Canonical Allele Identifier: CA1139663201

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 967215
• ClinVar RCV Id: RCV001242063 ; RCV001310061
• dbSNP Id: rs878853303

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32357791del , CM000675.2:g.32357791del	GRCh38
NC_000013.10:g.32931928del , CM000675.1:g.32931928del	GRCh37
NC_000013.9:g.31829928del	NCBI36
NG_012772.3:g.47312del , LRG_293:g.47312del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.7667del	ENSP00000434898.2:p.Asn2556MetfsTer?
ENST00000528762.2:c.7667del	ENSP00000433168.2:p.Asn2556MetfsTer?
ENST00000530893.7:c.7298del	ENSP00000499438.2:p.Asn2433MetfsTer?
ENST00000665585.2:c.7667del	ENSP00000499570.2:p.Asn2556MetfsTer?
ENST00000666593.2:c.7667del	ENSP00000499256.2:p.Asn2556MetfsTer?
ENST00000700202.2:c.7667del	ENSP00000514856.2:p.Asn2556MetfsTer?
ENST00000700202.1:c.134del	ENSP00000514856.1:p.Asn45MetfsTer?
ENST00000380152.8:c.7667del MANE Select	ENSP00000369497.3:p.Asn2556MetfsTer?
ENST00000544455.6:c.7667del	ENSP00000439902.1:p.Asn2556MetfsTer?
ENST00000614259.2:c.7667del	ENSP00000506251.1:p.Asn2556MetfsTer?
ENST00000665585.1:c.232del
ENST00000680887.1:c.7667del	ENSP00000505508.1:p.Asn2556MetfsTer?
ENST00000380152.7:c.7667del	ENSP00000369497.3:p.Asn2556MetfsTer?
ENST00000544455.5:c.7667del	ENSP00000439902.1:p.Asn2556MetfsTer?
ENST00000614259.1:n.7667del
NM_000059.3:c.7667del , LRG_293t1:c.7667del	NP_000050.2:p.Asn2556MetfsTer?
XM_011535203.1:c.7667del	XP_011533505.1:p.Asn2556MetfsTer?
XM_011535204.1:c.7571del	XP_011533506.1:p.Asn2524MetfsTer?
XM_011535205.1:c.7667del	XP_011533507.1:p.Asn2556MetfsTer?
NM_000059.4:c.7667del MANE Select	NP_000050.3:p.Asn2556MetfsTer?