Canonical Allele Identifier: CA915945534
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 666410
ClinVar RCV Id: RCV000824918
dbSNP Id: rs1586140436

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140781598_140781603del , CM000669.2:g.140781598_140781603del GRCh38
NC_000007.13:g.140481398_140481403del , CM000669.1:g.140481398_140481403del GRCh37
NC_000007.12:g.140127867_140127872del NCBI36
NG_007873.3:g.148163_148168del , LRG_299:g.148163_148168del

Transcript Alleles

HGVS Amino-acid change
ENST00000646891.2:c.1406_1411del MANE Select ENSP00000493543.1:p.Gly469_Thr470del
ENST00000288602.11:c.1526_1531del ENSP00000288602.7:p.Gly509_Thr510del
ENST00000479537.6:c.76_81del
ENST00000496384.7:c.1406_1411del ENSP00000419060.2:p.Gly469_Thr470del
ENST00000497784.2:c.*856_*861del ENSP00000420119.2:n.*856_*861del
ENST00000642228.1:c.*484_*489del ENSP00000493678.1:n.*484_*489del
ENST00000642875.1:n.848_853del
ENST00000644120.1:n.1796_1801del
ENST00000644650.1:c.502_507del
ENST00000644905.1:n.1495_1500del
ENST00000644969.2:c.1526_1531del MANE Plus Clinical ENSP00000496776.1:p.Gly509_Thr510del
ENST00000646334.1:n.536_541del
ENST00000646730.1:c.1406_1411del ENSP00000494784.1:p.Gly469_Thr470del
ENST00000646891.1:c.1406_1411del ENSP00000493543.1:p.Gly469_Thr470del
ENST00000647434.1:c.449_454del ENSP00000495132.1:p.Gly150_Thr151del
ENST00000288602.10:c.1406_1411del ENSP00000288602.6:p.Gly469_Thr470del
ENST00000496384.6:c.229_234del
ENST00000497784.1:c.1441_1446del ENSP00000420119.1:n.1441_1446del
NM_004333.4:c.1406_1411del , LRG_299t1:c.1406_1411del NP_004324.2:p.Gly469_Thr470del
XM_005250045.1:c.1406_1411del XP_005250102.1:p.Gly469_Thr470del
XM_005250046.1:c.1406_1411del XP_005250103.1:p.Gly469_Thr470del
XM_011516529.1:c.1406_1411del XP_011514831.1:p.Gly469_Thr470del
XM_011516530.1:c.1406_1411del XP_011514832.1:p.Gly469_Thr470del
XR_242190.1:n.1414_1419del
XR_927520.1:n.1414_1419del
XR_927521.1:n.1414_1419del
XR_927522.1:n.1414_1419del
XR_927523.1:n.1414_1419del
NM_001354609.1:c.1406_1411del NP_001341538.1:p.Gly469_Thr470del
NM_004333.5:c.1406_1411del NP_004324.2:p.Gly469_Thr470del
NR_148928.1:n.1711_1716del
XM_017012558.1:c.1526_1531del XP_016868047.1:p.Gly509_Thr510del
XM_017012559.1:c.1526_1531del XP_016868048.1:p.Gly509_Thr510del
XR_001744857.1:n.1534_1539del
XR_001744858.1:n.1534_1539del
NM_001354609.2:c.1406_1411del NP_001341538.1:p.Gly469_Thr470del
NM_001374244.1:c.1526_1531del NP_001361173.1:p.Gly509_Thr510del
NM_001374258.1:c.1526_1531del MANE Plus Clinical NP_001361187.1:p.Gly509_Thr510del
NM_004333.6:c.1406_1411del MANE Select NP_004324.2:p.Gly469_Thr470del
NM_001378467.1:c.1415_1420del NP_001365396.1:p.Gly472_Thr473del
NM_001378468.1:c.1406_1411del NP_001365397.1:p.Gly469_Thr470del
NM_001378469.1:c.1340_1345del NP_001365398.1:p.Gly447_Thr448del
NM_001378470.1:c.1304_1309del NP_001365399.1:p.Gly435_Thr436del
NM_001378471.1:c.1295_1300del NP_001365400.1:p.Gly432_Thr433del
NM_001378472.1:c.1250_1255del NP_001365401.1:p.Gly417_Thr418del
NM_001378473.1:c.1250_1255del NP_001365402.1:p.Gly417_Thr418del
NM_001378474.1:c.1406_1411del NP_001365403.1:p.Gly469_Thr470del
NM_001378475.1:c.1142_1147del NP_001365404.1:p.Gly381_Thr382del