Canonical Allele Identifier: CA2082830400
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32396960T= , CM000675.2:g.32396960T= GRCh38
NC_000013.10:g.32971097T= , CM000675.1:g.32971097T= GRCh37
NC_000013.9:g.31869097T= NCBI36
NG_012772.3:g.86481T= , LRG_293:g.86481T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000470094.2:c.*87T= ENSP00000434898.2:n.*87T=
ENST00000528762.2:c.*931T= ENSP00000433168.2:n.*931T=
ENST00000530893.7:c.9195T= ENSP00000499438.2:p.Asp3065=
ENST00000665585.2:c.*1126T= ENSP00000499570.2:n.*1126T=
ENST00000700202.2:c.9513T= ENSP00000514856.2:p.Asp3171=
ENST00000700202.1:c.1980T= ENSP00000514856.1:p.Asp660=
ENST00000700203.1:n.1691T=
ENST00000380152.8:c.9564T= MANE Select ENSP00000369497.3:p.Asp3188=
ENST00000544455.6:c.9564T= ENSP00000439902.1:p.Asp3188=
ENST00000614259.2:c.9572T= ENSP00000506251.1:n.9572T=
ENST00000665585.1:c.2442T=
ENST00000680887.1:c.9564T= ENSP00000505508.1:p.Asp3188=
ENST00000380152.7:c.9564T= ENSP00000369497.3:p.Asp3188=
ENST00000470094.1:c.647T=
ENST00000533776.1:n.152T=
ENST00000544455.5:c.9564T= ENSP00000439902.1:p.Asp3188=
NM_000059.3:c.9564T= , LRG_293t1:c.9564T= NP_000050.2:p.Asp3188=
XM_011535203.1:c.9564T= XP_011533505.1:p.Asp3188=
XM_011535204.1:c.9468T= XP_011533506.1:p.Asp3156=
NM_000059.4:c.9564T= MANE Select NP_000050.3:p.Asp3188=