Canonical Allele Identifier: CA2967272830
Gene: BRAF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140749376del , CM000669.2:g.140749376del GRCh38
NC_000007.13:g.140449176del , CM000669.1:g.140449176del GRCh37
NC_000007.12:g.140095645del NCBI36
NG_007873.3:g.180391del , LRG_299:g.180391del

Transcript Alleles

HGVS Amino-acid Change
ENST00000646891.2:c.1905del MANE Select ENSP00000493543.1:p.Gln636SerfsTer14
ENST00000288602.11:c.2025del ENSP00000288602.7:p.Gln676SerfsTer14
ENST00000479537.6:c.575del
ENST00000496384.7:c.1905del ENSP00000419060.2:p.Gln636SerfsTer14
ENST00000497784.2:c.*1355del ENSP00000420119.2:n.*1355del
ENST00000642228.1:c.*983del ENSP00000493678.1:n.*983del
ENST00000642875.1:n.1303del
ENST00000644120.1:n.2295del
ENST00000644650.1:c.1001del
ENST00000644905.1:n.2787del
ENST00000644969.2:c.2025del MANE Plus Clinical ENSP00000496776.1:p.Gln676SerfsTer14
ENST00000646730.1:c.*481del ENSP00000494784.1:n.*481del
ENST00000646891.1:c.1905del ENSP00000493543.1:p.Gln636SerfsTer14
ENST00000647434.1:c.782del ENSP00000495132.1:p.Phe261SerfsTer13
ENST00000288602.10:c.1905del ENSP00000288602.6:p.Gln636SerfsTer14
ENST00000479537.5:c.189del ENSP00000418033.1:p.Gln64SerfsTer14
ENST00000496384.6:c.728del
ENST00000497784.1:c.1940del ENSP00000420119.1:n.1940del
NM_004333.4:c.1905del , LRG_299t1:c.1905del NP_004324.2:p.Gln636SerfsTer14
XM_005250045.1:c.1905del XP_005250102.1:p.Gln636SerfsTer14
XM_005250046.1:c.1905del XP_005250103.1:p.Gln636SerfsTer14
XM_011516529.1:c.1905del XP_011514831.1:p.Gln636SerfsTer14
XM_011516530.1:c.1739del XP_011514832.1:p.Phe580SerfsTer13
XR_242190.1:n.1913del
XR_927520.1:n.1913del
XR_927521.1:n.1913del
XR_927522.1:n.1747del
XR_927523.1:n.1747del
NM_001354609.1:c.1905del NP_001341538.1:p.Gln636SerfsTer14
NM_004333.5:c.1905del NP_004324.2:p.Gln636SerfsTer14
NR_148928.1:n.3003del
XM_017012558.1:c.2025del XP_016868047.1:p.Gln676SerfsTer14
XM_017012559.1:c.2025del XP_016868048.1:p.Gln676SerfsTer14
XR_001744857.1:n.2033del
XR_001744858.1:n.1867del
NM_001354609.2:c.1905del NP_001341538.1:p.Gln636SerfsTer14
NM_001374244.1:c.2025del NP_001361173.1:p.Gln676SerfsTer14
NM_001374258.1:c.2025del MANE Plus Clinical NP_001361187.1:p.Gln676SerfsTer14
NM_004333.6:c.1905del MANE Select NP_004324.2:p.Gln636SerfsTer14
NM_001378467.1:c.1914del NP_001365396.1:p.Gln639SerfsTer14
NM_001378468.1:c.1905del NP_001365397.1:p.Gln636SerfsTer14
NM_001378469.1:c.1839del NP_001365398.1:p.Gln614SerfsTer14
NM_001378470.1:c.1803del NP_001365399.1:p.Gln602SerfsTer14
NM_001378471.1:c.1794del NP_001365400.1:p.Gln599SerfsTer14
NM_001378472.1:c.1749del NP_001365401.1:p.Gln584SerfsTer14
NM_001378473.1:c.1749del NP_001365402.1:p.Gln584SerfsTer14
NM_001378474.1:c.1905del NP_001365403.1:p.Gln636SerfsTer14
NM_001378475.1:c.1641del NP_001365404.1:p.Gln548SerfsTer14