Canonical Allele Identifier: CA1327076741

Gene: BARD1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214792434C= , CM000664.2:g.214792434C=	GRCh38
NC_000002.11:g.215657158C= , CM000664.1:g.215657158C=	GRCh37
NC_000002.10:g.215365403C=	NCBI36
NG_012047.2:g.22271G=
NG_012047.3:g.22278G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.227G= MANE Select	ENSP00000260947.4:p.Ser76=
ENST00000421162.2:c.215+4627G=	ENSP00000392245.2:n.215+4627G=
ENST00000613192.2:c.158+16978G=	ENSP00000483275.2:n.158+16978G=
ENST00000613374.5:c.158+16978G=	ENSP00000484464.1:n.158+16978G=
ENST00000613706.5:c.227G=	ENSP00000484976.2:p.Ser76=
ENST00000617164.5:c.170G=	ENSP00000480470.1:p.Ser57=
ENST00000619009.5:c.227G=	ENSP00000482293.1:p.Ser76=
ENST00000650978.1:c.69G=
ENST00000260947.8:c.227G=	ENSP00000260947.4:p.Ser76=
ENST00000421162.1:c.215+4627G=	ENSP00000392245.1:n.215+4627G=
ENST00000455743.5:c.215+4627G=	ENSP00000412186.1:n.215+4627G=
ENST00000471787.1:n.260-10925G=
ENST00000613192.1:c.73+16978G=	ENSP00000483275.1:n.73+16978G=
ENST00000613374.4:c.158+16978G=	ENSP00000484464.1:n.158+16978G=
ENST00000613706.4:c.215+4627G=	ENSP00000484976.1:n.215+4627G=
ENST00000617164.4:c.170G=	ENSP00000480470.1:p.Ser57=
ENST00000619009.4:c.227G=	ENSP00000482293.1:p.Ser76=
ENST00000620057.4:c.227G=	ENSP00000481988.1:p.Ser76=
NM_000465.3:c.227G=	NP_000456.2:p.Ser76=
NM_001282543.1:c.170G=	NP_001269472.1:p.Ser57=
NM_001282545.1:c.215+4627G=	NP_001269474.1:n.215+4627G=
NM_001282548.1:c.158+16978G=	NP_001269477.1:n.158+16978G=
NM_001282549.1:c.227G=	NP_001269478.1:p.Ser76=
NR_104212.1:n.357+4627G=
NR_104215.1:n.301-10925G=
NR_104216.1:n.369G=
XM_011511567.1:c.173G=	XP_011509869.1:p.Ser58=
XM_011511568.1:c.227G=	XP_011509870.1:p.Ser76=
XM_017004613.1:c.326G=	XP_016860102.1:p.Ser109=
XM_017004614.1:c.326G=	XP_016860103.1:p.Ser109=
XR_002959322.1:n.417G=
NM_000465.4:c.227G= MANE Select	NP_000456.2:p.Ser76=
NM_001282543.2:c.170G=	NP_001269472.1:p.Ser57=
NM_001282545.2:c.215+4627G=	NP_001269474.1:n.215+4627G=
NM_001282548.2:c.158+16978G=	NP_001269477.1:n.158+16978G=
NM_001282549.2:c.227G=	NP_001269478.1:p.Ser76=
NR_104212.2:n.329+4627G=
NR_104215.2:n.273-10925G=
NR_104216.2:n.341G=