Canonical Allele Identifier: CA369589054
Gene: BRAF HGNC NCBI

Linked Data

dbSNP Id: rs2129023988

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140781689G>C , CM000669.2:g.140781689G>C GRCh38
NC_000007.13:g.140481489G>C , CM000669.1:g.140481489G>C GRCh37
NC_000007.12:g.140127958G>C NCBI36
NG_007873.3:g.148076C>G , LRG_299:g.148076C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000646891.2:c.1319C>G MANE Select ENSP00000493543.1:p.Thr440Arg
ENST00000288602.11:c.1439C>G ENSP00000288602.7:p.Thr480Arg
ENST00000496384.7:c.1319C>G ENSP00000419060.2:p.Thr440Arg
ENST00000497784.2:c.*769C>G ENSP00000420119.2:n.*769C>G
ENST00000642228.1:c.*397C>G ENSP00000493678.1:n.*397C>G
ENST00000642875.1:n.761C>G
ENST00000644120.1:n.1709C>G
ENST00000644650.1:c.415C>G
ENST00000644905.1:n.1408C>G
ENST00000644969.2:c.1439C>G MANE Plus Clinical ENSP00000496776.1:p.Thr480Arg
ENST00000646334.1:n.449C>G
ENST00000646730.1:c.1319C>G ENSP00000494784.1:p.Thr440Arg
ENST00000646891.1:c.1319C>G ENSP00000493543.1:p.Thr440Arg
ENST00000647434.1:c.362C>G ENSP00000495132.1:p.Thr121Arg
ENST00000288602.10:c.1319C>G ENSP00000288602.6:p.Thr440Arg
ENST00000496384.6:c.142C>G
ENST00000497784.1:c.1354C>G ENSP00000420119.1:n.1354C>G
NM_004333.4:c.1319C>G , LRG_299t1:c.1319C>G NP_004324.2:p.Thr440Arg
XM_005250045.1:c.1319C>G XP_005250102.1:p.Thr440Arg
XM_005250046.1:c.1319C>G XP_005250103.1:p.Thr440Arg
XM_011516529.1:c.1319C>G XP_011514831.1:p.Thr440Arg
XM_011516530.1:c.1319C>G XP_011514832.1:p.Thr440Arg
XR_242190.1:n.1327C>G
XR_927520.1:n.1327C>G
XR_927521.1:n.1327C>G
XR_927522.1:n.1327C>G
XR_927523.1:n.1327C>G
NM_001354609.1:c.1319C>G NP_001341538.1:p.Thr440Arg
NM_004333.5:c.1319C>G NP_004324.2:p.Thr440Arg
NR_148928.1:n.1624C>G
XM_017012558.1:c.1439C>G XP_016868047.1:p.Thr480Arg
XM_017012559.1:c.1439C>G XP_016868048.1:p.Thr480Arg
XR_001744857.1:n.1447C>G
XR_001744858.1:n.1447C>G
NM_001354609.2:c.1319C>G NP_001341538.1:p.Thr440Arg
NM_001374244.1:c.1439C>G NP_001361173.1:p.Thr480Arg
NM_001374258.1:c.1439C>G MANE Plus Clinical NP_001361187.1:p.Thr480Arg
NM_004333.6:c.1319C>G MANE Select NP_004324.2:p.Thr440Arg
NM_001378467.1:c.1328C>G NP_001365396.1:p.Thr443Arg
NM_001378468.1:c.1319C>G NP_001365397.1:p.Thr440Arg
NM_001378469.1:c.1253C>G NP_001365398.1:p.Thr418Arg
NM_001378470.1:c.1217C>G NP_001365399.1:p.Thr406Arg
NM_001378471.1:c.1208C>G NP_001365400.1:p.Thr403Arg
NM_001378472.1:c.1163C>G NP_001365401.1:p.Thr388Arg
NM_001378473.1:c.1163C>G NP_001365402.1:p.Thr388Arg
NM_001378474.1:c.1319C>G NP_001365403.1:p.Thr440Arg
NM_001378475.1:c.1055C>G NP_001365404.1:p.Thr352Arg