Canonical Allele Identifier: CA369543859

Gene: BRAF

Linked Data

• MyVariant Identifiers: chr7:g.140453999G>T (hg19) ; chr7:g.140754199G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140754199G>T , CM000669.2:g.140754199G>T	GRCh38
NC_000007.13:g.140453999G>T , CM000669.1:g.140453999G>T	GRCh37
NC_000007.12:g.140100468G>T	NCBI36
NG_007873.3:g.175566C>A , LRG_299:g.175566C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000646891.2:c.1729C>A MANE Select	ENSP00000493543.1:p.Leu577Ile
ENST00000288602.11:c.1849C>A	ENSP00000288602.7:p.Leu617Ile
ENST00000479537.6:c.399C>A
ENST00000496384.7:c.1729C>A	ENSP00000419060.2:p.Leu577Ile
ENST00000497784.2:c.*1179C>A	ENSP00000420119.2:n.*1179C>A
ENST00000642228.1:c.*807C>A	ENSP00000493678.1:n.*807C>A
ENST00000642875.1:n.1259-4781C>A
ENST00000644120.1:n.2119C>A
ENST00000644650.1:c.825C>A
ENST00000644905.1:n.1818C>A
ENST00000644969.2:c.1849C>A MANE Plus Clinical	ENSP00000496776.1:p.Leu617Ile
ENST00000646730.1:c.*305C>A	ENSP00000494784.1:n.*305C>A
ENST00000646891.1:c.1729C>A	ENSP00000493543.1:p.Leu577Ile
ENST00000647434.1:c.738-4781C>A	ENSP00000495132.1:n.738-4781C>A
ENST00000288602.10:c.1729C>A	ENSP00000288602.6:p.Leu577Ile
ENST00000479537.5:c.13C>A	ENSP00000418033.1:p.Leu5Ile
ENST00000496384.6:c.552C>A
ENST00000497784.1:c.1764C>A	ENSP00000420119.1:n.1764C>A
NM_004333.4:c.1729C>A , LRG_299t1:c.1729C>A	NP_004324.2:p.Leu577Ile
XM_005250045.1:c.1729C>A	XP_005250102.1:p.Leu577Ile
XM_005250046.1:c.1729C>A	XP_005250103.1:p.Leu577Ile
XM_011516529.1:c.1729C>A	XP_011514831.1:p.Leu577Ile
XM_011516530.1:c.1695-4781C>A	XP_011514832.1:n.1695-4781C>A
XR_242190.1:n.1737C>A
XR_927520.1:n.1737C>A
XR_927521.1:n.1737C>A
XR_927522.1:n.1703-4781C>A
XR_927523.1:n.1703-4781C>A
NM_001354609.1:c.1729C>A	NP_001341538.1:p.Leu577Ile
NM_004333.5:c.1729C>A	NP_004324.2:p.Leu577Ile
NR_148928.1:n.2034C>A
XM_017012558.1:c.1849C>A	XP_016868047.1:p.Leu617Ile
XM_017012559.1:c.1849C>A	XP_016868048.1:p.Leu617Ile
XR_001744857.1:n.1857C>A
XR_001744858.1:n.1823-4781C>A
NM_001354609.2:c.1729C>A	NP_001341538.1:p.Leu577Ile
NM_001374244.1:c.1849C>A	NP_001361173.1:p.Leu617Ile
NM_001374258.1:c.1849C>A MANE Plus Clinical	NP_001361187.1:p.Leu617Ile
NM_004333.6:c.1729C>A MANE Select	NP_004324.2:p.Leu577Ile
NM_001378467.1:c.1738C>A	NP_001365396.1:p.Leu580Ile
NM_001378468.1:c.1729C>A	NP_001365397.1:p.Leu577Ile
NM_001378469.1:c.1663C>A	NP_001365398.1:p.Leu555Ile
NM_001378470.1:c.1627C>A	NP_001365399.1:p.Leu543Ile
NM_001378471.1:c.1618C>A	NP_001365400.1:p.Leu540Ile
NM_001378472.1:c.1573C>A	NP_001365401.1:p.Leu525Ile
NM_001378473.1:c.1573C>A	NP_001365402.1:p.Leu525Ile
NM_001378474.1:c.1729C>A	NP_001365403.1:p.Leu577Ile
NM_001378475.1:c.1465C>A	NP_001365404.1:p.Leu489Ile