Canonical Allele Identifier: CA168090462
Gene: BRAF HGNC NCBI

Linked Data

dbSNP Id: rs121913358
COSMIC: COSM1113

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140781601_140781603delinsGCT , CM000669.2:g.140781601_140781603delinsGCT GRCh38
NC_000007.13:g.140481401_140481403delinsGCT , CM000669.1:g.140481401_140481403delinsGCT GRCh37
NC_000007.12:g.140127870_140127872delinsGCT NCBI36
NG_007873.3:g.148162_148164delinsAGC , LRG_299:g.148162_148164delinsAGC

Transcript Alleles

HGVS Amino-acid change
ENST00000646891.2:c.1405_1407delinsAGC MANE Select ENSP00000493543.1:p.Gly469Ser
ENST00000288602.11:c.1525_1527delinsAGC ENSP00000288602.7:p.Gly509Ser
ENST00000479537.6:c.75_77delinsAGC
ENST00000496384.7:c.1405_1407delinsAGC ENSP00000419060.2:p.Gly469Ser
ENST00000497784.2:c.*855_*857delinsAGC ENSP00000420119.2:n.*855_*857delinsAGC
ENST00000642228.1:c.*483_*485delinsAGC ENSP00000493678.1:n.*483_*485delinsAGC
ENST00000642875.1:n.847_849delinsAGC
ENST00000644120.1:n.1795_1797delinsAGC
ENST00000644650.1:c.501_503delinsAGC
ENST00000644905.1:n.1494_1496delinsAGC
ENST00000644969.2:c.1525_1527delinsAGC MANE Plus Clinical ENSP00000496776.1:p.Gly509Ser
ENST00000646334.1:n.535_537delinsAGC
ENST00000646730.1:c.1405_1407delinsAGC ENSP00000494784.1:p.Gly469Ser
ENST00000646891.1:c.1405_1407delinsAGC ENSP00000493543.1:p.Gly469Ser
ENST00000647434.1:c.448_450delinsAGC ENSP00000495132.1:p.Gly150Ser
ENST00000288602.10:c.1405_1407delinsAGC ENSP00000288602.6:p.Gly469Ser
ENST00000496384.6:c.228_230delinsAGC
ENST00000497784.1:c.1440_1442delinsAGC ENSP00000420119.1:n.1440_1442delinsAGC
NM_004333.4:c.1405_1407delinsAGC , LRG_299t1:c.1405_1407delinsAGC NP_004324.2:p.Gly469Ser
XM_005250045.1:c.1405_1407delinsAGC XP_005250102.1:p.Gly469Ser
XM_005250046.1:c.1405_1407delinsAGC XP_005250103.1:p.Gly469Ser
XM_011516529.1:c.1405_1407delinsAGC XP_011514831.1:p.Gly469Ser
XM_011516530.1:c.1405_1407delinsAGC XP_011514832.1:p.Gly469Ser
XR_242190.1:n.1413_1415delinsAGC
XR_927520.1:n.1413_1415delinsAGC
XR_927521.1:n.1413_1415delinsAGC
XR_927522.1:n.1413_1415delinsAGC
XR_927523.1:n.1413_1415delinsAGC
NM_001354609.1:c.1405_1407delinsAGC NP_001341538.1:p.Gly469Ser
NM_004333.5:c.1405_1407delinsAGC NP_004324.2:p.Gly469Ser
NR_148928.1:n.1710_1712delinsAGC
XM_017012558.1:c.1525_1527delinsAGC XP_016868047.1:p.Gly509Ser
XM_017012559.1:c.1525_1527delinsAGC XP_016868048.1:p.Gly509Ser
XR_001744857.1:n.1533_1535delinsAGC
XR_001744858.1:n.1533_1535delinsAGC
NM_001354609.2:c.1405_1407delinsAGC NP_001341538.1:p.Gly469Ser
NM_001374244.1:c.1525_1527delinsAGC NP_001361173.1:p.Gly509Ser
NM_001374258.1:c.1525_1527delinsAGC MANE Plus Clinical NP_001361187.1:p.Gly509Ser
NM_004333.6:c.1405_1407delinsAGC MANE Select NP_004324.2:p.Gly469Ser
NM_001378467.1:c.1414_1416delinsAGC NP_001365396.1:p.Gly472Ser
NM_001378468.1:c.1405_1407delinsAGC NP_001365397.1:p.Gly469Ser
NM_001378469.1:c.1339_1341delinsAGC NP_001365398.1:p.Gly447Ser
NM_001378470.1:c.1303_1305delinsAGC NP_001365399.1:p.Gly435Ser
NM_001378471.1:c.1294_1296delinsAGC NP_001365400.1:p.Gly432Ser
NM_001378472.1:c.1249_1251delinsAGC NP_001365401.1:p.Gly417Ser
NM_001378473.1:c.1249_1251delinsAGC NP_001365402.1:p.Gly417Ser
NM_001378474.1:c.1405_1407delinsAGC NP_001365403.1:p.Gly469Ser
NM_001378475.1:c.1141_1143delinsAGC NP_001365404.1:p.Gly381Ser