Canonical Allele Identifier: CA2715966080

Gene: BRAF

Linked Data

• dbSNP Id: rs2129018293

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140776969del , CM000669.2:g.140776969del	GRCh38
NC_000007.13:g.140476769del , CM000669.1:g.140476769del	GRCh37
NC_000007.12:g.140123238del	NCBI36
NG_007873.3:g.152797del , LRG_299:g.152797del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646891.2:c.1638del MANE Select	ENSP00000493543.1:p.Lys547AsnfsTer4
ENST00000288602.11:c.1758del	ENSP00000288602.7:p.Lys587AsnfsTer4
ENST00000479537.6:c.308del
ENST00000496384.7:c.1638del	ENSP00000419060.2:p.Lys547AsnfsTer4
ENST00000497784.2:c.*1088del	ENSP00000420119.2:n.*1088del
ENST00000642228.1:c.*716del	ENSP00000493678.1:n.*716del
ENST00000642875.1:n.1202del
ENST00000644120.1:n.2028del
ENST00000644650.1:c.734del
ENST00000644905.1:n.1727del
ENST00000644969.2:c.1758del MANE Plus Clinical	ENSP00000496776.1:p.Lys587AsnfsTer4
ENST00000646730.1:c.1638del	ENSP00000494784.1:p.Lys547AsnfsTer4
ENST00000646891.1:c.1638del	ENSP00000493543.1:p.Lys547AsnfsTer4
ENST00000647434.1:c.681del	ENSP00000495132.1:p.Lys228AsnfsTer4
ENST00000288602.10:c.1638del	ENSP00000288602.6:p.Lys547AsnfsTer4
ENST00000496384.6:c.461del
ENST00000497784.1:c.1673del	ENSP00000420119.1:n.1673del
NM_004333.4:c.1638del , LRG_299t1:c.1638del	NP_004324.2:p.Lys547AsnfsTer4
XM_005250045.1:c.1638del	XP_005250102.1:p.Lys547AsnfsTer4
XM_005250046.1:c.1638del	XP_005250103.1:p.Lys547AsnfsTer4
XM_011516529.1:c.1638del	XP_011514831.1:p.Lys547AsnfsTer4
XM_011516530.1:c.1638del	XP_011514832.1:p.Lys547AsnfsTer4
XR_242190.1:n.1646del
XR_927520.1:n.1646del
XR_927521.1:n.1646del
XR_927522.1:n.1646del
XR_927523.1:n.1646del
NM_001354609.1:c.1638del	NP_001341538.1:p.Lys547AsnfsTer4
NM_004333.5:c.1638del	NP_004324.2:p.Lys547AsnfsTer4
NR_148928.1:n.1943del
XM_017012558.1:c.1758del	XP_016868047.1:p.Lys587AsnfsTer4
XM_017012559.1:c.1758del	XP_016868048.1:p.Lys587AsnfsTer4
XR_001744857.1:n.1766del
XR_001744858.1:n.1766del
NM_001354609.2:c.1638del	NP_001341538.1:p.Lys547AsnfsTer4
NM_001374244.1:c.1758del	NP_001361173.1:p.Lys587AsnfsTer4
NM_001374258.1:c.1758del MANE Plus Clinical	NP_001361187.1:p.Lys587AsnfsTer4
NM_004333.6:c.1638del MANE Select	NP_004324.2:p.Lys547AsnfsTer4
NM_001378467.1:c.1647del	NP_001365396.1:p.Lys550AsnfsTer4
NM_001378468.1:c.1638del	NP_001365397.1:p.Lys547AsnfsTer4
NM_001378469.1:c.1572del	NP_001365398.1:p.Lys525AsnfsTer4
NM_001378470.1:c.1536del	NP_001365399.1:p.Lys513AsnfsTer4
NM_001378471.1:c.1527del	NP_001365400.1:p.Lys510AsnfsTer4
NM_001378472.1:c.1482del	NP_001365401.1:p.Lys495AsnfsTer4
NM_001378473.1:c.1482del	NP_001365402.1:p.Lys495AsnfsTer4
NM_001378474.1:c.1638del	NP_001365403.1:p.Lys547AsnfsTer4
NM_001378475.1:c.1374del	NP_001365404.1:p.Lys459AsnfsTer4