Canonical Allele Identifier: CA1327053326
Gene: BARD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214745088A= , CM000664.2:g.214745088A= GRCh38
NC_000002.11:g.215609812A= , CM000664.1:g.215609812A= GRCh37
NC_000002.10:g.215318057A= NCBI36
NG_012047.2:g.69617T=
NG_012047.3:g.69624T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000260947.9:c.1882T= MANE Select ENSP00000260947.4:p.Cys628=
ENST00000421162.2:c.529T= ENSP00000392245.2:p.Cys177=
ENST00000613192.2:c.159-14580T= ENSP00000483275.2:n.159-14580T=
ENST00000613374.5:c.472T= ENSP00000484464.1:p.Cys158=
ENST00000613706.5:c.1474T= ENSP00000484976.2:p.Cys492=
ENST00000617164.5:c.1825T= ENSP00000480470.1:p.Cys609=
ENST00000619009.5:c.365-14580T= ENSP00000482293.1:n.365-14580T=
ENST00000650978.1:c.3257T=
ENST00000260947.8:c.1882T= ENSP00000260947.4:p.Cys628=
ENST00000421162.1:c.529T= ENSP00000392245.1:p.Cys177=
ENST00000455743.5:c.*1502T= ENSP00000412186.1:n.*1502T=
ENST00000613192.1:c.74-14580T= ENSP00000483275.1:n.74-14580T=
ENST00000613374.4:c.472T= ENSP00000484464.1:p.Cys158=
ENST00000613706.4:c.529T= ENSP00000484976.1:p.Cys177=
ENST00000617164.4:c.1825T= ENSP00000480470.1:p.Cys609=
ENST00000619009.4:c.365-14580T= ENSP00000482293.1:n.365-14580T=
ENST00000620057.4:c.*548T= ENSP00000481988.1:n.*548T=
NM_000465.3:c.1882T= NP_000456.2:p.Cys628=
NM_001282543.1:c.1825T= NP_001269472.1:p.Cys609=
NM_001282545.1:c.529T= NP_001269474.1:p.Cys177=
NM_001282548.1:c.472T= NP_001269477.1:p.Cys158=
NM_001282549.1:c.365-14580T= NP_001269478.1:n.365-14580T=
NR_104212.1:n.1875T=
NR_104215.1:n.1818T=
NR_104216.1:n.1074T=
XM_011511567.1:c.1828T= XP_011509869.1:p.Cys610=
XM_011511568.1:c.1882T= XP_011509870.1:p.Cys628=
XM_017004613.1:c.1981T= XP_016860102.1:p.Cys661=
XM_017004614.1:c.1981T= XP_016860103.1:p.Cys661=
XR_002959322.1:n.2072T=
NM_000465.4:c.1882T= MANE Select NP_000456.2:p.Cys628=
NM_001282543.2:c.1825T= NP_001269472.1:p.Cys609=
NM_001282545.2:c.529T= NP_001269474.1:p.Cys177=
NM_001282548.2:c.472T= NP_001269477.1:p.Cys158=
NM_001282549.2:c.365-14580T= NP_001269478.1:n.365-14580T=
NR_104212.2:n.1847T=
NR_104215.2:n.1790T=
NR_104216.2:n.1046T=