Canonical Allele Identifier: CA369542733
Gene: BRAF HGNC NCBI

Linked Data

dbSNP Id: rs2128998110
COSMIC: COSM33730

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140753282A>C , CM000669.2:g.140753282A>C GRCh38
NC_000007.13:g.140453082A>C , CM000669.1:g.140453082A>C GRCh37
NC_000007.12:g.140099551A>C NCBI36
NG_007873.3:g.176483T>G , LRG_299:g.176483T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000646891.2:c.1853T>G MANE Select ENSP00000493543.1:p.Leu618Trp
ENST00000288602.11:c.1973T>G ENSP00000288602.7:p.Leu658Trp
ENST00000479537.6:c.523T>G
ENST00000496384.7:c.1853T>G ENSP00000419060.2:p.Leu618Trp
ENST00000497784.2:c.*1303T>G ENSP00000420119.2:n.*1303T>G
ENST00000642228.1:c.*931T>G ENSP00000493678.1:n.*931T>G
ENST00000642875.1:n.1259-3864T>G
ENST00000644120.1:n.2243T>G
ENST00000644650.1:c.949T>G
ENST00000644905.1:n.2735T>G
ENST00000644969.2:c.1973T>G MANE Plus Clinical ENSP00000496776.1:p.Leu658Trp
ENST00000646730.1:c.*429T>G ENSP00000494784.1:n.*429T>G
ENST00000646891.1:c.1853T>G ENSP00000493543.1:p.Leu618Trp
ENST00000647434.1:c.738-3864T>G ENSP00000495132.1:n.738-3864T>G
ENST00000288602.10:c.1853T>G ENSP00000288602.6:p.Leu618Trp
ENST00000479537.5:c.137T>G ENSP00000418033.1:p.Leu46Trp
ENST00000496384.6:c.676T>G
ENST00000497784.1:c.1888T>G ENSP00000420119.1:n.1888T>G
NM_004333.4:c.1853T>G , LRG_299t1:c.1853T>G NP_004324.2:p.Leu618Trp
XM_005250045.1:c.1853T>G XP_005250102.1:p.Leu618Trp
XM_005250046.1:c.1853T>G XP_005250103.1:p.Leu618Trp
XM_011516529.1:c.1853T>G XP_011514831.1:p.Leu618Trp
XM_011516530.1:c.1695-3864T>G XP_011514832.1:n.1695-3864T>G
XR_242190.1:n.1861T>G
XR_927520.1:n.1861T>G
XR_927521.1:n.1861T>G
XR_927522.1:n.1703-3864T>G
XR_927523.1:n.1703-3864T>G
NM_001354609.1:c.1853T>G NP_001341538.1:p.Leu618Trp
NM_004333.5:c.1853T>G NP_004324.2:p.Leu618Trp
NR_148928.1:n.2951T>G
XM_017012558.1:c.1973T>G XP_016868047.1:p.Leu658Trp
XM_017012559.1:c.1973T>G XP_016868048.1:p.Leu658Trp
XR_001744857.1:n.1981T>G
XR_001744858.1:n.1823-3864T>G
NM_001354609.2:c.1853T>G NP_001341538.1:p.Leu618Trp
NM_001374244.1:c.1973T>G NP_001361173.1:p.Leu658Trp
NM_001374258.1:c.1973T>G MANE Plus Clinical NP_001361187.1:p.Leu658Trp
NM_004333.6:c.1853T>G MANE Select NP_004324.2:p.Leu618Trp
NM_001378467.1:c.1862T>G NP_001365396.1:p.Leu621Trp
NM_001378468.1:c.1853T>G NP_001365397.1:p.Leu618Trp
NM_001378469.1:c.1787T>G NP_001365398.1:p.Leu596Trp
NM_001378470.1:c.1751T>G NP_001365399.1:p.Leu584Trp
NM_001378471.1:c.1742T>G NP_001365400.1:p.Leu581Trp
NM_001378472.1:c.1697T>G NP_001365401.1:p.Leu566Trp
NM_001378473.1:c.1697T>G NP_001365402.1:p.Leu566Trp
NM_001378474.1:c.1853T>G NP_001365403.1:p.Leu618Trp
NM_001378475.1:c.1589T>G NP_001365404.1:p.Leu530Trp