Canonical Allele Identifier: CA1747725975
Gene: BRAF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140776968G= , CM000669.2:g.140776968G= GRCh38
NC_000007.13:g.140476768G= , CM000669.1:g.140476768G= GRCh37
NC_000007.12:g.140123237G= NCBI36
NG_007873.3:g.152797C= , LRG_299:g.152797C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000646891.2:c.1638C= MANE Select ENSP00000493543.1:p.Thr546=
ENST00000288602.11:c.1758C= ENSP00000288602.7:p.Thr586=
ENST00000479537.6:c.308C=
ENST00000496384.7:c.1638C= ENSP00000419060.2:p.Thr546=
ENST00000497784.2:c.*1088C= ENSP00000420119.2:n.*1088C=
ENST00000642228.1:c.*716C= ENSP00000493678.1:n.*716C=
ENST00000642875.1:n.1202C=
ENST00000644120.1:n.2028C=
ENST00000644650.1:c.734C=
ENST00000644905.1:n.1727C=
ENST00000644969.2:c.1758C= MANE Plus Clinical ENSP00000496776.1:p.Thr586=
ENST00000646730.1:c.1638C= ENSP00000494784.1:p.Thr546=
ENST00000646891.1:c.1638C= ENSP00000493543.1:p.Thr546=
ENST00000647434.1:c.681C= ENSP00000495132.1:p.Thr227=
ENST00000288602.10:c.1638C= ENSP00000288602.6:p.Thr546=
ENST00000496384.6:c.461C=
ENST00000497784.1:c.1673C= ENSP00000420119.1:n.1673C=
NM_004333.4:c.1638C= , LRG_299t1:c.1638C= NP_004324.2:p.Thr546=
XM_005250045.1:c.1638C= XP_005250102.1:p.Thr546=
XM_005250046.1:c.1638C= XP_005250103.1:p.Thr546=
XM_011516529.1:c.1638C= XP_011514831.1:p.Thr546=
XM_011516530.1:c.1638C= XP_011514832.1:p.Thr546=
XR_242190.1:n.1646C=
XR_927520.1:n.1646C=
XR_927521.1:n.1646C=
XR_927522.1:n.1646C=
XR_927523.1:n.1646C=
NM_001354609.1:c.1638C= NP_001341538.1:p.Thr546=
NM_004333.5:c.1638C= NP_004324.2:p.Thr546=
NR_148928.1:n.1943C=
XM_017012558.1:c.1758C= XP_016868047.1:p.Thr586=
XM_017012559.1:c.1758C= XP_016868048.1:p.Thr586=
XR_001744857.1:n.1766C=
XR_001744858.1:n.1766C=
NM_001354609.2:c.1638C= NP_001341538.1:p.Thr546=
NM_001374244.1:c.1758C= NP_001361173.1:p.Thr586=
NM_001374258.1:c.1758C= MANE Plus Clinical NP_001361187.1:p.Thr586=
NM_004333.6:c.1638C= MANE Select NP_004324.2:p.Thr546=
NM_001378467.1:c.1647C= NP_001365396.1:p.Thr549=
NM_001378468.1:c.1638C= NP_001365397.1:p.Thr546=
NM_001378469.1:c.1572C= NP_001365398.1:p.Thr524=
NM_001378470.1:c.1536C= NP_001365399.1:p.Thr512=
NM_001378471.1:c.1527C= NP_001365400.1:p.Thr509=
NM_001378472.1:c.1482C= NP_001365401.1:p.Thr494=
NM_001378473.1:c.1482C= NP_001365402.1:p.Thr494=
NM_001378474.1:c.1638C= NP_001365403.1:p.Thr546=
NM_001378475.1:c.1374C= NP_001365404.1:p.Thr458=