Canonical Allele Identifier: CA458115518

Gene: BRAF

Linked Data

• dbSNP Id: rs2129018319
• MyVariant Identifiers: chr7:g.140476777G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140776977G>A , CM000669.2:g.140776977G>A	GRCh38
NC_000007.13:g.140476777G>A , CM000669.1:g.140476777G>A	GRCh37
NC_000007.12:g.140123246G>A	NCBI36
NG_007873.3:g.152788C>T , LRG_299:g.152788C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646891.2:c.1629C>T MANE Select	ENSP00000493543.1:p.Ile543=
ENST00000288602.11:c.1749C>T	ENSP00000288602.7:p.Ile583=
ENST00000479537.6:c.299C>T
ENST00000496384.7:c.1629C>T	ENSP00000419060.2:p.Ile543=
ENST00000497784.2:c.*1079C>T	ENSP00000420119.2:n.*1079C>T
ENST00000642228.1:c.*707C>T	ENSP00000493678.1:n.*707C>T
ENST00000642875.1:n.1193C>T
ENST00000644120.1:n.2019C>T
ENST00000644650.1:c.725C>T
ENST00000644905.1:n.1718C>T
ENST00000644969.2:c.1749C>T MANE Plus Clinical	ENSP00000496776.1:p.Ile583=
ENST00000646730.1:c.1629C>T	ENSP00000494784.1:p.Ile543=
ENST00000646891.1:c.1629C>T	ENSP00000493543.1:p.Ile543=
ENST00000647434.1:c.672C>T	ENSP00000495132.1:p.Ile224=
ENST00000288602.10:c.1629C>T	ENSP00000288602.6:p.Ile543=
ENST00000496384.6:c.452C>T
ENST00000497784.1:c.1664C>T	ENSP00000420119.1:n.1664C>T
NM_004333.4:c.1629C>T , LRG_299t1:c.1629C>T	NP_004324.2:p.Ile543=
XM_005250045.1:c.1629C>T	XP_005250102.1:p.Ile543=
XM_005250046.1:c.1629C>T	XP_005250103.1:p.Ile543=
XM_011516529.1:c.1629C>T	XP_011514831.1:p.Ile543=
XM_011516530.1:c.1629C>T	XP_011514832.1:p.Ile543=
XR_242190.1:n.1637C>T
XR_927520.1:n.1637C>T
XR_927521.1:n.1637C>T
XR_927522.1:n.1637C>T
XR_927523.1:n.1637C>T
NM_001354609.1:c.1629C>T	NP_001341538.1:p.Ile543=
NM_004333.5:c.1629C>T	NP_004324.2:p.Ile543=
NR_148928.1:n.1934C>T
XM_017012558.1:c.1749C>T	XP_016868047.1:p.Ile583=
XM_017012559.1:c.1749C>T	XP_016868048.1:p.Ile583=
XR_001744857.1:n.1757C>T
XR_001744858.1:n.1757C>T
NM_001354609.2:c.1629C>T	NP_001341538.1:p.Ile543=
NM_001374244.1:c.1749C>T	NP_001361173.1:p.Ile583=
NM_001374258.1:c.1749C>T MANE Plus Clinical	NP_001361187.1:p.Ile583=
NM_004333.6:c.1629C>T MANE Select	NP_004324.2:p.Ile543=
NM_001378467.1:c.1638C>T	NP_001365396.1:p.Ile546=
NM_001378468.1:c.1629C>T	NP_001365397.1:p.Ile543=
NM_001378469.1:c.1563C>T	NP_001365398.1:p.Ile521=
NM_001378470.1:c.1527C>T	NP_001365399.1:p.Ile509=
NM_001378471.1:c.1518C>T	NP_001365400.1:p.Ile506=
NM_001378472.1:c.1473C>T	NP_001365401.1:p.Ile491=
NM_001378473.1:c.1473C>T	NP_001365402.1:p.Ile491=
NM_001378474.1:c.1629C>T	NP_001365403.1:p.Ile543=
NM_001378475.1:c.1365C>T	NP_001365404.1:p.Ile455=