Canonical Allele Identifier: CA1327046366

Gene: BARD1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214730432G= , CM000664.2:g.214730432G=	GRCh38
NC_000002.11:g.215595156G= , CM000664.1:g.215595156G=	GRCh37
NC_000002.10:g.215303401G=	NCBI36
NG_012047.2:g.84273C=
NG_012047.3:g.84280C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.1980C= MANE Select	ENSP00000260947.4:p.Ser660=
ENST00000421162.2:c.627C=	ENSP00000392245.2:p.Ser209=
ENST00000613192.2:c.*43C=	ENSP00000483275.2:n.*43C=
ENST00000613374.5:c.570C=	ENSP00000484464.1:p.Ser190=
ENST00000613706.5:c.1572C=	ENSP00000484976.2:p.Ser524=
ENST00000617164.5:c.1923C=	ENSP00000480470.1:p.Ser641=
ENST00000619009.5:c.441C=	ENSP00000482293.1:p.Ser147=
ENST00000650978.1:c.3355C=
ENST00000260947.8:c.1980C=	ENSP00000260947.4:p.Ser660=
ENST00000421162.1:c.627C=	ENSP00000392245.1:p.Ser209=
ENST00000432456.5:c.77C=
ENST00000455743.5:c.*1600C=	ENSP00000412186.1:n.*1600C=
ENST00000471590.5:n.315C=
ENST00000613192.1:c.150C=	ENSP00000483275.1:p.Ser50=
ENST00000613374.4:c.570C=	ENSP00000484464.1:p.Ser190=
ENST00000613706.4:c.627C=	ENSP00000484976.1:p.Ser209=
ENST00000617164.4:c.1923C=	ENSP00000480470.1:p.Ser641=
ENST00000619009.4:c.441C=	ENSP00000482293.1:p.Ser147=
ENST00000620057.4:c.*646C=	ENSP00000481988.1:n.*646C=
NM_000465.3:c.1980C=	NP_000456.2:p.Ser660=
NM_001282543.1:c.1923C=	NP_001269472.1:p.Ser641=
NM_001282545.1:c.627C=	NP_001269474.1:p.Ser209=
NM_001282548.1:c.570C=	NP_001269477.1:p.Ser190=
NM_001282549.1:c.441C=	NP_001269478.1:p.Ser147=
NR_104212.1:n.1973C=
NR_104215.1:n.1916C=
NR_104216.1:n.1172C=
XM_011511567.1:c.1926C=	XP_011509869.1:p.Ser642=
XM_017004613.1:c.2079C=	XP_016860102.1:p.Ser693=
XR_002959322.1:n.2170C=
NM_000465.4:c.1980C= MANE Select	NP_000456.2:p.Ser660=
NM_001282543.2:c.1923C=	NP_001269472.1:p.Ser641=
NM_001282545.2:c.627C=	NP_001269474.1:p.Ser209=
NM_001282548.2:c.570C=	NP_001269477.1:p.Ser190=
NM_001282549.2:c.441C=	NP_001269478.1:p.Ser147=
NR_104212.2:n.1945C=
NR_104215.2:n.1888C=
NR_104216.2:n.1144C=