Canonical Allele Identifier: CA1327085339

Gene: BARD1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214809664G= , CM000664.2:g.214809664G=	GRCh38
NC_000002.11:g.215674388G= , CM000664.1:g.215674388G=	GRCh37
NC_000002.10:g.215382633G=	NCBI36
NG_012047.2:g.5041C=
NG_012047.3:g.5048C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.-95C= MANE Select	ENSP00000260947.4:n.-95C=
ENST00000613192.2:c.-95C=	ENSP00000483275.2:n.-95C=
ENST00000613706.5:c.-95C=	ENSP00000484976.2:n.-95C=
ENST00000260947.8:c.-95C=	ENSP00000260947.4:n.-95C=
ENST00000421162.1:c.-95C=	ENSP00000392245.1:n.-95C=
ENST00000455743.5:c.-95C=	ENSP00000412186.1:n.-95C=
ENST00000471787.1:n.7C=
ENST00000613192.1:c.-180C=	ENSP00000483275.1:n.-180C=
ENST00000613374.4:c.-95C=	ENSP00000484464.1:n.-95C=
ENST00000613706.4:c.-95C=	ENSP00000484976.1:n.-95C=
ENST00000617164.4:c.-95C=	ENSP00000480470.1:n.-95C=
ENST00000619009.4:c.-95C=	ENSP00000482293.1:n.-95C=
NM_000465.3:c.-95C=	NP_000456.2:n.-95C=
NM_001282543.1:c.-95C=	NP_001269472.1:n.-95C=
NM_001282545.1:c.-95C=	NP_001269474.1:n.-95C=
NM_001282548.1:c.-95C=	NP_001269477.1:n.-95C=
NM_001282549.1:c.-95C=	NP_001269478.1:n.-95C=
NR_104212.1:n.48C=
NR_104215.1:n.48C=
NR_104216.1:n.48C=
XM_011511568.1:c.-95C=	XP_011509870.1:n.-95C=
NM_000465.4:c.-95C= MANE Select	NP_000456.2:n.-95C=
NM_001282543.2:c.-95C=	NP_001269472.1:n.-95C=
NM_001282545.2:c.-95C=	NP_001269474.1:n.-95C=
NM_001282548.2:c.-95C=	NP_001269477.1:n.-95C=
NM_001282549.2:c.-95C=	NP_001269478.1:n.-95C=
NR_104212.2:n.20C=
NR_104215.2:n.20C=
NR_104216.2:n.20C=