Canonical Allele Identifier: CA2622597135

Gene: BRCA2

Linked Data

• gnomAD v4: 13-32315729-CG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32315734del , CM000675.2:g.32315734del	GRCh38
NC_000013.10:g.32889871del , CM000675.1:g.32889871del	GRCh37
NC_000013.9:g.31787871del	NCBI36
NG_012772.3:g.5255del , LRG_293:g.5255del
NG_017006.1:g.1225del
NG_017006.2:g.4634del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.-40+67del	ENSP00000434898.2:n.-40+67del
ENST00000528762.2:c.-40+67del	ENSP00000433168.2:n.-40+67del
ENST00000530893.7:c.-405+67del	ENSP00000499438.2:n.-405+67del
ENST00000665585.2:c.-40+67del	ENSP00000499570.2:n.-40+67del
ENST00000666593.2:c.-40+67del	ENSP00000499256.2:n.-40+67del
ENST00000700202.2:c.-40+67del	ENSP00000514856.2:n.-40+67del
ENST00000700199.1:n.85+67del
ENST00000700200.1:n.85+67del
ENST00000700201.1:c.-40+67del	ENSP00000514855.1:n.-40+67del
ENST00000380152.8:c.-40+67del MANE Select	ENSP00000369497.3:n.-40+67del
ENST00000544455.6:c.-40+589del	ENSP00000439902.1:n.-40+589del
ENST00000380152.7:c.-40+67del	ENSP00000369497.3:n.-40+67del
ENST00000530893.6:n.163+67del
ENST00000544455.5:c.-40+67del	ENSP00000439902.1:n.-40+67del
NM_000059.3:c.-40+67del , LRG_293t1:c.-40+67del	NP_000050.2:n.-40+67del
XM_011535203.1:c.-40+589del	XP_011533505.1:n.-40+589del
XM_011535204.1:c.-40+67del	XP_011533506.1:n.-40+67del
XM_011535205.1:c.-40+67del	XP_011533507.1:n.-40+67del
NM_000059.4:c.-40+67del MANE Select	NP_000050.3:n.-40+67del