Canonical Allele Identifier: CA2701537330
Gene: BARD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214797131_214797132insAG , CM000664.2:g.214797131_214797132insAG GRCh38
NC_000002.11:g.215661855_215661856insAG , CM000664.1:g.215661855_215661856insAG GRCh37
NC_000002.10:g.215370100_215370101insAG NCBI36
NG_012047.2:g.17573_17574insCT
NG_012047.3:g.17580_17581insCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000260947.9:c.159-15_159-14insCT MANE Select ENSP00000260947.4:n.159-15_159-14insCT
ENST00000421162.2:c.159-15_159-14insCT ENSP00000392245.2:n.159-15_159-14insCT
ENST00000613192.2:c.158+12280_158+12281insCT ENSP00000483275.2:n.158+12280_158+12281insCT
ENST00000613374.5:c.158+12280_158+12281insCT ENSP00000484464.1:n.158+12280_158+12281insCT
ENST00000613706.5:c.159-15_159-14insCT ENSP00000484976.2:n.159-15_159-14insCT
ENST00000617164.5:c.159-4687_159-4686insCT ENSP00000480470.1:n.159-4687_159-4686insCT
ENST00000619009.5:c.159-15_159-14insCT ENSP00000482293.1:n.159-15_159-14insCT
ENST00000260947.8:c.159-15_159-14insCT ENSP00000260947.4:n.159-15_159-14insCT
ENST00000421162.1:c.159-15_159-14insCT ENSP00000392245.1:n.159-15_159-14insCT
ENST00000455743.5:c.159-15_159-14insCT ENSP00000412186.1:n.159-15_159-14insCT
ENST00000471787.1:n.259+12280_259+12281insCT
ENST00000479904.1:n.250-15_250-14insCT
ENST00000613192.1:c.73+12280_73+12281insCT ENSP00000483275.1:n.73+12280_73+12281insCT
ENST00000613374.4:c.158+12280_158+12281insCT ENSP00000484464.1:n.158+12280_158+12281insCT
ENST00000613706.4:c.159-15_159-14insCT ENSP00000484976.1:n.159-15_159-14insCT
ENST00000617164.4:c.159-4687_159-4686insCT ENSP00000480470.1:n.159-4687_159-4686insCT
ENST00000619009.4:c.159-15_159-14insCT ENSP00000482293.1:n.159-15_159-14insCT
ENST00000620057.4:c.159-15_159-14insCT ENSP00000481988.1:n.159-15_159-14insCT
NM_000465.3:c.159-15_159-14insCT NP_000456.2:n.159-15_159-14insCT
NM_001282543.1:c.159-4687_159-4686insCT NP_001269472.1:n.159-4687_159-4686insCT
NM_001282545.1:c.159-15_159-14insCT NP_001269474.1:n.159-15_159-14insCT
NM_001282548.1:c.158+12280_158+12281insCT NP_001269477.1:n.158+12280_158+12281insCT
NM_001282549.1:c.159-15_159-14insCT NP_001269478.1:n.159-15_159-14insCT
NR_104212.1:n.301-15_301-14insCT
NR_104215.1:n.300+12280_300+12281insCT
NR_104216.1:n.301-15_301-14insCT
XM_011511567.1:c.105-15_105-14insCT XP_011509869.1:n.105-15_105-14insCT
XM_011511568.1:c.159-15_159-14insCT XP_011509870.1:n.159-15_159-14insCT
XM_017004613.1:c.159-15_159-14insCT XP_016860102.1:n.159-15_159-14insCT
XM_017004614.1:c.159-15_159-14insCT XP_016860103.1:n.159-15_159-14insCT
XR_002959322.1:n.250-15_250-14insCT
NM_000465.4:c.159-15_159-14insCT MANE Select NP_000456.2:n.159-15_159-14insCT
NM_001282543.2:c.159-4687_159-4686insCT NP_001269472.1:n.159-4687_159-4686insCT
NM_001282545.2:c.159-15_159-14insCT NP_001269474.1:n.159-15_159-14insCT
NM_001282548.2:c.158+12280_158+12281insCT NP_001269477.1:n.158+12280_158+12281insCT
NM_001282549.2:c.159-15_159-14insCT NP_001269478.1:n.159-15_159-14insCT
NR_104212.2:n.273-15_273-14insCT
NR_104215.2:n.272+12280_272+12281insCT
NR_104216.2:n.273-15_273-14insCT