Canonical Allele Identifier: CA2082815595
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32356593_32356594delinsCG , CM000675.2:g.32356593_32356594delinsCG GRCh38
NC_000013.10:g.32930730_32930731delinsCG , CM000675.1:g.32930730_32930731delinsCG GRCh37
NC_000013.9:g.31828730_31828731delinsCG NCBI36
NG_012772.3:g.46114_46115delinsCG , LRG_293:g.46114_46115delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000470094.2:c.7601_7602delinsCG ENSP00000434898.2:p.Ala2534=
ENST00000528762.2:c.7601_7602delinsCG ENSP00000433168.2:p.Ala2534=
ENST00000530893.7:c.7232_7233delinsCG ENSP00000499438.2:p.Ala2411=
ENST00000665585.2:c.7601_7602delinsCG ENSP00000499570.2:p.Ala2534=
ENST00000666593.2:c.7601_7602delinsCG ENSP00000499256.2:p.Ala2534=
ENST00000700202.2:c.7601_7602delinsCG ENSP00000514856.2:p.Ala2534=
ENST00000700202.1:c.68_69delinsCG ENSP00000514856.1:p.Ala23=
ENST00000380152.8:c.7601_7602delinsCG MANE Select ENSP00000369497.3:p.Ala2534=
ENST00000544455.6:c.7601_7602delinsCG ENSP00000439902.1:p.Ala2534=
ENST00000614259.2:c.7601_7602delinsCG ENSP00000506251.1:p.Ala2534=
ENST00000665585.1:c.166_167delinsCG
ENST00000680887.1:c.7601_7602delinsCG ENSP00000505508.1:p.Ala2534=
ENST00000380152.7:c.7601_7602delinsCG ENSP00000369497.3:p.Ala2534=
ENST00000544455.5:c.7601_7602delinsCG ENSP00000439902.1:p.Ala2534=
ENST00000614259.1:n.7601_7602delinsCG
NM_000059.3:c.7601_7602delinsCG , LRG_293t1:c.7601_7602delinsCG NP_000050.2:p.Ala2534=
XM_011535203.1:c.7601_7602delinsCG XP_011533505.1:p.Ala2534=
XM_011535204.1:c.7505_7506delinsCG XP_011533506.1:p.Ala2502=
XM_011535205.1:c.7601_7602delinsCG XP_011533507.1:p.Ala2534=
NM_000059.4:c.7601_7602delinsCG MANE Select NP_000050.3:p.Ala2534=