Canonical Allele Identifier: CA369542827

Gene: BRAF

Linked Data

• dbSNP Id: rs2128998173
• MyVariant Identifiers: chr7:g.140453103T>A (hg19) ; chr7:g.140753303T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140753303T>A , CM000669.2:g.140753303T>A	GRCh38
NC_000007.13:g.140453103T>A , CM000669.1:g.140453103T>A	GRCh37
NC_000007.12:g.140099572T>A	NCBI36
NG_007873.3:g.176462A>T , LRG_299:g.176462A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000646891.2:c.1832A>T MANE Select	ENSP00000493543.1:p.Glu611Val
ENST00000288602.11:c.1952A>T	ENSP00000288602.7:p.Glu651Val
ENST00000479537.6:c.502A>T
ENST00000496384.7:c.1832A>T	ENSP00000419060.2:p.Glu611Val
ENST00000497784.2:c.*1282A>T	ENSP00000420119.2:n.*1282A>T
ENST00000642228.1:c.*910A>T	ENSP00000493678.1:n.*910A>T
ENST00000642875.1:n.1259-3885A>T
ENST00000644120.1:n.2222A>T
ENST00000644650.1:c.928A>T
ENST00000644905.1:n.2714A>T
ENST00000644969.2:c.1952A>T MANE Plus Clinical	ENSP00000496776.1:p.Glu651Val
ENST00000646730.1:c.*408A>T	ENSP00000494784.1:n.*408A>T
ENST00000646891.1:c.1832A>T	ENSP00000493543.1:p.Glu611Val
ENST00000647434.1:c.738-3885A>T	ENSP00000495132.1:n.738-3885A>T
ENST00000288602.10:c.1832A>T	ENSP00000288602.6:p.Glu611Val
ENST00000479537.5:c.116A>T	ENSP00000418033.1:p.Glu39Val
ENST00000496384.6:c.655A>T
ENST00000497784.1:c.1867A>T	ENSP00000420119.1:n.1867A>T
NM_004333.4:c.1832A>T , LRG_299t1:c.1832A>T	NP_004324.2:p.Glu611Val
XM_005250045.1:c.1832A>T	XP_005250102.1:p.Glu611Val
XM_005250046.1:c.1832A>T	XP_005250103.1:p.Glu611Val
XM_011516529.1:c.1832A>T	XP_011514831.1:p.Glu611Val
XM_011516530.1:c.1695-3885A>T	XP_011514832.1:n.1695-3885A>T
XR_242190.1:n.1840A>T
XR_927520.1:n.1840A>T
XR_927521.1:n.1840A>T
XR_927522.1:n.1703-3885A>T
XR_927523.1:n.1703-3885A>T
NM_001354609.1:c.1832A>T	NP_001341538.1:p.Glu611Val
NM_004333.5:c.1832A>T	NP_004324.2:p.Glu611Val
NR_148928.1:n.2930A>T
XM_017012558.1:c.1952A>T	XP_016868047.1:p.Glu651Val
XM_017012559.1:c.1952A>T	XP_016868048.1:p.Glu651Val
XR_001744857.1:n.1960A>T
XR_001744858.1:n.1823-3885A>T
NM_001354609.2:c.1832A>T	NP_001341538.1:p.Glu611Val
NM_001374244.1:c.1952A>T	NP_001361173.1:p.Glu651Val
NM_001374258.1:c.1952A>T MANE Plus Clinical	NP_001361187.1:p.Glu651Val
NM_004333.6:c.1832A>T MANE Select	NP_004324.2:p.Glu611Val
NM_001378467.1:c.1841A>T	NP_001365396.1:p.Glu614Val
NM_001378468.1:c.1832A>T	NP_001365397.1:p.Glu611Val
NM_001378469.1:c.1766A>T	NP_001365398.1:p.Glu589Val
NM_001378470.1:c.1730A>T	NP_001365399.1:p.Glu577Val
NM_001378471.1:c.1721A>T	NP_001365400.1:p.Glu574Val
NM_001378472.1:c.1676A>T	NP_001365401.1:p.Glu559Val
NM_001378473.1:c.1676A>T	NP_001365402.1:p.Glu559Val
NM_001378474.1:c.1832A>T	NP_001365403.1:p.Glu611Val
NM_001378475.1:c.1568A>T	NP_001365404.1:p.Glu523Val