Canonical Allele Identifier: CA10589371

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 266941
• ClinVar RCV Id: RCV000256688
• dbSNP Id: rs886040652
• MyVariant Identifiers: chr13:g.32914848dupA (hg19) ; chr13:g.32340711dupA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32340711dup , CM000675.2:g.32340711dup	GRCh38
NC_000013.10:g.32914848dup , CM000675.1:g.32914848dup	GRCh37
NC_000013.9:g.31812848dup	NCBI36
NG_012772.3:g.30232dup , LRG_293:g.30232dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000470094.2:c.6356dup	ENSP00000434898.2:p.Asn2119LysfsTer10
ENST00000528762.2:c.6356dup	ENSP00000433168.2:p.Asn2119LysfsTer10
ENST00000530893.7:c.5987dup	ENSP00000499438.2:p.Asn1996LysfsTer10
ENST00000665585.2:c.6356dup	ENSP00000499570.2:p.Asn2119LysfsTer10
ENST00000666593.2:c.6356dup	ENSP00000499256.2:p.Asn2119LysfsTer10
ENST00000700202.2:c.6356dup	ENSP00000514856.2:p.Asn2119LysfsTer10
ENST00000380152.8:c.6356dup MANE Select	ENSP00000369497.3:p.Asn2119LysfsTer10
ENST00000544455.6:c.6356dup	ENSP00000439902.1:p.Asn2119LysfsTer10
ENST00000614259.2:c.6356dup	ENSP00000506251.1:p.Asn2119LysfsTer10
ENST00000680887.1:c.6356dup	ENSP00000505508.1:p.Asn2119LysfsTer10
ENST00000380152.7:c.6356dup	ENSP00000369497.3:p.Asn2119LysfsTer10
ENST00000544455.5:c.6356dup	ENSP00000439902.1:p.Asn2119LysfsTer10
ENST00000614259.1:n.6356dup
NM_000059.3:c.6356dup , LRG_293t1:c.6356dup	NP_000050.2:p.Asn2119LysfsTer10
XM_011535203.1:c.6356dup	XP_011533505.1:p.Asn2119LysfsTer10
XM_011535204.1:c.6356dup	XP_011533506.1:p.Asn2119LysfsTer10
XM_011535205.1:c.6356dup	XP_011533507.1:p.Asn2119LysfsTer10
NM_000059.4:c.6356dup MANE Select	NP_000050.3:p.Asn2119LysfsTer10