Canonical Allele Identifier: CA1747725995
Gene: BRAF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140777027T= , CM000669.2:g.140777027T= GRCh38
NC_000007.13:g.140476827T= , CM000669.1:g.140476827T= GRCh37
NC_000007.12:g.140123296T= NCBI36
NG_007873.3:g.152738A= , LRG_299:g.152738A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000646891.2:c.1579A= MANE Select ENSP00000493543.1:p.Ile527=
ENST00000288602.11:c.1699A= ENSP00000288602.7:p.Ile567=
ENST00000479537.6:c.249A=
ENST00000496384.7:c.1579A= ENSP00000419060.2:p.Ile527=
ENST00000497784.2:c.*1029A= ENSP00000420119.2:n.*1029A=
ENST00000642228.1:c.*657A= ENSP00000493678.1:n.*657A=
ENST00000642875.1:n.1143A=
ENST00000644120.1:n.1969A=
ENST00000644650.1:c.675A=
ENST00000644905.1:n.1668A=
ENST00000644969.2:c.1699A= MANE Plus Clinical ENSP00000496776.1:p.Ile567=
ENST00000646730.1:c.1579A= ENSP00000494784.1:p.Ile527=
ENST00000646891.1:c.1579A= ENSP00000493543.1:p.Ile527=
ENST00000647434.1:c.622A= ENSP00000495132.1:p.Ile208=
ENST00000288602.10:c.1579A= ENSP00000288602.6:p.Ile527=
ENST00000496384.6:c.402A=
ENST00000497784.1:c.1614A= ENSP00000420119.1:n.1614A=
NM_004333.4:c.1579A= , LRG_299t1:c.1579A= NP_004324.2:p.Ile527=
XM_005250045.1:c.1579A= XP_005250102.1:p.Ile527=
XM_005250046.1:c.1579A= XP_005250103.1:p.Ile527=
XM_011516529.1:c.1579A= XP_011514831.1:p.Ile527=
XM_011516530.1:c.1579A= XP_011514832.1:p.Ile527=
XR_242190.1:n.1587A=
XR_927520.1:n.1587A=
XR_927521.1:n.1587A=
XR_927522.1:n.1587A=
XR_927523.1:n.1587A=
NM_001354609.1:c.1579A= NP_001341538.1:p.Ile527=
NM_004333.5:c.1579A= NP_004324.2:p.Ile527=
NR_148928.1:n.1884A=
XM_017012558.1:c.1699A= XP_016868047.1:p.Ile567=
XM_017012559.1:c.1699A= XP_016868048.1:p.Ile567=
XR_001744857.1:n.1707A=
XR_001744858.1:n.1707A=
NM_001354609.2:c.1579A= NP_001341538.1:p.Ile527=
NM_001374244.1:c.1699A= NP_001361173.1:p.Ile567=
NM_001374258.1:c.1699A= MANE Plus Clinical NP_001361187.1:p.Ile567=
NM_004333.6:c.1579A= MANE Select NP_004324.2:p.Ile527=
NM_001378467.1:c.1588A= NP_001365396.1:p.Ile530=
NM_001378468.1:c.1579A= NP_001365397.1:p.Ile527=
NM_001378469.1:c.1513A= NP_001365398.1:p.Ile505=
NM_001378470.1:c.1477A= NP_001365399.1:p.Ile493=
NM_001378471.1:c.1468A= NP_001365400.1:p.Ile490=
NM_001378472.1:c.1423A= NP_001365401.1:p.Ile475=
NM_001378473.1:c.1423A= NP_001365402.1:p.Ile475=
NM_001378474.1:c.1579A= NP_001365403.1:p.Ile527=
NM_001378475.1:c.1315A= NP_001365404.1:p.Ile439=