Canonical Allele Identifier: CA1327045097
Gene: BARD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214728024G= , CM000664.2:g.214728024G= GRCh38
NC_000002.11:g.215592748G= , CM000664.1:g.215592748G= GRCh37
NC_000002.10:g.215300993G= NCBI36
NG_012047.2:g.86681C=
NG_012047.3:g.86688C=

Transcript Alleles

HGVS Amino-acid change
ENST00000260947.9:c.*652C= MANE Select ENSP00000260947.4:n.*652C=
ENST00000260947.8:c.*652C= ENSP00000260947.4:n.*652C=
ENST00000613374.4:c.*652C= ENSP00000484464.1:n.*652C=
ENST00000613706.4:c.*652C= ENSP00000484976.1:n.*652C=
ENST00000617164.4:c.*652C= ENSP00000480470.1:n.*652C=
ENST00000619009.4:c.*652C= ENSP00000482293.1:n.*652C=
NM_000465.3:c.*652C= NP_000456.2:n.*652C=
NM_001282543.1:c.*652C= NP_001269472.1:n.*652C=
NM_001282545.1:c.*652C= NP_001269474.1:n.*652C=
NM_001282548.1:c.*652C= NP_001269477.1:n.*652C=
NM_001282549.1:c.*652C= NP_001269478.1:n.*652C=
NR_104212.1:n.2979C=
NR_104215.1:n.2922C=
NR_104216.1:n.2178C=
XM_011511567.1:c.*652C= XP_011509869.1:n.*652C=
XM_017004613.1:c.*652C= XP_016860102.1:n.*652C=
NM_000465.4:c.*652C= MANE Select NP_000456.2:n.*652C=
NM_001282543.2:c.*652C= NP_001269472.1:n.*652C=
NM_001282545.2:c.*652C= NP_001269474.1:n.*652C=
NM_001282548.2:c.*652C= NP_001269477.1:n.*652C=
NM_001282549.2:c.*652C= NP_001269478.1:n.*652C=
NR_104212.2:n.2951C=
NR_104215.2:n.2894C=
NR_104216.2:n.2150C=