Canonical Allele Identifier: CA1042201145
Gene: BARD1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214728666G>A , CM000664.2:g.214728666G>A GRCh38
NC_000002.11:g.215593390G>A , CM000664.1:g.215593390G>A GRCh37
NC_000002.10:g.215301635G>A NCBI36
NG_012047.2:g.86039C>T
NG_012047.3:g.86046C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000260947.9:c.*10C>T MANE Select ENSP00000260947.4:n.*10C>T
ENST00000613374.5:c.*10C>T ENSP00000484464.1:n.*10C>T
ENST00000613706.5:c.*10C>T ENSP00000484976.2:n.*10C>T
ENST00000617164.5:c.*10C>T ENSP00000480470.1:n.*10C>T
ENST00000619009.5:c.*10C>T ENSP00000482293.1:n.*10C>T
ENST00000650978.1:c.3719C>T
ENST00000260947.8:c.*10C>T ENSP00000260947.4:n.*10C>T
ENST00000432456.5:c.487C>T
ENST00000471590.5:n.679C>T
ENST00000613374.4:c.*10C>T ENSP00000484464.1:n.*10C>T
ENST00000613706.4:c.*10C>T ENSP00000484976.1:n.*10C>T
ENST00000617164.4:c.*10C>T ENSP00000480470.1:n.*10C>T
ENST00000619009.4:c.*10C>T ENSP00000482293.1:n.*10C>T
NM_000465.3:c.*10C>T NP_000456.2:n.*10C>T
NM_001282543.1:c.*10C>T NP_001269472.1:n.*10C>T
NM_001282545.1:c.*10C>T NP_001269474.1:n.*10C>T
NM_001282548.1:c.*10C>T NP_001269477.1:n.*10C>T
NM_001282549.1:c.*10C>T NP_001269478.1:n.*10C>T
NR_104212.1:n.2337C>T
NR_104215.1:n.2280C>T
NR_104216.1:n.1536C>T
XM_011511567.1:c.*10C>T XP_011509869.1:n.*10C>T
XM_017004613.1:c.*10C>T XP_016860102.1:n.*10C>T
XR_002959322.1:n.2710C>T
NM_000465.4:c.*10C>T MANE Select NP_000456.2:n.*10C>T
NM_001282543.2:c.*10C>T NP_001269472.1:n.*10C>T
NM_001282545.2:c.*10C>T NP_001269474.1:n.*10C>T
NM_001282548.2:c.*10C>T NP_001269477.1:n.*10C>T
NM_001282549.2:c.*10C>T NP_001269478.1:n.*10C>T
NR_104212.2:n.2309C>T
NR_104215.2:n.2252C>T
NR_104216.2:n.1508C>T