Canonical Allele Identifier: CA1747732035
Gene: BRAF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140800358A= , CM000669.2:g.140800358A= GRCh38
NC_000007.13:g.140500158A= , CM000669.1:g.140500158A= GRCh37
NC_000007.12:g.140146627A= NCBI36
NG_007873.3:g.129407T= , LRG_299:g.129407T=

Transcript Alleles

HGVS Amino-acid change
ENST00000646891.2:c.980+4T= MANE Select ENSP00000493543.1:n.980+4T=
ENST00000288602.11:c.980+4T= ENSP00000288602.7:n.980+4T=
ENST00000496384.7:c.980+4T= ENSP00000419060.2:n.980+4T=
ENST00000497784.2:c.*430+4T= ENSP00000420119.2:n.*430+4T=
ENST00000642228.1:c.*58+4T= ENSP00000493678.1:n.*58+4T=
ENST00000642272.1:n.1016T=
ENST00000642875.1:n.474+4T=
ENST00000644120.1:n.1422+4T=
ENST00000644650.1:c.76+4T=
ENST00000644905.1:n.1069+4T=
ENST00000644969.2:c.980+4T= MANE Plus Clinical ENSP00000496776.1:n.980+4T=
ENST00000646730.1:c.980+4T= ENSP00000494784.1:n.980+4T=
ENST00000646891.1:c.980+4T= ENSP00000493543.1:n.980+4T=
ENST00000647434.1:c.23+4T= ENSP00000495132.1:n.23+4T=
ENST00000288602.10:c.980+4T= ENSP00000288602.6:n.980+4T=
ENST00000497784.1:c.1015+4T= ENSP00000420119.1:n.1015+4T=
NM_004333.4:c.980+4T= , LRG_299t1:c.980+4T= NP_004324.2:n.980+4T=
XM_005250045.1:c.980+4T= XP_005250102.1:n.980+4T=
XM_005250046.1:c.980+4T= XP_005250103.1:n.980+4T=
XM_011516529.1:c.980+4T= XP_011514831.1:n.980+4T=
XM_011516530.1:c.980+4T= XP_011514832.1:n.980+4T=
XR_242190.1:n.988+4T=
XR_927520.1:n.988+4T=
XR_927521.1:n.988+4T=
XR_927522.1:n.988+4T=
XR_927523.1:n.988+4T=
NM_001354609.1:c.980+4T= NP_001341538.1:n.980+4T=
NM_004333.5:c.980+4T= NP_004324.2:n.980+4T=
NR_148928.1:n.1285+4T=
XM_017012558.1:c.980+4T= XP_016868047.1:n.980+4T=
XM_017012559.1:c.980+4T= XP_016868048.1:n.980+4T=
XR_001744857.1:n.988+4T=
XR_001744858.1:n.988+4T=
NM_001354609.2:c.980+4T= NP_001341538.1:n.980+4T=
NM_001374244.1:c.980+4T= NP_001361173.1:n.980+4T=
NM_001374258.1:c.980+4T= MANE Plus Clinical NP_001361187.1:n.980+4T=
NM_004333.6:c.980+4T= MANE Select NP_004324.2:n.980+4T=
NM_001378467.1:c.989+4T= NP_001365396.1:n.989+4T=
NM_001378468.1:c.980+4T= NP_001365397.1:n.980+4T=
NM_001378469.1:c.980+4T= NP_001365398.1:n.980+4T=
NM_001378470.1:c.878+4T= NP_001365399.1:n.878+4T=
NM_001378471.1:c.980+4T= NP_001365400.1:n.980+4T=
NM_001378472.1:c.824+4T= NP_001365401.1:n.824+4T=
NM_001378473.1:c.824+4T= NP_001365402.1:n.824+4T=
NM_001378474.1:c.980+4T= NP_001365403.1:n.980+4T=
NM_001378475.1:c.716+4T= NP_001365404.1:n.716+4T=