Canonical Allele Identifier: CA1747718259
Gene: BRAF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140781602_140781603delinsCC , CM000669.2:g.140781602_140781603delinsCC GRCh38
NC_000007.13:g.140481402_140481403delinsCC , CM000669.1:g.140481402_140481403delinsCC GRCh37
NC_000007.12:g.140127871_140127872delinsCC NCBI36
NG_007873.3:g.148162_148163delinsGG , LRG_299:g.148162_148163delinsGG

Transcript Alleles

HGVS Amino-acid change
ENST00000646891.2:c.1405_1406delinsGG MANE Select ENSP00000493543.1:p.Gly469=
ENST00000288602.11:c.1525_1526delinsGG ENSP00000288602.7:p.Gly509=
ENST00000479537.6:c.75_76delinsGG
ENST00000496384.7:c.1405_1406delinsGG ENSP00000419060.2:p.Gly469=
ENST00000497784.2:c.*855_*856delinsGG ENSP00000420119.2:n.*855_*856delinsGG
ENST00000642228.1:c.*483_*484delinsGG ENSP00000493678.1:n.*483_*484delinsGG
ENST00000642875.1:n.847_848delinsGG
ENST00000644120.1:n.1795_1796delinsGG
ENST00000644650.1:c.501_502delinsGG
ENST00000644905.1:n.1494_1495delinsGG
ENST00000644969.2:c.1525_1526delinsGG MANE Plus Clinical ENSP00000496776.1:p.Gly509=
ENST00000646334.1:n.535_536delinsGG
ENST00000646730.1:c.1405_1406delinsGG ENSP00000494784.1:p.Gly469=
ENST00000646891.1:c.1405_1406delinsGG ENSP00000493543.1:p.Gly469=
ENST00000647434.1:c.448_449delinsGG ENSP00000495132.1:p.Gly150=
ENST00000288602.10:c.1405_1406delinsGG ENSP00000288602.6:p.Gly469=
ENST00000496384.6:c.228_229delinsGG
ENST00000497784.1:c.1440_1441delinsGG ENSP00000420119.1:n.1440_1441delinsGG
NM_004333.4:c.1405_1406delinsGG , LRG_299t1:c.1405_1406delinsGG NP_004324.2:p.Gly469=
XM_005250045.1:c.1405_1406delinsGG XP_005250102.1:p.Gly469=
XM_005250046.1:c.1405_1406delinsGG XP_005250103.1:p.Gly469=
XM_011516529.1:c.1405_1406delinsGG XP_011514831.1:p.Gly469=
XM_011516530.1:c.1405_1406delinsGG XP_011514832.1:p.Gly469=
XR_242190.1:n.1413_1414delinsGG
XR_927520.1:n.1413_1414delinsGG
XR_927521.1:n.1413_1414delinsGG
XR_927522.1:n.1413_1414delinsGG
XR_927523.1:n.1413_1414delinsGG
NM_001354609.1:c.1405_1406delinsGG NP_001341538.1:p.Gly469=
NM_004333.5:c.1405_1406delinsGG NP_004324.2:p.Gly469=
NR_148928.1:n.1710_1711delinsGG
XM_017012558.1:c.1525_1526delinsGG XP_016868047.1:p.Gly509=
XM_017012559.1:c.1525_1526delinsGG XP_016868048.1:p.Gly509=
XR_001744857.1:n.1533_1534delinsGG
XR_001744858.1:n.1533_1534delinsGG
NM_001354609.2:c.1405_1406delinsGG NP_001341538.1:p.Gly469=
NM_001374244.1:c.1525_1526delinsGG NP_001361173.1:p.Gly509=
NM_001374258.1:c.1525_1526delinsGG MANE Plus Clinical NP_001361187.1:p.Gly509=
NM_004333.6:c.1405_1406delinsGG MANE Select NP_004324.2:p.Gly469=
NM_001378467.1:c.1414_1415delinsGG NP_001365396.1:p.Gly472=
NM_001378468.1:c.1405_1406delinsGG NP_001365397.1:p.Gly469=
NM_001378469.1:c.1339_1340delinsGG NP_001365398.1:p.Gly447=
NM_001378470.1:c.1303_1304delinsGG NP_001365399.1:p.Gly435=
NM_001378471.1:c.1294_1295delinsGG NP_001365400.1:p.Gly432=
NM_001378472.1:c.1249_1250delinsGG NP_001365401.1:p.Gly417=
NM_001378473.1:c.1249_1250delinsGG NP_001365402.1:p.Gly417=
NM_001378474.1:c.1405_1406delinsGG NP_001365403.1:p.Gly469=
NM_001378475.1:c.1141_1142delinsGG NP_001365404.1:p.Gly381=