Canonical Allele Identifier: CA165434
Gene: BRCA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 141449
dbSNP Id: rs276174915

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32379510_32379520del , CM000675.2:g.32379510_32379520del GRCh38
NC_000013.10:g.32953647_32953657del , CM000675.1:g.32953647_32953657del GRCh37
NC_000013.9:g.31851647_31851657del NCBI36
NG_012772.3:g.69031_69041del , LRG_293:g.69031_69041del

Transcript Alleles

HGVS Amino-acid change
ENST00000470094.2:c.8948_8953+5del
ENST00000528762.2:c.*315_*320+5del
ENST00000530893.7:c.8579_8584+5del
ENST00000665585.2:c.*510_*515+5del
ENST00000666593.2:c.8948_8953+5del
ENST00000700202.2:c.8948_8953+5del
ENST00000700202.1:c.1415_1420+5del
ENST00000700203.1:n.1075_1080+5del
ENST00000380152.8:c.8948_8953+5del
ENST00000544455.6:c.8948_8953+5del
ENST00000614259.2:c.8956_8961+5del
ENST00000665585.1:c.1826_1831+5del
ENST00000680887.1:c.8948_8953+5del
ENST00000380152.7:c.8948_8953+5del
ENST00000544455.5:c.8948_8953+5del
NM_000059.3:c.8948_8953+5del , LRG_293t1:c.8948_8953+5del
XM_011535203.1:c.8948_8953+5del
XM_011535204.1:c.8852_8857+5del
XM_011535205.1:c.8755-240_8755-230del XP_011533507.1:n.8755-240_8755-230del
NM_000059.4:c.8948_8953+5del