Canonical Allele Identifier: CA369538526

Gene: BRAF

Linked Data

• dbSNP Id: rs2130900815
• MyVariant Identifiers: chr7:g.140439728G>C (hg19) ; chr7:g.140739928G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140739928G>C , CM000669.2:g.140739928G>C	GRCh38
NC_000007.13:g.140439728G>C , CM000669.1:g.140439728G>C	GRCh37
NC_000007.12:g.140086197G>C	NCBI36
NG_007873.3:g.189837C>G , LRG_299:g.189837C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646891.2:c.2011C>G MANE Select	ENSP00000493543.1:p.Arg671Gly
ENST00000288602.11:c.2131C>G	ENSP00000288602.7:p.Arg711Gly
ENST00000479537.6:c.763C>G
ENST00000496384.7:c.2011C>G	ENSP00000419060.2:p.Arg671Gly
ENST00000497784.2:c.*1461C>G	ENSP00000420119.2:n.*1461C>G
ENST00000642228.1:c.*1089C>G	ENSP00000493678.1:n.*1089C>G
ENST00000642875.1:n.1409C>G
ENST00000644120.1:n.2401C>G
ENST00000644650.1:c.1310C>G
ENST00000644905.1:n.2893C>G
ENST00000644969.2:c.2131C>G MANE Plus Clinical	ENSP00000496776.1:p.Arg711Gly
ENST00000645443.1:n.1790C>G
ENST00000646730.1:c.*669C>G	ENSP00000494784.1:n.*669C>G
ENST00000646891.1:c.2011C>G	ENSP00000493543.1:p.Arg671Gly
ENST00000647434.1:c.888C>G	ENSP00000495132.1:n.888C>G
ENST00000288602.10:c.2011C>G	ENSP00000288602.6:p.Arg671Gly
ENST00000479537.5:c.377C>G	ENSP00000418033.1:n.377C>G
ENST00000496384.6:c.834C>G
ENST00000497784.1:c.2046C>G	ENSP00000420119.1:n.2046C>G
NM_004333.4:c.2011C>G , LRG_299t1:c.2011C>G	NP_004324.2:p.Arg671Gly
XM_005250045.1:c.2011C>G	XP_005250102.1:p.Arg671Gly
XM_005250046.1:c.2011C>G	XP_005250103.1:p.Arg671Gly
XM_011516529.1:c.2011C>G	XP_011514831.1:p.Arg671Gly
XR_242190.1:n.2101C>G
XR_927520.1:n.2140C>G
XR_927521.1:n.2222C>G
XR_927522.1:n.1853C>G
XR_927523.1:n.1935C>G
NM_001354609.1:c.2011C>G	NP_001341538.1:p.Arg671Gly
NM_004333.5:c.2011C>G	NP_004324.2:p.Arg671Gly
NR_148928.1:n.3109C>G
XM_017012558.1:c.2131C>G	XP_016868047.1:p.Arg711Gly
XM_017012559.1:c.2131C>G	XP_016868048.1:p.Arg711Gly
XR_001744857.1:n.2221C>G
XR_001744858.1:n.1973C>G
NM_001354609.2:c.2011C>G	NP_001341538.1:p.Arg671Gly
NM_001374244.1:c.2131C>G	NP_001361173.1:p.Arg711Gly
NM_001374258.1:c.2131C>G MANE Plus Clinical	NP_001361187.1:p.Arg711Gly
NM_004333.6:c.2011C>G MANE Select	NP_004324.2:p.Arg671Gly
NM_001378467.1:c.2020C>G	NP_001365396.1:p.Arg674Gly
NM_001378468.1:c.2011C>G	NP_001365397.1:p.Arg671Gly
NM_001378469.1:c.1945C>G	NP_001365398.1:p.Arg649Gly
NM_001378470.1:c.1909C>G	NP_001365399.1:p.Arg637Gly
NM_001378471.1:c.1900C>G	NP_001365400.1:p.Arg634Gly
NM_001378472.1:c.1855C>G	NP_001365401.1:p.Arg619Gly
NM_001378473.1:c.1855C>G	NP_001365402.1:p.Arg619Gly
NM_001378474.1:c.2011C>G	NP_001365403.1:p.Arg671Gly
NM_001378475.1:c.1747C>G	NP_001365404.1:p.Arg583Gly