Canonical Allele Identifier: CA2082822298
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32394723T= , CM000675.2:g.32394723T= GRCh38
NC_000013.10:g.32968860T= , CM000675.1:g.32968860T= GRCh37
NC_000013.9:g.31866860T= NCBI36
NG_012772.3:g.84244T= , LRG_293:g.84244T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000470094.2:c.9291T= ENSP00000434898.2:p.Cys3097=
ENST00000528762.2:c.*658T= ENSP00000433168.2:n.*658T=
ENST00000530893.7:c.8922T= ENSP00000499438.2:p.Cys2974=
ENST00000665585.2:c.*853T= ENSP00000499570.2:n.*853T=
ENST00000666593.2:c.*136T= ENSP00000499256.2:n.*136T=
ENST00000700202.2:c.9240T= ENSP00000514856.2:p.Cys3080=
ENST00000700202.1:c.1707T= ENSP00000514856.1:p.Cys569=
ENST00000700203.1:n.1418T=
ENST00000380152.8:c.9291T= MANE Select ENSP00000369497.3:p.Cys3097=
ENST00000544455.6:c.9291T= ENSP00000439902.1:p.Cys3097=
ENST00000614259.2:c.9299T= ENSP00000506251.1:n.9299T=
ENST00000665585.1:c.2169T=
ENST00000666593.1:c.313T= ENSP00000499256.1:n.313T=
ENST00000680887.1:c.9291T= ENSP00000505508.1:p.Cys3097=
ENST00000380152.7:c.9291T= ENSP00000369497.3:p.Cys3097=
ENST00000470094.1:c.248T=
ENST00000544455.5:c.9291T= ENSP00000439902.1:p.Cys3097=
NM_000059.3:c.9291T= , LRG_293t1:c.9291T= NP_000050.2:p.Cys3097=
XM_011535203.1:c.9291T= XP_011533505.1:p.Cys3097=
XM_011535204.1:c.9195T= XP_011533506.1:p.Cys3065=
NM_000059.4:c.9291T= MANE Select NP_000050.3:p.Cys3097=