Canonical Allele Identifier: CA021017

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 51742
• ClinVar RCV Id: RCV000577442 ; RCV000661890
• dbSNP Id: rs397507750
• MyVariant Identifiers: chr13:g.32913418_32913427del (hg19) ; chr13:g.32339281_32339290del (hg38)
• PubMed: PMID:22762150

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32339281_32339290del , CM000675.2:g.32339281_32339290del	GRCh38
NC_000013.10:g.32913418_32913427del , CM000675.1:g.32913418_32913427del	GRCh37
NC_000013.9:g.31811418_31811427del	NCBI36
NG_012772.3:g.28802_28811del , LRG_293:g.28802_28811del

Transcript Alleles

HGVS	Amino-acid change
ENST00000470094.2:c.4926_4935del	ENSP00000434898.2:p.Asn1642LysfsTer25
ENST00000528762.2:c.4926_4935del	ENSP00000433168.2:p.Asn1642LysfsTer25
ENST00000530893.7:c.4557_4566del	ENSP00000499438.2:p.Asn1519LysfsTer25
ENST00000665585.2:c.4926_4935del	ENSP00000499570.2:p.Asn1642LysfsTer25
ENST00000666593.2:c.4926_4935del	ENSP00000499256.2:p.Asn1642LysfsTer25
ENST00000700202.2:c.4926_4935del	ENSP00000514856.2:p.Asn1642LysfsTer25
ENST00000380152.8:c.4926_4935del MANE Select	ENSP00000369497.3:p.Asn1642LysfsTer25
ENST00000544455.6:c.4926_4935del	ENSP00000439902.1:p.Asn1642LysfsTer25
ENST00000614259.2:c.4926_4935del	ENSP00000506251.1:p.Asn1642LysfsTer25
ENST00000680887.1:c.4926_4935del	ENSP00000505508.1:p.Asn1642LysfsTer25
ENST00000380152.7:c.4926_4935del	ENSP00000369497.3:p.Asn1642LysfsTer25
ENST00000544455.5:c.4926_4935del	ENSP00000439902.1:p.Asn1642LysfsTer25
ENST00000614259.1:n.4926_4935del
NM_000059.3:c.4926_4935del , LRG_293t1:c.4926_4935del	NP_000050.2:p.Asn1642LysfsTer25
XM_011535203.1:c.4926_4935del	XP_011533505.1:p.Asn1642LysfsTer25
XM_011535204.1:c.4926_4935del	XP_011533506.1:p.Asn1642LysfsTer25
XM_011535205.1:c.4926_4935del	XP_011533507.1:p.Asn1642LysfsTer25
NM_000059.4:c.4926_4935del MANE Select	NP_000050.3:p.Asn1642LysfsTer25