Canonical Allele Identifier: CA1747718195
Gene: BRAF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140781596_140781602delinsACTGTTC , CM000669.2:g.140781596_140781602delinsACTGTTC GRCh38
NC_000007.13:g.140481396_140481402delinsACTGTTC , CM000669.1:g.140481396_140481402delinsACTGTTC GRCh37
NC_000007.12:g.140127865_140127871delinsACTGTTC NCBI36
NG_007873.3:g.148163_148169delinsGAACAGT , LRG_299:g.148163_148169delinsGAACAGT

Transcript Alleles

HGVS Amino-acid change
ENST00000646891.2:c.1406_1412delinsGAACAGT MANE Select ENSP00000493543.1:p.Gly469=
ENST00000288602.11:c.1526_1532delinsGAACAGT ENSP00000288602.7:p.Gly509=
ENST00000479537.6:c.76_82delinsGAACAGT
ENST00000496384.7:c.1406_1412delinsGAACAGT ENSP00000419060.2:p.Gly469=
ENST00000497784.2:c.*856_*862delinsGAACAGT ENSP00000420119.2:n.*856_*862delinsGAACAG...
ENST00000642228.1:c.*484_*490delinsGAACAGT ENSP00000493678.1:n.*484_*490delinsGAACAG...
ENST00000642875.1:n.848_854delinsGAACAGT
ENST00000644120.1:n.1796_1802delinsGAACAGT
ENST00000644650.1:c.502_508delinsGAACAGT
ENST00000644905.1:n.1495_1501delinsGAACAGT
ENST00000644969.2:c.1526_1532delinsGAACAGT MANE Plus Clinical ENSP00000496776.1:p.Gly509=
ENST00000646334.1:n.536_542delinsGAACAGT
ENST00000646730.1:c.1406_1412delinsGAACAGT ENSP00000494784.1:p.Gly469=
ENST00000646891.1:c.1406_1412delinsGAACAGT ENSP00000493543.1:p.Gly469=
ENST00000647434.1:c.449_455delinsGAACAGT ENSP00000495132.1:p.Gly150=
ENST00000288602.10:c.1406_1412delinsGAACAGT ENSP00000288602.6:p.Gly469=
ENST00000496384.6:c.229_235delinsGAACAGT
ENST00000497784.1:c.1441_1447delinsGAACAGT ENSP00000420119.1:n.1441_1447delinsGAACAG...
NM_004333.4:c.1406_1412delinsGAACAGT , LRG_299t1:c.1406_1412delinsGAACAGT NP_004324.2:p.Gly469=
XM_005250045.1:c.1406_1412delinsGAACAGT XP_005250102.1:p.Gly469=
XM_005250046.1:c.1406_1412delinsGAACAGT XP_005250103.1:p.Gly469=
XM_011516529.1:c.1406_1412delinsGAACAGT XP_011514831.1:p.Gly469=
XM_011516530.1:c.1406_1412delinsGAACAGT XP_011514832.1:p.Gly469=
XR_242190.1:n.1414_1420delinsGAACAGT
XR_927520.1:n.1414_1420delinsGAACAGT
XR_927521.1:n.1414_1420delinsGAACAGT
XR_927522.1:n.1414_1420delinsGAACAGT
XR_927523.1:n.1414_1420delinsGAACAGT
NM_001354609.1:c.1406_1412delinsGAACAGT NP_001341538.1:p.Gly469=
NM_004333.5:c.1406_1412delinsGAACAGT NP_004324.2:p.Gly469=
NR_148928.1:n.1711_1717delinsGAACAGT
XM_017012558.1:c.1526_1532delinsGAACAGT XP_016868047.1:p.Gly509=
XM_017012559.1:c.1526_1532delinsGAACAGT XP_016868048.1:p.Gly509=
XR_001744857.1:n.1534_1540delinsGAACAGT
XR_001744858.1:n.1534_1540delinsGAACAGT
NM_001354609.2:c.1406_1412delinsGAACAGT NP_001341538.1:p.Gly469=
NM_001374244.1:c.1526_1532delinsGAACAGT NP_001361173.1:p.Gly509=
NM_001374258.1:c.1526_1532delinsGAACAGT MANE Plus Clinical NP_001361187.1:p.Gly509=
NM_004333.6:c.1406_1412delinsGAACAGT MANE Select NP_004324.2:p.Gly469=
NM_001378467.1:c.1415_1421delinsGAACAGT NP_001365396.1:p.Gly472=
NM_001378468.1:c.1406_1412delinsGAACAGT NP_001365397.1:p.Gly469=
NM_001378469.1:c.1340_1346delinsGAACAGT NP_001365398.1:p.Gly447=
NM_001378470.1:c.1304_1310delinsGAACAGT NP_001365399.1:p.Gly435=
NM_001378471.1:c.1295_1301delinsGAACAGT NP_001365400.1:p.Gly432=
NM_001378472.1:c.1250_1256delinsGAACAGT NP_001365401.1:p.Gly417=
NM_001378473.1:c.1250_1256delinsGAACAGT NP_001365402.1:p.Gly417=
NM_001378474.1:c.1406_1412delinsGAACAGT NP_001365403.1:p.Gly469=
NM_001378475.1:c.1142_1148delinsGAACAGT NP_001365404.1:p.Gly381=