Canonical Allele Identifier: CA834224575
Gene: BRAF HGNC NCBI

Linked Data

dbSNP Id: rs1378296522

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140776974_140776976del , CM000669.2:g.140776974_140776976del GRCh38
NC_000007.13:g.140476774_140476776del , CM000669.1:g.140476774_140476776del GRCh37
NC_000007.12:g.140123243_140123245del NCBI36
NG_007873.3:g.152789_152791del , LRG_299:g.152789_152791del

Transcript Alleles

HGVS Amino-acid Change
ENST00000646891.2:c.1630_1632del MANE Select ENSP00000493543.1:p.Ile544del
ENST00000288602.11:c.1750_1752del ENSP00000288602.7:p.Ile584del
ENST00000479537.6:c.300_302del
ENST00000496384.7:c.1630_1632del ENSP00000419060.2:p.Ile544del
ENST00000497784.2:c.*1080_*1082del ENSP00000420119.2:n.*1080_*1082del
ENST00000642228.1:c.*708_*710del ENSP00000493678.1:n.*708_*710del
ENST00000642875.1:n.1194_1196del
ENST00000644120.1:n.2020_2022del
ENST00000644650.1:c.726_728del
ENST00000644905.1:n.1719_1721del
ENST00000644969.2:c.1750_1752del MANE Plus Clinical ENSP00000496776.1:p.Ile584del
ENST00000646730.1:c.1630_1632del ENSP00000494784.1:p.Ile544del
ENST00000646891.1:c.1630_1632del ENSP00000493543.1:p.Ile544del
ENST00000647434.1:c.673_675del ENSP00000495132.1:p.Ile225del
ENST00000288602.10:c.1630_1632del ENSP00000288602.6:p.Ile544del
ENST00000496384.6:c.453_455del
ENST00000497784.1:c.1665_1667del ENSP00000420119.1:n.1665_1667del
NM_004333.4:c.1630_1632del , LRG_299t1:c.1630_1632del NP_004324.2:p.Ile544del
XM_005250045.1:c.1630_1632del XP_005250102.1:p.Ile544del
XM_005250046.1:c.1630_1632del XP_005250103.1:p.Ile544del
XM_011516529.1:c.1630_1632del XP_011514831.1:p.Ile544del
XM_011516530.1:c.1630_1632del XP_011514832.1:p.Ile544del
XR_242190.1:n.1638_1640del
XR_927520.1:n.1638_1640del
XR_927521.1:n.1638_1640del
XR_927522.1:n.1638_1640del
XR_927523.1:n.1638_1640del
NM_001354609.1:c.1630_1632del NP_001341538.1:p.Ile544del
NM_004333.5:c.1630_1632del NP_004324.2:p.Ile544del
NR_148928.1:n.1935_1937del
XM_017012558.1:c.1750_1752del XP_016868047.1:p.Ile584del
XM_017012559.1:c.1750_1752del XP_016868048.1:p.Ile584del
XR_001744857.1:n.1758_1760del
XR_001744858.1:n.1758_1760del
NM_001354609.2:c.1630_1632del NP_001341538.1:p.Ile544del
NM_001374244.1:c.1750_1752del NP_001361173.1:p.Ile584del
NM_001374258.1:c.1750_1752del MANE Plus Clinical NP_001361187.1:p.Ile584del
NM_004333.6:c.1630_1632del MANE Select NP_004324.2:p.Ile544del
NM_001378467.1:c.1639_1641del NP_001365396.1:p.Ile547del
NM_001378468.1:c.1630_1632del NP_001365397.1:p.Ile544del
NM_001378469.1:c.1564_1566del NP_001365398.1:p.Ile522del
NM_001378470.1:c.1528_1530del NP_001365399.1:p.Ile510del
NM_001378471.1:c.1519_1521del NP_001365400.1:p.Ile507del
NM_001378472.1:c.1474_1476del NP_001365401.1:p.Ile492del
NM_001378473.1:c.1474_1476del NP_001365402.1:p.Ile492del
NM_001378474.1:c.1630_1632del NP_001365403.1:p.Ile544del
NM_001378475.1:c.1366_1368del NP_001365404.1:p.Ile456del