Canonical Allele Identifier: CA2573149349

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 1386112
• ClinVar RCV Id: RCV001871525
• dbSNP Id: rs2137516326

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32339680_32339689del , CM000675.2:g.32339680_32339689del	GRCh38
NC_000013.10:g.32913817_32913826del , CM000675.1:g.32913817_32913826del	GRCh37
NC_000013.9:g.31811817_31811826del	NCBI36
NG_012772.3:g.29201_29210del , LRG_293:g.29201_29210del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.5325_5334del	ENSP00000434898.2:p.Asn1778IlefsTer10
ENST00000528762.2:c.5325_5334del	ENSP00000433168.2:p.Asn1778IlefsTer10
ENST00000530893.7:c.4956_4965del	ENSP00000499438.2:p.Asn1655IlefsTer10
ENST00000665585.2:c.5325_5334del	ENSP00000499570.2:p.Asn1778IlefsTer10
ENST00000666593.2:c.5325_5334del	ENSP00000499256.2:p.Asn1778IlefsTer10
ENST00000700202.2:c.5325_5334del	ENSP00000514856.2:p.Asn1778IlefsTer10
ENST00000380152.8:c.5325_5334del MANE Select	ENSP00000369497.3:p.Asn1778IlefsTer10
ENST00000544455.6:c.5325_5334del	ENSP00000439902.1:p.Asn1778IlefsTer10
ENST00000614259.2:c.5325_5334del	ENSP00000506251.1:p.Asn1778IlefsTer10
ENST00000680887.1:c.5325_5334del	ENSP00000505508.1:p.Asn1778IlefsTer10
ENST00000380152.7:c.5325_5334del	ENSP00000369497.3:p.Asn1778IlefsTer10
ENST00000544455.5:c.5325_5334del	ENSP00000439902.1:p.Asn1778IlefsTer10
ENST00000614259.1:n.5325_5334del
NM_000059.3:c.5325_5334del , LRG_293t1:c.5325_5334del	NP_000050.2:p.Asn1778IlefsTer10
XM_011535203.1:c.5325_5334del	XP_011533505.1:p.Asn1778IlefsTer10
XM_011535204.1:c.5325_5334del	XP_011533506.1:p.Asn1778IlefsTer10
XM_011535205.1:c.5325_5334del	XP_011533507.1:p.Asn1778IlefsTer10
NM_000059.4:c.5325_5334del MANE Select	NP_000050.3:p.Asn1778IlefsTer10