Canonical Allele Identifier: CA1327046369

Gene: BARD1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214730436C= , CM000664.2:g.214730436C=	GRCh38
NC_000002.11:g.215595160C= , CM000664.1:g.215595160C=	GRCh37
NC_000002.10:g.215303405C=	NCBI36
NG_012047.2:g.84269G=
NG_012047.3:g.84276G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.1976G= MANE Select	ENSP00000260947.4:p.Arg659=
ENST00000421162.2:c.623G=	ENSP00000392245.2:p.Arg208=
ENST00000613192.2:c.*39G=	ENSP00000483275.2:n.*39G=
ENST00000613374.5:c.566G=	ENSP00000484464.1:p.Arg189=
ENST00000613706.5:c.1568G=	ENSP00000484976.2:p.Arg523=
ENST00000617164.5:c.1919G=	ENSP00000480470.1:p.Arg640=
ENST00000619009.5:c.437G=	ENSP00000482293.1:p.Arg146=
ENST00000650978.1:c.3351G=
ENST00000260947.8:c.1976G=	ENSP00000260947.4:p.Arg659=
ENST00000421162.1:c.623G=	ENSP00000392245.1:p.Arg208=
ENST00000432456.5:c.73G=
ENST00000455743.5:c.*1596G=	ENSP00000412186.1:n.*1596G=
ENST00000471590.5:n.311G=
ENST00000613192.1:c.146G=	ENSP00000483275.1:p.Arg49=
ENST00000613374.4:c.566G=	ENSP00000484464.1:p.Arg189=
ENST00000613706.4:c.623G=	ENSP00000484976.1:p.Arg208=
ENST00000617164.4:c.1919G=	ENSP00000480470.1:p.Arg640=
ENST00000619009.4:c.437G=	ENSP00000482293.1:p.Arg146=
ENST00000620057.4:c.*642G=	ENSP00000481988.1:n.*642G=
NM_000465.3:c.1976G=	NP_000456.2:p.Arg659=
NM_001282543.1:c.1919G=	NP_001269472.1:p.Arg640=
NM_001282545.1:c.623G=	NP_001269474.1:p.Arg208=
NM_001282548.1:c.566G=	NP_001269477.1:p.Arg189=
NM_001282549.1:c.437G=	NP_001269478.1:p.Arg146=
NR_104212.1:n.1969G=
NR_104215.1:n.1912G=
NR_104216.1:n.1168G=
XM_011511567.1:c.1922G=	XP_011509869.1:p.Arg641=
XM_017004613.1:c.2075G=	XP_016860102.1:p.Arg692=
XR_002959322.1:n.2166G=
NM_000465.4:c.1976G= MANE Select	NP_000456.2:p.Arg659=
NM_001282543.2:c.1919G=	NP_001269472.1:p.Arg640=
NM_001282545.2:c.623G=	NP_001269474.1:p.Arg208=
NM_001282548.2:c.566G=	NP_001269477.1:p.Arg189=
NM_001282549.2:c.437G=	NP_001269478.1:p.Arg146=
NR_104212.2:n.1941G=
NR_104215.2:n.1884G=
NR_104216.2:n.1140G=