Canonical Allele Identifier: CA645556780
Gene: BRAF HGNC NCBI

Linked Data

COSMIC: COSM347662

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140781602_140781603delinsAG , CM000669.2:g.140781602_140781603delinsAG GRCh38
NC_000007.13:g.140481402_140481403delinsAG , CM000669.1:g.140481402_140481403delinsAG GRCh37
NC_000007.12:g.140127871_140127872delinsAG NCBI36
NG_007873.3:g.148162_148163delinsCT , LRG_299:g.148162_148163delinsCT

Transcript Alleles

HGVS Amino-acid change
ENST00000646891.2:c.1405_1406delinsCT MANE Select ENSP00000493543.1:p.Gly469Leu
ENST00000288602.11:c.1525_1526delinsCT ENSP00000288602.7:p.Gly509Leu
ENST00000479537.6:c.75_76delinsCT
ENST00000496384.7:c.1405_1406delinsCT ENSP00000419060.2:p.Gly469Leu
ENST00000497784.2:c.*855_*856delinsCT ENSP00000420119.2:n.*855_*856delinsCT
ENST00000642228.1:c.*483_*484delinsCT ENSP00000493678.1:n.*483_*484delinsCT
ENST00000642875.1:n.847_848delinsCT
ENST00000644120.1:n.1795_1796delinsCT
ENST00000644650.1:c.501_502delinsCT
ENST00000644905.1:n.1494_1495delinsCT
ENST00000644969.2:c.1525_1526delinsCT MANE Plus Clinical ENSP00000496776.1:p.Gly509Leu
ENST00000646334.1:n.535_536delinsCT
ENST00000646730.1:c.1405_1406delinsCT ENSP00000494784.1:p.Gly469Leu
ENST00000646891.1:c.1405_1406delinsCT ENSP00000493543.1:p.Gly469Leu
ENST00000647434.1:c.448_449delinsCT ENSP00000495132.1:p.Gly150Leu
ENST00000288602.10:c.1405_1406delinsCT ENSP00000288602.6:p.Gly469Leu
ENST00000496384.6:c.228_229delinsCT
ENST00000497784.1:c.1440_1441delinsCT ENSP00000420119.1:n.1440_1441delinsCT
NM_004333.4:c.1405_1406delinsCT , LRG_299t1:c.1405_1406delinsCT NP_004324.2:p.Gly469Leu
XM_005250045.1:c.1405_1406delinsCT XP_005250102.1:p.Gly469Leu
XM_005250046.1:c.1405_1406delinsCT XP_005250103.1:p.Gly469Leu
XM_011516529.1:c.1405_1406delinsCT XP_011514831.1:p.Gly469Leu
XM_011516530.1:c.1405_1406delinsCT XP_011514832.1:p.Gly469Leu
XR_242190.1:n.1413_1414delinsCT
XR_927520.1:n.1413_1414delinsCT
XR_927521.1:n.1413_1414delinsCT
XR_927522.1:n.1413_1414delinsCT
XR_927523.1:n.1413_1414delinsCT
NM_001354609.1:c.1405_1406delinsCT NP_001341538.1:p.Gly469Leu
NM_004333.5:c.1405_1406delinsCT NP_004324.2:p.Gly469Leu
NR_148928.1:n.1710_1711delinsCT
XM_017012558.1:c.1525_1526delinsCT XP_016868047.1:p.Gly509Leu
XM_017012559.1:c.1525_1526delinsCT XP_016868048.1:p.Gly509Leu
XR_001744857.1:n.1533_1534delinsCT
XR_001744858.1:n.1533_1534delinsCT
NM_001354609.2:c.1405_1406delinsCT NP_001341538.1:p.Gly469Leu
NM_001374244.1:c.1525_1526delinsCT NP_001361173.1:p.Gly509Leu
NM_001374258.1:c.1525_1526delinsCT MANE Plus Clinical NP_001361187.1:p.Gly509Leu
NM_004333.6:c.1405_1406delinsCT MANE Select NP_004324.2:p.Gly469Leu
NM_001378467.1:c.1414_1415delinsCT NP_001365396.1:p.Gly472Leu
NM_001378468.1:c.1405_1406delinsCT NP_001365397.1:p.Gly469Leu
NM_001378469.1:c.1339_1340delinsCT NP_001365398.1:p.Gly447Leu
NM_001378470.1:c.1303_1304delinsCT NP_001365399.1:p.Gly435Leu
NM_001378471.1:c.1294_1295delinsCT NP_001365400.1:p.Gly432Leu
NM_001378472.1:c.1249_1250delinsCT NP_001365401.1:p.Gly417Leu
NM_001378473.1:c.1249_1250delinsCT NP_001365402.1:p.Gly417Leu
NM_001378474.1:c.1405_1406delinsCT NP_001365403.1:p.Gly469Leu
NM_001378475.1:c.1141_1142delinsCT NP_001365404.1:p.Gly381Leu