Canonical Allele Identifier: CA1327071525

Gene: BARD1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214781451_214781454delinsATTC , CM000664.2:g.214781451_214781454delinsATTC	GRCh38
NC_000002.11:g.215646175_215646178delinsATTC , CM000664.1:g.215646175_215646178delinsATTC	GRCh37
NC_000002.10:g.215354420_215354423delinsATTC	NCBI36
NG_012047.2:g.33251_33254delinsGAAT
NG_012047.3:g.33258_33261delinsGAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.420_423delinsGAAT MANE Select	ENSP00000260947.4:p.Lys140=
ENST00000421162.2:c.215+15607_215+15610delinsGAAT	ENSP00000392245.2:n.215+15607_215+15610delinsGAAT
ENST00000613192.2:c.158+27958_158+27961delinsGAAT	ENSP00000483275.2:n.158+27958_158+27961delinsGAAT
ENST00000613374.5:c.158+27958_158+27961delinsGAAT	ENSP00000484464.1:n.158+27958_158+27961delinsGAAT
ENST00000613706.5:c.420_423delinsGAAT	ENSP00000484976.2:p.Lys140=
ENST00000617164.5:c.363_366delinsGAAT	ENSP00000480470.1:p.Lys121=
ENST00000619009.5:c.364+10843_364+10846delinsGAAT	ENSP00000482293.1:n.364+10843_364+10846delinsGAAT
ENST00000650978.1:c.262_265delinsGAAT
ENST00000260947.8:c.420_423delinsGAAT	ENSP00000260947.4:p.Lys140=
ENST00000421162.1:c.215+15607_215+15610delinsGAAT	ENSP00000392245.1:n.215+15607_215+15610delinsGAAT
ENST00000455743.5:c.*40_*43delinsGAAT	ENSP00000412186.1:n.*40_*43delinsGAAT
ENST00000471787.1:n.315_318delinsGAAT
ENST00000613192.1:c.73+27958_73+27961delinsGAAT	ENSP00000483275.1:n.73+27958_73+27961delinsGAAT
ENST00000613374.4:c.158+27958_158+27961delinsGAAT	ENSP00000484464.1:n.158+27958_158+27961delinsGAAT
ENST00000613706.4:c.215+15607_215+15610delinsGAAT	ENSP00000484976.1:n.215+15607_215+15610delinsGAAT
ENST00000617164.4:c.363_366delinsGAAT	ENSP00000480470.1:p.Lys121=
ENST00000619009.4:c.364+10843_364+10846delinsGAAT	ENSP00000482293.1:n.364+10843_364+10846delinsGAAT
ENST00000620057.4:c.364+10843_364+10846delinsGAAT	ENSP00000481988.1:n.364+10843_364+10846delinsGAAT
NM_000465.3:c.420_423delinsGAAT	NP_000456.2:p.Lys140=
NM_001282543.1:c.363_366delinsGAAT	NP_001269472.1:p.Lys121=
NM_001282545.1:c.215+15607_215+15610delinsGAAT	NP_001269474.1:n.215+15607_215+15610delinsGAAT
NM_001282548.1:c.158+27958_158+27961delinsGAAT	NP_001269477.1:n.158+27958_158+27961delinsGAAT
NM_001282549.1:c.364+10843_364+10846delinsGAAT	NP_001269478.1:n.364+10843_364+10846delinsGAAT
NR_104212.1:n.413_416delinsGAAT
NR_104215.1:n.356_359delinsGAAT
NR_104216.1:n.506+10843_506+10846delinsGAAT
XM_011511567.1:c.366_369delinsGAAT	XP_011509869.1:p.Lys122=
XM_011511568.1:c.420_423delinsGAAT	XP_011509870.1:p.Lys140=
XM_017004613.1:c.519_522delinsGAAT	XP_016860102.1:p.Lys173=
XM_017004614.1:c.519_522delinsGAAT	XP_016860103.1:p.Lys173=
XR_002959322.1:n.610_613delinsGAAT
NM_000465.4:c.420_423delinsGAAT MANE Select	NP_000456.2:p.Lys140=
NM_001282543.2:c.363_366delinsGAAT	NP_001269472.1:p.Lys121=
NM_001282545.2:c.215+15607_215+15610delinsGAAT	NP_001269474.1:n.215+15607_215+15610delinsGAAT
NM_001282548.2:c.158+27958_158+27961delinsGAAT	NP_001269477.1:n.158+27958_158+27961delinsGAAT
NM_001282549.2:c.364+10843_364+10846delinsGAAT	NP_001269478.1:n.364+10843_364+10846delinsGAAT
NR_104212.2:n.385_388delinsGAAT
NR_104215.2:n.328_331delinsGAAT
NR_104216.2:n.478+10843_478+10846delinsGAAT