Canonical Allele Identifier: CA1327076880

Gene: BARD1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214792720_214792721delinsAG , CM000664.2:g.214792720_214792721delinsAG	GRCh38
NC_000002.11:g.215657444_215657445delinsAG , CM000664.1:g.215657444_215657445delinsAG	GRCh37
NC_000002.10:g.215365689_215365690delinsAG	NCBI36
NG_012047.2:g.21984_21985delinsCT
NG_012047.3:g.21991_21992delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.216-276_216-275delinsCT MANE Select	ENSP00000260947.4:n.216-276_216-275delinsCT
ENST00000421162.2:c.215+4340_215+4341delinsCT	ENSP00000392245.2:n.215+4340_215+4341delinsCT
ENST00000613192.2:c.158+16691_158+16692delinsCT	ENSP00000483275.2:n.158+16691_158+16692delinsCT
ENST00000613374.5:c.158+16691_158+16692delinsCT	ENSP00000484464.1:n.158+16691_158+16692delinsCT
ENST00000613706.5:c.216-276_216-275delinsCT	ENSP00000484976.2:n.216-276_216-275delinsCT
ENST00000617164.5:c.159-276_159-275delinsCT	ENSP00000480470.1:n.159-276_159-275delinsCT
ENST00000619009.5:c.216-276_216-275delinsCT	ENSP00000482293.1:n.216-276_216-275delinsCT
ENST00000650978.1:c.58-276_58-275delinsCT
ENST00000260947.8:c.216-276_216-275delinsCT	ENSP00000260947.4:n.216-276_216-275delinsCT
ENST00000421162.1:c.215+4340_215+4341delinsCT	ENSP00000392245.1:n.215+4340_215+4341delinsCT
ENST00000455743.5:c.215+4340_215+4341delinsCT	ENSP00000412186.1:n.215+4340_215+4341delinsCT
ENST00000471787.1:n.260-11212_260-11211delinsCT
ENST00000613192.1:c.73+16691_73+16692delinsCT	ENSP00000483275.1:n.73+16691_73+16692delinsCT
ENST00000613374.4:c.158+16691_158+16692delinsCT	ENSP00000484464.1:n.158+16691_158+16692delinsCT
ENST00000613706.4:c.215+4340_215+4341delinsCT	ENSP00000484976.1:n.215+4340_215+4341delinsCT
ENST00000617164.4:c.159-276_159-275delinsCT	ENSP00000480470.1:n.159-276_159-275delinsCT
ENST00000619009.4:c.216-276_216-275delinsCT	ENSP00000482293.1:n.216-276_216-275delinsCT
ENST00000620057.4:c.216-276_216-275delinsCT	ENSP00000481988.1:n.216-276_216-275delinsCT
NM_000465.3:c.216-276_216-275delinsCT	NP_000456.2:n.216-276_216-275delinsCT
NM_001282543.1:c.159-276_159-275delinsCT	NP_001269472.1:n.159-276_159-275delinsCT
NM_001282545.1:c.215+4340_215+4341delinsCT	NP_001269474.1:n.215+4340_215+4341delinsCT
NM_001282548.1:c.158+16691_158+16692delinsCT	NP_001269477.1:n.158+16691_158+16692delinsCT
NM_001282549.1:c.216-276_216-275delinsCT	NP_001269478.1:n.216-276_216-275delinsCT
NR_104212.1:n.357+4340_357+4341delinsCT
NR_104215.1:n.301-11212_301-11211delinsCT
NR_104216.1:n.358-276_358-275delinsCT
XM_011511567.1:c.162-276_162-275delinsCT	XP_011509869.1:n.162-276_162-275delinsCT
XM_011511568.1:c.216-276_216-275delinsCT	XP_011509870.1:n.216-276_216-275delinsCT
XM_017004613.1:c.315-276_315-275delinsCT	XP_016860102.1:n.315-276_315-275delinsCT
XM_017004614.1:c.315-276_315-275delinsCT	XP_016860103.1:n.315-276_315-275delinsCT
XR_002959322.1:n.406-276_406-275delinsCT
NM_000465.4:c.216-276_216-275delinsCT MANE Select	NP_000456.2:n.216-276_216-275delinsCT
NM_001282543.2:c.159-276_159-275delinsCT	NP_001269472.1:n.159-276_159-275delinsCT
NM_001282545.2:c.215+4340_215+4341delinsCT	NP_001269474.1:n.215+4340_215+4341delinsCT
NM_001282548.2:c.158+16691_158+16692delinsCT	NP_001269477.1:n.158+16691_158+16692delinsCT
NM_001282549.2:c.216-276_216-275delinsCT	NP_001269478.1:n.216-276_216-275delinsCT
NR_104212.2:n.329+4340_329+4341delinsCT
NR_104215.2:n.273-11212_273-11211delinsCT
NR_104216.2:n.330-276_330-275delinsCT