Canonical Allele Identifier: CA1747710404
Gene: BRAF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140754233A= , CM000669.2:g.140754233A= GRCh38
NC_000007.13:g.140454033A= , CM000669.1:g.140454033A= GRCh37
NC_000007.12:g.140100502A= NCBI36
NG_007873.3:g.175532T= , LRG_299:g.175532T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000646891.2:c.1695T= MANE Select ENSP00000493543.1:p.Asp565=
ENST00000288602.11:c.1815T= ENSP00000288602.7:p.Asp605=
ENST00000479537.6:c.365T=
ENST00000496384.7:c.1695T= ENSP00000419060.2:p.Asp565=
ENST00000497784.2:c.*1145T= ENSP00000420119.2:n.*1145T=
ENST00000642228.1:c.*773T= ENSP00000493678.1:n.*773T=
ENST00000642875.1:n.1259-4815T=
ENST00000644120.1:n.2085T=
ENST00000644650.1:c.791T=
ENST00000644905.1:n.1784T=
ENST00000644969.2:c.1815T= MANE Plus Clinical ENSP00000496776.1:p.Asp605=
ENST00000646730.1:c.*271T= ENSP00000494784.1:n.*271T=
ENST00000646891.1:c.1695T= ENSP00000493543.1:p.Asp565=
ENST00000647434.1:c.738-4815T= ENSP00000495132.1:n.738-4815T=
ENST00000288602.10:c.1695T= ENSP00000288602.6:p.Asp565=
ENST00000496384.6:c.518T=
ENST00000497784.1:c.1730T= ENSP00000420119.1:n.1730T=
NM_004333.4:c.1695T= , LRG_299t1:c.1695T= NP_004324.2:p.Asp565=
XM_005250045.1:c.1695T= XP_005250102.1:p.Asp565=
XM_005250046.1:c.1695T= XP_005250103.1:p.Asp565=
XM_011516529.1:c.1695T= XP_011514831.1:p.Asp565=
XM_011516530.1:c.1695-4815T= XP_011514832.1:n.1695-4815T=
XR_242190.1:n.1703T=
XR_927520.1:n.1703T=
XR_927521.1:n.1703T=
XR_927522.1:n.1703-4815T=
XR_927523.1:n.1703-4815T=
NM_001354609.1:c.1695T= NP_001341538.1:p.Asp565=
NM_004333.5:c.1695T= NP_004324.2:p.Asp565=
NR_148928.1:n.2000T=
XM_017012558.1:c.1815T= XP_016868047.1:p.Asp605=
XM_017012559.1:c.1815T= XP_016868048.1:p.Asp605=
XR_001744857.1:n.1823T=
XR_001744858.1:n.1823-4815T=
NM_001354609.2:c.1695T= NP_001341538.1:p.Asp565=
NM_001374244.1:c.1815T= NP_001361173.1:p.Asp605=
NM_001374258.1:c.1815T= MANE Plus Clinical NP_001361187.1:p.Asp605=
NM_004333.6:c.1695T= MANE Select NP_004324.2:p.Asp565=
NM_001378467.1:c.1704T= NP_001365396.1:p.Asp568=
NM_001378468.1:c.1695T= NP_001365397.1:p.Asp565=
NM_001378469.1:c.1629T= NP_001365398.1:p.Asp543=
NM_001378470.1:c.1593T= NP_001365399.1:p.Asp531=
NM_001378471.1:c.1584T= NP_001365400.1:p.Asp528=
NM_001378472.1:c.1539T= NP_001365401.1:p.Asp513=
NM_001378473.1:c.1539T= NP_001365402.1:p.Asp513=
NM_001378474.1:c.1695T= NP_001365403.1:p.Asp565=
NM_001378475.1:c.1431T= NP_001365404.1:p.Asp477=