Canonical Allele Identifier: CA645556776

Gene: BRAF

Linked Data

• COSMIC: COSM1731736

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140778050_140778058del , CM000669.2:g.140778050_140778058del	GRCh38
NC_000007.13:g.140477850_140477858del , CM000669.1:g.140477850_140477858del	GRCh37
NC_000007.12:g.140124319_140124327del	NCBI36
NG_007873.3:g.151707_151715del , LRG_299:g.151707_151715del

Transcript Alleles

HGVS	Amino-acid change
ENST00000646891.2:c.1450_1458del MANE Select	ENSP00000493543.1:p.Met484_Asn486del
ENST00000288602.11:c.1570_1578del	ENSP00000288602.7:p.Met524_Asn526del
ENST00000479537.6:c.120_128del
ENST00000496384.7:c.1450_1458del	ENSP00000419060.2:p.Met484_Asn486del
ENST00000497784.2:c.*900_*908del	ENSP00000420119.2:n.*900_*908del
ENST00000642228.1:c.*528_*536del	ENSP00000493678.1:n.*528_*536del
ENST00000642875.1:n.1014_1022del
ENST00000644120.1:n.1840_1848del
ENST00000644650.1:c.546_554del
ENST00000644905.1:n.1539_1547del
ENST00000644969.2:c.1570_1578del MANE Plus Clinical	ENSP00000496776.1:p.Met524_Asn526del
ENST00000646730.1:c.1450_1458del	ENSP00000494784.1:p.Met484_Asn486del
ENST00000646891.1:c.1450_1458del	ENSP00000493543.1:p.Met484_Asn486del
ENST00000647434.1:c.493_501del	ENSP00000495132.1:p.Met165_Asn167del
ENST00000288602.10:c.1450_1458del	ENSP00000288602.6:p.Met484_Asn486del
ENST00000496384.6:c.273_281del
ENST00000497784.1:c.1485_1493del	ENSP00000420119.1:n.1485_1493del
NM_004333.4:c.1450_1458del , LRG_299t1:c.1450_1458del	NP_004324.2:p.Met484_Asn486del
XM_005250045.1:c.1450_1458del	XP_005250102.1:p.Met484_Asn486del
XM_005250046.1:c.1450_1458del	XP_005250103.1:p.Met484_Asn486del
XM_011516529.1:c.1450_1458del	XP_011514831.1:p.Met484_Asn486del
XM_011516530.1:c.1450_1458del	XP_011514832.1:p.Met484_Asn486del
XR_242190.1:n.1458_1466del
XR_927520.1:n.1458_1466del
XR_927521.1:n.1458_1466del
XR_927522.1:n.1458_1466del
XR_927523.1:n.1458_1466del
NM_001354609.1:c.1450_1458del	NP_001341538.1:p.Met484_Asn486del
NM_004333.5:c.1450_1458del	NP_004324.2:p.Met484_Asn486del
NR_148928.1:n.1755_1763del
XM_017012558.1:c.1570_1578del	XP_016868047.1:p.Met524_Asn526del
XM_017012559.1:c.1570_1578del	XP_016868048.1:p.Met524_Asn526del
XR_001744857.1:n.1578_1586del
XR_001744858.1:n.1578_1586del
NM_001354609.2:c.1450_1458del	NP_001341538.1:p.Met484_Asn486del
NM_001374244.1:c.1570_1578del	NP_001361173.1:p.Met524_Asn526del
NM_001374258.1:c.1570_1578del MANE Plus Clinical	NP_001361187.1:p.Met524_Asn526del
NM_004333.6:c.1450_1458del MANE Select	NP_004324.2:p.Met484_Asn486del
NM_001378467.1:c.1459_1467del	NP_001365396.1:p.Met487_Asn489del
NM_001378468.1:c.1450_1458del	NP_001365397.1:p.Met484_Asn486del
NM_001378469.1:c.1384_1392del	NP_001365398.1:p.Met462_Asn464del
NM_001378470.1:c.1348_1356del	NP_001365399.1:p.Met450_Asn452del
NM_001378471.1:c.1339_1347del	NP_001365400.1:p.Met447_Asn449del
NM_001378472.1:c.1294_1302del	NP_001365401.1:p.Met432_Asn434del
NM_001378473.1:c.1294_1302del	NP_001365402.1:p.Met432_Asn434del
NM_001378474.1:c.1450_1458del	NP_001365403.1:p.Met484_Asn486del
NM_001378475.1:c.1186_1194del	NP_001365404.1:p.Met396_Asn398del