Canonical Allele Identifier: CA1327053325
Gene: BARD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214745087C= , CM000664.2:g.214745087C= GRCh38
NC_000002.11:g.215609811C= , CM000664.1:g.215609811C= GRCh37
NC_000002.10:g.215318056C= NCBI36
NG_012047.2:g.69618G=
NG_012047.3:g.69625G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000260947.9:c.1883G= MANE Select ENSP00000260947.4:p.Cys628=
ENST00000421162.2:c.530G= ENSP00000392245.2:p.Cys177=
ENST00000613192.2:c.159-14579G= ENSP00000483275.2:n.159-14579G=
ENST00000613374.5:c.473G= ENSP00000484464.1:p.Cys158=
ENST00000613706.5:c.1475G= ENSP00000484976.2:p.Cys492=
ENST00000617164.5:c.1826G= ENSP00000480470.1:p.Cys609=
ENST00000619009.5:c.365-14579G= ENSP00000482293.1:n.365-14579G=
ENST00000650978.1:c.3258G=
ENST00000260947.8:c.1883G= ENSP00000260947.4:p.Cys628=
ENST00000421162.1:c.530G= ENSP00000392245.1:p.Cys177=
ENST00000455743.5:c.*1503G= ENSP00000412186.1:n.*1503G=
ENST00000613192.1:c.74-14579G= ENSP00000483275.1:n.74-14579G=
ENST00000613374.4:c.473G= ENSP00000484464.1:p.Cys158=
ENST00000613706.4:c.530G= ENSP00000484976.1:p.Cys177=
ENST00000617164.4:c.1826G= ENSP00000480470.1:p.Cys609=
ENST00000619009.4:c.365-14579G= ENSP00000482293.1:n.365-14579G=
ENST00000620057.4:c.*549G= ENSP00000481988.1:n.*549G=
NM_000465.3:c.1883G= NP_000456.2:p.Cys628=
NM_001282543.1:c.1826G= NP_001269472.1:p.Cys609=
NM_001282545.1:c.530G= NP_001269474.1:p.Cys177=
NM_001282548.1:c.473G= NP_001269477.1:p.Cys158=
NM_001282549.1:c.365-14579G= NP_001269478.1:n.365-14579G=
NR_104212.1:n.1876G=
NR_104215.1:n.1819G=
NR_104216.1:n.1075G=
XM_011511567.1:c.1829G= XP_011509869.1:p.Cys610=
XM_011511568.1:c.1883G= XP_011509870.1:p.Cys628=
XM_017004613.1:c.1982G= XP_016860102.1:p.Cys661=
XM_017004614.1:c.1982G= XP_016860103.1:p.Cys661=
XR_002959322.1:n.2073G=
NM_000465.4:c.1883G= MANE Select NP_000456.2:p.Cys628=
NM_001282543.2:c.1826G= NP_001269472.1:p.Cys609=
NM_001282545.2:c.530G= NP_001269474.1:p.Cys177=
NM_001282548.2:c.473G= NP_001269477.1:p.Cys158=
NM_001282549.2:c.365-14579G= NP_001269478.1:n.365-14579G=
NR_104212.2:n.1848G=
NR_104215.2:n.1791G=
NR_104216.2:n.1047G=