Canonical Allele Identifier: CA350451299
Gene: BARD1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214730495A>T , CM000664.2:g.214730495A>T GRCh38
NC_000002.11:g.215595219A>T , CM000664.1:g.215595219A>T GRCh37
NC_000002.10:g.215303464A>T NCBI36
NG_012047.2:g.84210T>A
NG_012047.3:g.84217T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000260947.9:c.1917T>A MANE Select ENSP00000260947.4:p.Cys639Ter
ENST00000421162.2:c.564T>A ENSP00000392245.2:p.Cys188Ter
ENST00000613192.2:c.172T>A ENSP00000483275.2:p.Ser58Thr
ENST00000613374.5:c.507T>A ENSP00000484464.1:p.Cys169Ter
ENST00000613706.5:c.1509T>A ENSP00000484976.2:p.Cys503Ter
ENST00000617164.5:c.1860T>A ENSP00000480470.1:p.Cys620Ter
ENST00000619009.5:c.378T>A ENSP00000482293.1:p.Cys126Ter
ENST00000650978.1:c.3292T>A
ENST00000260947.8:c.1917T>A ENSP00000260947.4:p.Cys639Ter
ENST00000421162.1:c.564T>A ENSP00000392245.1:p.Cys188Ter
ENST00000432456.5:c.14T>A
ENST00000455743.5:c.*1537T>A ENSP00000412186.1:n.*1537T>A
ENST00000471590.5:n.252T>A
ENST00000613192.1:c.87T>A ENSP00000483275.1:p.Cys29Ter
ENST00000613374.4:c.507T>A ENSP00000484464.1:p.Cys169Ter
ENST00000613706.4:c.564T>A ENSP00000484976.1:p.Cys188Ter
ENST00000617164.4:c.1860T>A ENSP00000480470.1:p.Cys620Ter
ENST00000619009.4:c.378T>A ENSP00000482293.1:p.Cys126Ter
ENST00000620057.4:c.*583T>A ENSP00000481988.1:n.*583T>A
NM_000465.3:c.1917T>A NP_000456.2:p.Cys639Ter
NM_001282543.1:c.1860T>A NP_001269472.1:p.Cys620Ter
NM_001282545.1:c.564T>A NP_001269474.1:p.Cys188Ter
NM_001282548.1:c.507T>A NP_001269477.1:p.Cys169Ter
NM_001282549.1:c.378T>A NP_001269478.1:p.Cys126Ter
NR_104212.1:n.1910T>A
NR_104215.1:n.1853T>A
NR_104216.1:n.1109T>A
XM_011511567.1:c.1863T>A XP_011509869.1:p.Cys621Ter
XM_017004613.1:c.2016T>A XP_016860102.1:p.Cys672Ter
XR_002959322.1:n.2107T>A
NM_000465.4:c.1917T>A MANE Select NP_000456.2:p.Cys639Ter
NM_001282543.2:c.1860T>A NP_001269472.1:p.Cys620Ter
NM_001282545.2:c.564T>A NP_001269474.1:p.Cys188Ter
NM_001282548.2:c.507T>A NP_001269477.1:p.Cys169Ter
NM_001282549.2:c.378T>A NP_001269478.1:p.Cys126Ter
NR_104212.2:n.1882T>A
NR_104215.2:n.1825T>A
NR_104216.2:n.1081T>A