Canonical Allele Identifier: CA1327076768

Gene: BARD1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214792458_214792462delinsTAAAA , CM000664.2:g.214792458_214792462delinsTAAAA	GRCh38
NC_000002.11:g.215657182_215657186delinsTAAAA , CM000664.1:g.215657182_215657186delinsTAAAA	GRCh37
NC_000002.10:g.215365427_215365431delinsTAAAA	NCBI36
NG_012047.2:g.22243_22247delinsTTTTA
NG_012047.3:g.22250_22254delinsTTTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.216-17_216-13delinsTTTTA MANE Select	ENSP00000260947.4:n.216-17_216-13delinsTTTTA
ENST00000421162.2:c.215+4599_215+4603delinsTTTTA	ENSP00000392245.2:n.215+4599_215+4603delinsTTTTA
ENST00000613192.2:c.158+16950_158+16954delinsTTTTA	ENSP00000483275.2:n.158+16950_158+16954delinsTTTTA
ENST00000613374.5:c.158+16950_158+16954delinsTTTTA	ENSP00000484464.1:n.158+16950_158+16954delinsTTTTA
ENST00000613706.5:c.216-17_216-13delinsTTTTA	ENSP00000484976.2:n.216-17_216-13delinsTTTTA
ENST00000617164.5:c.159-17_159-13delinsTTTTA	ENSP00000480470.1:n.159-17_159-13delinsTTTTA
ENST00000619009.5:c.216-17_216-13delinsTTTTA	ENSP00000482293.1:n.216-17_216-13delinsTTTTA
ENST00000650978.1:c.58-17_58-13delinsTTTTA
ENST00000260947.8:c.216-17_216-13delinsTTTTA	ENSP00000260947.4:n.216-17_216-13delinsTTTTA
ENST00000421162.1:c.215+4599_215+4603delinsTTTTA	ENSP00000392245.1:n.215+4599_215+4603delinsTTTTA
ENST00000455743.5:c.215+4599_215+4603delinsTTTTA	ENSP00000412186.1:n.215+4599_215+4603delinsTTTTA
ENST00000471787.1:n.260-10953_260-10949delinsTTTTA
ENST00000613192.1:c.73+16950_73+16954delinsTTTTA	ENSP00000483275.1:n.73+16950_73+16954delinsTTTTA
ENST00000613374.4:c.158+16950_158+16954delinsTTTTA	ENSP00000484464.1:n.158+16950_158+16954delinsTTTTA
ENST00000613706.4:c.215+4599_215+4603delinsTTTTA	ENSP00000484976.1:n.215+4599_215+4603delinsTTTTA
ENST00000617164.4:c.159-17_159-13delinsTTTTA	ENSP00000480470.1:n.159-17_159-13delinsTTTTA
ENST00000619009.4:c.216-17_216-13delinsTTTTA	ENSP00000482293.1:n.216-17_216-13delinsTTTTA
ENST00000620057.4:c.216-17_216-13delinsTTTTA	ENSP00000481988.1:n.216-17_216-13delinsTTTTA
NM_000465.3:c.216-17_216-13delinsTTTTA	NP_000456.2:n.216-17_216-13delinsTTTTA
NM_001282543.1:c.159-17_159-13delinsTTTTA	NP_001269472.1:n.159-17_159-13delinsTTTTA
NM_001282545.1:c.215+4599_215+4603delinsTTTTA	NP_001269474.1:n.215+4599_215+4603delinsTTTTA
NM_001282548.1:c.158+16950_158+16954delinsTTTTA	NP_001269477.1:n.158+16950_158+16954delinsTTTTA
NM_001282549.1:c.216-17_216-13delinsTTTTA	NP_001269478.1:n.216-17_216-13delinsTTTTA
NR_104212.1:n.357+4599_357+4603delinsTTTTA
NR_104215.1:n.301-10953_301-10949delinsTTTTA
NR_104216.1:n.358-17_358-13delinsTTTTA
XM_011511567.1:c.162-17_162-13delinsTTTTA	XP_011509869.1:n.162-17_162-13delinsTTTTA
XM_011511568.1:c.216-17_216-13delinsTTTTA	XP_011509870.1:n.216-17_216-13delinsTTTTA
XM_017004613.1:c.315-17_315-13delinsTTTTA	XP_016860102.1:n.315-17_315-13delinsTTTTA
XM_017004614.1:c.315-17_315-13delinsTTTTA	XP_016860103.1:n.315-17_315-13delinsTTTTA
XR_002959322.1:n.406-17_406-13delinsTTTTA
NM_000465.4:c.216-17_216-13delinsTTTTA MANE Select	NP_000456.2:n.216-17_216-13delinsTTTTA
NM_001282543.2:c.159-17_159-13delinsTTTTA	NP_001269472.1:n.159-17_159-13delinsTTTTA
NM_001282545.2:c.215+4599_215+4603delinsTTTTA	NP_001269474.1:n.215+4599_215+4603delinsTTTTA
NM_001282548.2:c.158+16950_158+16954delinsTTTTA	NP_001269477.1:n.158+16950_158+16954delinsTTTTA
NM_001282549.2:c.216-17_216-13delinsTTTTA	NP_001269478.1:n.216-17_216-13delinsTTTTA
NR_104212.2:n.329+4599_329+4603delinsTTTTA
NR_104215.2:n.273-10953_273-10949delinsTTTTA
NR_104216.2:n.330-17_330-13delinsTTTTA