Canonical Allele Identifier: CA2082772543

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32315528_32315539delinsACTGCTGCGCCT , CM000675.2:g.32315528_32315539delinsACTGCTGCGCCT	GRCh38
NC_000013.10:g.32889665_32889676delinsACTGCTGCGCCT , CM000675.1:g.32889665_32889676delinsACTGCTGCGCCT	GRCh37
NC_000013.9:g.31787665_31787676delinsACTGCTGCGCCT	NCBI36
NG_012772.3:g.5049_5060delinsACTGCTGCGCCT , LRG_293:g.5049_5060delinsACTGCTGCGCCT
NG_017006.1:g.1416_1427delinsAGGCGCAGCAGT
NG_017006.2:g.4825_4836delinsAGGCGCAGCAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.-179_-168delinsACTGCTGCGCCT	ENSP00000434898.2:n.-179_-168delinsACTGCTGCGCCT
ENST00000528762.2:c.-179_-168delinsACTGCTGCGCCT	ENSP00000433168.2:n.-179_-168delinsACTGCTGCGCCT
ENST00000530893.7:c.-544_-533delinsACTGCTGCGCCT	ENSP00000499438.2:n.-544_-533delinsACTGCTGCGCCT
ENST00000665585.2:c.-179_-168delinsACTGCTGCGCCT	ENSP00000499570.2:n.-179_-168delinsACTGCTGCGCCT
ENST00000666593.2:c.-179_-168delinsACTGCTGCGCCT	ENSP00000499256.2:n.-179_-168delinsACTGCTGCGCCT
ENST00000700202.2:c.-179_-168delinsACTGCTGCGCCT	ENSP00000514856.2:n.-179_-168delinsACTGCTGCGCCT
ENST00000380152.8:c.-179_-168delinsACTGCTGCGCCT MANE Select	ENSP00000369497.3:n.-179_-168delinsACTGCTGCGCCT
ENST00000544455.6:c.-40+383_-40+394delinsACTGCTGCGCCT	ENSP00000439902.1:n.-40+383_-40+394delinsACTGCTGCGCCT
ENST00000380152.7:c.-179_-168delinsACTGCTGCGCCT	ENSP00000369497.3:n.-179_-168delinsACTGCTGCGCCT
ENST00000530893.6:n.24_35delinsACTGCTGCGCCT
ENST00000544455.5:c.-179_-168delinsACTGCTGCGCCT	ENSP00000439902.1:n.-179_-168delinsACTGCTGCGCCT
NM_000059.3:c.-179_-168delinsACTGCTGCGCCT , LRG_293t1:c.-179_-168delinsACTGCTGCGCCT	NP_000050.2:n.-179_-168delinsACTGCTGCGCCT
XM_011535203.1:c.-40+383_-40+394delinsACTGCTGCGCCT	XP_011533505.1:n.-40+383_-40+394delinsACTGCTGCGCCT
XM_011535204.1:c.-179_-168delinsACTGCTGCGCCT	XP_011533506.1:n.-179_-168delinsACTGCTGCGCCT
XM_011535205.1:c.-179_-168delinsACTGCTGCGCCT	XP_011533507.1:n.-179_-168delinsACTGCTGCGCCT
NM_000059.4:c.-179_-168delinsACTGCTGCGCCT MANE Select	NP_000050.3:n.-179_-168delinsACTGCTGCGCCT