Canonical Allele Identifier: CA2082782361
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32319089_32319155delinsTAAGTCTTAATTGGTTTGAAGAACTTTCTTCAGAAGCTCCACCCTATAATTCTGAACCTGCAGAAGA , CM000675.2:g.32319089_32319155delinsTAAGTCTTAATTGGTTTGAAGAACTTTCTTCAGAAGCTCCACCCTATAATTCTGAACCTGCAGAAGA GRCh38
NC_000013.10:g.32893226_32893292delinsTAAGTCTTAATTGGTTTGAAGAACTTTCTTCAGAAGCTCCACCCTATAATTCTGAACCTGCAGAAGA , CM000675.1:g.32893226_32893292delinsTAAGTCTTAATTGGTTTGAAGAACTTTCTTCAGAAGCTCCACCCTATAATTCTGAACCTGCAGAAGA GRCh37
NC_000013.9:g.31791226_31791292delinsTAAGTCTTAATTGGTTTGAAGAACTTTCTTCAGAAGCTCCACCCTATAATTCTGAACCTGCAGAAGA NCBI36
NG_012772.3:g.8610_8676delinsTAAGTCTTAATTGGTTTGAAGAACTTTCTTCAGAAGCTCCACCCTATAATTCTGAACCTGCAGAAGA , LRG_293:g.8610_8676delinsTAAGTCTTAATTGGTTTGAAGAACTTTCTTCAGAAGCTCCACCCTATAATTCTGAACCTGCAGAAGA
NG_017006.2:g.1209_1275delinsTCTTCTGCAGGTTCAGAATTATAGGGTGGAGCTTCTGAAGAAAGTTCTTCAAACCAATTAAGACTTA

Transcript Alleles

HGVS Amino-acid change
ENST00000470094.2:c.80_146delinsTAAGTCTTAATTGGTTTGAAGAACTTTCTTCAGAAGCTCCACCCTATAATTCTGAACCTGCAGAAGA ENSP00000434898.2:p.Ile27=
ENST00000528762.2:c.80_146delinsTAAGTCTTAATTGGTTTGAAGAACTTTCTTCAGAAGCTCCACCCTATAATTCTGAACCTGCAGAAGA ENSP00000433168.2:p.Ile27=
ENST00000530893.7:c.-290_-224delinsTAAGTCTTAATTGGTTTGAAGAACTTTCTTCAGAAGCTCCACCCTATAATTCTGAACCTGCAGAAGA ENSP00000499438.2:n.-290_-224delinsTAAGTC...
ENST00000665585.2:c.80_146delinsTAAGTCTTAATTGGTTTGAAGAACTTTCTTCAGAAGCTCCACCCTATAATTCTGAACCTGCAGAAGA ENSP00000499570.2:p.Ile27=
ENST00000666593.2:c.80_146delinsTAAGTCTTAATTGGTTTGAAGAACTTTCTTCAGAAGCTCCACCCTATAATTCTGAACCTGCAGAAGA ENSP00000499256.2:p.Ile27=
ENST00000700202.2:c.80_146delinsTAAGTCTTAATTGGTTTGAAGAACTTTCTTCAGAAGCTCCACCCTATAATTCTGAACCTGCAGAAGA ENSP00000514856.2:p.Ile27=
ENST00000700200.1:n.191+2562_191+2628delinsTAAGTCTTAATTGGTTTGAAGAACTTTCTTCAGAAGCTCCACCCTATAATTCTGAACCTGCAGAAGA
ENST00000700201.1:c.80_146delinsTAAGTCTTAATTGGTTTGAAGAACTTTCTTCAGAAGCTCCACCCTATAATTCTGAACCTGCAGAAGA ENSP00000514855.1:p.Ile27=
ENST00000380152.8:c.80_146delinsTAAGTCTTAATTGGTTTGAAGAACTTTCTTCAGAAGCTCCACCCTATAATTCTGAACCTGCAGAAGA MANE Select ENSP00000369497.3:p.Ile27=
ENST00000544455.6:c.80_146delinsTAAGTCTTAATTGGTTTGAAGAACTTTCTTCAGAAGCTCCACCCTATAATTCTGAACCTGCAGAAGA ENSP00000439902.1:p.Ile27=
ENST00000614259.2:c.80_146delinsTAAGTCTTAATTGGTTTGAAGAACTTTCTTCAGAAGCTCCACCCTATAATTCTGAACCTGCAGAAGA ENSP00000506251.1:p.Ile27=
ENST00000680887.1:c.80_146delinsTAAGTCTTAATTGGTTTGAAGAACTTTCTTCAGAAGCTCCACCCTATAATTCTGAACCTGCAGAAGA ENSP00000505508.1:p.Ile27=
ENST00000380152.7:c.80_146delinsTAAGTCTTAATTGGTTTGAAGAACTTTCTTCAGAAGCTCCACCCTATAATTCTGAACCTGCAGAAGA ENSP00000369497.3:p.Ile27=
ENST00000530893.6:n.278_344delinsTAAGTCTTAATTGGTTTGAAGAACTTTCTTCAGAAGCTCCACCCTATAATTCTGAACCTGCAGAAGA
ENST00000544455.5:c.80_146delinsTAAGTCTTAATTGGTTTGAAGAACTTTCTTCAGAAGCTCCACCCTATAATTCTGAACCTGCAGAAGA ENSP00000439902.1:p.Ile27=
ENST00000614259.1:n.80_146delinsTAAGTCTTAATTGGTTTGAAGAACTTTCTTCAGAAGCTCCACCCTATAATTCTGAACCTGCAGAAGA
NM_000059.3:c.80_146delinsTAAGTCTTAATTGGTTTGAAGAACTTTCTTCAGAAGCTCCACCCTATAATTCTGAACCTGCAGAAGA , LRG_293t1:c.80_146delinsTAAGTCTTAATTGGTTTGAAGAACTTTCTTCAGAAGCTCCACCCTATAATTCTGAACCTGCAGAAGA NP_000050.2:p.Ile27=
XM_011535203.1:c.80_146delinsTAAGTCTTAATTGGTTTGAAGAACTTTCTTCAGAAGCTCCACCCTATAATTCTGAACCTGCAGAAGA XP_011533505.1:p.Ile27=
XM_011535204.1:c.80_146delinsTAAGTCTTAATTGGTTTGAAGAACTTTCTTCAGAAGCTCCACCCTATAATTCTGAACCTGCAGAAGA XP_011533506.1:p.Ile27=
XM_011535205.1:c.80_146delinsTAAGTCTTAATTGGTTTGAAGAACTTTCTTCAGAAGCTCCACCCTATAATTCTGAACCTGCAGAAGA XP_011533507.1:p.Ile27=
NM_000059.4:c.80_146delinsTAAGTCTTAATTGGTTTGAAGAACTTTCTTCAGAAGCTCCACCCTATAATTCTGAACCTGCAGAAGA MANE Select NP_000050.3:p.Ile27=