Canonical Allele Identifier: CA2586971185
Gene: BARD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214728661del , CM000664.2:g.214728661del GRCh38
NC_000002.11:g.215593385del , CM000664.1:g.215593385del GRCh37
NC_000002.10:g.215301630del NCBI36
NG_012047.2:g.86044del
NG_012047.3:g.86051del

Transcript Alleles

HGVS Amino-acid change
ENST00000260947.9:c.*15del MANE Select ENSP00000260947.4:n.*15del
ENST00000613374.5:c.*15del ENSP00000484464.1:n.*15del
ENST00000613706.5:c.*15del ENSP00000484976.2:n.*15del
ENST00000617164.5:c.*15del ENSP00000480470.1:n.*15del
ENST00000619009.5:c.*15del ENSP00000482293.1:n.*15del
ENST00000650978.1:c.3724del
ENST00000260947.8:c.*15del ENSP00000260947.4:n.*15del
ENST00000432456.5:c.492del
ENST00000471590.5:n.684del
ENST00000613374.4:c.*15del ENSP00000484464.1:n.*15del
ENST00000613706.4:c.*15del ENSP00000484976.1:n.*15del
ENST00000617164.4:c.*15del ENSP00000480470.1:n.*15del
ENST00000619009.4:c.*15del ENSP00000482293.1:n.*15del
NM_000465.3:c.*15del NP_000456.2:n.*15del
NM_001282543.1:c.*15del NP_001269472.1:n.*15del
NM_001282545.1:c.*15del NP_001269474.1:n.*15del
NM_001282548.1:c.*15del NP_001269477.1:n.*15del
NM_001282549.1:c.*15del NP_001269478.1:n.*15del
NR_104212.1:n.2342del
NR_104215.1:n.2285del
NR_104216.1:n.1541del
XM_011511567.1:c.*15del XP_011509869.1:n.*15del
XM_017004613.1:c.*15del XP_016860102.1:n.*15del
XR_002959322.1:n.2715del
NM_000465.4:c.*15del MANE Select NP_000456.2:n.*15del
NM_001282543.2:c.*15del NP_001269472.1:n.*15del
NM_001282545.2:c.*15del NP_001269474.1:n.*15del
NM_001282548.2:c.*15del NP_001269477.1:n.*15del
NM_001282549.2:c.*15del NP_001269478.1:n.*15del
NR_104212.2:n.2314del
NR_104215.2:n.2257del
NR_104216.2:n.1513del