Canonical Allele Identifier: CA369538536

Gene: BRAF

Linked Data

• dbSNP Id: rs2130900851
• MyVariant Identifiers: chr7:g.140439730C>G (hg19) ; chr7:g.140739930C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140739930C>G , CM000669.2:g.140739930C>G	GRCh38
NC_000007.13:g.140439730C>G , CM000669.1:g.140439730C>G	GRCh37
NC_000007.12:g.140086199C>G	NCBI36
NG_007873.3:g.189835G>C , LRG_299:g.189835G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000646891.2:c.2009G>C MANE Select	ENSP00000493543.1:p.Gly670Ala
ENST00000288602.11:c.2129G>C	ENSP00000288602.7:p.Gly710Ala
ENST00000479537.6:c.761G>C
ENST00000496384.7:c.2009G>C	ENSP00000419060.2:p.Gly670Ala
ENST00000497784.2:c.*1459G>C	ENSP00000420119.2:n.*1459G>C
ENST00000642228.1:c.*1087G>C	ENSP00000493678.1:n.*1087G>C
ENST00000642875.1:n.1407G>C
ENST00000644120.1:n.2399G>C
ENST00000644650.1:c.1308G>C
ENST00000644905.1:n.2891G>C
ENST00000644969.2:c.2129G>C MANE Plus Clinical	ENSP00000496776.1:p.Gly710Ala
ENST00000645443.1:n.1788G>C
ENST00000646730.1:c.*667G>C	ENSP00000494784.1:n.*667G>C
ENST00000646891.1:c.2009G>C	ENSP00000493543.1:p.Gly670Ala
ENST00000647434.1:c.886G>C	ENSP00000495132.1:n.886G>C
ENST00000288602.10:c.2009G>C	ENSP00000288602.6:p.Gly670Ala
ENST00000479537.5:c.375G>C	ENSP00000418033.1:n.375G>C
ENST00000496384.6:c.832G>C
ENST00000497784.1:c.2044G>C	ENSP00000420119.1:n.2044G>C
NM_004333.4:c.2009G>C , LRG_299t1:c.2009G>C	NP_004324.2:p.Gly670Ala
XM_005250045.1:c.2009G>C	XP_005250102.1:p.Gly670Ala
XM_005250046.1:c.2009G>C	XP_005250103.1:p.Gly670Ala
XM_011516529.1:c.2009G>C	XP_011514831.1:p.Gly670Ala
XR_242190.1:n.2099G>C
XR_927520.1:n.2138G>C
XR_927521.1:n.2220G>C
XR_927522.1:n.1851G>C
XR_927523.1:n.1933G>C
NM_001354609.1:c.2009G>C	NP_001341538.1:p.Gly670Ala
NM_004333.5:c.2009G>C	NP_004324.2:p.Gly670Ala
NR_148928.1:n.3107G>C
XM_017012558.1:c.2129G>C	XP_016868047.1:p.Gly710Ala
XM_017012559.1:c.2129G>C	XP_016868048.1:p.Gly710Ala
XR_001744857.1:n.2219G>C
XR_001744858.1:n.1971G>C
NM_001354609.2:c.2009G>C	NP_001341538.1:p.Gly670Ala
NM_001374244.1:c.2129G>C	NP_001361173.1:p.Gly710Ala
NM_001374258.1:c.2129G>C MANE Plus Clinical	NP_001361187.1:p.Gly710Ala
NM_004333.6:c.2009G>C MANE Select	NP_004324.2:p.Gly670Ala
NM_001378467.1:c.2018G>C	NP_001365396.1:p.Gly673Ala
NM_001378468.1:c.2009G>C	NP_001365397.1:p.Gly670Ala
NM_001378469.1:c.1943G>C	NP_001365398.1:p.Gly648Ala
NM_001378470.1:c.1907G>C	NP_001365399.1:p.Gly636Ala
NM_001378471.1:c.1898G>C	NP_001365400.1:p.Gly633Ala
NM_001378472.1:c.1853G>C	NP_001365401.1:p.Gly618Ala
NM_001378473.1:c.1853G>C	NP_001365402.1:p.Gly618Ala
NM_001378474.1:c.2009G>C	NP_001365403.1:p.Gly670Ala
NM_001378475.1:c.1745G>C	NP_001365404.1:p.Gly582Ala