Canonical Allele Identifier: CA891842037

Gene: BRAF

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140777087_140777088insGTGGAATAG , CM000669.2:g.140777087_140777088insGTGGAATAG	GRCh38
NC_000007.13:g.140476887_140476888insGTGGAATAG , CM000669.1:g.140476887_140476888insGTGGAATAG	GRCh37
NC_000007.12:g.140123356_140123357insGTGGAATAG	NCBI36
NG_007873.3:g.152677_152678insCTATTCCAC , LRG_299:g.152677_152678insCTATTCCAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646891.2:c.1518_1519insCTATTCCAC MANE Select	ENSP00000493543.1:p.Arg506_Lys507insLeuPheHis
ENST00000288602.11:c.1638_1639insCTATTCCAC	ENSP00000288602.7:p.Arg546_Lys547insLeuPheHis
ENST00000479537.6:c.188_189insCTATTCCAC
ENST00000496384.7:c.1518_1519insCTATTCCAC	ENSP00000419060.2:p.Arg506_Lys507insLeuPheHis
ENST00000497784.2:c.*968_*969insCTATTCCAC	ENSP00000420119.2:n.*968_*969insCTATTCCAC
ENST00000642228.1:c.*596_*597insCTATTCCAC	ENSP00000493678.1:n.*596_*597insCTATTCCAC
ENST00000642875.1:n.1082_1083insCTATTCCAC
ENST00000644120.1:n.1908_1909insCTATTCCAC
ENST00000644650.1:c.614_615insCTATTCCAC
ENST00000644905.1:n.1607_1608insCTATTCCAC
ENST00000644969.2:c.1638_1639insCTATTCCAC MANE Plus Clinical	ENSP00000496776.1:p.Arg546_Lys547insLeuPheHis
ENST00000646730.1:c.1518_1519insCTATTCCAC	ENSP00000494784.1:p.Arg506_Lys507insLeuPheHis
ENST00000646891.1:c.1518_1519insCTATTCCAC	ENSP00000493543.1:p.Arg506_Lys507insLeuPheHis
ENST00000647434.1:c.561_562insCTATTCCAC	ENSP00000495132.1:p.Arg187_Lys188insLeuPheHis
ENST00000288602.10:c.1518_1519insCTATTCCAC	ENSP00000288602.6:p.Arg506_Lys507insLeuPheHis
ENST00000496384.6:c.341_342insCTATTCCAC
ENST00000497784.1:c.1553_1554insCTATTCCAC	ENSP00000420119.1:n.1553_1554insCTATTCCAC
NM_004333.4:c.1518_1519insCTATTCCAC , LRG_299t1:c.1518_1519insCTATTCCAC	NP_004324.2:p.Arg506_Lys507insLeuPheHis
XM_005250045.1:c.1518_1519insCTATTCCAC	XP_005250102.1:p.Arg506_Lys507insLeuPheHis
XM_005250046.1:c.1518_1519insCTATTCCAC	XP_005250103.1:p.Arg506_Lys507insLeuPheHis
XM_011516529.1:c.1518_1519insCTATTCCAC	XP_011514831.1:p.Arg506_Lys507insLeuPheHis
XM_011516530.1:c.1518_1519insCTATTCCAC	XP_011514832.1:p.Arg506_Lys507insLeuPheHis
XR_242190.1:n.1526_1527insCTATTCCAC
XR_927520.1:n.1526_1527insCTATTCCAC
XR_927521.1:n.1526_1527insCTATTCCAC
XR_927522.1:n.1526_1527insCTATTCCAC
XR_927523.1:n.1526_1527insCTATTCCAC
NM_001354609.1:c.1518_1519insCTATTCCAC	NP_001341538.1:p.Arg506_Lys507insLeuPheHis
NM_004333.5:c.1518_1519insCTATTCCAC	NP_004324.2:p.Arg506_Lys507insLeuPheHis
NR_148928.1:n.1823_1824insCTATTCCAC
XM_017012558.1:c.1638_1639insCTATTCCAC	XP_016868047.1:p.Arg546_Lys547insLeuPheHis
XM_017012559.1:c.1638_1639insCTATTCCAC	XP_016868048.1:p.Arg546_Lys547insLeuPheHis
XR_001744857.1:n.1646_1647insCTATTCCAC
XR_001744858.1:n.1646_1647insCTATTCCAC
NM_001354609.2:c.1518_1519insCTATTCCAC	NP_001341538.1:p.Arg506_Lys507insLeuPheHis
NM_001374244.1:c.1638_1639insCTATTCCAC	NP_001361173.1:p.Arg546_Lys547insLeuPheHis
NM_001374258.1:c.1638_1639insCTATTCCAC MANE Plus Clinical	NP_001361187.1:p.Arg546_Lys547insLeuPheHis
NM_004333.6:c.1518_1519insCTATTCCAC MANE Select	NP_004324.2:p.Arg506_Lys507insLeuPheHis
NM_001378467.1:c.1527_1528insCTATTCCAC	NP_001365396.1:p.Arg509_Lys510insLeuPheHis
NM_001378468.1:c.1518_1519insCTATTCCAC	NP_001365397.1:p.Arg506_Lys507insLeuPheHis
NM_001378469.1:c.1452_1453insCTATTCCAC	NP_001365398.1:p.Arg484_Lys485insLeuPheHis
NM_001378470.1:c.1416_1417insCTATTCCAC	NP_001365399.1:p.Arg472_Lys473insLeuPheHis
NM_001378471.1:c.1407_1408insCTATTCCAC	NP_001365400.1:p.Arg469_Lys470insLeuPheHis
NM_001378472.1:c.1362_1363insCTATTCCAC	NP_001365401.1:p.Arg454_Lys455insLeuPheHis
NM_001378473.1:c.1362_1363insCTATTCCAC	NP_001365402.1:p.Arg454_Lys455insLeuPheHis
NM_001378474.1:c.1518_1519insCTATTCCAC	NP_001365403.1:p.Arg506_Lys507insLeuPheHis
NM_001378475.1:c.1254_1255insCTATTCCAC	NP_001365404.1:p.Arg418_Lys419insLeuPheHis