Canonical Allele Identifier: CA331825
Gene: BARD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 127747
dbSNP Id: rs587780036

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214781098T>C , CM000664.2:g.214781098T>C GRCh38
NC_000002.11:g.215645822T>C , CM000664.1:g.215645822T>C GRCh37
NC_000002.10:g.215354067T>C NCBI36
NG_012047.2:g.33607A>G
NG_012047.3:g.33614A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000260947.9:c.776A>G MANE Select ENSP00000260947.4:p.Asp259Gly
ENST00000421162.2:c.215+15963A>G ENSP00000392245.2:n.215+15963A>G
ENST00000613192.2:c.158+28314A>G ENSP00000483275.2:n.158+28314A>G
ENST00000613374.5:c.158+28314A>G ENSP00000484464.1:n.158+28314A>G
ENST00000613706.5:c.776A>G ENSP00000484976.2:p.Asp259Gly
ENST00000617164.5:c.719A>G ENSP00000480470.1:p.Asp240Gly
ENST00000619009.5:c.364+11199A>G ENSP00000482293.1:n.364+11199A>G
ENST00000650978.1:c.618A>G
ENST00000260947.8:c.776A>G ENSP00000260947.4:p.Asp259Gly
ENST00000421162.1:c.215+15963A>G ENSP00000392245.1:n.215+15963A>G
ENST00000455743.5:c.*396A>G ENSP00000412186.1:n.*396A>G
ENST00000471787.1:n.671A>G
ENST00000613192.1:c.73+28314A>G ENSP00000483275.1:n.73+28314A>G
ENST00000613374.4:c.158+28314A>G ENSP00000484464.1:n.158+28314A>G
ENST00000613706.4:c.215+15963A>G ENSP00000484976.1:n.215+15963A>G
ENST00000617164.4:c.719A>G ENSP00000480470.1:p.Asp240Gly
ENST00000619009.4:c.364+11199A>G ENSP00000482293.1:n.364+11199A>G
ENST00000620057.4:c.364+11199A>G ENSP00000481988.1:n.364+11199A>G
NM_000465.3:c.776A>G NP_000456.2:p.Asp259Gly
NM_001282543.1:c.719A>G NP_001269472.1:p.Asp240Gly
NM_001282545.1:c.215+15963A>G NP_001269474.1:n.215+15963A>G
NM_001282548.1:c.158+28314A>G NP_001269477.1:n.158+28314A>G
NM_001282549.1:c.364+11199A>G NP_001269478.1:n.364+11199A>G
NR_104212.1:n.769A>G
NR_104215.1:n.712A>G
NR_104216.1:n.506+11199A>G
XM_011511567.1:c.722A>G XP_011509869.1:p.Asp241Gly
XM_011511568.1:c.776A>G XP_011509870.1:p.Asp259Gly
XM_017004613.1:c.875A>G XP_016860102.1:p.Asp292Gly
XM_017004614.1:c.875A>G XP_016860103.1:p.Asp292Gly
XR_002959322.1:n.966A>G
NM_000465.4:c.776A>G MANE Select NP_000456.2:p.Asp259Gly
NM_001282543.2:c.719A>G NP_001269472.1:p.Asp240Gly
NM_001282545.2:c.215+15963A>G NP_001269474.1:n.215+15963A>G
NM_001282548.2:c.158+28314A>G NP_001269477.1:n.158+28314A>G
NM_001282549.2:c.364+11199A>G NP_001269478.1:n.364+11199A>G
NR_104212.2:n.741A>G
NR_104215.2:n.684A>G
NR_104216.2:n.478+11199A>G