Canonical Allele Identifier: CA2082772686

Gene: BRCA2

Linked Data

• dbSNP Id: rs2072247317

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32315561_32315562del , CM000675.2:g.32315561_32315562del	GRCh38
NC_000013.10:g.32889698_32889699del , CM000675.1:g.32889698_32889699del	GRCh37
NC_000013.9:g.31787698_31787699del	NCBI36
NG_012772.3:g.5082_5083del , LRG_293:g.5082_5083del
NG_017006.1:g.1395_1396del
NG_017006.2:g.4804_4805del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.-146_-145del	ENSP00000434898.2:n.-146_-145del
ENST00000528762.2:c.-146_-145del	ENSP00000433168.2:n.-146_-145del
ENST00000530893.7:c.-511_-510del	ENSP00000499438.2:n.-511_-510del
ENST00000665585.2:c.-146_-145del	ENSP00000499570.2:n.-146_-145del
ENST00000666593.2:c.-146_-145del	ENSP00000499256.2:n.-146_-145del
ENST00000700202.2:c.-146_-145del	ENSP00000514856.2:n.-146_-145del
ENST00000380152.8:c.-146_-145del MANE Select	ENSP00000369497.3:n.-146_-145del
ENST00000544455.6:c.-40+416_-40+417del	ENSP00000439902.1:n.-40+416_-40+417del
ENST00000380152.7:c.-146_-145del	ENSP00000369497.3:n.-146_-145del
ENST00000530893.6:n.57_58del
ENST00000544455.5:c.-146_-145del	ENSP00000439902.1:n.-146_-145del
NM_000059.3:c.-146_-145del , LRG_293t1:c.-146_-145del	NP_000050.2:n.-146_-145del
XM_011535203.1:c.-40+416_-40+417del	XP_011533505.1:n.-40+416_-40+417del
XM_011535204.1:c.-146_-145del	XP_011533506.1:n.-146_-145del
XM_011535205.1:c.-146_-145del	XP_011533507.1:n.-146_-145del
NM_000059.4:c.-146_-145del MANE Select	NP_000050.3:n.-146_-145del