Canonical Allele Identifier: CA356998

Gene: BRAF

Linked Data

• ClinVar Variation Id: 223139
• ClinVar RCV Id: RCV000208751
• dbSNP Id: rs869025607
• MyVariant Identifiers: chr7:g.140481398_140481400del (hg19) ; chr7:g.140781598_140781600del (hg38)
• PubMed: PMID:20301365

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140781599_140781601del , CM000669.2:g.140781599_140781601del	GRCh38
NC_000007.13:g.140481399_140481401del , CM000669.1:g.140481399_140481401del	GRCh37
NC_000007.12:g.140127868_140127870del	NCBI36
NG_007873.3:g.148165_148167del , LRG_299:g.148165_148167del

Transcript Alleles

HGVS	Amino-acid change
ENST00000646891.2:c.1408_1410del MANE Select	ENSP00000493543.1:p.Thr470del
ENST00000288602.11:c.1528_1530del	ENSP00000288602.7:p.Thr510del
ENST00000479537.6:c.78_80del
ENST00000496384.7:c.1408_1410del	ENSP00000419060.2:p.Thr470del
ENST00000497784.2:c.*858_*860del	ENSP00000420119.2:n.*858_*860del
ENST00000642228.1:c.*486_*488del	ENSP00000493678.1:n.*486_*488del
ENST00000642875.1:n.850_852del
ENST00000644120.1:n.1798_1800del
ENST00000644650.1:c.504_506del
ENST00000644905.1:n.1497_1499del
ENST00000644969.2:c.1528_1530del MANE Plus Clinical	ENSP00000496776.1:p.Thr510del
ENST00000646334.1:n.538_540del
ENST00000646730.1:c.1408_1410del	ENSP00000494784.1:p.Thr470del
ENST00000646891.1:c.1408_1410del	ENSP00000493543.1:p.Thr470del
ENST00000647434.1:c.451_453del	ENSP00000495132.1:p.Thr151del
ENST00000288602.10:c.1408_1410del	ENSP00000288602.6:p.Thr470del
ENST00000496384.6:c.231_233del
ENST00000497784.1:c.1443_1445del	ENSP00000420119.1:n.1443_1445del
NM_004333.4:c.1408_1410del , LRG_299t1:c.1408_1410del	NP_004324.2:p.Thr470del
XM_005250045.1:c.1408_1410del	XP_005250102.1:p.Thr470del
XM_005250046.1:c.1408_1410del	XP_005250103.1:p.Thr470del
XM_011516529.1:c.1408_1410del	XP_011514831.1:p.Thr470del
XM_011516530.1:c.1408_1410del	XP_011514832.1:p.Thr470del
XR_242190.1:n.1416_1418del
XR_927520.1:n.1416_1418del
XR_927521.1:n.1416_1418del
XR_927522.1:n.1416_1418del
XR_927523.1:n.1416_1418del
NM_001354609.1:c.1408_1410del	NP_001341538.1:p.Thr470del
NM_004333.5:c.1408_1410del	NP_004324.2:p.Thr470del
NR_148928.1:n.1713_1715del
XM_017012558.1:c.1528_1530del	XP_016868047.1:p.Thr510del
XM_017012559.1:c.1528_1530del	XP_016868048.1:p.Thr510del
XR_001744857.1:n.1536_1538del
XR_001744858.1:n.1536_1538del
NM_001354609.2:c.1408_1410del	NP_001341538.1:p.Thr470del
NM_001374244.1:c.1528_1530del	NP_001361173.1:p.Thr510del
NM_001374258.1:c.1528_1530del MANE Plus Clinical	NP_001361187.1:p.Thr510del
NM_004333.6:c.1408_1410del MANE Select	NP_004324.2:p.Thr470del
NM_001378467.1:c.1417_1419del	NP_001365396.1:p.Thr473del
NM_001378468.1:c.1408_1410del	NP_001365397.1:p.Thr470del
NM_001378469.1:c.1342_1344del	NP_001365398.1:p.Thr448del
NM_001378470.1:c.1306_1308del	NP_001365399.1:p.Thr436del
NM_001378471.1:c.1297_1299del	NP_001365400.1:p.Thr433del
NM_001378472.1:c.1252_1254del	NP_001365401.1:p.Thr418del
NM_001378473.1:c.1252_1254del	NP_001365402.1:p.Thr418del
NM_001378474.1:c.1408_1410del	NP_001365403.1:p.Thr470del
NM_001378475.1:c.1144_1146del	NP_001365404.1:p.Thr382del