Canonical Allele Identifier: CA2540121249
Gene: BARD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214809341_214809342insCGATCGGCGTGTCCGG , CM000664.2:g.214809341_214809342insCGATCGGCGTGTCCGG GRCh38
NC_000002.11:g.215674065_215674066insCGATCGGCGTGTCCGG , CM000664.1:g.215674065_215674066insCGATCGGCGTGTCCGG GRCh37
NC_000002.10:g.215382310_215382311insCGATCGGCGTGTCCGG NCBI36
NG_012047.2:g.5363_5364insCCGGACACGCCGATCG
NG_012047.3:g.5370_5371insCCGGACACGCCGATCG

Transcript Alleles

HGVS Amino-acid change
ENST00000260947.9:c.158+70_158+71insCCGGACACGCCGATCG MANE Select ENSP00000260947.4:n.158+70_158+71insCCGGA...
ENST00000421162.2:c.158+70_158+71insCCGGACACGCCGATCG ENSP00000392245.2:n.158+70_158+71insCCGGA...
ENST00000613192.2:c.158+70_158+71insCCGGACACGCCGATCG ENSP00000483275.2:n.158+70_158+71insCCGGA...
ENST00000613374.5:c.158+70_158+71insCCGGACACGCCGATCG ENSP00000484464.1:n.158+70_158+71insCCGGA...
ENST00000613706.5:c.158+70_158+71insCCGGACACGCCGATCG ENSP00000484976.2:n.158+70_158+71insCCGGA...
ENST00000617164.5:c.158+70_158+71insCCGGACACGCCGATCG ENSP00000480470.1:n.158+70_158+71insCCGGA...
ENST00000619009.5:c.158+70_158+71insCCGGACACGCCGATCG ENSP00000482293.1:n.158+70_158+71insCCGGA...
ENST00000260947.8:c.158+70_158+71insCCGGACACGCCGATCG ENSP00000260947.4:n.158+70_158+71insCCGGA...
ENST00000421162.1:c.158+70_158+71insCCGGACACGCCGATCG ENSP00000392245.1:n.158+70_158+71insCCGGA...
ENST00000455743.5:c.158+70_158+71insCCGGACACGCCGATCG ENSP00000412186.1:n.158+70_158+71insCCGGA...
ENST00000471787.1:n.259+70_259+71insCCGGACACGCCGATCG
ENST00000479904.1:n.249+70_249+71insCCGGACACGCCGATCG
ENST00000613192.1:c.73+70_73+71insCCGGACACGCCGATCG ENSP00000483275.1:n.73+70_73+71insCCGGACA...
ENST00000613374.4:c.158+70_158+71insCCGGACACGCCGATCG ENSP00000484464.1:n.158+70_158+71insCCGGA...
ENST00000613706.4:c.158+70_158+71insCCGGACACGCCGATCG ENSP00000484976.1:n.158+70_158+71insCCGGA...
ENST00000617164.4:c.158+70_158+71insCCGGACACGCCGATCG ENSP00000480470.1:n.158+70_158+71insCCGGA...
ENST00000619009.4:c.158+70_158+71insCCGGACACGCCGATCG ENSP00000482293.1:n.158+70_158+71insCCGGA...
ENST00000620057.4:c.158+70_158+71insCCGGACACGCCGATCG ENSP00000481988.1:n.158+70_158+71insCCGGA...
NM_000465.3:c.158+70_158+71insCCGGACACGCCGATCG NP_000456.2:n.158+70_158+71insCCGGACACGCC...
NM_001282543.1:c.158+70_158+71insCCGGACACGCCGATCG NP_001269472.1:n.158+70_158+71insCCGGACAC...
NM_001282545.1:c.158+70_158+71insCCGGACACGCCGATCG NP_001269474.1:n.158+70_158+71insCCGGACAC...
NM_001282548.1:c.158+70_158+71insCCGGACACGCCGATCG NP_001269477.1:n.158+70_158+71insCCGGACAC...
NM_001282549.1:c.158+70_158+71insCCGGACACGCCGATCG NP_001269478.1:n.158+70_158+71insCCGGACAC...
NR_104212.1:n.300+70_300+71insCCGGACACGCCGATCG
NR_104215.1:n.300+70_300+71insCCGGACACGCCGATCG
NR_104216.1:n.300+70_300+71insCCGGACACGCCGATCG
XM_011511568.1:c.158+70_158+71insCCGGACACGCCGATCG XP_011509870.1:n.158+70_158+71insCCGGACAC...
XM_017004613.1:c.158+70_158+71insCCGGACACGCCGATCG XP_016860102.1:n.158+70_158+71insCCGGACAC...
XM_017004614.1:c.158+70_158+71insCCGGACACGCCGATCG XP_016860103.1:n.158+70_158+71insCCGGACAC...
XR_002959322.1:n.249+70_249+71insCCGGACACGCCGATCG
NM_000465.4:c.158+70_158+71insCCGGACACGCCGATCG MANE Select NP_000456.2:n.158+70_158+71insCCGGACACGCC...
NM_001282543.2:c.158+70_158+71insCCGGACACGCCGATCG NP_001269472.1:n.158+70_158+71insCCGGACAC...
NM_001282545.2:c.158+70_158+71insCCGGACACGCCGATCG NP_001269474.1:n.158+70_158+71insCCGGACAC...
NM_001282548.2:c.158+70_158+71insCCGGACACGCCGATCG NP_001269477.1:n.158+70_158+71insCCGGACAC...
NM_001282549.2:c.158+70_158+71insCCGGACACGCCGATCG NP_001269478.1:n.158+70_158+71insCCGGACAC...
NR_104212.2:n.272+70_272+71insCCGGACACGCCGATCG
NR_104215.2:n.272+70_272+71insCCGGACACGCCGATCG
NR_104216.2:n.272+70_272+71insCCGGACACGCCGATCG