Canonical Allele Identifier: CA1327045338

Gene: BARD1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214728500T= , CM000664.2:g.214728500T=	GRCh38
NC_000002.11:g.215593224T= , CM000664.1:g.215593224T=	GRCh37
NC_000002.10:g.215301469T=	NCBI36
NG_012047.2:g.86205A=
NG_012047.3:g.86212A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.*176A= MANE Select	ENSP00000260947.4:n.*176A=
ENST00000260947.8:c.*176A=	ENSP00000260947.4:n.*176A=
ENST00000471590.5:n.845A=
ENST00000613374.4:c.*176A=	ENSP00000484464.1:n.*176A=
ENST00000613706.4:c.*176A=	ENSP00000484976.1:n.*176A=
ENST00000617164.4:c.*176A=	ENSP00000480470.1:n.*176A=
ENST00000619009.4:c.*176A=	ENSP00000482293.1:n.*176A=
NM_000465.3:c.*176A=	NP_000456.2:n.*176A=
NM_001282543.1:c.*176A=	NP_001269472.1:n.*176A=
NM_001282545.1:c.*176A=	NP_001269474.1:n.*176A=
NM_001282548.1:c.*176A=	NP_001269477.1:n.*176A=
NM_001282549.1:c.*176A=	NP_001269478.1:n.*176A=
NR_104212.1:n.2503A=
NR_104215.1:n.2446A=
NR_104216.1:n.1702A=
XM_011511567.1:c.*176A=	XP_011509869.1:n.*176A=
XM_017004613.1:c.*176A=	XP_016860102.1:n.*176A=
NM_000465.4:c.*176A= MANE Select	NP_000456.2:n.*176A=
NM_001282543.2:c.*176A=	NP_001269472.1:n.*176A=
NM_001282545.2:c.*176A=	NP_001269474.1:n.*176A=
NM_001282548.2:c.*176A=	NP_001269477.1:n.*176A=
NM_001282549.2:c.*176A=	NP_001269478.1:n.*176A=
NR_104212.2:n.2475A=
NR_104215.2:n.2418A=
NR_104216.2:n.1674A=