Canonical Allele Identifier: CA369588279

Gene: BRAF

Linked Data

• MyVariant Identifiers: chr7:g.140476862A>C (hg19) ; chr7:g.140777062A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140777062A>C , CM000669.2:g.140777062A>C	GRCh38
NC_000007.13:g.140476862A>C , CM000669.1:g.140476862A>C	GRCh37
NC_000007.12:g.140123331A>C	NCBI36
NG_007873.3:g.152703T>G , LRG_299:g.152703T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646891.2:c.1544T>G MANE Select	ENSP00000493543.1:p.Leu515Arg
ENST00000288602.11:c.1664T>G	ENSP00000288602.7:p.Leu555Arg
ENST00000479537.6:c.214T>G
ENST00000496384.7:c.1544T>G	ENSP00000419060.2:p.Leu515Arg
ENST00000497784.2:c.*994T>G	ENSP00000420119.2:n.*994T>G
ENST00000642228.1:c.*622T>G	ENSP00000493678.1:n.*622T>G
ENST00000642875.1:n.1108T>G
ENST00000644120.1:n.1934T>G
ENST00000644650.1:c.640T>G
ENST00000644905.1:n.1633T>G
ENST00000644969.2:c.1664T>G MANE Plus Clinical	ENSP00000496776.1:p.Leu555Arg
ENST00000646730.1:c.1544T>G	ENSP00000494784.1:p.Leu515Arg
ENST00000646891.1:c.1544T>G	ENSP00000493543.1:p.Leu515Arg
ENST00000647434.1:c.587T>G	ENSP00000495132.1:p.Leu196Arg
ENST00000288602.10:c.1544T>G	ENSP00000288602.6:p.Leu515Arg
ENST00000496384.6:c.367T>G
ENST00000497784.1:c.1579T>G	ENSP00000420119.1:n.1579T>G
NM_004333.4:c.1544T>G , LRG_299t1:c.1544T>G	NP_004324.2:p.Leu515Arg
XM_005250045.1:c.1544T>G	XP_005250102.1:p.Leu515Arg
XM_005250046.1:c.1544T>G	XP_005250103.1:p.Leu515Arg
XM_011516529.1:c.1544T>G	XP_011514831.1:p.Leu515Arg
XM_011516530.1:c.1544T>G	XP_011514832.1:p.Leu515Arg
XR_242190.1:n.1552T>G
XR_927520.1:n.1552T>G
XR_927521.1:n.1552T>G
XR_927522.1:n.1552T>G
XR_927523.1:n.1552T>G
NM_001354609.1:c.1544T>G	NP_001341538.1:p.Leu515Arg
NM_004333.5:c.1544T>G	NP_004324.2:p.Leu515Arg
NR_148928.1:n.1849T>G
XM_017012558.1:c.1664T>G	XP_016868047.1:p.Leu555Arg
XM_017012559.1:c.1664T>G	XP_016868048.1:p.Leu555Arg
XR_001744857.1:n.1672T>G
XR_001744858.1:n.1672T>G
NM_001354609.2:c.1544T>G	NP_001341538.1:p.Leu515Arg
NM_001374244.1:c.1664T>G	NP_001361173.1:p.Leu555Arg
NM_001374258.1:c.1664T>G MANE Plus Clinical	NP_001361187.1:p.Leu555Arg
NM_004333.6:c.1544T>G MANE Select	NP_004324.2:p.Leu515Arg
NM_001378467.1:c.1553T>G	NP_001365396.1:p.Leu518Arg
NM_001378468.1:c.1544T>G	NP_001365397.1:p.Leu515Arg
NM_001378469.1:c.1478T>G	NP_001365398.1:p.Leu493Arg
NM_001378470.1:c.1442T>G	NP_001365399.1:p.Leu481Arg
NM_001378471.1:c.1433T>G	NP_001365400.1:p.Leu478Arg
NM_001378472.1:c.1388T>G	NP_001365401.1:p.Leu463Arg
NM_001378473.1:c.1388T>G	NP_001365402.1:p.Leu463Arg
NM_001378474.1:c.1544T>G	NP_001365403.1:p.Leu515Arg
NM_001378475.1:c.1280T>G	NP_001365404.1:p.Leu427Arg