Canonical Allele Identifier: CA919242564
Gene: BRCA2 HGNC NCBI

Linked Data

dbSNP Id: rs1593897395

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32336996_32336998del , CM000675.2:g.32336996_32336998del GRCh38
NC_000013.10:g.32911133_32911135del , CM000675.1:g.32911133_32911135del GRCh37
NC_000013.9:g.31809133_31809135del NCBI36
NG_012772.3:g.26517_26519del , LRG_293:g.26517_26519del

Transcript Alleles

HGVS Amino-acid Change
ENST00000470094.2:c.2641_2643del ENSP00000434898.2:p.Glu881del
ENST00000528762.2:c.2641_2643del ENSP00000433168.2:p.Glu881del
ENST00000530893.7:c.2272_2274del ENSP00000499438.2:p.Glu758del
ENST00000665585.2:c.2641_2643del ENSP00000499570.2:p.Glu881del
ENST00000666593.2:c.2641_2643del ENSP00000499256.2:p.Glu881del
ENST00000700202.2:c.2641_2643del ENSP00000514856.2:p.Glu881del
ENST00000380152.8:c.2641_2643del MANE Select ENSP00000369497.3:p.Glu881del
ENST00000544455.6:c.2641_2643del ENSP00000439902.1:p.Glu881del
ENST00000614259.2:c.2641_2643del ENSP00000506251.1:p.Glu881del
ENST00000680887.1:c.2641_2643del ENSP00000505508.1:p.Glu881del
ENST00000380152.7:c.2641_2643del ENSP00000369497.3:p.Glu881del
ENST00000544455.5:c.2641_2643del ENSP00000439902.1:p.Glu881del
ENST00000614259.1:n.2641_2643del
NM_000059.3:c.2641_2643del , LRG_293t1:c.2641_2643del NP_000050.2:p.Glu881del
XM_011535203.1:c.2641_2643del XP_011533505.1:p.Glu881del
XM_011535204.1:c.2641_2643del XP_011533506.1:p.Glu881del
XM_011535205.1:c.2641_2643del XP_011533507.1:p.Glu881del
NM_000059.4:c.2641_2643del MANE Select NP_000050.3:p.Glu881del