Canonical Allele Identifier: CA2622597014

Gene: BRCA2

Linked Data

• gnomAD v4: 13-32315567-CG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32315569del , CM000675.2:g.32315569del	GRCh38
NC_000013.10:g.32889706del , CM000675.1:g.32889706del	GRCh37
NC_000013.9:g.31787706del	NCBI36
NG_012772.3:g.5090del , LRG_293:g.5090del
NG_017006.1:g.1387del
NG_017006.2:g.4796del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.-138del	ENSP00000434898.2:n.-138del
ENST00000528762.2:c.-138del	ENSP00000433168.2:n.-138del
ENST00000530893.7:c.-503del	ENSP00000499438.2:n.-503del
ENST00000665585.2:c.-138del	ENSP00000499570.2:n.-138del
ENST00000666593.2:c.-138del	ENSP00000499256.2:n.-138del
ENST00000700202.2:c.-138del	ENSP00000514856.2:n.-138del
ENST00000380152.8:c.-138del MANE Select	ENSP00000369497.3:n.-138del
ENST00000544455.6:c.-40+424del	ENSP00000439902.1:n.-40+424del
ENST00000380152.7:c.-138del	ENSP00000369497.3:n.-138del
ENST00000530893.6:n.65del
ENST00000544455.5:c.-138del	ENSP00000439902.1:n.-138del
NM_000059.3:c.-138del , LRG_293t1:c.-138del	NP_000050.2:n.-138del
XM_011535203.1:c.-40+424del	XP_011533505.1:n.-40+424del
XM_011535204.1:c.-138del	XP_011533506.1:n.-138del
XM_011535205.1:c.-138del	XP_011533507.1:n.-138del
NM_000059.4:c.-138del MANE Select	NP_000050.3:n.-138del