Canonical Allele Identifier: CA369587781

Gene: BRAF

Linked Data

• dbSNP Id: rs2129018164
• MyVariant Identifiers: chr7:g.140476722G>C (hg19) ; chr7:g.140776922G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140776922G>C , CM000669.2:g.140776922G>C	GRCh38
NC_000007.13:g.140476722G>C , CM000669.1:g.140476722G>C	GRCh37
NC_000007.12:g.140123191G>C	NCBI36
NG_007873.3:g.152843C>G , LRG_299:g.152843C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646891.2:c.1684C>G MANE Select	ENSP00000493543.1:p.Gln562Glu
ENST00000288602.11:c.1804C>G	ENSP00000288602.7:p.Gln602Glu
ENST00000479537.6:c.354C>G
ENST00000496384.7:c.1684C>G	ENSP00000419060.2:p.Gln562Glu
ENST00000497784.2:c.*1134C>G	ENSP00000420119.2:n.*1134C>G
ENST00000642228.1:c.*762C>G	ENSP00000493678.1:n.*762C>G
ENST00000642875.1:n.1248C>G
ENST00000644120.1:n.2074C>G
ENST00000644650.1:c.780C>G
ENST00000644905.1:n.1773C>G
ENST00000644969.2:c.1804C>G MANE Plus Clinical	ENSP00000496776.1:p.Gln602Glu
ENST00000646730.1:c.1684C>G	ENSP00000494784.1:p.Gln562Glu
ENST00000646891.1:c.1684C>G	ENSP00000493543.1:p.Gln562Glu
ENST00000647434.1:c.727C>G	ENSP00000495132.1:p.Gln243Glu
ENST00000288602.10:c.1684C>G	ENSP00000288602.6:p.Gln562Glu
ENST00000496384.6:c.507C>G
ENST00000497784.1:c.1719C>G	ENSP00000420119.1:n.1719C>G
NM_004333.4:c.1684C>G , LRG_299t1:c.1684C>G	NP_004324.2:p.Gln562Glu
XM_005250045.1:c.1684C>G	XP_005250102.1:p.Gln562Glu
XM_005250046.1:c.1684C>G	XP_005250103.1:p.Gln562Glu
XM_011516529.1:c.1684C>G	XP_011514831.1:p.Gln562Glu
XM_011516530.1:c.1684C>G	XP_011514832.1:p.Gln562Glu
XR_242190.1:n.1692C>G
XR_927520.1:n.1692C>G
XR_927521.1:n.1692C>G
XR_927522.1:n.1692C>G
XR_927523.1:n.1692C>G
NM_001354609.1:c.1684C>G	NP_001341538.1:p.Gln562Glu
NM_004333.5:c.1684C>G	NP_004324.2:p.Gln562Glu
NR_148928.1:n.1989C>G
XM_017012558.1:c.1804C>G	XP_016868047.1:p.Gln602Glu
XM_017012559.1:c.1804C>G	XP_016868048.1:p.Gln602Glu
XR_001744857.1:n.1812C>G
XR_001744858.1:n.1812C>G
NM_001354609.2:c.1684C>G	NP_001341538.1:p.Gln562Glu
NM_001374244.1:c.1804C>G	NP_001361173.1:p.Gln602Glu
NM_001374258.1:c.1804C>G MANE Plus Clinical	NP_001361187.1:p.Gln602Glu
NM_004333.6:c.1684C>G MANE Select	NP_004324.2:p.Gln562Glu
NM_001378467.1:c.1693C>G	NP_001365396.1:p.Gln565Glu
NM_001378468.1:c.1684C>G	NP_001365397.1:p.Gln562Glu
NM_001378469.1:c.1618C>G	NP_001365398.1:p.Gln540Glu
NM_001378470.1:c.1582C>G	NP_001365399.1:p.Gln528Glu
NM_001378471.1:c.1573C>G	NP_001365400.1:p.Gln525Glu
NM_001378472.1:c.1528C>G	NP_001365401.1:p.Gln510Glu
NM_001378473.1:c.1528C>G	NP_001365402.1:p.Gln510Glu
NM_001378474.1:c.1684C>G	NP_001365403.1:p.Gln562Glu
NM_001378475.1:c.1420C>G	NP_001365404.1:p.Gln474Glu