Canonical Allele Identifier: CA1327076691
Gene: BARD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214792369_214792379delinsTTATCTTCAAG , CM000664.2:g.214792369_214792379delinsTTATCTTCAAG GRCh38
NC_000002.11:g.215657093_215657103delinsTTATCTTCAAG , CM000664.1:g.215657093_215657103delinsTTATCTTCAAG GRCh37
NC_000002.10:g.215365338_215365348delinsTTATCTTCAAG NCBI36
NG_012047.2:g.22326_22336delinsCTTGAAGATAA
NG_012047.3:g.22333_22343delinsCTTGAAGATAA

Transcript Alleles

HGVS Amino-acid change
ENST00000260947.9:c.282_292delinsCTTGAAGATAA MANE Select ENSP00000260947.4:p.Asp94=
ENST00000421162.2:c.215+4682_215+4692delinsCTTGAAGATAA ENSP00000392245.2:n.215+4682_215+4692deli...
ENST00000613192.2:c.158+17033_158+17043delinsCTTGAAGATAA ENSP00000483275.2:n.158+17033_158+17043de...
ENST00000613374.5:c.158+17033_158+17043delinsCTTGAAGATAA ENSP00000484464.1:n.158+17033_158+17043de...
ENST00000613706.5:c.282_292delinsCTTGAAGATAA ENSP00000484976.2:p.Asp94=
ENST00000617164.5:c.225_235delinsCTTGAAGATAA ENSP00000480470.1:p.Asp75=
ENST00000619009.5:c.282_292delinsCTTGAAGATAA ENSP00000482293.1:p.Asp94=
ENST00000650978.1:c.124_134delinsCTTGAAGATAA
ENST00000260947.8:c.282_292delinsCTTGAAGATAA ENSP00000260947.4:p.Asp94=
ENST00000421162.1:c.215+4682_215+4692delinsCTTGAAGATAA ENSP00000392245.1:n.215+4682_215+4692deli...
ENST00000455743.5:c.215+4682_215+4692delinsCTTGAAGATAA ENSP00000412186.1:n.215+4682_215+4692deli...
ENST00000471787.1:n.260-10870_260-10860delinsCTTGAAGATAA
ENST00000613192.1:c.73+17033_73+17043delinsCTTGAAGATAA ENSP00000483275.1:n.73+17033_73+17043deli...
ENST00000613374.4:c.158+17033_158+17043delinsCTTGAAGATAA ENSP00000484464.1:n.158+17033_158+17043de...
ENST00000613706.4:c.215+4682_215+4692delinsCTTGAAGATAA ENSP00000484976.1:n.215+4682_215+4692deli...
ENST00000617164.4:c.225_235delinsCTTGAAGATAA ENSP00000480470.1:p.Asp75=
ENST00000619009.4:c.282_292delinsCTTGAAGATAA ENSP00000482293.1:p.Asp94=
ENST00000620057.4:c.282_292delinsCTTGAAGATAA ENSP00000481988.1:p.Asp94=
NM_000465.3:c.282_292delinsCTTGAAGATAA NP_000456.2:p.Asp94=
NM_001282543.1:c.225_235delinsCTTGAAGATAA NP_001269472.1:p.Asp75=
NM_001282545.1:c.215+4682_215+4692delinsCTTGAAGATAA NP_001269474.1:n.215+4682_215+4692delinsC...
NM_001282548.1:c.158+17033_158+17043delinsCTTGAAGATAA NP_001269477.1:n.158+17033_158+17043delin...
NM_001282549.1:c.282_292delinsCTTGAAGATAA NP_001269478.1:p.Asp94=
NR_104212.1:n.357+4682_357+4692delinsCTTGAAGATAA
NR_104215.1:n.301-10870_301-10860delinsCTTGAAGATAA
NR_104216.1:n.424_434delinsCTTGAAGATAA
XM_011511567.1:c.228_238delinsCTTGAAGATAA XP_011509869.1:p.Asp76=
XM_011511568.1:c.282_292delinsCTTGAAGATAA XP_011509870.1:p.Asp94=
XM_017004613.1:c.381_391delinsCTTGAAGATAA XP_016860102.1:p.Asp127=
XM_017004614.1:c.381_391delinsCTTGAAGATAA XP_016860103.1:p.Asp127=
XR_002959322.1:n.472_482delinsCTTGAAGATAA
NM_000465.4:c.282_292delinsCTTGAAGATAA MANE Select NP_000456.2:p.Asp94=
NM_001282543.2:c.225_235delinsCTTGAAGATAA NP_001269472.1:p.Asp75=
NM_001282545.2:c.215+4682_215+4692delinsCTTGAAGATAA NP_001269474.1:n.215+4682_215+4692delinsC...
NM_001282548.2:c.158+17033_158+17043delinsCTTGAAGATAA NP_001269477.1:n.158+17033_158+17043delin...
NM_001282549.2:c.282_292delinsCTTGAAGATAA NP_001269478.1:p.Asp94=
NR_104212.2:n.329+4682_329+4692delinsCTTGAAGATAA
NR_104215.2:n.273-10870_273-10860delinsCTTGAAGATAA
NR_104216.2:n.396_406delinsCTTGAAGATAA