-20del
XM_011516529.1:c.1315-24_1315-20del XP_011514831.1:n.1315-24_1315-20del
XM_011516530.1:c.1315-24_1315-20del XP_011514832.1:n.1315-24_1315-20del
XR_242190.1:n.1323-24_1323-20del
XR_927520.1:n.1323-24_1323-20del
XR_927521.1:n.1323-24_1323-20del
XR_927522.1:n.1323-24_1323-20del
XR_927523.1:n.1323-24_1323-20del
NM_001354609.1:c.1315-24_1315-20del NP_001341538.1:n.1315-24_1315-20del
NM_004333.5:c.1315-24_1315-20del NP_004324.2:n.1315-24_1315-20del
NR_148928.1:n.1620-24_1620-20del
XM_017012558.1:c.1435-24_1435-20del XP_016868047.1:n.1435-24_1435-20del
XM_017012559.1:c.1435-24_1435-20del XP_016868048.1:n.1435-24_1435-20del
XR_001744857.1:n.1443-24_1443-20del
XR_001744858.1:n.1443-24_1443-20del
NM_001354609.2:c.1315-24_1315-20del NP_001341538.1:n.1315-24_1315-20del
NM_001374244.1:c.1435-24_1435-20del NP_001361173.1:n.1435-24_1435-20del
NM_001374258.1:c.1435-24_1435-20del MANE Plus Clinical NP_001361187.1:n.1435-24_1435-20del
NM_004333.6:c.1315-24_1315-20del MANE Select NP_004324.2:n.1315-24_1315-20del
NM_001378467.1:c.1324-24_1324-20del NP_001365396.1:n.1324-24_1324-20del
NM_001378468.1:c.1315-24_1315-20del NP_001365397.1:n.1315-24_1315-20del
NM_001378469.1:c.1249-24_1249-20del NP_001365398.1:n.1249-24_1249-20del
NM_001378470.1:c.1213-24_1213-20del NP_001365399.1:n.1213-24_1213-20del
NM_001378471.1:c.1204-24_1204-20del NP_001365400.1:n.1204-24_1204-20del
NM_001378472.1:c.1159-24_1159-20del NP_001365401.1:n.1159-24_1159-20del
NM_001378473.1:c.1159-24_1159-20del NP_001365402.1:n.1159-24_1159-20del
NM_001378474.1:c.1315-24_1315-20del NP_001365403.1:n.1315-24_1315-20del
NM_001378475.1:c.1051-24_1051-20del NP_001365404.1:n.1051-24_1051-20del