Canonical Allele Identifier: CA2701482483
Gene: BARD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214728630C>T , CM000664.2:g.214728630C>T GRCh38
NC_000002.11:g.215593354C>T , CM000664.1:g.215593354C>T GRCh37
NC_000002.10:g.215301599C>T NCBI36
NG_012047.2:g.86075G>A
NG_012047.3:g.86082G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000260947.9:c.*46G>A MANE Select ENSP00000260947.4:n.*46G>A
ENST00000613374.5:c.*46G>A ENSP00000484464.1:n.*46G>A
ENST00000613706.5:c.*46G>A ENSP00000484976.2:n.*46G>A
ENST00000617164.5:c.*46G>A ENSP00000480470.1:n.*46G>A
ENST00000619009.5:c.*46G>A ENSP00000482293.1:n.*46G>A
ENST00000650978.1:c.3755G>A
ENST00000260947.8:c.*46G>A ENSP00000260947.4:n.*46G>A
ENST00000432456.5:c.523G>A
ENST00000471590.5:n.715G>A
ENST00000613374.4:c.*46G>A ENSP00000484464.1:n.*46G>A
ENST00000613706.4:c.*46G>A ENSP00000484976.1:n.*46G>A
ENST00000617164.4:c.*46G>A ENSP00000480470.1:n.*46G>A
ENST00000619009.4:c.*46G>A ENSP00000482293.1:n.*46G>A
NM_000465.3:c.*46G>A NP_000456.2:n.*46G>A
NM_001282543.1:c.*46G>A NP_001269472.1:n.*46G>A
NM_001282545.1:c.*46G>A NP_001269474.1:n.*46G>A
NM_001282548.1:c.*46G>A NP_001269477.1:n.*46G>A
NM_001282549.1:c.*46G>A NP_001269478.1:n.*46G>A
NR_104212.1:n.2373G>A
NR_104215.1:n.2316G>A
NR_104216.1:n.1572G>A
XM_011511567.1:c.*46G>A XP_011509869.1:n.*46G>A
XM_017004613.1:c.*46G>A XP_016860102.1:n.*46G>A
XR_002959322.1:n.2746G>A
NM_000465.4:c.*46G>A MANE Select NP_000456.2:n.*46G>A
NM_001282543.2:c.*46G>A NP_001269472.1:n.*46G>A
NM_001282545.2:c.*46G>A NP_001269474.1:n.*46G>A
NM_001282548.2:c.*46G>A NP_001269477.1:n.*46G>A
NM_001282549.2:c.*46G>A NP_001269478.1:n.*46G>A
NR_104212.2:n.2345G>A
NR_104215.2:n.2288G>A
NR_104216.2:n.1544G>A