Canonical Allele Identifier: CA2662972070

Gene: BARD1

Linked Data

• gnomAD v4: 2-214792458-TAAAAA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214792470_214792474del , CM000664.2:g.214792470_214792474del	GRCh38
NC_000002.11:g.215657194_215657198del , CM000664.1:g.215657194_215657198del	GRCh37
NC_000002.10:g.215365439_215365443del	NCBI36
NG_012047.2:g.22242_22246del
NG_012047.3:g.22249_22253del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.216-18_216-14del MANE Select	ENSP00000260947.4:n.216-18_216-14del
ENST00000421162.2:c.215+4598_215+4602del	ENSP00000392245.2:n.215+4598_215+4602del
ENST00000613192.2:c.158+16949_158+16953del	ENSP00000483275.2:n.158+16949_158+16953del
ENST00000613374.5:c.158+16949_158+16953del	ENSP00000484464.1:n.158+16949_158+16953del
ENST00000613706.5:c.216-18_216-14del	ENSP00000484976.2:n.216-18_216-14del
ENST00000617164.5:c.159-18_159-14del	ENSP00000480470.1:n.159-18_159-14del
ENST00000619009.5:c.216-18_216-14del	ENSP00000482293.1:n.216-18_216-14del
ENST00000650978.1:c.58-18_58-14del
ENST00000260947.8:c.216-18_216-14del	ENSP00000260947.4:n.216-18_216-14del
ENST00000421162.1:c.215+4598_215+4602del	ENSP00000392245.1:n.215+4598_215+4602del
ENST00000455743.5:c.215+4598_215+4602del	ENSP00000412186.1:n.215+4598_215+4602del
ENST00000471787.1:n.260-10954_260-10950del
ENST00000613192.1:c.73+16949_73+16953del	ENSP00000483275.1:n.73+16949_73+16953del
ENST00000613374.4:c.158+16949_158+16953del	ENSP00000484464.1:n.158+16949_158+16953del
ENST00000613706.4:c.215+4598_215+4602del	ENSP00000484976.1:n.215+4598_215+4602del
ENST00000617164.4:c.159-18_159-14del	ENSP00000480470.1:n.159-18_159-14del
ENST00000619009.4:c.216-18_216-14del	ENSP00000482293.1:n.216-18_216-14del
ENST00000620057.4:c.216-18_216-14del	ENSP00000481988.1:n.216-18_216-14del
NM_000465.3:c.216-18_216-14del	NP_000456.2:n.216-18_216-14del
NM_001282543.1:c.159-18_159-14del	NP_001269472.1:n.159-18_159-14del
NM_001282545.1:c.215+4598_215+4602del	NP_001269474.1:n.215+4598_215+4602del
NM_001282548.1:c.158+16949_158+16953del	NP_001269477.1:n.158+16949_158+16953del
NM_001282549.1:c.216-18_216-14del	NP_001269478.1:n.216-18_216-14del
NR_104212.1:n.357+4598_357+4602del
NR_104215.1:n.301-10954_301-10950del
NR_104216.1:n.358-18_358-14del
XM_011511567.1:c.162-18_162-14del	XP_011509869.1:n.162-18_162-14del
XM_011511568.1:c.216-18_216-14del	XP_011509870.1:n.216-18_216-14del
XM_017004613.1:c.315-18_315-14del	XP_016860102.1:n.315-18_315-14del
XM_017004614.1:c.315-18_315-14del	XP_016860103.1:n.315-18_315-14del
XR_002959322.1:n.406-18_406-14del
NM_000465.4:c.216-18_216-14del MANE Select	NP_000456.2:n.216-18_216-14del
NM_001282543.2:c.159-18_159-14del	NP_001269472.1:n.159-18_159-14del
NM_001282545.2:c.215+4598_215+4602del	NP_001269474.1:n.215+4598_215+4602del
NM_001282548.2:c.158+16949_158+16953del	NP_001269477.1:n.158+16949_158+16953del
NM_001282549.2:c.216-18_216-14del	NP_001269478.1:n.216-18_216-14del
NR_104212.2:n.329+4598_329+4602del
NR_104215.2:n.273-10954_273-10950del
NR_104216.2:n.330-18_330-14del