Canonical Allele Identifier: CA1327076777

Gene: BARD1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214792473_214792475delinsAAG , CM000664.2:g.214792473_214792475delinsAAG	GRCh38
NC_000002.11:g.215657197_215657199delinsAAG , CM000664.1:g.215657197_215657199delinsAAG	GRCh37
NC_000002.10:g.215365442_215365444delinsAAG	NCBI36
NG_012047.2:g.22230_22232delinsCTT
NG_012047.3:g.22237_22239delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.216-30_216-28delinsCTT MANE Select	ENSP00000260947.4:n.216-30_216-28delinsCTT
ENST00000421162.2:c.215+4586_215+4588delinsCTT	ENSP00000392245.2:n.215+4586_215+4588delinsCTT
ENST00000613192.2:c.158+16937_158+16939delinsCTT	ENSP00000483275.2:n.158+16937_158+16939delinsCTT
ENST00000613374.5:c.158+16937_158+16939delinsCTT	ENSP00000484464.1:n.158+16937_158+16939delinsCTT
ENST00000613706.5:c.216-30_216-28delinsCTT	ENSP00000484976.2:n.216-30_216-28delinsCTT
ENST00000617164.5:c.159-30_159-28delinsCTT	ENSP00000480470.1:n.159-30_159-28delinsCTT
ENST00000619009.5:c.216-30_216-28delinsCTT	ENSP00000482293.1:n.216-30_216-28delinsCTT
ENST00000650978.1:c.58-30_58-28delinsCTT
ENST00000260947.8:c.216-30_216-28delinsCTT	ENSP00000260947.4:n.216-30_216-28delinsCTT
ENST00000421162.1:c.215+4586_215+4588delinsCTT	ENSP00000392245.1:n.215+4586_215+4588delinsCTT
ENST00000455743.5:c.215+4586_215+4588delinsCTT	ENSP00000412186.1:n.215+4586_215+4588delinsCTT
ENST00000471787.1:n.260-10966_260-10964delinsCTT
ENST00000613192.1:c.73+16937_73+16939delinsCTT	ENSP00000483275.1:n.73+16937_73+16939delinsCTT
ENST00000613374.4:c.158+16937_158+16939delinsCTT	ENSP00000484464.1:n.158+16937_158+16939delinsCTT
ENST00000613706.4:c.215+4586_215+4588delinsCTT	ENSP00000484976.1:n.215+4586_215+4588delinsCTT
ENST00000617164.4:c.159-30_159-28delinsCTT	ENSP00000480470.1:n.159-30_159-28delinsCTT
ENST00000619009.4:c.216-30_216-28delinsCTT	ENSP00000482293.1:n.216-30_216-28delinsCTT
ENST00000620057.4:c.216-30_216-28delinsCTT	ENSP00000481988.1:n.216-30_216-28delinsCTT
NM_000465.3:c.216-30_216-28delinsCTT	NP_000456.2:n.216-30_216-28delinsCTT
NM_001282543.1:c.159-30_159-28delinsCTT	NP_001269472.1:n.159-30_159-28delinsCTT
NM_001282545.1:c.215+4586_215+4588delinsCTT	NP_001269474.1:n.215+4586_215+4588delinsCTT
NM_001282548.1:c.158+16937_158+16939delinsCTT	NP_001269477.1:n.158+16937_158+16939delinsCTT
NM_001282549.1:c.216-30_216-28delinsCTT	NP_001269478.1:n.216-30_216-28delinsCTT
NR_104212.1:n.357+4586_357+4588delinsCTT
NR_104215.1:n.301-10966_301-10964delinsCTT
NR_104216.1:n.358-30_358-28delinsCTT
XM_011511567.1:c.162-30_162-28delinsCTT	XP_011509869.1:n.162-30_162-28delinsCTT
XM_011511568.1:c.216-30_216-28delinsCTT	XP_011509870.1:n.216-30_216-28delinsCTT
XM_017004613.1:c.315-30_315-28delinsCTT	XP_016860102.1:n.315-30_315-28delinsCTT
XM_017004614.1:c.315-30_315-28delinsCTT	XP_016860103.1:n.315-30_315-28delinsCTT
XR_002959322.1:n.406-30_406-28delinsCTT
NM_000465.4:c.216-30_216-28delinsCTT MANE Select	NP_000456.2:n.216-30_216-28delinsCTT
NM_001282543.2:c.159-30_159-28delinsCTT	NP_001269472.1:n.159-30_159-28delinsCTT
NM_001282545.2:c.215+4586_215+4588delinsCTT	NP_001269474.1:n.215+4586_215+4588delinsCTT
NM_001282548.2:c.158+16937_158+16939delinsCTT	NP_001269477.1:n.158+16937_158+16939delinsCTT
NM_001282549.2:c.216-30_216-28delinsCTT	NP_001269478.1:n.216-30_216-28delinsCTT
NR_104212.2:n.329+4586_329+4588delinsCTT
NR_104215.2:n.273-10966_273-10964delinsCTT
NR_104216.2:n.330-30_330-28delinsCTT