Canonical Allele Identifier: CA458115766

Gene: BRAF

Linked Data

• dbSNP Id: rs2129019598
• MyVariant Identifiers: chr7:g.140477832A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140778032A>T , CM000669.2:g.140778032A>T	GRCh38
NC_000007.13:g.140477832A>T , CM000669.1:g.140477832A>T	GRCh37
NC_000007.12:g.140124301A>T	NCBI36
NG_007873.3:g.151733T>A , LRG_299:g.151733T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000646891.2:c.1476T>A MANE Select	ENSP00000493543.1:p.Pro492=
ENST00000288602.11:c.1596T>A	ENSP00000288602.7:p.Pro532=
ENST00000479537.6:c.146T>A
ENST00000496384.7:c.1476T>A	ENSP00000419060.2:p.Pro492=
ENST00000497784.2:c.*926T>A	ENSP00000420119.2:n.*926T>A
ENST00000642228.1:c.*554T>A	ENSP00000493678.1:n.*554T>A
ENST00000642875.1:n.1040T>A
ENST00000644120.1:n.1866T>A
ENST00000644650.1:c.572T>A
ENST00000644905.1:n.1565T>A
ENST00000644969.2:c.1596T>A MANE Plus Clinical	ENSP00000496776.1:p.Pro532=
ENST00000646730.1:c.1476T>A	ENSP00000494784.1:p.Pro492=
ENST00000646891.1:c.1476T>A	ENSP00000493543.1:p.Pro492=
ENST00000647434.1:c.519T>A	ENSP00000495132.1:p.Pro173=
ENST00000288602.10:c.1476T>A	ENSP00000288602.6:p.Pro492=
ENST00000496384.6:c.299T>A
ENST00000497784.1:c.1511T>A	ENSP00000420119.1:n.1511T>A
NM_004333.4:c.1476T>A , LRG_299t1:c.1476T>A	NP_004324.2:p.Pro492=
XM_005250045.1:c.1476T>A	XP_005250102.1:p.Pro492=
XM_005250046.1:c.1476T>A	XP_005250103.1:p.Pro492=
XM_011516529.1:c.1476T>A	XP_011514831.1:p.Pro492=
XM_011516530.1:c.1476T>A	XP_011514832.1:p.Pro492=
XR_242190.1:n.1484T>A
XR_927520.1:n.1484T>A
XR_927521.1:n.1484T>A
XR_927522.1:n.1484T>A
XR_927523.1:n.1484T>A
NM_001354609.1:c.1476T>A	NP_001341538.1:p.Pro492=
NM_004333.5:c.1476T>A	NP_004324.2:p.Pro492=
NR_148928.1:n.1781T>A
XM_017012558.1:c.1596T>A	XP_016868047.1:p.Pro532=
XM_017012559.1:c.1596T>A	XP_016868048.1:p.Pro532=
XR_001744857.1:n.1604T>A
XR_001744858.1:n.1604T>A
NM_001354609.2:c.1476T>A	NP_001341538.1:p.Pro492=
NM_001374244.1:c.1596T>A	NP_001361173.1:p.Pro532=
NM_001374258.1:c.1596T>A MANE Plus Clinical	NP_001361187.1:p.Pro532=
NM_004333.6:c.1476T>A MANE Select	NP_004324.2:p.Pro492=
NM_001378467.1:c.1485T>A	NP_001365396.1:p.Pro495=
NM_001378468.1:c.1476T>A	NP_001365397.1:p.Pro492=
NM_001378469.1:c.1410T>A	NP_001365398.1:p.Pro470=
NM_001378470.1:c.1374T>A	NP_001365399.1:p.Pro458=
NM_001378471.1:c.1365T>A	NP_001365400.1:p.Pro455=
NM_001378472.1:c.1320T>A	NP_001365401.1:p.Pro440=
NM_001378473.1:c.1320T>A	NP_001365402.1:p.Pro440=
NM_001378474.1:c.1476T>A	NP_001365403.1:p.Pro492=
NM_001378475.1:c.1212T>A	NP_001365404.1:p.Pro404=