Canonical Allele Identifier: CA2580087432
Gene: BRCA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2039775
ClinVar RCV Id: RCV002886011

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32362688_32362697del , CM000675.2:g.32362688_32362697del GRCh38
NC_000013.10:g.32936825_32936834del , CM000675.1:g.32936825_32936834del GRCh37
NC_000013.9:g.31834825_31834834del NCBI36
NG_012772.3:g.52209_52218del , LRG_293:g.52209_52218del

Transcript Alleles

HGVS Amino-acid change
ENST00000470094.2:c.7971_7976+4del
ENST00000528762.2:c.7971_7976+4del
ENST00000530893.7:c.7602_7607+4del
ENST00000665585.2:c.7971_7976+4del
ENST00000666593.2:c.7971_7976+4del
ENST00000700202.2:c.7971_7976+4del
ENST00000700202.1:c.438_443+4del
ENST00000380152.8:c.7971_7976+4del
ENST00000544455.6:c.7971_7976+4del
ENST00000614259.2:c.7979_7984+4del
ENST00000665585.1:c.536_541+4del
ENST00000680887.1:c.7971_7976+4del
ENST00000380152.7:c.7971_7976+4del
ENST00000544455.5:c.7971_7976+4del
NM_000059.3:c.7971_7976+4del , LRG_293t1:c.7971_7976+4del
XM_011535203.1:c.7971_7976+4del
XM_011535204.1:c.7875_7880+4del
XM_011535205.1:c.7971_7976+4del
NM_000059.4:c.7971_7976+4del