Canonical Allele Identifier: CA1327071578
Gene: BARD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214781518A= , CM000664.2:g.214781518A= GRCh38
NC_000002.11:g.215646242A= , CM000664.1:g.215646242A= GRCh37
NC_000002.10:g.215354487A= NCBI36
NG_012047.2:g.33187T=
NG_012047.3:g.33194T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000260947.9:c.365-9T= MANE Select ENSP00000260947.4:n.365-9T=
ENST00000421162.2:c.215+15543T= ENSP00000392245.2:n.215+15543T=
ENST00000613192.2:c.158+27894T= ENSP00000483275.2:n.158+27894T=
ENST00000613374.5:c.158+27894T= ENSP00000484464.1:n.158+27894T=
ENST00000613706.5:c.365-9T= ENSP00000484976.2:n.365-9T=
ENST00000617164.5:c.308-9T= ENSP00000480470.1:n.308-9T=
ENST00000619009.5:c.364+10779T= ENSP00000482293.1:n.364+10779T=
ENST00000650978.1:c.207-9T=
ENST00000260947.8:c.365-9T= ENSP00000260947.4:n.365-9T=
ENST00000421162.1:c.215+15543T= ENSP00000392245.1:n.215+15543T=
ENST00000455743.5:c.216-9T= ENSP00000412186.1:n.216-9T=
ENST00000471787.1:n.260-9T=
ENST00000613192.1:c.73+27894T= ENSP00000483275.1:n.73+27894T=
ENST00000613374.4:c.158+27894T= ENSP00000484464.1:n.158+27894T=
ENST00000613706.4:c.215+15543T= ENSP00000484976.1:n.215+15543T=
ENST00000617164.4:c.308-9T= ENSP00000480470.1:n.308-9T=
ENST00000619009.4:c.364+10779T= ENSP00000482293.1:n.364+10779T=
ENST00000620057.4:c.364+10779T= ENSP00000481988.1:n.364+10779T=
NM_000465.3:c.365-9T= NP_000456.2:n.365-9T=
NM_001282543.1:c.308-9T= NP_001269472.1:n.308-9T=
NM_001282545.1:c.215+15543T= NP_001269474.1:n.215+15543T=
NM_001282548.1:c.158+27894T= NP_001269477.1:n.158+27894T=
NM_001282549.1:c.364+10779T= NP_001269478.1:n.364+10779T=
NR_104212.1:n.358-9T=
NR_104215.1:n.301-9T=
NR_104216.1:n.506+10779T=
XM_011511567.1:c.311-9T= XP_011509869.1:n.311-9T=
XM_011511568.1:c.365-9T= XP_011509870.1:n.365-9T=
XM_017004613.1:c.464-9T= XP_016860102.1:n.464-9T=
XM_017004614.1:c.464-9T= XP_016860103.1:n.464-9T=
XR_002959322.1:n.555-9T=
NM_000465.4:c.365-9T= MANE Select NP_000456.2:n.365-9T=
NM_001282543.2:c.308-9T= NP_001269472.1:n.308-9T=
NM_001282545.2:c.215+15543T= NP_001269474.1:n.215+15543T=
NM_001282548.2:c.158+27894T= NP_001269477.1:n.158+27894T=
NM_001282549.2:c.364+10779T= NP_001269478.1:n.364+10779T=
NR_104212.2:n.330-9T=
NR_104215.2:n.273-9T=
NR_104216.2:n.478+10779T=