Canonical Allele Identifier: CA1747718457
Gene: BRAF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140781708_140781709delinsTA , CM000669.2:g.140781708_140781709delinsTA GRCh38
NC_000007.13:g.140481508_140481509delinsTA , CM000669.1:g.140481508_140481509delinsTA GRCh37
NC_000007.12:g.140127977_140127978delinsTA NCBI36
NG_007873.3:g.148056_148057delinsTA , LRG_299:g.148056_148057delinsTA

Transcript Alleles

HGVS Amino-acid change
ENST00000646891.2:c.1315-16_1315-15delinsTA MANE Select ENSP00000493543.1:n.1315-16_1315-15delins...
ENST00000288602.11:c.1435-16_1435-15delinsTA ENSP00000288602.7:n.1435-16_1435-15delins...
ENST00000496384.7:c.1315-16_1315-15delinsTA ENSP00000419060.2:n.1315-16_1315-15delins...
ENST00000497784.2:c.*765-16_*765-15delinsTA ENSP00000420119.2:n.*765-16_*765-15delins...
ENST00000642228.1:c.*393-16_*393-15delinsTA ENSP00000493678.1:n.*393-16_*393-15delins...
ENST00000642875.1:n.757-16_757-15delinsTA
ENST00000644120.1:n.1705-16_1705-15delinsTA
ENST00000644650.1:c.411-16_411-15delinsTA
ENST00000644905.1:n.1404-16_1404-15delinsTA
ENST00000644969.2:c.1435-16_1435-15delinsTA MANE Plus Clinical ENSP00000496776.1:n.1435-16_1435-15delins...
ENST00000646334.1:n.445-16_445-15delinsTA
ENST00000646730.1:c.1315-16_1315-15delinsTA ENSP00000494784.1:n.1315-16_1315-15delins...
ENST00000646891.1:c.1315-16_1315-15delinsTA ENSP00000493543.1:n.1315-16_1315-15delins...
ENST00000647434.1:c.358-16_358-15delinsTA ENSP00000495132.1:n.358-16_358-15delinsTA...
ENST00000288602.10:c.1315-16_1315-15delinsTA ENSP00000288602.6:n.1315-16_1315-15delins...
ENST00000496384.6:c.138-16_138-15delinsTA
ENST00000497784.1:c.1350-16_1350-15delinsTA ENSP00000420119.1:n.1350-16_1350-15delins...
NM_004333.4:c.1315-16_1315-15delinsTA , LRG_299t1:c.1315-16_1315-15delinsTA NP_004324.2:n.1315-16_1315-15delinsTA
XM_005250045.1:c.1315-16_1315-15delinsTA XP_005250102.1:n.1315-16_1315-15delinsTA
XM_005250046.1:c.1315-16_1315-15delinsTA XP_005250103.1:n.1315-16_1315-15delinsTA
XM_011516529.1:c.1315-16_1315-15delinsTA XP_011514831.1:n.1315-16_1315-15delinsTA
XM_011516530.1:c.1315-16_1315-15delinsTA XP_011514832.1:n.1315-16_1315-15delinsTA
XR_242190.1:n.1323-16_1323-15delinsTA
XR_927520.1:n.1323-16_1323-15delinsTA
XR_927521.1:n.1323-16_1323-15delinsTA
XR_927522.1:n.1323-16_1323-15delinsTA
XR_927523.1:n.1323-16_1323-15delinsTA
NM_001354609.1:c.1315-16_1315-15delinsTA NP_001341538.1:n.1315-16_1315-15delinsTA
NM_004333.5:c.1315-16_1315-15delinsTA NP_004324.2:n.1315-16_1315-15delinsTA
NR_148928.1:n.1620-16_1620-15delinsTA
XM_017012558.1:c.1435-16_1435-15delinsTA XP_016868047.1:n.1435-16_1435-15delinsTA
XM_017012559.1:c.1435-16_1435-15delinsTA XP_016868048.1:n.1435-16_1435-15delinsTA
XR_001744857.1:n.1443-16_1443-15delinsTA
XR_001744858.1:n.1443-16_1443-15delinsTA
NM_001354609.2:c.1315-16_1315-15delinsTA NP_001341538.1:n.1315-16_1315-15delinsTA
NM_001374244.1:c.1435-16_1435-15delinsTA NP_001361173.1:n.1435-16_1435-15delinsTA
NM_001374258.1:c.1435-16_1435-15delinsTA MANE Plus Clinical NP_001361187.1:n.1435-16_1435-15delinsTA
NM_004333.6:c.1315-16_1315-15delinsTA MANE Select NP_004324.2:n.1315-16_1315-15delinsTA
NM_001378467.1:c.1324-16_1324-15delinsTA NP_001365396.1:n.1324-16_1324-15delinsTA
NM_001378468.1:c.1315-16_1315-15delinsTA NP_001365397.1:n.1315-16_1315-15delinsTA
NM_001378469.1:c.1249-16_1249-15delinsTA NP_001365398.1:n.1249-16_1249-15delinsTA
NM_001378470.1:c.1213-16_1213-15delinsTA NP_001365399.1:n.1213-16_1213-15delinsTA
NM_001378471.1:c.1204-16_1204-15delinsTA NP_001365400.1:n.1204-16_1204-15delinsTA
NM_001378472.1:c.1159-16_1159-15delinsTA NP_001365401.1:n.1159-16_1159-15delinsTA
NM_001378473.1:c.1159-16_1159-15delinsTA NP_001365402.1:n.1159-16_1159-15delinsTA
NM_001378474.1:c.1315-16_1315-15delinsTA NP_001365403.1:n.1315-16_1315-15delinsTA
NM_001378475.1:c.1051-16_1051-15delinsTA NP_001365404.1:n.1051-16_1051-15delinsTA