Canonical Allele Identifier: CA1747718583
Gene: BRAF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140781839_140781840delinsAG , CM000669.2:g.140781839_140781840delinsAG GRCh38
NC_000007.13:g.140481639_140481640delinsAG , CM000669.1:g.140481639_140481640delinsAG GRCh37
NC_000007.12:g.140128108_140128109delinsAG NCBI36
NG_007873.3:g.147925_147926delinsCT , LRG_299:g.147925_147926delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000646891.2:c.1315-147_1315-146delinsCT MANE Select ENSP00000493543.1:n.1315-147_1315-146delinsCT
ENST00000288602.11:c.1435-147_1435-146delinsCT ENSP00000288602.7:n.1435-147_1435-146delinsCT
ENST00000496384.7:c.1315-147_1315-146delinsCT ENSP00000419060.2:n.1315-147_1315-146delinsCT
ENST00000497784.2:c.*765-147_*765-146delinsCT ENSP00000420119.2:n.*765-147_*765-146delinsCT
ENST00000642228.1:c.*393-147_*393-146delinsCT ENSP00000493678.1:n.*393-147_*393-146delinsCT
ENST00000642875.1:n.757-147_757-146delinsCT
ENST00000644120.1:n.1705-147_1705-146delinsCT
ENST00000644650.1:c.411-147_411-146delinsCT
ENST00000644905.1:n.1404-147_1404-146delinsCT
ENST00000644969.2:c.1435-147_1435-146delinsCT MANE Plus Clinical ENSP00000496776.1:n.1435-147_1435-146delinsCT
ENST00000646334.1:n.445-147_445-146delinsCT
ENST00000646730.1:c.1315-147_1315-146delinsCT ENSP00000494784.1:n.1315-147_1315-146delinsCT
ENST00000646891.1:c.1315-147_1315-146delinsCT ENSP00000493543.1:n.1315-147_1315-146delinsCT
ENST00000647434.1:c.358-147_358-146delinsCT ENSP00000495132.1:n.358-147_358-146delinsCT
ENST00000288602.10:c.1315-147_1315-146delinsCT ENSP00000288602.6:n.1315-147_1315-146delinsCT
ENST00000496384.6:c.138-147_138-146delinsCT
ENST00000497784.1:c.1350-147_1350-146delinsCT ENSP00000420119.1:n.1350-147_1350-146delinsCT
NM_004333.4:c.1315-147_1315-146delinsCT , LRG_299t1:c.1315-147_1315-146delinsCT NP_004324.2:n.1315-147_1315-146delinsCT
XM_005250045.1:c.1315-147_1315-146delinsCT XP_005250102.1:n.1315-147_1315-146delinsCT
XM_005250046.1:c.1315-147_1315-146delinsCT XP_005250103.1:n.1315-147_1315-146delinsCT
XM_011516529.1:c.1315-147_1315-146delinsCT XP_011514831.1:n.1315-147_1315-146delinsCT
XM_011516530.1:c.1315-147_1315-146delinsCT XP_011514832.1:n.1315-147_1315-146delinsCT
XR_242190.1:n.1323-147_1323-146delinsCT
XR_927520.1:n.1323-147_1323-146delinsCT
XR_927521.1:n.1323-147_1323-146delinsCT
XR_927522.1:n.1323-147_1323-146delinsCT
XR_927523.1:n.1323-147_1323-146delinsCT
NM_001354609.1:c.1315-147_1315-146delinsCT NP_001341538.1:n.1315-147_1315-146delinsCT
NM_004333.5:c.1315-147_1315-146delinsCT NP_004324.2:n.1315-147_1315-146delinsCT
NR_148928.1:n.1620-147_1620-146delinsCT
XM_017012558.1:c.1435-147_1435-146delinsCT XP_016868047.1:n.1435-147_1435-146delinsCT
XM_017012559.1:c.1435-147_1435-146delinsCT XP_016868048.1:n.1435-147_1435-146delinsCT
XR_001744857.1:n.1443-147_1443-146delinsCT
XR_001744858.1:n.1443-147_1443-146delinsCT
NM_001354609.2:c.1315-147_1315-146delinsCT NP_001341538.1:n.1315-147_1315-146delinsCT
NM_001374244.1:c.1435-147_1435-146delinsCT NP_001361173.1:n.1435-147_1435-146delinsCT
NM_001374258.1:c.1435-147_1435-146delinsCT MANE Plus Clinical NP_001361187.1:n.1435-147_1435-146delinsCT
NM_004333.6:c.1315-147_1315-146delinsCT MANE Select NP_004324.2:n.1315-147_1315-146delinsCT
NM_001378467.1:c.1324-147_1324-146delinsCT NP_001365396.1:n.1324-147_1324-146delinsCT
NM_001378468.1:c.1315-147_1315-146delinsCT NP_001365397.1:n.1315-147_1315-146delinsCT
NM_001378469.1:c.1249-147_1249-146delinsCT NP_001365398.1:n.1249-147_1249-146delinsCT
NM_001378470.1:c.1213-147_1213-146delinsCT NP_001365399.1:n.1213-147_1213-146delinsCT
NM_001378471.1:c.1204-147_1204-146delinsCT NP_001365400.1:n.1204-147_1204-146delinsCT
NM_001378472.1:c.1159-147_1159-146delinsCT NP_001365401.1:n.1159-147_1159-146delinsCT
NM_001378473.1:c.1159-147_1159-146delinsCT NP_001365402.1:n.1159-147_1159-146delinsCT
NM_001378474.1:c.1315-147_1315-146delinsCT NP_001365403.1:n.1315-147_1315-146delinsCT
NM_001378475.1:c.1051-147_1051-146delinsCT NP_001365404.1:n.1051-147_1051-146delinsCT