Canonical Allele Identifier: CA2727671141

Gene: BRCA2

Linked Data

• dbSNP Id: rs2137462584

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32331076del , CM000675.2:g.32331076del	GRCh38
NC_000013.10:g.32905213del , CM000675.1:g.32905213del	GRCh37
NC_000013.9:g.31803213del	NCBI36
NG_012772.3:g.20597del , LRG_293:g.20597del

Transcript Alleles

HGVS	Amino-acid change
ENST00000470094.2:c.793+46del	ENSP00000434898.2:n.793+46del
ENST00000528762.2:c.793+46del	ENSP00000433168.2:n.793+46del
ENST00000530893.7:c.424+46del	ENSP00000499438.2:n.424+46del
ENST00000665585.2:c.793+46del	ENSP00000499570.2:n.793+46del
ENST00000666593.2:c.793+46del	ENSP00000499256.2:n.793+46del
ENST00000700202.2:c.793+46del	ENSP00000514856.2:n.793+46del
ENST00000700201.1:c.*572+46del	ENSP00000514855.1:n.*572+46del
ENST00000380152.8:c.793+46del MANE Select	ENSP00000369497.3:n.793+46del
ENST00000544455.6:c.793+46del	ENSP00000439902.1:n.793+46del
ENST00000614259.2:c.793+46del	ENSP00000506251.1:n.793+46del
ENST00000680887.1:c.793+46del	ENSP00000505508.1:n.793+46del
ENST00000380152.7:c.793+46del	ENSP00000369497.3:n.793+46del
ENST00000530893.6:n.991+46del
ENST00000544455.5:c.793+46del	ENSP00000439902.1:n.793+46del
ENST00000614259.1:n.793+46del
NM_000059.3:c.793+46del , LRG_293t1:c.793+46del	NP_000050.2:n.793+46del
XM_011535203.1:c.793+46del	XP_011533505.1:n.793+46del
XM_011535204.1:c.793+46del	XP_011533506.1:n.793+46del
XM_011535205.1:c.793+46del	XP_011533507.1:n.793+46del
NM_000059.4:c.793+46del MANE Select	NP_000050.3:n.793+46del