Canonical Allele Identifier: CA10602514

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 267655
• ClinVar RCV Id: RCV000258399
• MyVariant Identifiers: chr13:g.32891818_32895723del (hg19) ; chr13:g.32317681_32321586del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32317681_32321586del , CM000675.2:g.32317681_32321586del	GRCh38
NC_000013.10:g.32891818_32895723del , CM000675.1:g.32891818_32895723del	GRCh37
NC_000013.9:g.31789818_31793723del	NCBI36
NG_012772.3:g.7202_11107del , LRG_293:g.7202_11107del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.67+1154_316+2261del
ENST00000528762.2:c.67+1154_316+2261del
ENST00000530893.7:c.-303+1158_-54+2261del
ENST00000665585.2:c.67+1154_316+2261del
ENST00000666593.2:c.67+1154_316+2261del
ENST00000700202.2:c.67+1154_316+2261del
ENST00000700200.1:n.191+1154_192-3494del
ENST00000700201.1:c.67+1154_316+2261del
ENST00000380152.8:c.67+1154_316+2261del
ENST00000544455.6:c.67+1154_316+2261del
ENST00000614259.2:c.67+1154_316+2261del
ENST00000680887.1:c.67+1154_316+2261del
ENST00000380152.7:c.67+1154_316+2261del
ENST00000530893.6:n.265+1158_514+2261del
ENST00000544455.5:c.67+1154_316+2261del
ENST00000614259.1:n.67+1154_316+2261del
NM_000059.3:c.67+1154_316+2261del , LRG_293t1:c.67+1154_316+2261del
XM_011535203.1:c.67+1154_316+2261del
XM_011535204.1:c.67+1154_316+2261del
XM_011535205.1:c.67+1154_316+2261del
NM_000059.4:c.67+1154_316+2261del