Canonical Allele Identifier: CA457985403

Gene: BRAF

Linked Data

• MyVariant Identifiers: chr7:g.140439624T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140739824T>A , CM000669.2:g.140739824T>A	GRCh38
NC_000007.13:g.140439624T>A , CM000669.1:g.140439624T>A	GRCh37
NC_000007.12:g.140086093T>A	NCBI36
NG_007873.3:g.189941A>T , LRG_299:g.189941A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000646891.2:c.2115A>T MANE Select	ENSP00000493543.1:p.Pro705=
ENST00000288602.11:c.2235A>T	ENSP00000288602.7:p.Pro745=
ENST00000479537.6:c.867A>T
ENST00000496384.7:c.2115A>T	ENSP00000419060.2:p.Pro705=
ENST00000497784.2:c.*1565A>T	ENSP00000420119.2:n.*1565A>T
ENST00000642228.1:c.*1193A>T	ENSP00000493678.1:n.*1193A>T
ENST00000642875.1:n.1513A>T
ENST00000644120.1:n.2505A>T
ENST00000644650.1:c.1414A>T
ENST00000644905.1:n.2997A>T
ENST00000644969.2:c.2235A>T MANE Plus Clinical	ENSP00000496776.1:p.Pro745=
ENST00000645443.1:n.1894A>T
ENST00000646730.1:c.*773A>T	ENSP00000494784.1:n.*773A>T
ENST00000646891.1:c.2115A>T	ENSP00000493543.1:p.Pro705=
ENST00000647434.1:c.992A>T	ENSP00000495132.1:n.992A>T
ENST00000288602.10:c.2115A>T	ENSP00000288602.6:p.Pro705=
ENST00000479537.5:c.481A>T	ENSP00000418033.1:n.481A>T
ENST00000496384.6:c.938A>T
ENST00000497784.1:c.2150A>T	ENSP00000420119.1:n.2150A>T
NM_004333.4:c.2115A>T , LRG_299t1:c.2115A>T	NP_004324.2:p.Pro705=
XM_005250045.1:c.2115A>T	XP_005250102.1:p.Pro705=
XM_005250046.1:c.2115A>T	XP_005250103.1:p.Pro705=
XM_011516529.1:c.2115A>T	XP_011514831.1:p.Pro705=
XR_242190.1:n.2205A>T
XR_927520.1:n.2244A>T
XR_927521.1:n.2326A>T
XR_927522.1:n.1957A>T
XR_927523.1:n.2039A>T
NM_001354609.1:c.2115A>T	NP_001341538.1:p.Pro705=
NM_004333.5:c.2115A>T	NP_004324.2:p.Pro705=
NR_148928.1:n.3213A>T
XM_017012558.1:c.2235A>T	XP_016868047.1:p.Pro745=
XM_017012559.1:c.2235A>T	XP_016868048.1:p.Pro745=
XR_001744857.1:n.2325A>T
XR_001744858.1:n.2077A>T
NM_001354609.2:c.2115A>T	NP_001341538.1:p.Pro705=
NM_001374244.1:c.2235A>T	NP_001361173.1:p.Pro745=
NM_001374258.1:c.2235A>T MANE Plus Clinical	NP_001361187.1:p.Pro745=
NM_004333.6:c.2115A>T MANE Select	NP_004324.2:p.Pro705=
NM_001378467.1:c.2124A>T	NP_001365396.1:p.Pro708=
NM_001378468.1:c.2115A>T	NP_001365397.1:p.Pro705=
NM_001378469.1:c.2049A>T	NP_001365398.1:p.Pro683=
NM_001378470.1:c.2013A>T	NP_001365399.1:p.Pro671=
NM_001378471.1:c.2004A>T	NP_001365400.1:p.Pro668=
NM_001378472.1:c.1959A>T	NP_001365401.1:p.Pro653=
NM_001378473.1:c.1959A>T	NP_001365402.1:p.Pro653=
NM_001378474.1:c.2115A>T	NP_001365403.1:p.Pro705=
NM_001378475.1:c.1851A>T	NP_001365404.1:p.Pro617=