Canonical Allele Identifier: CA1327045091
Gene: BARD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214728016T= , CM000664.2:g.214728016T= GRCh38
NC_000002.11:g.215592740T= , CM000664.1:g.215592740T= GRCh37
NC_000002.10:g.215300985T= NCBI36
NG_012047.2:g.86689A=
NG_012047.3:g.86696A=

Transcript Alleles

HGVS Amino-acid change
ENST00000260947.9:c.*660A= MANE Select ENSP00000260947.4:n.*660A=
ENST00000260947.8:c.*660A= ENSP00000260947.4:n.*660A=
ENST00000613374.4:c.*660A= ENSP00000484464.1:n.*660A=
ENST00000613706.4:c.*660A= ENSP00000484976.1:n.*660A=
ENST00000617164.4:c.*660A= ENSP00000480470.1:n.*660A=
ENST00000619009.4:c.*660A= ENSP00000482293.1:n.*660A=
NM_000465.3:c.*660A= NP_000456.2:n.*660A=
NM_001282543.1:c.*660A= NP_001269472.1:n.*660A=
NM_001282545.1:c.*660A= NP_001269474.1:n.*660A=
NM_001282548.1:c.*660A= NP_001269477.1:n.*660A=
NM_001282549.1:c.*660A= NP_001269478.1:n.*660A=
NR_104212.1:n.2987A=
NR_104215.1:n.2930A=
NR_104216.1:n.2186A=
XM_011511567.1:c.*660A= XP_011509869.1:n.*660A=
XM_017004613.1:c.*660A= XP_016860102.1:n.*660A=
NM_000465.4:c.*660A= MANE Select NP_000456.2:n.*660A=
NM_001282543.2:c.*660A= NP_001269472.1:n.*660A=
NM_001282545.2:c.*660A= NP_001269474.1:n.*660A=
NM_001282548.2:c.*660A= NP_001269477.1:n.*660A=
NM_001282549.2:c.*660A= NP_001269478.1:n.*660A=
NR_104212.2:n.2959A=
NR_104215.2:n.2902A=
NR_104216.2:n.2158A=