Canonical Allele Identifier: CA369543278

Gene: BRAF

Linked Data

• dbSNP Id: rs2128998452
• MyVariant Identifiers: chr7:g.140453176C>A (hg19) ; chr7:g.140753376C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140753376C>A , CM000669.2:g.140753376C>A	GRCh38
NC_000007.13:g.140453176C>A , CM000669.1:g.140453176C>A	GRCh37
NC_000007.12:g.140099645C>A	NCBI36
NG_007873.3:g.176389G>T , LRG_299:g.176389G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000646891.2:c.1759G>T MANE Select	ENSP00000493543.1:p.Asp587Tyr
ENST00000288602.11:c.1879G>T	ENSP00000288602.7:p.Asp627Tyr
ENST00000479537.6:c.429G>T
ENST00000496384.7:c.1759G>T	ENSP00000419060.2:p.Asp587Tyr
ENST00000497784.2:c.*1209G>T	ENSP00000420119.2:n.*1209G>T
ENST00000642228.1:c.*837G>T	ENSP00000493678.1:n.*837G>T
ENST00000642875.1:n.1259-3958G>T
ENST00000644120.1:n.2149G>T
ENST00000644650.1:c.855G>T
ENST00000644905.1:n.2641G>T
ENST00000644969.2:c.1879G>T MANE Plus Clinical	ENSP00000496776.1:p.Asp627Tyr
ENST00000646730.1:c.*335G>T	ENSP00000494784.1:n.*335G>T
ENST00000646891.1:c.1759G>T	ENSP00000493543.1:p.Asp587Tyr
ENST00000647434.1:c.738-3958G>T	ENSP00000495132.1:n.738-3958G>T
ENST00000288602.10:c.1759G>T	ENSP00000288602.6:p.Asp587Tyr
ENST00000479537.5:c.43G>T	ENSP00000418033.1:p.Asp15Tyr
ENST00000496384.6:c.582G>T
ENST00000497784.1:c.1794G>T	ENSP00000420119.1:n.1794G>T
NM_004333.4:c.1759G>T , LRG_299t1:c.1759G>T	NP_004324.2:p.Asp587Tyr
XM_005250045.1:c.1759G>T	XP_005250102.1:p.Asp587Tyr
XM_005250046.1:c.1759G>T	XP_005250103.1:p.Asp587Tyr
XM_011516529.1:c.1759G>T	XP_011514831.1:p.Asp587Tyr
XM_011516530.1:c.1695-3958G>T	XP_011514832.1:n.1695-3958G>T
XR_242190.1:n.1767G>T
XR_927520.1:n.1767G>T
XR_927521.1:n.1767G>T
XR_927522.1:n.1703-3958G>T
XR_927523.1:n.1703-3958G>T
NM_001354609.1:c.1759G>T	NP_001341538.1:p.Asp587Tyr
NM_004333.5:c.1759G>T	NP_004324.2:p.Asp587Tyr
NR_148928.1:n.2857G>T
XM_017012558.1:c.1879G>T	XP_016868047.1:p.Asp627Tyr
XM_017012559.1:c.1879G>T	XP_016868048.1:p.Asp627Tyr
XR_001744857.1:n.1887G>T
XR_001744858.1:n.1823-3958G>T
NM_001354609.2:c.1759G>T	NP_001341538.1:p.Asp587Tyr
NM_001374244.1:c.1879G>T	NP_001361173.1:p.Asp627Tyr
NM_001374258.1:c.1879G>T MANE Plus Clinical	NP_001361187.1:p.Asp627Tyr
NM_004333.6:c.1759G>T MANE Select	NP_004324.2:p.Asp587Tyr
NM_001378467.1:c.1768G>T	NP_001365396.1:p.Asp590Tyr
NM_001378468.1:c.1759G>T	NP_001365397.1:p.Asp587Tyr
NM_001378469.1:c.1693G>T	NP_001365398.1:p.Asp565Tyr
NM_001378470.1:c.1657G>T	NP_001365399.1:p.Asp553Tyr
NM_001378471.1:c.1648G>T	NP_001365400.1:p.Asp550Tyr
NM_001378472.1:c.1603G>T	NP_001365401.1:p.Asp535Tyr
NM_001378473.1:c.1603G>T	NP_001365402.1:p.Asp535Tyr
NM_001378474.1:c.1759G>T	NP_001365403.1:p.Asp587Tyr
NM_001378475.1:c.1495G>T	NP_001365404.1:p.Asp499Tyr