Canonical Allele Identifier: CA1327076711

Gene: BARD1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214792394_214792395delinsCG , CM000664.2:g.214792394_214792395delinsCG	GRCh38
NC_000002.11:g.215657118_215657119delinsCG , CM000664.1:g.215657118_215657119delinsCG	GRCh37
NC_000002.10:g.215365363_215365364delinsCG	NCBI36
NG_012047.2:g.22310_22311delinsCG
NG_012047.3:g.22317_22318delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.266_267delinsCG MANE Select	ENSP00000260947.4:p.Pro89=
ENST00000421162.2:c.215+4666_215+4667delinsCG	ENSP00000392245.2:n.215+4666_215+4667delinsCG
ENST00000613192.2:c.158+17017_158+17018delinsCG	ENSP00000483275.2:n.158+17017_158+17018delinsCG
ENST00000613374.5:c.158+17017_158+17018delinsCG	ENSP00000484464.1:n.158+17017_158+17018delinsCG
ENST00000613706.5:c.266_267delinsCG	ENSP00000484976.2:p.Pro89=
ENST00000617164.5:c.209_210delinsCG	ENSP00000480470.1:p.Pro70=
ENST00000619009.5:c.266_267delinsCG	ENSP00000482293.1:p.Pro89=
ENST00000650978.1:c.108_109delinsCG
ENST00000260947.8:c.266_267delinsCG	ENSP00000260947.4:p.Pro89=
ENST00000421162.1:c.215+4666_215+4667delinsCG	ENSP00000392245.1:n.215+4666_215+4667delinsCG
ENST00000455743.5:c.215+4666_215+4667delinsCG	ENSP00000412186.1:n.215+4666_215+4667delinsCG
ENST00000471787.1:n.260-10886_260-10885delinsCG
ENST00000613192.1:c.73+17017_73+17018delinsCG	ENSP00000483275.1:n.73+17017_73+17018delinsCG
ENST00000613374.4:c.158+17017_158+17018delinsCG	ENSP00000484464.1:n.158+17017_158+17018delinsCG
ENST00000613706.4:c.215+4666_215+4667delinsCG	ENSP00000484976.1:n.215+4666_215+4667delinsCG
ENST00000617164.4:c.209_210delinsCG	ENSP00000480470.1:p.Pro70=
ENST00000619009.4:c.266_267delinsCG	ENSP00000482293.1:p.Pro89=
ENST00000620057.4:c.266_267delinsCG	ENSP00000481988.1:p.Pro89=
NM_000465.3:c.266_267delinsCG	NP_000456.2:p.Pro89=
NM_001282543.1:c.209_210delinsCG	NP_001269472.1:p.Pro70=
NM_001282545.1:c.215+4666_215+4667delinsCG	NP_001269474.1:n.215+4666_215+4667delinsCG
NM_001282548.1:c.158+17017_158+17018delinsCG	NP_001269477.1:n.158+17017_158+17018delinsCG
NM_001282549.1:c.266_267delinsCG	NP_001269478.1:p.Pro89=
NR_104212.1:n.357+4666_357+4667delinsCG
NR_104215.1:n.301-10886_301-10885delinsCG
NR_104216.1:n.408_409delinsCG
XM_011511567.1:c.212_213delinsCG	XP_011509869.1:p.Pro71=
XM_011511568.1:c.266_267delinsCG	XP_011509870.1:p.Pro89=
XM_017004613.1:c.365_366delinsCG	XP_016860102.1:p.Pro122=
XM_017004614.1:c.365_366delinsCG	XP_016860103.1:p.Pro122=
XR_002959322.1:n.456_457delinsCG
NM_000465.4:c.266_267delinsCG MANE Select	NP_000456.2:p.Pro89=
NM_001282543.2:c.209_210delinsCG	NP_001269472.1:p.Pro70=
NM_001282545.2:c.215+4666_215+4667delinsCG	NP_001269474.1:n.215+4666_215+4667delinsCG
NM_001282548.2:c.158+17017_158+17018delinsCG	NP_001269477.1:n.158+17017_158+17018delinsCG
NM_001282549.2:c.266_267delinsCG	NP_001269478.1:p.Pro89=
NR_104212.2:n.329+4666_329+4667delinsCG
NR_104215.2:n.273-10886_273-10885delinsCG
NR_104216.2:n.380_381delinsCG