Canonical Allele Identifier: CA1327046364

Gene: BARD1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214730429C= , CM000664.2:g.214730429C=	GRCh38
NC_000002.11:g.215595153C= , CM000664.1:g.215595153C=	GRCh37
NC_000002.10:g.215303398C=	NCBI36
NG_012047.2:g.84276G=
NG_012047.3:g.84283G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.1983G= MANE Select	ENSP00000260947.4:p.Arg661=
ENST00000421162.2:c.630G=	ENSP00000392245.2:p.Arg210=
ENST00000613192.2:c.*46G=	ENSP00000483275.2:n.*46G=
ENST00000613374.5:c.573G=	ENSP00000484464.1:p.Arg191=
ENST00000613706.5:c.1575G=	ENSP00000484976.2:p.Arg525=
ENST00000617164.5:c.1926G=	ENSP00000480470.1:p.Arg642=
ENST00000619009.5:c.444G=	ENSP00000482293.1:p.Arg148=
ENST00000650978.1:c.3358G=
ENST00000260947.8:c.1983G=	ENSP00000260947.4:p.Arg661=
ENST00000421162.1:c.630G=	ENSP00000392245.1:p.Arg210=
ENST00000432456.5:c.80G=
ENST00000455743.5:c.*1603G=	ENSP00000412186.1:n.*1603G=
ENST00000471590.5:n.318G=
ENST00000613192.1:c.153G=	ENSP00000483275.1:p.Arg51=
ENST00000613374.4:c.573G=	ENSP00000484464.1:p.Arg191=
ENST00000613706.4:c.630G=	ENSP00000484976.1:p.Arg210=
ENST00000617164.4:c.1926G=	ENSP00000480470.1:p.Arg642=
ENST00000619009.4:c.444G=	ENSP00000482293.1:p.Arg148=
ENST00000620057.4:c.*649G=	ENSP00000481988.1:n.*649G=
NM_000465.3:c.1983G=	NP_000456.2:p.Arg661=
NM_001282543.1:c.1926G=	NP_001269472.1:p.Arg642=
NM_001282545.1:c.630G=	NP_001269474.1:p.Arg210=
NM_001282548.1:c.573G=	NP_001269477.1:p.Arg191=
NM_001282549.1:c.444G=	NP_001269478.1:p.Arg148=
NR_104212.1:n.1976G=
NR_104215.1:n.1919G=
NR_104216.1:n.1175G=
XM_011511567.1:c.1929G=	XP_011509869.1:p.Arg643=
XM_017004613.1:c.2082G=	XP_016860102.1:p.Arg694=
XR_002959322.1:n.2173G=
NM_000465.4:c.1983G= MANE Select	NP_000456.2:p.Arg661=
NM_001282543.2:c.1926G=	NP_001269472.1:p.Arg642=
NM_001282545.2:c.630G=	NP_001269474.1:p.Arg210=
NM_001282548.2:c.573G=	NP_001269477.1:p.Arg191=
NM_001282549.2:c.444G=	NP_001269478.1:p.Arg148=
NR_104212.2:n.1948G=
NR_104215.2:n.1891G=
NR_104216.2:n.1147G=