Canonical Allele Identifier: CA168091333
Gene: BRAF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140782627T>C , CM000669.2:g.140782627T>C GRCh38
NC_000007.13:g.140482427T>C , CM000669.1:g.140482427T>C GRCh37
NC_000007.12:g.140128896T>C NCBI36
NG_007873.3:g.147138A>G , LRG_299:g.147138A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000646891.2:c.1314+394A>G MANE Select ENSP00000493543.1:n.1314+394A>G
ENST00000288602.11:c.1434+394A>G ENSP00000288602.7:n.1434+394A>G
ENST00000496384.7:c.1314+394A>G ENSP00000419060.2:n.1314+394A>G
ENST00000497784.2:c.*764+394A>G ENSP00000420119.2:n.*764+394A>G
ENST00000642228.1:c.*392+394A>G ENSP00000493678.1:n.*392+394A>G
ENST00000642875.1:n.756+394A>G
ENST00000644120.1:n.1704+394A>G
ENST00000644650.1:c.410+394A>G
ENST00000644905.1:n.1403+394A>G
ENST00000644969.2:c.1434+394A>G MANE Plus Clinical ENSP00000496776.1:n.1434+394A>G
ENST00000646334.1:n.444+394A>G
ENST00000646730.1:c.1314+394A>G ENSP00000494784.1:n.1314+394A>G
ENST00000646891.1:c.1314+394A>G ENSP00000493543.1:n.1314+394A>G
ENST00000647434.1:c.357+394A>G ENSP00000495132.1:n.357+394A>G
ENST00000288602.10:c.1314+394A>G ENSP00000288602.6:n.1314+394A>G
ENST00000496384.6:c.137+394A>G
ENST00000497784.1:c.1349+394A>G ENSP00000420119.1:n.1349+394A>G
NM_004333.4:c.1314+394A>G , LRG_299t1:c.1314+394A>G NP_004324.2:n.1314+394A>G
XM_005250045.1:c.1314+394A>G XP_005250102.1:n.1314+394A>G
XM_005250046.1:c.1314+394A>G XP_005250103.1:n.1314+394A>G
XM_011516529.1:c.1314+394A>G XP_011514831.1:n.1314+394A>G
XM_011516530.1:c.1314+394A>G XP_011514832.1:n.1314+394A>G
XR_242190.1:n.1322+394A>G
XR_927520.1:n.1322+394A>G
XR_927521.1:n.1322+394A>G
XR_927522.1:n.1322+394A>G
XR_927523.1:n.1322+394A>G
NM_001354609.1:c.1314+394A>G NP_001341538.1:n.1314+394A>G
NM_004333.5:c.1314+394A>G NP_004324.2:n.1314+394A>G
NR_148928.1:n.1619+394A>G
XM_017012558.1:c.1434+394A>G XP_016868047.1:n.1434+394A>G
XM_017012559.1:c.1434+394A>G XP_016868048.1:n.1434+394A>G
XR_001744857.1:n.1442+394A>G
XR_001744858.1:n.1442+394A>G
NM_001354609.2:c.1314+394A>G NP_001341538.1:n.1314+394A>G
NM_001374244.1:c.1434+394A>G NP_001361173.1:n.1434+394A>G
NM_001374258.1:c.1434+394A>G MANE Plus Clinical NP_001361187.1:n.1434+394A>G
NM_004333.6:c.1314+394A>G MANE Select NP_004324.2:n.1314+394A>G
NM_001378467.1:c.1323+394A>G NP_001365396.1:n.1323+394A>G
NM_001378468.1:c.1314+394A>G NP_001365397.1:n.1314+394A>G
NM_001378469.1:c.1248+394A>G NP_001365398.1:n.1248+394A>G
NM_001378470.1:c.1212+394A>G NP_001365399.1:n.1212+394A>G
NM_001378471.1:c.1203+394A>G NP_001365400.1:n.1203+394A>G
NM_001378472.1:c.1158+394A>G NP_001365401.1:n.1158+394A>G
NM_001378473.1:c.1158+394A>G NP_001365402.1:n.1158+394A>G
NM_001378474.1:c.1314+394A>G NP_001365403.1:n.1314+394A>G
NM_001378475.1:c.1050+394A>G NP_001365404.1:n.1050+394A>G