Canonical Allele Identifier: CA919242832

Gene: BRCA2

Linked Data

• dbSNP Id: rs1566244634

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32362495_32362507del , CM000675.2:g.32362495_32362507del	GRCh38
NC_000013.10:g.32936632_32936644del , CM000675.1:g.32936632_32936644del	GRCh37
NC_000013.9:g.31834632_31834644del	NCBI36
NG_012772.3:g.52016_52028del , LRG_293:g.52016_52028del

Transcript Alleles

HGVS	Amino-acid change
ENST00000470094.2:c.7806-28_7806-16del	ENSP00000434898.2:n.7806-28_7806-16del
ENST00000528762.2:c.7806-28_7806-16del	ENSP00000433168.2:n.7806-28_7806-16del
ENST00000530893.7:c.7437-28_7437-16del	ENSP00000499438.2:n.7437-28_7437-16del
ENST00000665585.2:c.7806-28_7806-16del	ENSP00000499570.2:n.7806-28_7806-16del
ENST00000666593.2:c.7806-28_7806-16del	ENSP00000499256.2:n.7806-28_7806-16del
ENST00000700202.2:c.7806-28_7806-16del	ENSP00000514856.2:n.7806-28_7806-16del
ENST00000700202.1:c.273-28_273-16del	ENSP00000514856.1:n.273-28_273-16del
ENST00000380152.8:c.7806-28_7806-16del MANE Select	ENSP00000369497.3:n.7806-28_7806-16del
ENST00000544455.6:c.7806-28_7806-16del	ENSP00000439902.1:n.7806-28_7806-16del
ENST00000614259.2:c.7806-20_7806-8del	ENSP00000506251.1:n.7806-20_7806-8del
ENST00000665585.1:c.371-28_371-16del
ENST00000680887.1:c.7806-28_7806-16del	ENSP00000505508.1:n.7806-28_7806-16del
ENST00000380152.7:c.7806-28_7806-16del	ENSP00000369497.3:n.7806-28_7806-16del
ENST00000544455.5:c.7806-28_7806-16del	ENSP00000439902.1:n.7806-28_7806-16del
ENST00000614259.1:n.7806-20_7806-8del
NM_000059.3:c.7806-28_7806-16del , LRG_293t1:c.7806-28_7806-16del	NP_000050.2:n.7806-28_7806-16del
XM_011535203.1:c.7806-28_7806-16del	XP_011533505.1:n.7806-28_7806-16del
XM_011535204.1:c.7710-28_7710-16del	XP_011533506.1:n.7710-28_7710-16del
XM_011535205.1:c.7806-28_7806-16del	XP_011533507.1:n.7806-28_7806-16del
NM_000059.4:c.7806-28_7806-16del MANE Select	NP_000050.3:n.7806-28_7806-16del