Canonical Allele Identifier: CA645556773

Gene: BRAF

Linked Data

• COSMIC: COSM5761459

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140778035_140778049del , CM000669.2:g.140778035_140778049del	GRCh38
NC_000007.13:g.140477835_140477849del , CM000669.1:g.140477835_140477849del	GRCh37
NC_000007.12:g.140124304_140124318del	NCBI36
NG_007873.3:g.151716_151730del , LRG_299:g.151716_151730del

Transcript Alleles

HGVS	Amino-acid change
ENST00000646891.2:c.1459_1473del MANE Select	ENSP00000493543.1:p.Val487_Thr491del
ENST00000288602.11:c.1579_1593del	ENSP00000288602.7:p.Val527_Thr531del
ENST00000479537.6:c.129_143del
ENST00000496384.7:c.1459_1473del	ENSP00000419060.2:p.Val487_Thr491del
ENST00000497784.2:c.*909_*923del	ENSP00000420119.2:n.*909_*923del
ENST00000642228.1:c.*537_*551del	ENSP00000493678.1:n.*537_*551del
ENST00000642875.1:n.1023_1037del
ENST00000644120.1:n.1849_1863del
ENST00000644650.1:c.555_569del
ENST00000644905.1:n.1548_1562del
ENST00000644969.2:c.1579_1593del MANE Plus Clinical	ENSP00000496776.1:p.Val527_Thr531del
ENST00000646730.1:c.1459_1473del	ENSP00000494784.1:p.Val487_Thr491del
ENST00000646891.1:c.1459_1473del	ENSP00000493543.1:p.Val487_Thr491del
ENST00000647434.1:c.502_516del	ENSP00000495132.1:p.Val168_Thr172del
ENST00000288602.10:c.1459_1473del	ENSP00000288602.6:p.Val487_Thr491del
ENST00000496384.6:c.282_296del
ENST00000497784.1:c.1494_1508del	ENSP00000420119.1:n.1494_1508del
NM_004333.4:c.1459_1473del , LRG_299t1:c.1459_1473del	NP_004324.2:p.Val487_Thr491del
XM_005250045.1:c.1459_1473del	XP_005250102.1:p.Val487_Thr491del
XM_005250046.1:c.1459_1473del	XP_005250103.1:p.Val487_Thr491del
XM_011516529.1:c.1459_1473del	XP_011514831.1:p.Val487_Thr491del
XM_011516530.1:c.1459_1473del	XP_011514832.1:p.Val487_Thr491del
XR_242190.1:n.1467_1481del
XR_927520.1:n.1467_1481del
XR_927521.1:n.1467_1481del
XR_927522.1:n.1467_1481del
XR_927523.1:n.1467_1481del
NM_001354609.1:c.1459_1473del	NP_001341538.1:p.Val487_Thr491del
NM_004333.5:c.1459_1473del	NP_004324.2:p.Val487_Thr491del
NR_148928.1:n.1764_1778del
XM_017012558.1:c.1579_1593del	XP_016868047.1:p.Val527_Thr531del
XM_017012559.1:c.1579_1593del	XP_016868048.1:p.Val527_Thr531del
XR_001744857.1:n.1587_1601del
XR_001744858.1:n.1587_1601del
NM_001354609.2:c.1459_1473del	NP_001341538.1:p.Val487_Thr491del
NM_001374244.1:c.1579_1593del	NP_001361173.1:p.Val527_Thr531del
NM_001374258.1:c.1579_1593del MANE Plus Clinical	NP_001361187.1:p.Val527_Thr531del
NM_004333.6:c.1459_1473del MANE Select	NP_004324.2:p.Val487_Thr491del
NM_001378467.1:c.1468_1482del	NP_001365396.1:p.Val490_Thr494del
NM_001378468.1:c.1459_1473del	NP_001365397.1:p.Val487_Thr491del
NM_001378469.1:c.1393_1407del	NP_001365398.1:p.Val465_Thr469del
NM_001378470.1:c.1357_1371del	NP_001365399.1:p.Val453_Thr457del
NM_001378471.1:c.1348_1362del	NP_001365400.1:p.Val450_Thr454del
NM_001378472.1:c.1303_1317del	NP_001365401.1:p.Val435_Thr439del
NM_001378473.1:c.1303_1317del	NP_001365402.1:p.Val435_Thr439del
NM_001378474.1:c.1459_1473del	NP_001365403.1:p.Val487_Thr491del
NM_001378475.1:c.1195_1209del	NP_001365404.1:p.Val399_Thr403del