Canonical Allele Identifier: CA2082770084
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32333131_32333132delinsCT , CM000675.2:g.32333131_32333132delinsCT GRCh38
NC_000013.10:g.32907268_32907269delinsCT , CM000675.1:g.32907268_32907269delinsCT GRCh37
NC_000013.9:g.31805268_31805269delinsCT NCBI36
NG_012772.3:g.22652_22653delinsCT , LRG_293:g.22652_22653delinsCT

Transcript Alleles

HGVS Amino-acid change
ENST00000470094.2:c.1653_1654delinsCT ENSP00000434898.2:p.Asp551=
ENST00000528762.2:c.1653_1654delinsCT ENSP00000433168.2:p.Asp551=
ENST00000530893.7:c.1284_1285delinsCT ENSP00000499438.2:p.Asp428=
ENST00000665585.2:c.1653_1654delinsCT ENSP00000499570.2:p.Asp551=
ENST00000666593.2:c.1653_1654delinsCT ENSP00000499256.2:p.Asp551=
ENST00000700202.2:c.1653_1654delinsCT ENSP00000514856.2:p.Asp551=
ENST00000700201.1:c.*1432_*1433delinsCT ENSP00000514855.1:n.*1432_*1433delinsCT
ENST00000380152.8:c.1653_1654delinsCT MANE Select ENSP00000369497.3:p.Asp551=
ENST00000544455.6:c.1653_1654delinsCT ENSP00000439902.1:p.Asp551=
ENST00000614259.2:c.1653_1654delinsCT ENSP00000506251.1:p.Asp551=
ENST00000680887.1:c.1653_1654delinsCT ENSP00000505508.1:p.Asp551=
ENST00000380152.7:c.1653_1654delinsCT ENSP00000369497.3:p.Asp551=
ENST00000530893.6:n.1851_1852delinsCT
ENST00000544455.5:c.1653_1654delinsCT ENSP00000439902.1:p.Asp551=
ENST00000614259.1:n.1653_1654delinsCT
NM_000059.3:c.1653_1654delinsCT , LRG_293t1:c.1653_1654delinsCT NP_000050.2:p.Asp551=
XM_011535203.1:c.1653_1654delinsCT XP_011533505.1:p.Asp551=
XM_011535204.1:c.1653_1654delinsCT XP_011533506.1:p.Asp551=
XM_011535205.1:c.1653_1654delinsCT XP_011533507.1:p.Asp551=
NM_000059.4:c.1653_1654delinsCT MANE Select NP_000050.3:p.Asp551=