Canonical Allele Identifier: CA2662971955

Gene: BARD1

Linked Data

• gnomAD v4: 2-214792150-TAAAAAA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214792163_214792168del , CM000664.2:g.214792163_214792168del	GRCh38
NC_000002.11:g.215656887_215656892del , CM000664.1:g.215656887_215656892del	GRCh37
NC_000002.10:g.215365132_215365137del	NCBI36
NG_012047.2:g.22549_22554del
NG_012047.3:g.22556_22561del

Transcript Alleles

HGVS	Amino-acid change
ENST00000260947.9:c.364+141_364+146del MANE Select	ENSP00000260947.4:n.364+141_364+146del
ENST00000421162.2:c.215+4905_215+4910del	ENSP00000392245.2:n.215+4905_215+4910del
ENST00000613192.2:c.158+17256_158+17261del	ENSP00000483275.2:n.158+17256_158+17261de...
ENST00000613374.5:c.158+17256_158+17261del	ENSP00000484464.1:n.158+17256_158+17261de...
ENST00000613706.5:c.364+141_364+146del	ENSP00000484976.2:n.364+141_364+146del
ENST00000617164.5:c.307+141_307+146del	ENSP00000480470.1:n.307+141_307+146del
ENST00000619009.5:c.364+141_364+146del	ENSP00000482293.1:n.364+141_364+146del
ENST00000650978.1:c.206+141_206+146del
ENST00000260947.8:c.364+141_364+146del	ENSP00000260947.4:n.364+141_364+146del
ENST00000421162.1:c.215+4905_215+4910del	ENSP00000392245.1:n.215+4905_215+4910del
ENST00000455743.5:c.215+4905_215+4910del	ENSP00000412186.1:n.215+4905_215+4910del
ENST00000471787.1:n.260-10647_260-10642del
ENST00000613192.1:c.73+17256_73+17261del	ENSP00000483275.1:n.73+17256_73+17261del
ENST00000613374.4:c.158+17256_158+17261del	ENSP00000484464.1:n.158+17256_158+17261de...
ENST00000613706.4:c.215+4905_215+4910del	ENSP00000484976.1:n.215+4905_215+4910del
ENST00000617164.4:c.307+141_307+146del	ENSP00000480470.1:n.307+141_307+146del
ENST00000619009.4:c.364+141_364+146del	ENSP00000482293.1:n.364+141_364+146del
ENST00000620057.4:c.364+141_364+146del	ENSP00000481988.1:n.364+141_364+146del
NM_000465.3:c.364+141_364+146del	NP_000456.2:n.364+141_364+146del
NM_001282543.1:c.307+141_307+146del	NP_001269472.1:n.307+141_307+146del
NM_001282545.1:c.215+4905_215+4910del	NP_001269474.1:n.215+4905_215+4910del
NM_001282548.1:c.158+17256_158+17261del	NP_001269477.1:n.158+17256_158+17261del
NM_001282549.1:c.364+141_364+146del	NP_001269478.1:n.364+141_364+146del
NR_104212.1:n.357+4905_357+4910del
NR_104215.1:n.301-10647_301-10642del
NR_104216.1:n.506+141_506+146del
XM_011511567.1:c.310+141_310+146del	XP_011509869.1:n.310+141_310+146del
XM_011511568.1:c.364+141_364+146del	XP_011509870.1:n.364+141_364+146del
XM_017004613.1:c.463+141_463+146del	XP_016860102.1:n.463+141_463+146del
XM_017004614.1:c.463+141_463+146del	XP_016860103.1:n.463+141_463+146del
XR_002959322.1:n.554+141_554+146del
NM_000465.4:c.364+141_364+146del MANE Select	NP_000456.2:n.364+141_364+146del
NM_001282543.2:c.307+141_307+146del	NP_001269472.1:n.307+141_307+146del
NM_001282545.2:c.215+4905_215+4910del	NP_001269474.1:n.215+4905_215+4910del
NM_001282548.2:c.158+17256_158+17261del	NP_001269477.1:n.158+17256_158+17261del
NM_001282549.2:c.364+141_364+146del	NP_001269478.1:n.364+141_364+146del
NR_104212.2:n.329+4905_329+4910del
NR_104215.2:n.273-10647_273-10642del
NR_104216.2:n.478+141_478+146del