Canonical Allele Identifier: CA10577852
Gene: BARD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 229715
dbSNP Id: rs201798163

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214792367A>T , CM000664.2:g.214792367A>T GRCh38
NC_000002.11:g.215657091A>T , CM000664.1:g.215657091A>T GRCh37
NC_000002.10:g.215365336A>T NCBI36
NG_012047.2:g.22338T>A
NG_012047.3:g.22345T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000260947.9:c.294T>A MANE Select ENSP00000260947.4:p.Asn98Lys
ENST00000421162.2:c.215+4694T>A ENSP00000392245.2:n.215+4694T>A
ENST00000613192.2:c.158+17045T>A ENSP00000483275.2:n.158+17045T>A
ENST00000613374.5:c.158+17045T>A ENSP00000484464.1:n.158+17045T>A
ENST00000613706.5:c.294T>A ENSP00000484976.2:p.Asn98Lys
ENST00000617164.5:c.237T>A ENSP00000480470.1:p.Asn79Lys
ENST00000619009.5:c.294T>A ENSP00000482293.1:p.Asn98Lys
ENST00000650978.1:c.136T>A
ENST00000260947.8:c.294T>A ENSP00000260947.4:p.Asn98Lys
ENST00000421162.1:c.215+4694T>A ENSP00000392245.1:n.215+4694T>A
ENST00000455743.5:c.215+4694T>A ENSP00000412186.1:n.215+4694T>A
ENST00000471787.1:n.260-10858T>A
ENST00000613192.1:c.73+17045T>A ENSP00000483275.1:n.73+17045T>A
ENST00000613374.4:c.158+17045T>A ENSP00000484464.1:n.158+17045T>A
ENST00000613706.4:c.215+4694T>A ENSP00000484976.1:n.215+4694T>A
ENST00000617164.4:c.237T>A ENSP00000480470.1:p.Asn79Lys
ENST00000619009.4:c.294T>A ENSP00000482293.1:p.Asn98Lys
ENST00000620057.4:c.294T>A ENSP00000481988.1:p.Asn98Lys
NM_000465.3:c.294T>A NP_000456.2:p.Asn98Lys
NM_001282543.1:c.237T>A NP_001269472.1:p.Asn79Lys
NM_001282545.1:c.215+4694T>A NP_001269474.1:n.215+4694T>A
NM_001282548.1:c.158+17045T>A NP_001269477.1:n.158+17045T>A
NM_001282549.1:c.294T>A NP_001269478.1:p.Asn98Lys
NR_104212.1:n.357+4694T>A
NR_104215.1:n.301-10858T>A
NR_104216.1:n.436T>A
XM_011511567.1:c.240T>A XP_011509869.1:p.Asn80Lys
XM_011511568.1:c.294T>A XP_011509870.1:p.Asn98Lys
XM_017004613.1:c.393T>A XP_016860102.1:p.Asn131Lys
XM_017004614.1:c.393T>A XP_016860103.1:p.Asn131Lys
XR_002959322.1:n.484T>A
NM_000465.4:c.294T>A MANE Select NP_000456.2:p.Asn98Lys
NM_001282543.2:c.237T>A NP_001269472.1:p.Asn79Lys
NM_001282545.2:c.215+4694T>A NP_001269474.1:n.215+4694T>A
NM_001282548.2:c.158+17045T>A NP_001269477.1:n.158+17045T>A
NM_001282549.2:c.294T>A NP_001269478.1:p.Asn98Lys
NR_104212.2:n.329+4694T>A
NR_104215.2:n.273-10858T>A
NR_104216.2:n.408T>A