Canonical Allele Identifier: CA2580077582

Gene: BRAF

Linked Data

• ClinVar Variation Id: 1711784
• ClinVar RCV Id: RCV002293329

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140781630_140781631insA , CM000669.2:g.140781630_140781631insA	GRCh38
NC_000007.13:g.140481430_140481431insA , CM000669.1:g.140481430_140481431insA	GRCh37
NC_000007.12:g.140127899_140127900insA	NCBI36
NG_007873.3:g.148134_148135insT , LRG_299:g.148134_148135insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646891.2:c.1377_1378insT MANE Select	ENSP00000493543.1:p.Gly460TrpfsTer20
ENST00000288602.11:c.1497_1498insT	ENSP00000288602.7:p.Gly500TrpfsTer20
ENST00000479537.6:c.47_48insT
ENST00000496384.7:c.1377_1378insT	ENSP00000419060.2:p.Gly460TrpfsTer20
ENST00000497784.2:c.*827_*828insT	ENSP00000420119.2:n.*827_*828insT
ENST00000642228.1:c.*455_*456insT	ENSP00000493678.1:n.*455_*456insT
ENST00000642875.1:n.819_820insT
ENST00000644120.1:n.1767_1768insT
ENST00000644650.1:c.473_474insT
ENST00000644905.1:n.1466_1467insT
ENST00000644969.2:c.1497_1498insT MANE Plus Clinical	ENSP00000496776.1:p.Gly500TrpfsTer20
ENST00000646334.1:n.507_508insT
ENST00000646730.1:c.1377_1378insT	ENSP00000494784.1:p.Gly460TrpfsTer20
ENST00000646891.1:c.1377_1378insT	ENSP00000493543.1:p.Gly460TrpfsTer20
ENST00000647434.1:c.420_421insT	ENSP00000495132.1:p.Gly141TrpfsTer20
ENST00000288602.10:c.1377_1378insT	ENSP00000288602.6:p.Gly460TrpfsTer20
ENST00000496384.6:c.200_201insT
ENST00000497784.1:c.1412_1413insT	ENSP00000420119.1:n.1412_1413insT
NM_004333.4:c.1377_1378insT , LRG_299t1:c.1377_1378insT	NP_004324.2:p.Gly460TrpfsTer20
XM_005250045.1:c.1377_1378insT	XP_005250102.1:p.Gly460TrpfsTer20
XM_005250046.1:c.1377_1378insT	XP_005250103.1:p.Gly460TrpfsTer20
XM_011516529.1:c.1377_1378insT	XP_011514831.1:p.Gly460TrpfsTer20
XM_011516530.1:c.1377_1378insT	XP_011514832.1:p.Gly460TrpfsTer20
XR_242190.1:n.1385_1386insT
XR_927520.1:n.1385_1386insT
XR_927521.1:n.1385_1386insT
XR_927522.1:n.1385_1386insT
XR_927523.1:n.1385_1386insT
NM_001354609.1:c.1377_1378insT	NP_001341538.1:p.Gly460TrpfsTer20
NM_004333.5:c.1377_1378insT	NP_004324.2:p.Gly460TrpfsTer20
NR_148928.1:n.1682_1683insT
XM_017012558.1:c.1497_1498insT	XP_016868047.1:p.Gly500TrpfsTer20
XM_017012559.1:c.1497_1498insT	XP_016868048.1:p.Gly500TrpfsTer20
XR_001744857.1:n.1505_1506insT
XR_001744858.1:n.1505_1506insT
NM_001354609.2:c.1377_1378insT	NP_001341538.1:p.Gly460TrpfsTer20
NM_001374244.1:c.1497_1498insT	NP_001361173.1:p.Gly500TrpfsTer20
NM_001374258.1:c.1497_1498insT MANE Plus Clinical	NP_001361187.1:p.Gly500TrpfsTer20
NM_004333.6:c.1377_1378insT MANE Select	NP_004324.2:p.Gly460TrpfsTer20
NM_001378467.1:c.1386_1387insT	NP_001365396.1:p.Gly463TrpfsTer20
NM_001378468.1:c.1377_1378insT	NP_001365397.1:p.Gly460TrpfsTer20
NM_001378469.1:c.1311_1312insT	NP_001365398.1:p.Gly438TrpfsTer20
NM_001378470.1:c.1275_1276insT	NP_001365399.1:p.Gly426TrpfsTer20
NM_001378471.1:c.1266_1267insT	NP_001365400.1:p.Gly423TrpfsTer20
NM_001378472.1:c.1221_1222insT	NP_001365401.1:p.Gly408TrpfsTer20
NM_001378473.1:c.1221_1222insT	NP_001365402.1:p.Gly408TrpfsTer20
NM_001378474.1:c.1377_1378insT	NP_001365403.1:p.Gly460TrpfsTer20
NM_001378475.1:c.1113_1114insT	NP_001365404.1:p.Gly372TrpfsTer20