Canonical Allele Identifier: CA1747718608
Gene: BRAF HGNC NCBI

Linked Data

dbSNP Id: rs1800909798

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140781867_140781872del , CM000669.2:g.140781867_140781872del GRCh38
NC_000007.13:g.140481667_140481672del , CM000669.1:g.140481667_140481672del GRCh37
NC_000007.12:g.140128136_140128141del NCBI36
NG_007873.3:g.147897_147902del , LRG_299:g.147897_147902del

Transcript Alleles

HGVS Amino-acid Change
ENST00000646891.2:c.1315-175_1315-170del MANE Select ENSP00000493543.1:n.1315-175_1315-170del
ENST00000288602.11:c.1435-175_1435-170del ENSP00000288602.7:n.1435-175_1435-170del
ENST00000496384.7:c.1315-175_1315-170del ENSP00000419060.2:n.1315-175_1315-170del
ENST00000497784.2:c.*765-175_*765-170del ENSP00000420119.2:n.*765-175_*765-170del
ENST00000642228.1:c.*393-175_*393-170del ENSP00000493678.1:n.*393-175_*393-170del
ENST00000642875.1:n.757-175_757-170del
ENST00000644120.1:n.1705-175_1705-170del
ENST00000644650.1:c.411-175_411-170del
ENST00000644905.1:n.1404-175_1404-170del
ENST00000644969.2:c.1435-175_1435-170del MANE Plus Clinical ENSP00000496776.1:n.1435-175_1435-170del
ENST00000646334.1:n.445-175_445-170del
ENST00000646730.1:c.1315-175_1315-170del ENSP00000494784.1:n.1315-175_1315-170del
ENST00000646891.1:c.1315-175_1315-170del ENSP00000493543.1:n.1315-175_1315-170del
ENST00000647434.1:c.358-175_358-170del ENSP00000495132.1:n.358-175_358-170del
ENST00000288602.10:c.1315-175_1315-170del ENSP00000288602.6:n.1315-175_1315-170del
ENST00000496384.6:c.138-175_138-170del
ENST00000497784.1:c.1350-175_1350-170del ENSP00000420119.1:n.1350-175_1350-170del
NM_004333.4:c.1315-175_1315-170del , LRG_299t1:c.1315-175_1315-170del NP_004324.2:n.1315-175_1315-170del
XM_005250045.1:c.1315-175_1315-170del XP_005250102.1:n.1315-175_1315-170del
XM_005250046.1:c.1315-175_1315-170del XP_005250103.1:n.1315-175_1315-170del
XM_011516529.1:c.1315-175_1315-170del XP_011514831.1:n.1315-175_1315-170del
XM_011516530.1:c.1315-175_1315-170del XP_011514832.1:n.1315-175_1315-170del
XR_242190.1:n.1323-175_1323-170del
XR_927520.1:n.1323-175_1323-170del
XR_927521.1:n.1323-175_1323-170del
XR_927522.1:n.1323-175_1323-170del
XR_927523.1:n.1323-175_1323-170del
NM_001354609.1:c.1315-175_1315-170del NP_001341538.1:n.1315-175_1315-170del
NM_004333.5:c.1315-175_1315-170del NP_004324.2:n.1315-175_1315-170del
NR_148928.1:n.1620-175_1620-170del
XM_017012558.1:c.1435-175_1435-170del XP_016868047.1:n.1435-175_1435-170del
XM_017012559.1:c.1435-175_1435-170del XP_016868048.1:n.1435-175_1435-170del
XR_001744857.1:n.1443-175_1443-170del
XR_001744858.1:n.1443-175_1443-170del
NM_001354609.2:c.1315-175_1315-170del NP_001341538.1:n.1315-175_1315-170del
NM_001374244.1:c.1435-175_1435-170del NP_001361173.1:n.1435-175_1435-170del
NM_001374258.1:c.1435-175_1435-170del MANE Plus Clinical NP_001361187.1:n.1435-175_1435-170del
NM_004333.6:c.1315-175_1315-170del MANE Select NP_004324.2:n.1315-175_1315-170del
NM_001378467.1:c.1324-175_1324-170del NP_001365396.1:n.1324-175_1324-170del
NM_001378468.1:c.1315-175_1315-170del NP_001365397.1:n.1315-175_1315-170del
NM_001378469.1:c.1249-175_1249-170del NP_001365398.1:n.1249-175_1249-170del
NM_001378470.1:c.1213-175_1213-170del NP_001365399.1:n.1213-175_1213-170del
NM_001378471.1:c.1204-175_1204-170del NP_001365400.1:n.1204-175_1204-170del
NM_001378472.1:c.1159-175_1159-170del NP_001365401.1:n.1159-175_1159-170del
NM_001378473.1:c.1159-175_1159-170del NP_001365402.1:n.1159-175_1159-170del
NM_001378474.1:c.1315-175_1315-170del NP_001365403.1:n.1315-175_1315-170del
NM_001378475.1:c.1051-175_1051-170del NP_001365404.1:n.1051-175_1051-170del