Canonical Allele Identifier: CA1327045557

Gene: BARD1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214728827G= , CM000664.2:g.214728827G=	GRCh38
NC_000002.11:g.215593551G= , CM000664.1:g.215593551G=	GRCh37
NC_000002.10:g.215301796G=	NCBI36
NG_012047.2:g.85878C=
NG_012047.3:g.85885C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.2183C= MANE Select	ENSP00000260947.4:p.Ser728=
ENST00000421162.2:c.830C=	ENSP00000392245.2:p.Ser277=
ENST00000613192.2:c.*246C=	ENSP00000483275.2:n.*246C=
ENST00000613374.5:c.773C=	ENSP00000484464.1:p.Ser258=
ENST00000613706.5:c.1775C=	ENSP00000484976.2:p.Ser592=
ENST00000617164.5:c.2126C=	ENSP00000480470.1:p.Ser709=
ENST00000619009.5:c.644C=	ENSP00000482293.1:p.Ser215=
ENST00000650978.1:c.3558C=
ENST00000260947.8:c.2183C=	ENSP00000260947.4:p.Ser728=
ENST00000432456.5:c.326C=
ENST00000455743.5:c.*1803C=	ENSP00000412186.1:n.*1803C=
ENST00000471590.5:n.518C=
ENST00000613192.1:c.353C=	ENSP00000483275.1:p.Ser118=
ENST00000613374.4:c.773C=	ENSP00000484464.1:p.Ser258=
ENST00000613706.4:c.830C=	ENSP00000484976.1:p.Ser277=
ENST00000617164.4:c.2126C=	ENSP00000480470.1:p.Ser709=
ENST00000619009.4:c.644C=	ENSP00000482293.1:p.Ser215=
ENST00000620057.4:c.*849C=	ENSP00000481988.1:n.*849C=
NM_000465.3:c.2183C=	NP_000456.2:p.Ser728=
NM_001282543.1:c.2126C=	NP_001269472.1:p.Ser709=
NM_001282545.1:c.830C=	NP_001269474.1:p.Ser277=
NM_001282548.1:c.773C=	NP_001269477.1:p.Ser258=
NM_001282549.1:c.644C=	NP_001269478.1:p.Ser215=
NR_104212.1:n.2176C=
NR_104215.1:n.2119C=
NR_104216.1:n.1375C=
XM_011511567.1:c.2129C=	XP_011509869.1:p.Ser710=
XM_017004613.1:c.2282C=	XP_016860102.1:p.Ser761=
XR_002959322.1:n.2549C=
NM_000465.4:c.2183C= MANE Select	NP_000456.2:p.Ser728=
NM_001282543.2:c.2126C=	NP_001269472.1:p.Ser709=
NM_001282545.2:c.830C=	NP_001269474.1:p.Ser277=
NM_001282548.2:c.773C=	NP_001269477.1:p.Ser258=
NM_001282549.2:c.644C=	NP_001269478.1:p.Ser215=
NR_104212.2:n.2148C=
NR_104215.2:n.2091C=
NR_104216.2:n.1347C=