Canonical Allele Identifier: CA020410

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 51669
• ClinVar RCV Id: RCV003460583
• dbSNP Id: rs80359457
• MyVariant Identifiers: chr13:g.32913043_32913046del (hg19) ; chr13:g.32338906_32338909del (hg38)
• PubMed: PMID:17688236 ; PMID:26295337

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32338906_32338909del , CM000675.2:g.32338906_32338909del	GRCh38
NC_000013.10:g.32913043_32913046del , CM000675.1:g.32913043_32913046del	GRCh37
NC_000013.9:g.31811043_31811046del	NCBI36
NG_012772.3:g.28427_28430del , LRG_293:g.28427_28430del

Transcript Alleles

HGVS	Amino-acid change
ENST00000470094.2:c.4551_4554del	ENSP00000434898.2:p.Lys1517AsnfsTer25
ENST00000528762.2:c.4551_4554del	ENSP00000433168.2:p.Lys1517AsnfsTer25
ENST00000530893.7:c.4182_4185del	ENSP00000499438.2:p.Lys1394AsnfsTer25
ENST00000665585.2:c.4551_4554del	ENSP00000499570.2:p.Lys1517AsnfsTer25
ENST00000666593.2:c.4551_4554del	ENSP00000499256.2:p.Lys1517AsnfsTer25
ENST00000700202.2:c.4551_4554del	ENSP00000514856.2:p.Lys1517AsnfsTer25
ENST00000380152.8:c.4551_4554del MANE Select	ENSP00000369497.3:p.Lys1517AsnfsTer25
ENST00000544455.6:c.4551_4554del	ENSP00000439902.1:p.Lys1517AsnfsTer25
ENST00000614259.2:c.4551_4554del	ENSP00000506251.1:p.Lys1517AsnfsTer25
ENST00000680887.1:c.4551_4554del	ENSP00000505508.1:p.Lys1517AsnfsTer25
ENST00000380152.7:c.4551_4554del	ENSP00000369497.3:p.Lys1517AsnfsTer25
ENST00000544455.5:c.4551_4554del	ENSP00000439902.1:p.Lys1517AsnfsTer25
ENST00000614259.1:n.4551_4554del
NM_000059.3:c.4551_4554del , LRG_293t1:c.4551_4554del	NP_000050.2:p.Lys1517AsnfsTer25
XM_011535203.1:c.4551_4554del	XP_011533505.1:p.Lys1517AsnfsTer25
XM_011535204.1:c.4551_4554del	XP_011533506.1:p.Lys1517AsnfsTer25
XM_011535205.1:c.4551_4554del	XP_011533507.1:p.Lys1517AsnfsTer25
NM_000059.4:c.4551_4554del MANE Select	NP_000050.3:p.Lys1517AsnfsTer25