Canonical Allele Identifier: CA1327085351

Gene: BARD1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214809678G= , CM000664.2:g.214809678G=	GRCh38
NC_000002.11:g.215674402G= , CM000664.1:g.215674402G=	GRCh37
NC_000002.10:g.215382647G=	NCBI36
NG_012047.2:g.5027C=
NG_012047.3:g.5034C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.-109C= MANE Select	ENSP00000260947.4:n.-109C=
ENST00000613192.2:c.-109C=	ENSP00000483275.2:n.-109C=
ENST00000613706.5:c.-109C=	ENSP00000484976.2:n.-109C=
ENST00000260947.8:c.-109C=	ENSP00000260947.4:n.-109C=
ENST00000421162.1:c.-109C=	ENSP00000392245.1:n.-109C=
ENST00000613192.1:c.-194C=	ENSP00000483275.1:n.-194C=
ENST00000613374.4:c.-109C=	ENSP00000484464.1:n.-109C=
ENST00000613706.4:c.-109C=	ENSP00000484976.1:n.-109C=
ENST00000617164.4:c.-109C=	ENSP00000480470.1:n.-109C=
ENST00000619009.4:c.-109C=	ENSP00000482293.1:n.-109C=
NM_000465.3:c.-109C=	NP_000456.2:n.-109C=
NM_001282543.1:c.-109C=	NP_001269472.1:n.-109C=
NM_001282545.1:c.-109C=	NP_001269474.1:n.-109C=
NM_001282548.1:c.-109C=	NP_001269477.1:n.-109C=
NM_001282549.1:c.-109C=	NP_001269478.1:n.-109C=
NR_104212.1:n.34C=
NR_104215.1:n.34C=
NR_104216.1:n.34C=
XM_011511568.1:c.-109C=	XP_011509870.1:n.-109C=
NM_000465.4:c.-109C= MANE Select	NP_000456.2:n.-109C=
NM_001282543.2:c.-109C=	NP_001269472.1:n.-109C=
NM_001282545.2:c.-109C=	NP_001269474.1:n.-109C=
NM_001282548.2:c.-109C=	NP_001269477.1:n.-109C=
NM_001282549.2:c.-109C=	NP_001269478.1:n.-109C=
NR_104212.2:n.6C=
NR_104215.2:n.6C=
NR_104216.2:n.6C=