Canonical Allele Identifier: CA1327046379
Gene: BARD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214730449C= , CM000664.2:g.214730449C= GRCh38
NC_000002.11:g.215595173C= , CM000664.1:g.215595173C= GRCh37
NC_000002.10:g.215303418C= NCBI36
NG_012047.2:g.84256G=
NG_012047.3:g.84263G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000260947.9:c.1963G= MANE Select ENSP00000260947.4:p.Glu655=
ENST00000421162.2:c.610G= ENSP00000392245.2:p.Glu204=
ENST00000613192.2:c.*26G= ENSP00000483275.2:n.*26G=
ENST00000613374.5:c.553G= ENSP00000484464.1:p.Glu185=
ENST00000613706.5:c.1555G= ENSP00000484976.2:p.Glu519=
ENST00000617164.5:c.1906G= ENSP00000480470.1:p.Glu636=
ENST00000619009.5:c.424G= ENSP00000482293.1:p.Glu142=
ENST00000650978.1:c.3338G=
ENST00000260947.8:c.1963G= ENSP00000260947.4:p.Glu655=
ENST00000421162.1:c.610G= ENSP00000392245.1:p.Glu204=
ENST00000432456.5:c.60G=
ENST00000455743.5:c.*1583G= ENSP00000412186.1:n.*1583G=
ENST00000471590.5:n.298G=
ENST00000613192.1:c.133G= ENSP00000483275.1:p.Glu45=
ENST00000613374.4:c.553G= ENSP00000484464.1:p.Glu185=
ENST00000613706.4:c.610G= ENSP00000484976.1:p.Glu204=
ENST00000617164.4:c.1906G= ENSP00000480470.1:p.Glu636=
ENST00000619009.4:c.424G= ENSP00000482293.1:p.Glu142=
ENST00000620057.4:c.*629G= ENSP00000481988.1:n.*629G=
NM_000465.3:c.1963G= NP_000456.2:p.Glu655=
NM_001282543.1:c.1906G= NP_001269472.1:p.Glu636=
NM_001282545.1:c.610G= NP_001269474.1:p.Glu204=
NM_001282548.1:c.553G= NP_001269477.1:p.Glu185=
NM_001282549.1:c.424G= NP_001269478.1:p.Glu142=
NR_104212.1:n.1956G=
NR_104215.1:n.1899G=
NR_104216.1:n.1155G=
XM_011511567.1:c.1909G= XP_011509869.1:p.Glu637=
XM_017004613.1:c.2062G= XP_016860102.1:p.Glu688=
XR_002959322.1:n.2153G=
NM_000465.4:c.1963G= MANE Select NP_000456.2:p.Glu655=
NM_001282543.2:c.1906G= NP_001269472.1:p.Glu636=
NM_001282545.2:c.610G= NP_001269474.1:p.Glu204=
NM_001282548.2:c.553G= NP_001269477.1:p.Glu185=
NM_001282549.2:c.424G= NP_001269478.1:p.Glu142=
NR_104212.2:n.1928G=
NR_104215.2:n.1871G=
NR_104216.2:n.1127G=