Canonical Allele Identifier: CA2082828284
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32376683A= , CM000675.2:g.32376683A= GRCh38
NC_000013.10:g.32950820A= , CM000675.1:g.32950820A= GRCh37
NC_000013.9:g.31848820A= NCBI36
NG_012772.3:g.66204A= , LRG_293:g.66204A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000470094.2:c.8646A= ENSP00000434898.2:p.Lys2882=
ENST00000528762.2:c.*13A= ENSP00000433168.2:n.*13A=
ENST00000530893.7:c.8277A= ENSP00000499438.2:p.Lys2759=
ENST00000665585.2:c.*208A= ENSP00000499570.2:n.*208A=
ENST00000666593.2:c.8646A= ENSP00000499256.2:p.Lys2882=
ENST00000700202.2:c.8646A= ENSP00000514856.2:p.Lys2882=
ENST00000700202.1:c.1113A= ENSP00000514856.1:p.Lys371=
ENST00000700203.1:n.773A=
ENST00000380152.8:c.8646A= MANE Select ENSP00000369497.3:p.Lys2882=
ENST00000544455.6:c.8646A= ENSP00000439902.1:p.Lys2882=
ENST00000614259.2:c.8654A= ENSP00000506251.1:n.8654A=
ENST00000665585.1:c.1524A=
ENST00000680887.1:c.8646A= ENSP00000505508.1:p.Lys2882=
ENST00000380152.7:c.8646A= ENSP00000369497.3:p.Lys2882=
ENST00000528762.1:c.208A= ENSP00000433168.1:n.208A=
ENST00000544455.5:c.8646A= ENSP00000439902.1:p.Lys2882=
NM_000059.3:c.8646A= , LRG_293t1:c.8646A= NP_000050.2:p.Lys2882=
XM_011535203.1:c.8646A= XP_011533505.1:p.Lys2882=
XM_011535204.1:c.8550A= XP_011533506.1:p.Lys2850=
XM_011535205.1:c.8646A= XP_011533507.1:p.Lys2882=
NM_000059.4:c.8646A= MANE Select NP_000050.3:p.Lys2882=