Canonical Allele Identifier: CA1327076874

Gene: BARD1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214792704_214792705delinsAG , CM000664.2:g.214792704_214792705delinsAG	GRCh38
NC_000002.11:g.215657428_215657429delinsAG , CM000664.1:g.215657428_215657429delinsAG	GRCh37
NC_000002.10:g.215365673_215365674delinsAG	NCBI36
NG_012047.2:g.22000_22001delinsCT
NG_012047.3:g.22007_22008delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.216-260_216-259delinsCT MANE Select	ENSP00000260947.4:n.216-260_216-259delinsCT
ENST00000421162.2:c.215+4356_215+4357delinsCT	ENSP00000392245.2:n.215+4356_215+4357delinsCT
ENST00000613192.2:c.158+16707_158+16708delinsCT	ENSP00000483275.2:n.158+16707_158+16708delinsCT
ENST00000613374.5:c.158+16707_158+16708delinsCT	ENSP00000484464.1:n.158+16707_158+16708delinsCT
ENST00000613706.5:c.216-260_216-259delinsCT	ENSP00000484976.2:n.216-260_216-259delinsCT
ENST00000617164.5:c.159-260_159-259delinsCT	ENSP00000480470.1:n.159-260_159-259delinsCT
ENST00000619009.5:c.216-260_216-259delinsCT	ENSP00000482293.1:n.216-260_216-259delinsCT
ENST00000650978.1:c.58-260_58-259delinsCT
ENST00000260947.8:c.216-260_216-259delinsCT	ENSP00000260947.4:n.216-260_216-259delinsCT
ENST00000421162.1:c.215+4356_215+4357delinsCT	ENSP00000392245.1:n.215+4356_215+4357delinsCT
ENST00000455743.5:c.215+4356_215+4357delinsCT	ENSP00000412186.1:n.215+4356_215+4357delinsCT
ENST00000471787.1:n.260-11196_260-11195delinsCT
ENST00000613192.1:c.73+16707_73+16708delinsCT	ENSP00000483275.1:n.73+16707_73+16708delinsCT
ENST00000613374.4:c.158+16707_158+16708delinsCT	ENSP00000484464.1:n.158+16707_158+16708delinsCT
ENST00000613706.4:c.215+4356_215+4357delinsCT	ENSP00000484976.1:n.215+4356_215+4357delinsCT
ENST00000617164.4:c.159-260_159-259delinsCT	ENSP00000480470.1:n.159-260_159-259delinsCT
ENST00000619009.4:c.216-260_216-259delinsCT	ENSP00000482293.1:n.216-260_216-259delinsCT
ENST00000620057.4:c.216-260_216-259delinsCT	ENSP00000481988.1:n.216-260_216-259delinsCT
NM_000465.3:c.216-260_216-259delinsCT	NP_000456.2:n.216-260_216-259delinsCT
NM_001282543.1:c.159-260_159-259delinsCT	NP_001269472.1:n.159-260_159-259delinsCT
NM_001282545.1:c.215+4356_215+4357delinsCT	NP_001269474.1:n.215+4356_215+4357delinsCT
NM_001282548.1:c.158+16707_158+16708delinsCT	NP_001269477.1:n.158+16707_158+16708delinsCT
NM_001282549.1:c.216-260_216-259delinsCT	NP_001269478.1:n.216-260_216-259delinsCT
NR_104212.1:n.357+4356_357+4357delinsCT
NR_104215.1:n.301-11196_301-11195delinsCT
NR_104216.1:n.358-260_358-259delinsCT
XM_011511567.1:c.162-260_162-259delinsCT	XP_011509869.1:n.162-260_162-259delinsCT
XM_011511568.1:c.216-260_216-259delinsCT	XP_011509870.1:n.216-260_216-259delinsCT
XM_017004613.1:c.315-260_315-259delinsCT	XP_016860102.1:n.315-260_315-259delinsCT
XM_017004614.1:c.315-260_315-259delinsCT	XP_016860103.1:n.315-260_315-259delinsCT
XR_002959322.1:n.406-260_406-259delinsCT
NM_000465.4:c.216-260_216-259delinsCT MANE Select	NP_000456.2:n.216-260_216-259delinsCT
NM_001282543.2:c.159-260_159-259delinsCT	NP_001269472.1:n.159-260_159-259delinsCT
NM_001282545.2:c.215+4356_215+4357delinsCT	NP_001269474.1:n.215+4356_215+4357delinsCT
NM_001282548.2:c.158+16707_158+16708delinsCT	NP_001269477.1:n.158+16707_158+16708delinsCT
NM_001282549.2:c.216-260_216-259delinsCT	NP_001269478.1:n.216-260_216-259delinsCT
NR_104212.2:n.329+4356_329+4357delinsCT
NR_104215.2:n.273-11196_273-11195delinsCT
NR_104216.2:n.330-260_330-259delinsCT