Canonical Allele Identifier: CA2662969687
Gene: BARD1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214728547_214728552del , CM000664.2:g.214728547_214728552del GRCh38
NC_000002.11:g.215593271_215593276del , CM000664.1:g.215593271_215593276del GRCh37
NC_000002.10:g.215301516_215301521del NCBI36
NG_012047.2:g.86162_86167del
NG_012047.3:g.86169_86174del

Transcript Alleles

HGVS Amino-acid Change
ENST00000260947.9:c.*133_*138del MANE Select ENSP00000260947.4:n.*133_*138del
ENST00000260947.8:c.*133_*138del ENSP00000260947.4:n.*133_*138del
ENST00000432456.5:c.610_615del
ENST00000471590.5:n.802_807del
ENST00000613374.4:c.*133_*138del ENSP00000484464.1:n.*133_*138del
ENST00000613706.4:c.*133_*138del ENSP00000484976.1:n.*133_*138del
ENST00000617164.4:c.*133_*138del ENSP00000480470.1:n.*133_*138del
ENST00000619009.4:c.*133_*138del ENSP00000482293.1:n.*133_*138del
NM_000465.3:c.*133_*138del NP_000456.2:n.*133_*138del
NM_001282543.1:c.*133_*138del NP_001269472.1:n.*133_*138del
NM_001282545.1:c.*133_*138del NP_001269474.1:n.*133_*138del
NM_001282548.1:c.*133_*138del NP_001269477.1:n.*133_*138del
NM_001282549.1:c.*133_*138del NP_001269478.1:n.*133_*138del
NR_104212.1:n.2460_2465del
NR_104215.1:n.2403_2408del
NR_104216.1:n.1659_1664del
XM_011511567.1:c.*133_*138del XP_011509869.1:n.*133_*138del
XM_017004613.1:c.*133_*138del XP_016860102.1:n.*133_*138del
XR_002959322.1:n.2833_2838del
NM_000465.4:c.*133_*138del MANE Select NP_000456.2:n.*133_*138del
NM_001282543.2:c.*133_*138del NP_001269472.1:n.*133_*138del
NM_001282545.2:c.*133_*138del NP_001269474.1:n.*133_*138del
NM_001282548.2:c.*133_*138del NP_001269477.1:n.*133_*138del
NM_001282549.2:c.*133_*138del NP_001269478.1:n.*133_*138del
NR_104212.2:n.2432_2437del
NR_104215.2:n.2375_2380del
NR_104216.2:n.1631_1636del