Canonical Allele Identifier: CA2825002122
Gene: BRCA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3148664
ClinVar RCV Id: RCV004442558

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32333049dup , CM000675.2:g.32333049dup GRCh38
NC_000013.10:g.32907186dup , CM000675.1:g.32907186dup GRCh37
NC_000013.9:g.31805186dup NCBI36
NG_012772.3:g.22570dup , LRG_293:g.22570dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000470094.2:c.1571dup ENSP00000434898.2:p.Met524IlefsTer3
ENST00000528762.2:c.1571dup ENSP00000433168.2:p.Met524IlefsTer3
ENST00000530893.7:c.1202dup ENSP00000499438.2:p.Met401IlefsTer3
ENST00000665585.2:c.1571dup ENSP00000499570.2:p.Met524IlefsTer3
ENST00000666593.2:c.1571dup ENSP00000499256.2:p.Met524IlefsTer3
ENST00000700202.2:c.1571dup ENSP00000514856.2:p.Met524IlefsTer3
ENST00000700201.1:c.*1350dup ENSP00000514855.1:n.*1350dup
ENST00000380152.8:c.1571dup MANE Select ENSP00000369497.3:p.Met524IlefsTer3
ENST00000544455.6:c.1571dup ENSP00000439902.1:p.Met524IlefsTer3
ENST00000614259.2:c.1571dup ENSP00000506251.1:p.Met524IlefsTer3
ENST00000680887.1:c.1571dup ENSP00000505508.1:p.Met524IlefsTer3
ENST00000380152.7:c.1571dup ENSP00000369497.3:p.Met524IlefsTer3
ENST00000530893.6:n.1769dup
ENST00000544455.5:c.1571dup ENSP00000439902.1:p.Met524IlefsTer3
ENST00000614259.1:n.1571dup
NM_000059.3:c.1571dup , LRG_293t1:c.1571dup NP_000050.2:p.Met524IlefsTer3
XM_011535203.1:c.1571dup XP_011533505.1:p.Met524IlefsTer3
XM_011535204.1:c.1571dup XP_011533506.1:p.Met524IlefsTer3
XM_011535205.1:c.1571dup XP_011533507.1:p.Met524IlefsTer3
NM_000059.4:c.1571dup MANE Select NP_000050.3:p.Met524IlefsTer3