Canonical Allele Identifier: CA458115494

Gene: BRAF

Linked Data

• dbSNP Id: rs1443228172
• MyVariant Identifiers: chr7:g.140476747A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140776947A>T , CM000669.2:g.140776947A>T	GRCh38
NC_000007.13:g.140476747A>T , CM000669.1:g.140476747A>T	GRCh37
NC_000007.12:g.140123216A>T	NCBI36
NG_007873.3:g.152818T>A , LRG_299:g.152818T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646891.2:c.1659T>A MANE Select	ENSP00000493543.1:p.Leu553=
ENST00000288602.11:c.1779T>A	ENSP00000288602.7:p.Leu593=
ENST00000479537.6:c.329T>A
ENST00000496384.7:c.1659T>A	ENSP00000419060.2:p.Leu553=
ENST00000497784.2:c.*1109T>A	ENSP00000420119.2:n.*1109T>A
ENST00000642228.1:c.*737T>A	ENSP00000493678.1:n.*737T>A
ENST00000642875.1:n.1223T>A
ENST00000644120.1:n.2049T>A
ENST00000644650.1:c.755T>A
ENST00000644905.1:n.1748T>A
ENST00000644969.2:c.1779T>A MANE Plus Clinical	ENSP00000496776.1:p.Leu593=
ENST00000646730.1:c.1659T>A	ENSP00000494784.1:p.Leu553=
ENST00000646891.1:c.1659T>A	ENSP00000493543.1:p.Leu553=
ENST00000647434.1:c.702T>A	ENSP00000495132.1:p.Leu234=
ENST00000288602.10:c.1659T>A	ENSP00000288602.6:p.Leu553=
ENST00000496384.6:c.482T>A
ENST00000497784.1:c.1694T>A	ENSP00000420119.1:n.1694T>A
NM_004333.4:c.1659T>A , LRG_299t1:c.1659T>A	NP_004324.2:p.Leu553=
XM_005250045.1:c.1659T>A	XP_005250102.1:p.Leu553=
XM_005250046.1:c.1659T>A	XP_005250103.1:p.Leu553=
XM_011516529.1:c.1659T>A	XP_011514831.1:p.Leu553=
XM_011516530.1:c.1659T>A	XP_011514832.1:p.Leu553=
XR_242190.1:n.1667T>A
XR_927520.1:n.1667T>A
XR_927521.1:n.1667T>A
XR_927522.1:n.1667T>A
XR_927523.1:n.1667T>A
NM_001354609.1:c.1659T>A	NP_001341538.1:p.Leu553=
NM_004333.5:c.1659T>A	NP_004324.2:p.Leu553=
NR_148928.1:n.1964T>A
XM_017012558.1:c.1779T>A	XP_016868047.1:p.Leu593=
XM_017012559.1:c.1779T>A	XP_016868048.1:p.Leu593=
XR_001744857.1:n.1787T>A
XR_001744858.1:n.1787T>A
NM_001354609.2:c.1659T>A	NP_001341538.1:p.Leu553=
NM_001374244.1:c.1779T>A	NP_001361173.1:p.Leu593=
NM_001374258.1:c.1779T>A MANE Plus Clinical	NP_001361187.1:p.Leu593=
NM_004333.6:c.1659T>A MANE Select	NP_004324.2:p.Leu553=
NM_001378467.1:c.1668T>A	NP_001365396.1:p.Leu556=
NM_001378468.1:c.1659T>A	NP_001365397.1:p.Leu553=
NM_001378469.1:c.1593T>A	NP_001365398.1:p.Leu531=
NM_001378470.1:c.1557T>A	NP_001365399.1:p.Leu519=
NM_001378471.1:c.1548T>A	NP_001365400.1:p.Leu516=
NM_001378472.1:c.1503T>A	NP_001365401.1:p.Leu501=
NM_001378473.1:c.1503T>A	NP_001365402.1:p.Leu501=
NM_001378474.1:c.1659T>A	NP_001365403.1:p.Leu553=
NM_001378475.1:c.1395T>A	NP_001365404.1:p.Leu465=