Canonical Allele Identifier: CA1327071529

Gene: BARD1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214781454_214781461delinsCTTCTTGT , CM000664.2:g.214781454_214781461delinsCTTCTTGT	GRCh38
NC_000002.11:g.215646178_215646185delinsCTTCTTGT , CM000664.1:g.215646178_215646185delinsCTTCTTGT	GRCh37
NC_000002.10:g.215354423_215354430delinsCTTCTTGT	NCBI36
NG_012047.2:g.33244_33251delinsACAAGAAG
NG_012047.3:g.33251_33258delinsACAAGAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.413_420delinsACAAGAAG MANE Select	ENSP00000260947.4:p.Asn138=
ENST00000421162.2:c.215+15600_215+15607delinsACAAGAAG	ENSP00000392245.2:n.215+15600_215+15607delinsACAAGAAG
ENST00000613192.2:c.158+27951_158+27958delinsACAAGAAG	ENSP00000483275.2:n.158+27951_158+27958delinsACAAGAAG
ENST00000613374.5:c.158+27951_158+27958delinsACAAGAAG	ENSP00000484464.1:n.158+27951_158+27958delinsACAAGAAG
ENST00000613706.5:c.413_420delinsACAAGAAG	ENSP00000484976.2:p.Asn138=
ENST00000617164.5:c.356_363delinsACAAGAAG	ENSP00000480470.1:p.Asn119=
ENST00000619009.5:c.364+10836_364+10843delinsACAAGAAG	ENSP00000482293.1:n.364+10836_364+10843delinsACAAGAAG
ENST00000650978.1:c.255_262delinsACAAGAAG
ENST00000260947.8:c.413_420delinsACAAGAAG	ENSP00000260947.4:p.Asn138=
ENST00000421162.1:c.215+15600_215+15607delinsACAAGAAG	ENSP00000392245.1:n.215+15600_215+15607delinsACAAGAAG
ENST00000455743.5:c.*33_*40delinsACAAGAAG	ENSP00000412186.1:n.*33_*40delinsACAAGAAG
ENST00000471787.1:n.308_315delinsACAAGAAG
ENST00000613192.1:c.73+27951_73+27958delinsACAAGAAG	ENSP00000483275.1:n.73+27951_73+27958delinsACAAGAAG
ENST00000613374.4:c.158+27951_158+27958delinsACAAGAAG	ENSP00000484464.1:n.158+27951_158+27958delinsACAAGAAG
ENST00000613706.4:c.215+15600_215+15607delinsACAAGAAG	ENSP00000484976.1:n.215+15600_215+15607delinsACAAGAAG
ENST00000617164.4:c.356_363delinsACAAGAAG	ENSP00000480470.1:p.Asn119=
ENST00000619009.4:c.364+10836_364+10843delinsACAAGAAG	ENSP00000482293.1:n.364+10836_364+10843delinsACAAGAAG
ENST00000620057.4:c.364+10836_364+10843delinsACAAGAAG	ENSP00000481988.1:n.364+10836_364+10843delinsACAAGAAG
NM_000465.3:c.413_420delinsACAAGAAG	NP_000456.2:p.Asn138=
NM_001282543.1:c.356_363delinsACAAGAAG	NP_001269472.1:p.Asn119=
NM_001282545.1:c.215+15600_215+15607delinsACAAGAAG	NP_001269474.1:n.215+15600_215+15607delinsACAAGAAG
NM_001282548.1:c.158+27951_158+27958delinsACAAGAAG	NP_001269477.1:n.158+27951_158+27958delinsACAAGAAG
NM_001282549.1:c.364+10836_364+10843delinsACAAGAAG	NP_001269478.1:n.364+10836_364+10843delinsACAAGAAG
NR_104212.1:n.406_413delinsACAAGAAG
NR_104215.1:n.349_356delinsACAAGAAG
NR_104216.1:n.506+10836_506+10843delinsACAAGAAG
XM_011511567.1:c.359_366delinsACAAGAAG	XP_011509869.1:p.Asn120=
XM_011511568.1:c.413_420delinsACAAGAAG	XP_011509870.1:p.Asn138=
XM_017004613.1:c.512_519delinsACAAGAAG	XP_016860102.1:p.Asn171=
XM_017004614.1:c.512_519delinsACAAGAAG	XP_016860103.1:p.Asn171=
XR_002959322.1:n.603_610delinsACAAGAAG
NM_000465.4:c.413_420delinsACAAGAAG MANE Select	NP_000456.2:p.Asn138=
NM_001282543.2:c.356_363delinsACAAGAAG	NP_001269472.1:p.Asn119=
NM_001282545.2:c.215+15600_215+15607delinsACAAGAAG	NP_001269474.1:n.215+15600_215+15607delinsACAAGAAG
NM_001282548.2:c.158+27951_158+27958delinsACAAGAAG	NP_001269477.1:n.158+27951_158+27958delinsACAAGAAG
NM_001282549.2:c.364+10836_364+10843delinsACAAGAAG	NP_001269478.1:n.364+10836_364+10843delinsACAAGAAG
NR_104212.2:n.378_385delinsACAAGAAG
NR_104215.2:n.321_328delinsACAAGAAG
NR_104216.2:n.478+10836_478+10843delinsACAAGAAG