Canonical Allele Identifier: CA369588439

Gene: BRAF

Linked Data

• MyVariant Identifiers: chr7:g.140477831G>T (hg19) ; chr7:g.140778031G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140778031G>T , CM000669.2:g.140778031G>T	GRCh38
NC_000007.13:g.140477831G>T , CM000669.1:g.140477831G>T	GRCh37
NC_000007.12:g.140124300G>T	NCBI36
NG_007873.3:g.151734C>A , LRG_299:g.151734C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646891.2:c.1477C>A MANE Select	ENSP00000493543.1:p.Gln493Lys
ENST00000288602.11:c.1597C>A	ENSP00000288602.7:p.Gln533Lys
ENST00000479537.6:c.147C>A
ENST00000496384.7:c.1477C>A	ENSP00000419060.2:p.Gln493Lys
ENST00000497784.2:c.*927C>A	ENSP00000420119.2:n.*927C>A
ENST00000642228.1:c.*555C>A	ENSP00000493678.1:n.*555C>A
ENST00000642875.1:n.1041C>A
ENST00000644120.1:n.1867C>A
ENST00000644650.1:c.573C>A
ENST00000644905.1:n.1566C>A
ENST00000644969.2:c.1597C>A MANE Plus Clinical	ENSP00000496776.1:p.Gln533Lys
ENST00000646730.1:c.1477C>A	ENSP00000494784.1:p.Gln493Lys
ENST00000646891.1:c.1477C>A	ENSP00000493543.1:p.Gln493Lys
ENST00000647434.1:c.520C>A	ENSP00000495132.1:p.Gln174Lys
ENST00000288602.10:c.1477C>A	ENSP00000288602.6:p.Gln493Lys
ENST00000496384.6:c.300C>A
ENST00000497784.1:c.1512C>A	ENSP00000420119.1:n.1512C>A
NM_004333.4:c.1477C>A , LRG_299t1:c.1477C>A	NP_004324.2:p.Gln493Lys
XM_005250045.1:c.1477C>A	XP_005250102.1:p.Gln493Lys
XM_005250046.1:c.1477C>A	XP_005250103.1:p.Gln493Lys
XM_011516529.1:c.1477C>A	XP_011514831.1:p.Gln493Lys
XM_011516530.1:c.1477C>A	XP_011514832.1:p.Gln493Lys
XR_242190.1:n.1485C>A
XR_927520.1:n.1485C>A
XR_927521.1:n.1485C>A
XR_927522.1:n.1485C>A
XR_927523.1:n.1485C>A
NM_001354609.1:c.1477C>A	NP_001341538.1:p.Gln493Lys
NM_004333.5:c.1477C>A	NP_004324.2:p.Gln493Lys
NR_148928.1:n.1782C>A
XM_017012558.1:c.1597C>A	XP_016868047.1:p.Gln533Lys
XM_017012559.1:c.1597C>A	XP_016868048.1:p.Gln533Lys
XR_001744857.1:n.1605C>A
XR_001744858.1:n.1605C>A
NM_001354609.2:c.1477C>A	NP_001341538.1:p.Gln493Lys
NM_001374244.1:c.1597C>A	NP_001361173.1:p.Gln533Lys
NM_001374258.1:c.1597C>A MANE Plus Clinical	NP_001361187.1:p.Gln533Lys
NM_004333.6:c.1477C>A MANE Select	NP_004324.2:p.Gln493Lys
NM_001378467.1:c.1486C>A	NP_001365396.1:p.Gln496Lys
NM_001378468.1:c.1477C>A	NP_001365397.1:p.Gln493Lys
NM_001378469.1:c.1411C>A	NP_001365398.1:p.Gln471Lys
NM_001378470.1:c.1375C>A	NP_001365399.1:p.Gln459Lys
NM_001378471.1:c.1366C>A	NP_001365400.1:p.Gln456Lys
NM_001378472.1:c.1321C>A	NP_001365401.1:p.Gln441Lys
NM_001378473.1:c.1321C>A	NP_001365402.1:p.Gln441Lys
NM_001378474.1:c.1477C>A	NP_001365403.1:p.Gln493Lys
NM_001378475.1:c.1213C>A	NP_001365404.1:p.Gln405Lys