Canonical Allele Identifier: CA834227158

Gene: BRAF

Linked Data

• dbSNP Id: rs1219519655
• MyVariant Identifiers: chr7:g.140481316_140481317del (hg19) ; chr7:g.140781516_140781517del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140781518_140781519del , CM000669.2:g.140781518_140781519del	GRCh38
NC_000007.13:g.140481318_140481319del , CM000669.1:g.140481318_140481319del	GRCh37
NC_000007.12:g.140127787_140127788del	NCBI36
NG_007873.3:g.148248_148249del , LRG_299:g.148248_148249del

Transcript Alleles

HGVS	Amino-acid change
ENST00000646891.2:c.1432+59_1432+60del MANE Select	ENSP00000493543.1:n.1432+59_1432+60del
ENST00000288602.11:c.1552+59_1552+60del	ENSP00000288602.7:n.1552+59_1552+60del
ENST00000479537.6:c.102+59_102+60del
ENST00000496384.7:c.1432+59_1432+60del	ENSP00000419060.2:n.1432+59_1432+60del
ENST00000497784.2:c.*882+59_*882+60del	ENSP00000420119.2:n.*882+59_*882+60del
ENST00000642228.1:c.*510+59_*510+60del	ENSP00000493678.1:n.*510+59_*510+60del
ENST00000642875.1:n.874+59_874+60del
ENST00000644120.1:n.1822+59_1822+60del
ENST00000644650.1:c.528+59_528+60del
ENST00000644905.1:n.1521+59_1521+60del
ENST00000644969.2:c.1552+59_1552+60del MANE Plus Clinical	ENSP00000496776.1:n.1552+59_1552+60del
ENST00000646334.1:n.621_622del
ENST00000646730.1:c.1432+59_1432+60del	ENSP00000494784.1:n.1432+59_1432+60del
ENST00000646891.1:c.1432+59_1432+60del	ENSP00000493543.1:n.1432+59_1432+60del
ENST00000647434.1:c.475+59_475+60del	ENSP00000495132.1:n.475+59_475+60del
ENST00000288602.10:c.1432+59_1432+60del	ENSP00000288602.6:n.1432+59_1432+60del
ENST00000496384.6:c.255+59_255+60del
ENST00000497784.1:c.1467+59_1467+60del	ENSP00000420119.1:n.1467+59_1467+60del
NM_004333.4:c.1432+59_1432+60del , LRG_299t1:c.1432+59_1432+60del	NP_004324.2:n.1432+59_1432+60del
XM_005250045.1:c.1432+59_1432+60del	XP_005250102.1:n.1432+59_1432+60del
XM_005250046.1:c.1432+59_1432+60del	XP_005250103.1:n.1432+59_1432+60del
XM_011516529.1:c.1432+59_1432+60del	XP_011514831.1:n.1432+59_1432+60del
XM_011516530.1:c.1432+59_1432+60del	XP_011514832.1:n.1432+59_1432+60del
XR_242190.1:n.1440+59_1440+60del
XR_927520.1:n.1440+59_1440+60del
XR_927521.1:n.1440+59_1440+60del
XR_927522.1:n.1440+59_1440+60del
XR_927523.1:n.1440+59_1440+60del
NM_001354609.1:c.1432+59_1432+60del	NP_001341538.1:n.1432+59_1432+60del
NM_004333.5:c.1432+59_1432+60del	NP_004324.2:n.1432+59_1432+60del
NR_148928.1:n.1737+59_1737+60del
XM_017012558.1:c.1552+59_1552+60del	XP_016868047.1:n.1552+59_1552+60del
XM_017012559.1:c.1552+59_1552+60del	XP_016868048.1:n.1552+59_1552+60del
XR_001744857.1:n.1560+59_1560+60del
XR_001744858.1:n.1560+59_1560+60del
NM_001354609.2:c.1432+59_1432+60del	NP_001341538.1:n.1432+59_1432+60del
NM_001374244.1:c.1552+59_1552+60del	NP_001361173.1:n.1552+59_1552+60del
NM_001374258.1:c.1552+59_1552+60del MANE Plus Clinical	NP_001361187.1:n.1552+59_1552+60del
NM_004333.6:c.1432+59_1432+60del MANE Select	NP_004324.2:n.1432+59_1432+60del
NM_001378467.1:c.1441+59_1441+60del	NP_001365396.1:n.1441+59_1441+60del
NM_001378468.1:c.1432+59_1432+60del	NP_001365397.1:n.1432+59_1432+60del
NM_001378469.1:c.1366+59_1366+60del	NP_001365398.1:n.1366+59_1366+60del
NM_001378470.1:c.1330+59_1330+60del	NP_001365399.1:n.1330+59_1330+60del
NM_001378471.1:c.1321+59_1321+60del	NP_001365400.1:n.1321+59_1321+60del
NM_001378472.1:c.1276+59_1276+60del	NP_001365401.1:n.1276+59_1276+60del
NM_001378473.1:c.1276+59_1276+60del	NP_001365402.1:n.1276+59_1276+60del
NM_001378474.1:c.1432+59_1432+60del	NP_001365403.1:n.1432+59_1432+60del
NM_001378475.1:c.1168+59_1168+60del	NP_001365404.1:n.1168+59_1168+60del