Canonical Allele Identifier: CA2090042
Gene: BARD1 HGNC NCBI

Linked Data

dbSNP Id: rs779498054

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214728649A>T , CM000664.2:g.214728649A>T GRCh38
NC_000002.11:g.215593373A>T , CM000664.1:g.215593373A>T GRCh37
NC_000002.10:g.215301618A>T NCBI36
NG_012047.2:g.86056T>A
NG_012047.3:g.86063T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000260947.9:c.*27T>A MANE Select ENSP00000260947.4:n.*27T>A
ENST00000613374.5:c.*27T>A ENSP00000484464.1:n.*27T>A
ENST00000613706.5:c.*27T>A ENSP00000484976.2:n.*27T>A
ENST00000617164.5:c.*27T>A ENSP00000480470.1:n.*27T>A
ENST00000619009.5:c.*27T>A ENSP00000482293.1:n.*27T>A
ENST00000650978.1:c.3736T>A
ENST00000260947.8:c.*27T>A ENSP00000260947.4:n.*27T>A
ENST00000432456.5:c.504T>A
ENST00000471590.5:n.696T>A
ENST00000613374.4:c.*27T>A ENSP00000484464.1:n.*27T>A
ENST00000613706.4:c.*27T>A ENSP00000484976.1:n.*27T>A
ENST00000617164.4:c.*27T>A ENSP00000480470.1:n.*27T>A
ENST00000619009.4:c.*27T>A ENSP00000482293.1:n.*27T>A
NM_000465.3:c.*27T>A NP_000456.2:n.*27T>A
NM_001282543.1:c.*27T>A NP_001269472.1:n.*27T>A
NM_001282545.1:c.*27T>A NP_001269474.1:n.*27T>A
NM_001282548.1:c.*27T>A NP_001269477.1:n.*27T>A
NM_001282549.1:c.*27T>A NP_001269478.1:n.*27T>A
NR_104212.1:n.2354T>A
NR_104215.1:n.2297T>A
NR_104216.1:n.1553T>A
XM_011511567.1:c.*27T>A XP_011509869.1:n.*27T>A
XM_017004613.1:c.*27T>A XP_016860102.1:n.*27T>A
XR_002959322.1:n.2727T>A
NM_000465.4:c.*27T>A MANE Select NP_000456.2:n.*27T>A
NM_001282543.2:c.*27T>A NP_001269472.1:n.*27T>A
NM_001282545.2:c.*27T>A NP_001269474.1:n.*27T>A
NM_001282548.2:c.*27T>A NP_001269477.1:n.*27T>A
NM_001282549.2:c.*27T>A NP_001269478.1:n.*27T>A
NR_104212.2:n.2326T>A
NR_104215.2:n.2269T>A
NR_104216.2:n.1525T>A