Canonical Allele Identifier: CA1747718607
Gene: BRAF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140781862_140781868delinsCTTAAAT , CM000669.2:g.140781862_140781868delinsCTTAAAT GRCh38
NC_000007.13:g.140481662_140481668delinsCTTAAAT , CM000669.1:g.140481662_140481668delinsCTTAAAT GRCh37
NC_000007.12:g.140128131_140128137delinsCTTAAAT NCBI36
NG_007873.3:g.147897_147903delinsATTTAAG , LRG_299:g.147897_147903delinsATTTAAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000646891.2:c.1315-175_1315-169delinsATTTAAG MANE Select ENSP00000493543.1:n.1315-175_1315-169delinsATTTAAG
ENST00000288602.11:c.1435-175_1435-169delinsATTTAAG ENSP00000288602.7:n.1435-175_1435-169delinsATTTAAG
ENST00000496384.7:c.1315-175_1315-169delinsATTTAAG ENSP00000419060.2:n.1315-175_1315-169delinsATTTAAG
ENST00000497784.2:c.*765-175_*765-169delinsATTTAAG ENSP00000420119.2:n.*765-175_*765-169delinsATTTAAG
ENST00000642228.1:c.*393-175_*393-169delinsATTTAAG ENSP00000493678.1:n.*393-175_*393-169delinsATTTAAG
ENST00000642875.1:n.757-175_757-169delinsATTTAAG
ENST00000644120.1:n.1705-175_1705-169delinsATTTAAG
ENST00000644650.1:c.411-175_411-169delinsATTTAAG
ENST00000644905.1:n.1404-175_1404-169delinsATTTAAG
ENST00000644969.2:c.1435-175_1435-169delinsATTTAAG MANE Plus Clinical ENSP00000496776.1:n.1435-175_1435-169delinsATTTAAG
ENST00000646334.1:n.445-175_445-169delinsATTTAAG
ENST00000646730.1:c.1315-175_1315-169delinsATTTAAG ENSP00000494784.1:n.1315-175_1315-169delinsATTTAAG
ENST00000646891.1:c.1315-175_1315-169delinsATTTAAG ENSP00000493543.1:n.1315-175_1315-169delinsATTTAAG
ENST00000647434.1:c.358-175_358-169delinsATTTAAG ENSP00000495132.1:n.358-175_358-169delinsATTTAAG
ENST00000288602.10:c.1315-175_1315-169delinsATTTAAG ENSP00000288602.6:n.1315-175_1315-169delinsATTTAAG
ENST00000496384.6:c.138-175_138-169delinsATTTAAG
ENST00000497784.1:c.1350-175_1350-169delinsATTTAAG ENSP00000420119.1:n.1350-175_1350-169delinsATTTAAG
NM_004333.4:c.1315-175_1315-169delinsATTTAAG , LRG_299t1:c.1315-175_1315-169delinsATTTAAG NP_004324.2:n.1315-175_1315-169delinsATTTAAG
XM_005250045.1:c.1315-175_1315-169delinsATTTAAG XP_005250102.1:n.1315-175_1315-169delinsATTTAAG
XM_005250046.1:c.1315-175_1315-169delinsATTTAAG XP_005250103.1:n.1315-175_1315-169delinsATTTAAG
XM_011516529.1:c.1315-175_1315-169delinsATTTAAG XP_011514831.1:n.1315-175_1315-169delinsATTTAAG
XM_011516530.1:c.1315-175_1315-169delinsATTTAAG XP_011514832.1:n.1315-175_1315-169delinsATTTAAG
XR_242190.1:n.1323-175_1323-169delinsATTTAAG
XR_927520.1:n.1323-175_1323-169delinsATTTAAG
XR_927521.1:n.1323-175_1323-169delinsATTTAAG
XR_927522.1:n.1323-175_1323-169delinsATTTAAG
XR_927523.1:n.1323-175_1323-169delinsATTTAAG
NM_001354609.1:c.1315-175_1315-169delinsATTTAAG NP_001341538.1:n.1315-175_1315-169delinsATTTAAG
NM_004333.5:c.1315-175_1315-169delinsATTTAAG NP_004324.2:n.1315-175_1315-169delinsATTTAAG
NR_148928.1:n.1620-175_1620-169delinsATTTAAG
XM_017012558.1:c.1435-175_1435-169delinsATTTAAG XP_016868047.1:n.1435-175_1435-169delinsATTTAAG
XM_017012559.1:c.1435-175_1435-169delinsATTTAAG XP_016868048.1:n.1435-175_1435-169delinsATTTAAG
XR_001744857.1:n.1443-175_1443-169delinsATTTAAG
XR_001744858.1:n.1443-175_1443-169delinsATTTAAG
NM_001354609.2:c.1315-175_1315-169delinsATTTAAG NP_001341538.1:n.1315-175_1315-169delinsATTTAAG
NM_001374244.1:c.1435-175_1435-169delinsATTTAAG NP_001361173.1:n.1435-175_1435-169delinsATTTAAG
NM_001374258.1:c.1435-175_1435-169delinsATTTAAG MANE Plus Clinical NP_001361187.1:n.1435-175_1435-169delinsATTTAAG
NM_004333.6:c.1315-175_1315-169delinsATTTAAG MANE Select NP_004324.2:n.1315-175_1315-169delinsATTTAAG
NM_001378467.1:c.1324-175_1324-169delinsATTTAAG NP_001365396.1:n.1324-175_1324-169delinsATTTAAG
NM_001378468.1:c.1315-175_1315-169delinsATTTAAG NP_001365397.1:n.1315-175_1315-169delinsATTTAAG
NM_001378469.1:c.1249-175_1249-169delinsATTTAAG NP_001365398.1:n.1249-175_1249-169delinsATTTAAG
NM_001378470.1:c.1213-175_1213-169delinsATTTAAG NP_001365399.1:n.1213-175_1213-169delinsATTTAAG
NM_001378471.1:c.1204-175_1204-169delinsATTTAAG NP_001365400.1:n.1204-175_1204-169delinsATTTAAG
NM_001378472.1:c.1159-175_1159-169delinsATTTAAG NP_001365401.1:n.1159-175_1159-169delinsATTTAAG
NM_001378473.1:c.1159-175_1159-169delinsATTTAAG NP_001365402.1:n.1159-175_1159-169delinsATTTAAG
NM_001378474.1:c.1315-175_1315-169delinsATTTAAG NP_001365403.1:n.1315-175_1315-169delinsATTTAAG
NM_001378475.1:c.1051-175_1051-169delinsATTTAAG NP_001365404.1:n.1051-175_1051-169delinsATTTAAG