Canonical Allele Identifier: CA1327071579
Gene: BARD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214781521A= , CM000664.2:g.214781521A= GRCh38
NC_000002.11:g.215646245A= , CM000664.1:g.215646245A= GRCh37
NC_000002.10:g.215354490A= NCBI36
NG_012047.2:g.33184T=
NG_012047.3:g.33191T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000260947.9:c.365-12T= MANE Select ENSP00000260947.4:n.365-12T=
ENST00000421162.2:c.215+15540T= ENSP00000392245.2:n.215+15540T=
ENST00000613192.2:c.158+27891T= ENSP00000483275.2:n.158+27891T=
ENST00000613374.5:c.158+27891T= ENSP00000484464.1:n.158+27891T=
ENST00000613706.5:c.365-12T= ENSP00000484976.2:n.365-12T=
ENST00000617164.5:c.308-12T= ENSP00000480470.1:n.308-12T=
ENST00000619009.5:c.364+10776T= ENSP00000482293.1:n.364+10776T=
ENST00000650978.1:c.207-12T=
ENST00000260947.8:c.365-12T= ENSP00000260947.4:n.365-12T=
ENST00000421162.1:c.215+15540T= ENSP00000392245.1:n.215+15540T=
ENST00000455743.5:c.216-12T= ENSP00000412186.1:n.216-12T=
ENST00000471787.1:n.260-12T=
ENST00000613192.1:c.73+27891T= ENSP00000483275.1:n.73+27891T=
ENST00000613374.4:c.158+27891T= ENSP00000484464.1:n.158+27891T=
ENST00000613706.4:c.215+15540T= ENSP00000484976.1:n.215+15540T=
ENST00000617164.4:c.308-12T= ENSP00000480470.1:n.308-12T=
ENST00000619009.4:c.364+10776T= ENSP00000482293.1:n.364+10776T=
ENST00000620057.4:c.364+10776T= ENSP00000481988.1:n.364+10776T=
NM_000465.3:c.365-12T= NP_000456.2:n.365-12T=
NM_001282543.1:c.308-12T= NP_001269472.1:n.308-12T=
NM_001282545.1:c.215+15540T= NP_001269474.1:n.215+15540T=
NM_001282548.1:c.158+27891T= NP_001269477.1:n.158+27891T=
NM_001282549.1:c.364+10776T= NP_001269478.1:n.364+10776T=
NR_104212.1:n.358-12T=
NR_104215.1:n.301-12T=
NR_104216.1:n.506+10776T=
XM_011511567.1:c.311-12T= XP_011509869.1:n.311-12T=
XM_011511568.1:c.365-12T= XP_011509870.1:n.365-12T=
XM_017004613.1:c.464-12T= XP_016860102.1:n.464-12T=
XM_017004614.1:c.464-12T= XP_016860103.1:n.464-12T=
XR_002959322.1:n.555-12T=
NM_000465.4:c.365-12T= MANE Select NP_000456.2:n.365-12T=
NM_001282543.2:c.308-12T= NP_001269472.1:n.308-12T=
NM_001282545.2:c.215+15540T= NP_001269474.1:n.215+15540T=
NM_001282548.2:c.158+27891T= NP_001269477.1:n.158+27891T=
NM_001282549.2:c.364+10776T= NP_001269478.1:n.364+10776T=
NR_104212.2:n.330-12T=
NR_104215.2:n.273-12T=
NR_104216.2:n.478+10776T=