Canonical Allele Identifier: CA1327053345
Gene: BARD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214745111C= , CM000664.2:g.214745111C= GRCh38
NC_000002.11:g.215609835C= , CM000664.1:g.215609835C= GRCh37
NC_000002.10:g.215318080C= NCBI36
NG_012047.2:g.69594G=
NG_012047.3:g.69601G=

Transcript Alleles

HGVS Amino-acid change
ENST00000260947.9:c.1859G= MANE Select ENSP00000260947.4:p.Cys620=
ENST00000421162.2:c.506G= ENSP00000392245.2:p.Cys169=
ENST00000613192.2:c.159-14603G= ENSP00000483275.2:n.159-14603G=
ENST00000613374.5:c.449G= ENSP00000484464.1:p.Cys150=
ENST00000613706.5:c.1451G= ENSP00000484976.2:p.Cys484=
ENST00000617164.5:c.1802G= ENSP00000480470.1:p.Cys601=
ENST00000619009.5:c.365-14603G= ENSP00000482293.1:n.365-14603G=
ENST00000650978.1:c.3234G=
ENST00000260947.8:c.1859G= ENSP00000260947.4:p.Cys620=
ENST00000421162.1:c.506G= ENSP00000392245.1:p.Cys169=
ENST00000455743.5:c.*1479G= ENSP00000412186.1:n.*1479G=
ENST00000613192.1:c.74-14603G= ENSP00000483275.1:n.74-14603G=
ENST00000613374.4:c.449G= ENSP00000484464.1:p.Cys150=
ENST00000613706.4:c.506G= ENSP00000484976.1:p.Cys169=
ENST00000617164.4:c.1802G= ENSP00000480470.1:p.Cys601=
ENST00000619009.4:c.365-14603G= ENSP00000482293.1:n.365-14603G=
ENST00000620057.4:c.*525G= ENSP00000481988.1:n.*525G=
NM_000465.3:c.1859G= NP_000456.2:p.Cys620=
NM_001282543.1:c.1802G= NP_001269472.1:p.Cys601=
NM_001282545.1:c.506G= NP_001269474.1:p.Cys169=
NM_001282548.1:c.449G= NP_001269477.1:p.Cys150=
NM_001282549.1:c.365-14603G= NP_001269478.1:n.365-14603G=
NR_104212.1:n.1852G=
NR_104215.1:n.1795G=
NR_104216.1:n.1051G=
XM_011511567.1:c.1805G= XP_011509869.1:p.Cys602=
XM_011511568.1:c.1859G= XP_011509870.1:p.Cys620=
XM_017004613.1:c.1958G= XP_016860102.1:p.Cys653=
XM_017004614.1:c.1958G= XP_016860103.1:p.Cys653=
XR_002959322.1:n.2049G=
NM_000465.4:c.1859G= MANE Select NP_000456.2:p.Cys620=
NM_001282543.2:c.1802G= NP_001269472.1:p.Cys601=
NM_001282545.2:c.506G= NP_001269474.1:p.Cys169=
NM_001282548.2:c.449G= NP_001269477.1:p.Cys150=
NM_001282549.2:c.365-14603G= NP_001269478.1:n.365-14603G=
NR_104212.2:n.1824G=
NR_104215.2:n.1767G=
NR_104216.2:n.1023G=