Canonical Allele Identifier: CA2715968138

Gene: BRAF

Linked Data

• dbSNP Id: rs2129018393

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140777012_140777013del , CM000669.2:g.140777012_140777013del	GRCh38
NC_000007.13:g.140476812_140476813del , CM000669.1:g.140476812_140476813del	GRCh37
NC_000007.12:g.140123281_140123282del	NCBI36
NG_007873.3:g.152755_152756del , LRG_299:g.152755_152756del

Transcript Alleles

HGVS	Amino-acid change
ENST00000646891.2:c.1596_1597del MANE Select	ENSP00000493543.1:p.Cys532Ter
ENST00000288602.11:c.1716_1717del	ENSP00000288602.7:p.Cys572Ter
ENST00000479537.6:c.266_267del
ENST00000496384.7:c.1596_1597del	ENSP00000419060.2:p.Cys532Ter
ENST00000497784.2:c.*1046_*1047del	ENSP00000420119.2:n.*1046_*1047del
ENST00000642228.1:c.*674_*675del	ENSP00000493678.1:n.*674_*675del
ENST00000642875.1:n.1160_1161del
ENST00000644120.1:n.1986_1987del
ENST00000644650.1:c.692_693del
ENST00000644905.1:n.1685_1686del
ENST00000644969.2:c.1716_1717del MANE Plus Clinical	ENSP00000496776.1:p.Cys572Ter
ENST00000646730.1:c.1596_1597del	ENSP00000494784.1:p.Cys532Ter
ENST00000646891.1:c.1596_1597del	ENSP00000493543.1:p.Cys532Ter
ENST00000647434.1:c.639_640del	ENSP00000495132.1:p.Cys213Ter
ENST00000288602.10:c.1596_1597del	ENSP00000288602.6:p.Cys532Ter
ENST00000496384.6:c.419_420del
ENST00000497784.1:c.1631_1632del	ENSP00000420119.1:n.1631_1632del
NM_004333.4:c.1596_1597del , LRG_299t1:c.1596_1597del	NP_004324.2:p.Cys532Ter
XM_005250045.1:c.1596_1597del	XP_005250102.1:p.Cys532Ter
XM_005250046.1:c.1596_1597del	XP_005250103.1:p.Cys532Ter
XM_011516529.1:c.1596_1597del	XP_011514831.1:p.Cys532Ter
XM_011516530.1:c.1596_1597del	XP_011514832.1:p.Cys532Ter
XR_242190.1:n.1604_1605del
XR_927520.1:n.1604_1605del
XR_927521.1:n.1604_1605del
XR_927522.1:n.1604_1605del
XR_927523.1:n.1604_1605del
NM_001354609.1:c.1596_1597del	NP_001341538.1:p.Cys532Ter
NM_004333.5:c.1596_1597del	NP_004324.2:p.Cys532Ter
NR_148928.1:n.1901_1902del
XM_017012558.1:c.1716_1717del	XP_016868047.1:p.Cys572Ter
XM_017012559.1:c.1716_1717del	XP_016868048.1:p.Cys572Ter
XR_001744857.1:n.1724_1725del
XR_001744858.1:n.1724_1725del
NM_001354609.2:c.1596_1597del	NP_001341538.1:p.Cys532Ter
NM_001374244.1:c.1716_1717del	NP_001361173.1:p.Cys572Ter
NM_001374258.1:c.1716_1717del MANE Plus Clinical	NP_001361187.1:p.Cys572Ter
NM_004333.6:c.1596_1597del MANE Select	NP_004324.2:p.Cys532Ter
NM_001378467.1:c.1605_1606del	NP_001365396.1:p.Cys535Ter
NM_001378468.1:c.1596_1597del	NP_001365397.1:p.Cys532Ter
NM_001378469.1:c.1530_1531del	NP_001365398.1:p.Cys510Ter
NM_001378470.1:c.1494_1495del	NP_001365399.1:p.Cys498Ter
NM_001378471.1:c.1485_1486del	NP_001365400.1:p.Cys495Ter
NM_001378472.1:c.1440_1441del	NP_001365401.1:p.Cys480Ter
NM_001378473.1:c.1440_1441del	NP_001365402.1:p.Cys480Ter
NM_001378474.1:c.1596_1597del	NP_001365403.1:p.Cys532Ter
NM_001378475.1:c.1332_1333del	NP_001365404.1:p.Cys444Ter