Canonical Allele Identifier: CA2727946054

Gene: BRCA2

Linked Data

• dbSNP Id: rs2137670256

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32399181del , CM000675.2:g.32399181del	GRCh38
NC_000013.10:g.32973318del , CM000675.1:g.32973318del	GRCh37
NC_000013.9:g.31871318del	NCBI36
NG_012772.3:g.88702del , LRG_293:g.88702del

Transcript Alleles

HGVS	Amino-acid change
ENST00000470094.2:c.*1191del	ENSP00000434898.2:n.*1191del
ENST00000530893.7:c.*411del	ENSP00000499438.2:n.*411del
ENST00000380152.8:c.*411del MANE Select	ENSP00000369497.3:n.*411del
ENST00000544455.6:c.*411del	ENSP00000439902.1:n.*411del
ENST00000614259.2:c.10676del	ENSP00000506251.1:n.10676del
ENST00000680887.1:c.*411del	ENSP00000505508.1:n.*411del
ENST00000380152.7:c.*411del	ENSP00000369497.3:n.*411del
ENST00000544455.5:c.*411del	ENSP00000439902.1:n.*411del
NM_000059.3:c.*411del , LRG_293t1:c.*411del	NP_000050.2:n.*411del
XM_011535203.1:c.*411del	XP_011533505.1:n.*411del
XM_011535204.1:c.*411del	XP_011533506.1:n.*411del
NM_000059.4:c.*411del MANE Select	NP_000050.3:n.*411del