Canonical Allele Identifier: CA1327085301

Gene: BARD1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214809618G= , CM000664.2:g.214809618G=	GRCh38
NC_000002.11:g.215674342G= , CM000664.1:g.215674342G=	GRCh37
NC_000002.10:g.215382587G=	NCBI36
NG_012047.2:g.5087C=
NG_012047.3:g.5094C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000260947.9:c.-49C= MANE Select	ENSP00000260947.4:n.-49C=
ENST00000613192.2:c.-49C=	ENSP00000483275.2:n.-49C=
ENST00000613374.5:c.-49C=	ENSP00000484464.1:n.-49C=
ENST00000613706.5:c.-49C=	ENSP00000484976.2:n.-49C=
ENST00000617164.5:c.-49C=	ENSP00000480470.1:n.-49C=
ENST00000260947.8:c.-49C=	ENSP00000260947.4:n.-49C=
ENST00000421162.1:c.-49C=	ENSP00000392245.1:n.-49C=
ENST00000455743.5:c.-49C=	ENSP00000412186.1:n.-49C=
ENST00000471787.1:n.53C=
ENST00000479904.1:n.43C=
ENST00000613192.1:c.-134C=	ENSP00000483275.1:n.-134C=
ENST00000613374.4:c.-49C=	ENSP00000484464.1:n.-49C=
ENST00000613706.4:c.-49C=	ENSP00000484976.1:n.-49C=
ENST00000617164.4:c.-49C=	ENSP00000480470.1:n.-49C=
ENST00000619009.4:c.-49C=	ENSP00000482293.1:n.-49C=
ENST00000620057.4:c.-49C=	ENSP00000481988.1:n.-49C=
NM_000465.3:c.-49C=	NP_000456.2:n.-49C=
NM_001282543.1:c.-49C=	NP_001269472.1:n.-49C=
NM_001282545.1:c.-49C=	NP_001269474.1:n.-49C=
NM_001282548.1:c.-49C=	NP_001269477.1:n.-49C=
NM_001282549.1:c.-49C=	NP_001269478.1:n.-49C=
NR_104212.1:n.94C=
NR_104215.1:n.94C=
NR_104216.1:n.94C=
XM_011511568.1:c.-49C=	XP_011509870.1:n.-49C=
XM_017004613.1:c.-49C=	XP_016860102.1:n.-49C=
XM_017004614.1:c.-49C=	XP_016860103.1:n.-49C=
XR_002959322.1:n.43C=
NM_000465.4:c.-49C= MANE Select	NP_000456.2:n.-49C=
NM_001282543.2:c.-49C=	NP_001269472.1:n.-49C=
NM_001282545.2:c.-49C=	NP_001269474.1:n.-49C=
NM_001282548.2:c.-49C=	NP_001269477.1:n.-49C=
NM_001282549.2:c.-49C=	NP_001269478.1:n.-49C=
NR_104212.2:n.66C=
NR_104215.2:n.66C=
NR_104216.2:n.66C=