Canonical Allele Identifier: CA2573149191

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 1370317
• ClinVar RCV Id: RCV001877102
• dbSNP Id: rs886040652

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32340710_32340711del , CM000675.2:g.32340710_32340711del	GRCh38
NC_000013.10:g.32914847_32914848del , CM000675.1:g.32914847_32914848del	GRCh37
NC_000013.9:g.31812847_31812848del	NCBI36
NG_012772.3:g.30231_30232del , LRG_293:g.30231_30232del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.6355_6356del	ENSP00000434898.2:p.Asn2119LeufsTer9
ENST00000528762.2:c.6355_6356del	ENSP00000433168.2:p.Asn2119LeufsTer9
ENST00000530893.7:c.5986_5987del	ENSP00000499438.2:p.Asn1996LeufsTer9
ENST00000665585.2:c.6355_6356del	ENSP00000499570.2:p.Asn2119LeufsTer9
ENST00000666593.2:c.6355_6356del	ENSP00000499256.2:p.Asn2119LeufsTer9
ENST00000700202.2:c.6355_6356del	ENSP00000514856.2:p.Asn2119LeufsTer9
ENST00000380152.8:c.6355_6356del MANE Select	ENSP00000369497.3:p.Asn2119LeufsTer9
ENST00000544455.6:c.6355_6356del	ENSP00000439902.1:p.Asn2119LeufsTer9
ENST00000614259.2:c.6355_6356del	ENSP00000506251.1:p.Asn2119LeufsTer9
ENST00000680887.1:c.6355_6356del	ENSP00000505508.1:p.Asn2119LeufsTer9
ENST00000380152.7:c.6355_6356del	ENSP00000369497.3:p.Asn2119LeufsTer9
ENST00000544455.5:c.6355_6356del	ENSP00000439902.1:p.Asn2119LeufsTer9
ENST00000614259.1:n.6355_6356del
NM_000059.3:c.6355_6356del , LRG_293t1:c.6355_6356del	NP_000050.2:p.Asn2119LeufsTer9
XM_011535203.1:c.6355_6356del	XP_011533505.1:p.Asn2119LeufsTer9
XM_011535204.1:c.6355_6356del	XP_011533506.1:p.Asn2119LeufsTer9
XM_011535205.1:c.6355_6356del	XP_011533507.1:p.Asn2119LeufsTer9
NM_000059.4:c.6355_6356del MANE Select	NP_000050.3:p.Asn2119LeufsTer9