Canonical Allele Identifier: CA1747725961
Gene: BRAF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140776923T= , CM000669.2:g.140776923T= GRCh38
NC_000007.13:g.140476723T= , CM000669.1:g.140476723T= GRCh37
NC_000007.12:g.140123192T= NCBI36
NG_007873.3:g.152842A= , LRG_299:g.152842A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000646891.2:c.1683A= MANE Select ENSP00000493543.1:p.Ala561=
ENST00000288602.11:c.1803A= ENSP00000288602.7:p.Ala601=
ENST00000479537.6:c.353A=
ENST00000496384.7:c.1683A= ENSP00000419060.2:p.Ala561=
ENST00000497784.2:c.*1133A= ENSP00000420119.2:n.*1133A=
ENST00000642228.1:c.*761A= ENSP00000493678.1:n.*761A=
ENST00000642875.1:n.1247A=
ENST00000644120.1:n.2073A=
ENST00000644650.1:c.779A=
ENST00000644905.1:n.1772A=
ENST00000644969.2:c.1803A= MANE Plus Clinical ENSP00000496776.1:p.Ala601=
ENST00000646730.1:c.1683A= ENSP00000494784.1:p.Ala561=
ENST00000646891.1:c.1683A= ENSP00000493543.1:p.Ala561=
ENST00000647434.1:c.726A= ENSP00000495132.1:p.Ala242=
ENST00000288602.10:c.1683A= ENSP00000288602.6:p.Ala561=
ENST00000496384.6:c.506A=
ENST00000497784.1:c.1718A= ENSP00000420119.1:n.1718A=
NM_004333.4:c.1683A= , LRG_299t1:c.1683A= NP_004324.2:p.Ala561=
XM_005250045.1:c.1683A= XP_005250102.1:p.Ala561=
XM_005250046.1:c.1683A= XP_005250103.1:p.Ala561=
XM_011516529.1:c.1683A= XP_011514831.1:p.Ala561=
XM_011516530.1:c.1683A= XP_011514832.1:p.Ala561=
XR_242190.1:n.1691A=
XR_927520.1:n.1691A=
XR_927521.1:n.1691A=
XR_927522.1:n.1691A=
XR_927523.1:n.1691A=
NM_001354609.1:c.1683A= NP_001341538.1:p.Ala561=
NM_004333.5:c.1683A= NP_004324.2:p.Ala561=
NR_148928.1:n.1988A=
XM_017012558.1:c.1803A= XP_016868047.1:p.Ala601=
XM_017012559.1:c.1803A= XP_016868048.1:p.Ala601=
XR_001744857.1:n.1811A=
XR_001744858.1:n.1811A=
NM_001354609.2:c.1683A= NP_001341538.1:p.Ala561=
NM_001374244.1:c.1803A= NP_001361173.1:p.Ala601=
NM_001374258.1:c.1803A= MANE Plus Clinical NP_001361187.1:p.Ala601=
NM_004333.6:c.1683A= MANE Select NP_004324.2:p.Ala561=
NM_001378467.1:c.1692A= NP_001365396.1:p.Ala564=
NM_001378468.1:c.1683A= NP_001365397.1:p.Ala561=
NM_001378469.1:c.1617A= NP_001365398.1:p.Ala539=
NM_001378470.1:c.1581A= NP_001365399.1:p.Ala527=
NM_001378471.1:c.1572A= NP_001365400.1:p.Ala524=
NM_001378472.1:c.1527A= NP_001365401.1:p.Ala509=
NM_001378473.1:c.1527A= NP_001365402.1:p.Ala509=
NM_001378474.1:c.1683A= NP_001365403.1:p.Ala561=
NM_001378475.1:c.1419A= NP_001365404.1:p.Ala473=