Canonical Allele Identifier: CA369542758

Gene: BRAF

Linked Data

• dbSNP Id: rs2128998130
• MyVariant Identifiers: chr7:g.140453088G>T (hg19) ; chr7:g.140753288G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140753288G>T , CM000669.2:g.140753288G>T	GRCh38
NC_000007.13:g.140453088G>T , CM000669.1:g.140453088G>T	GRCh37
NC_000007.12:g.140099557G>T	NCBI36
NG_007873.3:g.176477C>A , LRG_299:g.176477C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000646891.2:c.1847C>A MANE Select	ENSP00000493543.1:p.Ser616Tyr
ENST00000288602.11:c.1967C>A	ENSP00000288602.7:p.Ser656Tyr
ENST00000479537.6:c.517C>A
ENST00000496384.7:c.1847C>A	ENSP00000419060.2:p.Ser616Tyr
ENST00000497784.2:c.*1297C>A	ENSP00000420119.2:n.*1297C>A
ENST00000642228.1:c.*925C>A	ENSP00000493678.1:n.*925C>A
ENST00000642875.1:n.1259-3870C>A
ENST00000644120.1:n.2237C>A
ENST00000644650.1:c.943C>A
ENST00000644905.1:n.2729C>A
ENST00000644969.2:c.1967C>A MANE Plus Clinical	ENSP00000496776.1:p.Ser656Tyr
ENST00000646730.1:c.*423C>A	ENSP00000494784.1:n.*423C>A
ENST00000646891.1:c.1847C>A	ENSP00000493543.1:p.Ser616Tyr
ENST00000647434.1:c.738-3870C>A	ENSP00000495132.1:n.738-3870C>A
ENST00000288602.10:c.1847C>A	ENSP00000288602.6:p.Ser616Tyr
ENST00000479537.5:c.131C>A	ENSP00000418033.1:p.Ser44Tyr
ENST00000496384.6:c.670C>A
ENST00000497784.1:c.1882C>A	ENSP00000420119.1:n.1882C>A
NM_004333.4:c.1847C>A , LRG_299t1:c.1847C>A	NP_004324.2:p.Ser616Tyr
XM_005250045.1:c.1847C>A	XP_005250102.1:p.Ser616Tyr
XM_005250046.1:c.1847C>A	XP_005250103.1:p.Ser616Tyr
XM_011516529.1:c.1847C>A	XP_011514831.1:p.Ser616Tyr
XM_011516530.1:c.1695-3870C>A	XP_011514832.1:n.1695-3870C>A
XR_242190.1:n.1855C>A
XR_927520.1:n.1855C>A
XR_927521.1:n.1855C>A
XR_927522.1:n.1703-3870C>A
XR_927523.1:n.1703-3870C>A
NM_001354609.1:c.1847C>A	NP_001341538.1:p.Ser616Tyr
NM_004333.5:c.1847C>A	NP_004324.2:p.Ser616Tyr
NR_148928.1:n.2945C>A
XM_017012558.1:c.1967C>A	XP_016868047.1:p.Ser656Tyr
XM_017012559.1:c.1967C>A	XP_016868048.1:p.Ser656Tyr
XR_001744857.1:n.1975C>A
XR_001744858.1:n.1823-3870C>A
NM_001354609.2:c.1847C>A	NP_001341538.1:p.Ser616Tyr
NM_001374244.1:c.1967C>A	NP_001361173.1:p.Ser656Tyr
NM_001374258.1:c.1967C>A MANE Plus Clinical	NP_001361187.1:p.Ser656Tyr
NM_004333.6:c.1847C>A MANE Select	NP_004324.2:p.Ser616Tyr
NM_001378467.1:c.1856C>A	NP_001365396.1:p.Ser619Tyr
NM_001378468.1:c.1847C>A	NP_001365397.1:p.Ser616Tyr
NM_001378469.1:c.1781C>A	NP_001365398.1:p.Ser594Tyr
NM_001378470.1:c.1745C>A	NP_001365399.1:p.Ser582Tyr
NM_001378471.1:c.1736C>A	NP_001365400.1:p.Ser579Tyr
NM_001378472.1:c.1691C>A	NP_001365401.1:p.Ser564Tyr
NM_001378473.1:c.1691C>A	NP_001365402.1:p.Ser564Tyr
NM_001378474.1:c.1847C>A	NP_001365403.1:p.Ser616Tyr
NM_001378475.1:c.1583C>A	NP_001365404.1:p.Ser528Tyr