Canonical Allele Identifier: CA2082835098
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32398293T= , CM000675.2:g.32398293T= GRCh38
NC_000013.10:g.32972430T= , CM000675.1:g.32972430T= GRCh37
NC_000013.9:g.31870430T= NCBI36
NG_012772.3:g.87814T= , LRG_293:g.87814T=

Transcript Alleles

HGVS Amino-acid change
ENST00000470094.2:c.*303T= ENSP00000434898.2:n.*303T=
ENST00000528762.2:c.*1147T= ENSP00000433168.2:n.*1147T=
ENST00000530893.7:c.9411T= ENSP00000499438.2:p.Asp3137=
ENST00000665585.2:c.*1342T= ENSP00000499570.2:n.*1342T=
ENST00000700202.2:c.9729T= ENSP00000514856.2:p.Asp3243=
ENST00000700202.1:c.2196T= ENSP00000514856.1:p.Asp732=
ENST00000700203.1:n.1907T=
ENST00000380152.8:c.9780T= MANE Select ENSP00000369497.3:p.Asp3260=
ENST00000544455.6:c.9780T= ENSP00000439902.1:p.Asp3260=
ENST00000614259.2:c.9788T= ENSP00000506251.1:n.9788T=
ENST00000680887.1:c.9780T= ENSP00000505508.1:p.Asp3260=
ENST00000380152.7:c.9780T= ENSP00000369497.3:p.Asp3260=
ENST00000533776.1:n.368T=
ENST00000544455.5:c.9780T= ENSP00000439902.1:p.Asp3260=
NM_000059.3:c.9780T= , LRG_293t1:c.9780T= NP_000050.2:p.Asp3260=
XM_011535203.1:c.9780T= XP_011533505.1:p.Asp3260=
XM_011535204.1:c.9684T= XP_011533506.1:p.Asp3228=
NM_000059.4:c.9780T= MANE Select NP_000050.3:p.Asp3260=