Canonical Allele Identifier: CA350458012
Gene: BARD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 495877
dbSNP Id: rs1553622698

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214781467G>A , CM000664.2:g.214781467G>A GRCh38
NC_000002.11:g.215646191G>A , CM000664.1:g.215646191G>A GRCh37
NC_000002.10:g.215354436G>A NCBI36
NG_012047.2:g.33238C>T
NG_012047.3:g.33245C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000260947.9:c.407C>T MANE Select ENSP00000260947.4:p.Ala136Val
ENST00000421162.2:c.215+15594C>T ENSP00000392245.2:n.215+15594C>T
ENST00000613192.2:c.158+27945C>T ENSP00000483275.2:n.158+27945C>T
ENST00000613374.5:c.158+27945C>T ENSP00000484464.1:n.158+27945C>T
ENST00000613706.5:c.407C>T ENSP00000484976.2:p.Ala136Val
ENST00000617164.5:c.350C>T ENSP00000480470.1:p.Ala117Val
ENST00000619009.5:c.364+10830C>T ENSP00000482293.1:n.364+10830C>T
ENST00000650978.1:c.249C>T
ENST00000260947.8:c.407C>T ENSP00000260947.4:p.Ala136Val
ENST00000421162.1:c.215+15594C>T ENSP00000392245.1:n.215+15594C>T
ENST00000455743.5:c.*27C>T ENSP00000412186.1:n.*27C>T
ENST00000471787.1:n.302C>T
ENST00000613192.1:c.73+27945C>T ENSP00000483275.1:n.73+27945C>T
ENST00000613374.4:c.158+27945C>T ENSP00000484464.1:n.158+27945C>T
ENST00000613706.4:c.215+15594C>T ENSP00000484976.1:n.215+15594C>T
ENST00000617164.4:c.350C>T ENSP00000480470.1:p.Ala117Val
ENST00000619009.4:c.364+10830C>T ENSP00000482293.1:n.364+10830C>T
ENST00000620057.4:c.364+10830C>T ENSP00000481988.1:n.364+10830C>T
NM_000465.3:c.407C>T NP_000456.2:p.Ala136Val
NM_001282543.1:c.350C>T NP_001269472.1:p.Ala117Val
NM_001282545.1:c.215+15594C>T NP_001269474.1:n.215+15594C>T
NM_001282548.1:c.158+27945C>T NP_001269477.1:n.158+27945C>T
NM_001282549.1:c.364+10830C>T NP_001269478.1:n.364+10830C>T
NR_104212.1:n.400C>T
NR_104215.1:n.343C>T
NR_104216.1:n.506+10830C>T
XM_011511567.1:c.353C>T XP_011509869.1:p.Ala118Val
XM_011511568.1:c.407C>T XP_011509870.1:p.Ala136Val
XM_017004613.1:c.506C>T XP_016860102.1:p.Ala169Val
XM_017004614.1:c.506C>T XP_016860103.1:p.Ala169Val
XR_002959322.1:n.597C>T
NM_000465.4:c.407C>T MANE Select NP_000456.2:p.Ala136Val
NM_001282543.2:c.350C>T NP_001269472.1:p.Ala117Val
NM_001282545.2:c.215+15594C>T NP_001269474.1:n.215+15594C>T
NM_001282548.2:c.158+27945C>T NP_001269477.1:n.158+27945C>T
NM_001282549.2:c.364+10830C>T NP_001269478.1:n.364+10830C>T
NR_104212.2:n.372C>T
NR_104215.2:n.315C>T
NR_104216.2:n.478+10830C>T