Canonical Allele Identifier: CA1327053348
Gene: BARD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214745117A= , CM000664.2:g.214745117A= GRCh38
NC_000002.11:g.215609841A= , CM000664.1:g.215609841A= GRCh37
NC_000002.10:g.215318086A= NCBI36
NG_012047.2:g.69588T=
NG_012047.3:g.69595T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000260947.9:c.1853T= MANE Select ENSP00000260947.4:p.Leu618=
ENST00000421162.2:c.500T= ENSP00000392245.2:p.Leu167=
ENST00000613192.2:c.159-14609T= ENSP00000483275.2:n.159-14609T=
ENST00000613374.5:c.443T= ENSP00000484464.1:p.Leu148=
ENST00000613706.5:c.1445T= ENSP00000484976.2:p.Leu482=
ENST00000617164.5:c.1796T= ENSP00000480470.1:p.Leu599=
ENST00000619009.5:c.365-14609T= ENSP00000482293.1:n.365-14609T=
ENST00000650978.1:c.3228T=
ENST00000260947.8:c.1853T= ENSP00000260947.4:p.Leu618=
ENST00000421162.1:c.500T= ENSP00000392245.1:p.Leu167=
ENST00000455743.5:c.*1473T= ENSP00000412186.1:n.*1473T=
ENST00000613192.1:c.74-14609T= ENSP00000483275.1:n.74-14609T=
ENST00000613374.4:c.443T= ENSP00000484464.1:p.Leu148=
ENST00000613706.4:c.500T= ENSP00000484976.1:p.Leu167=
ENST00000617164.4:c.1796T= ENSP00000480470.1:p.Leu599=
ENST00000619009.4:c.365-14609T= ENSP00000482293.1:n.365-14609T=
ENST00000620057.4:c.*519T= ENSP00000481988.1:n.*519T=
NM_000465.3:c.1853T= NP_000456.2:p.Leu618=
NM_001282543.1:c.1796T= NP_001269472.1:p.Leu599=
NM_001282545.1:c.500T= NP_001269474.1:p.Leu167=
NM_001282548.1:c.443T= NP_001269477.1:p.Leu148=
NM_001282549.1:c.365-14609T= NP_001269478.1:n.365-14609T=
NR_104212.1:n.1846T=
NR_104215.1:n.1789T=
NR_104216.1:n.1045T=
XM_011511567.1:c.1799T= XP_011509869.1:p.Leu600=
XM_011511568.1:c.1853T= XP_011509870.1:p.Leu618=
XM_017004613.1:c.1952T= XP_016860102.1:p.Leu651=
XM_017004614.1:c.1952T= XP_016860103.1:p.Leu651=
XR_002959322.1:n.2043T=
NM_000465.4:c.1853T= MANE Select NP_000456.2:p.Leu618=
NM_001282543.2:c.1796T= NP_001269472.1:p.Leu599=
NM_001282545.2:c.500T= NP_001269474.1:p.Leu167=
NM_001282548.2:c.443T= NP_001269477.1:p.Leu148=
NM_001282549.2:c.365-14609T= NP_001269478.1:n.365-14609T=
NR_104212.2:n.1818T=
NR_104215.2:n.1761T=
NR_104216.2:n.1017T=