Canonical Allele Identifier: CA1327045587
Gene: BARD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214728865C= , CM000664.2:g.214728865C= GRCh38
NC_000002.11:g.215593589C= , CM000664.1:g.215593589C= GRCh37
NC_000002.10:g.215301834C= NCBI36
NG_012047.2:g.85840G=
NG_012047.3:g.85847G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000260947.9:c.2145G= MANE Select ENSP00000260947.4:p.Gln715=
ENST00000421162.2:c.792G= ENSP00000392245.2:p.Gln264=
ENST00000613192.2:c.*208G= ENSP00000483275.2:n.*208G=
ENST00000613374.5:c.735G= ENSP00000484464.1:p.Gln245=
ENST00000613706.5:c.1737G= ENSP00000484976.2:p.Gln579=
ENST00000617164.5:c.2088G= ENSP00000480470.1:p.Gln696=
ENST00000619009.5:c.606G= ENSP00000482293.1:p.Gln202=
ENST00000650978.1:c.3520G=
ENST00000260947.8:c.2145G= ENSP00000260947.4:p.Gln715=
ENST00000432456.5:c.288G=
ENST00000455743.5:c.*1765G= ENSP00000412186.1:n.*1765G=
ENST00000471590.5:n.480G=
ENST00000613192.1:c.315G= ENSP00000483275.1:p.Gln105=
ENST00000613374.4:c.735G= ENSP00000484464.1:p.Gln245=
ENST00000613706.4:c.792G= ENSP00000484976.1:p.Gln264=
ENST00000617164.4:c.2088G= ENSP00000480470.1:p.Gln696=
ENST00000619009.4:c.606G= ENSP00000482293.1:p.Gln202=
ENST00000620057.4:c.*811G= ENSP00000481988.1:n.*811G=
NM_000465.3:c.2145G= NP_000456.2:p.Gln715=
NM_001282543.1:c.2088G= NP_001269472.1:p.Gln696=
NM_001282545.1:c.792G= NP_001269474.1:p.Gln264=
NM_001282548.1:c.735G= NP_001269477.1:p.Gln245=
NM_001282549.1:c.606G= NP_001269478.1:p.Gln202=
NR_104212.1:n.2138G=
NR_104215.1:n.2081G=
NR_104216.1:n.1337G=
XM_011511567.1:c.2091G= XP_011509869.1:p.Gln697=
XM_017004613.1:c.2244G= XP_016860102.1:p.Gln748=
XR_002959322.1:n.2511G=
NM_000465.4:c.2145G= MANE Select NP_000456.2:p.Gln715=
NM_001282543.2:c.2088G= NP_001269472.1:p.Gln696=
NM_001282545.2:c.792G= NP_001269474.1:p.Gln264=
NM_001282548.2:c.735G= NP_001269477.1:p.Gln245=
NM_001282549.2:c.606G= NP_001269478.1:p.Gln202=
NR_104212.2:n.2110G=
NR_104215.2:n.2053G=
NR_104216.2:n.1309G=