Canonical Allele Identifier: CA1327046374

Gene: BARD1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214730442G= , CM000664.2:g.214730442G=	GRCh38
NC_000002.11:g.215595166G= , CM000664.1:g.215595166G=	GRCh37
NC_000002.10:g.215303411G=	NCBI36
NG_012047.2:g.84263C=
NG_012047.3:g.84270C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.1970C= MANE Select	ENSP00000260947.4:p.Pro657=
ENST00000421162.2:c.617C=	ENSP00000392245.2:p.Pro206=
ENST00000613192.2:c.*33C=	ENSP00000483275.2:n.*33C=
ENST00000613374.5:c.560C=	ENSP00000484464.1:p.Pro187=
ENST00000613706.5:c.1562C=	ENSP00000484976.2:p.Pro521=
ENST00000617164.5:c.1913C=	ENSP00000480470.1:p.Pro638=
ENST00000619009.5:c.431C=	ENSP00000482293.1:p.Pro144=
ENST00000650978.1:c.3345C=
ENST00000260947.8:c.1970C=	ENSP00000260947.4:p.Pro657=
ENST00000421162.1:c.617C=	ENSP00000392245.1:p.Pro206=
ENST00000432456.5:c.67C=
ENST00000455743.5:c.*1590C=	ENSP00000412186.1:n.*1590C=
ENST00000471590.5:n.305C=
ENST00000613192.1:c.140C=	ENSP00000483275.1:p.Pro47=
ENST00000613374.4:c.560C=	ENSP00000484464.1:p.Pro187=
ENST00000613706.4:c.617C=	ENSP00000484976.1:p.Pro206=
ENST00000617164.4:c.1913C=	ENSP00000480470.1:p.Pro638=
ENST00000619009.4:c.431C=	ENSP00000482293.1:p.Pro144=
ENST00000620057.4:c.*636C=	ENSP00000481988.1:n.*636C=
NM_000465.3:c.1970C=	NP_000456.2:p.Pro657=
NM_001282543.1:c.1913C=	NP_001269472.1:p.Pro638=
NM_001282545.1:c.617C=	NP_001269474.1:p.Pro206=
NM_001282548.1:c.560C=	NP_001269477.1:p.Pro187=
NM_001282549.1:c.431C=	NP_001269478.1:p.Pro144=
NR_104212.1:n.1963C=
NR_104215.1:n.1906C=
NR_104216.1:n.1162C=
XM_011511567.1:c.1916C=	XP_011509869.1:p.Pro639=
XM_017004613.1:c.2069C=	XP_016860102.1:p.Pro690=
XR_002959322.1:n.2160C=
NM_000465.4:c.1970C= MANE Select	NP_000456.2:p.Pro657=
NM_001282543.2:c.1913C=	NP_001269472.1:p.Pro638=
NM_001282545.2:c.617C=	NP_001269474.1:p.Pro206=
NM_001282548.2:c.560C=	NP_001269477.1:p.Pro187=
NM_001282549.2:c.431C=	NP_001269478.1:p.Pro144=
NR_104212.2:n.1935C=
NR_104215.2:n.1878C=
NR_104216.2:n.1134C=