Canonical Allele Identifier: CA1327071115
Gene: BARD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214780859_214780860delinsTG , CM000664.2:g.214780859_214780860delinsTG GRCh38
NC_000002.11:g.215645583_215645584delinsTG , CM000664.1:g.215645583_215645584delinsTG GRCh37
NC_000002.10:g.215353828_215353829delinsTG NCBI36
NG_012047.2:g.33845_33846delinsCA
NG_012047.3:g.33852_33853delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000260947.9:c.1014_1015delinsCA MANE Select ENSP00000260947.4:p.Thr338=
ENST00000421162.2:c.215+16201_215+16202delinsCA ENSP00000392245.2:n.215+16201_215+16202delinsCA
ENST00000613192.2:c.158+28552_158+28553delinsCA ENSP00000483275.2:n.158+28552_158+28553delinsCA
ENST00000613374.5:c.159-28305_159-28304delinsCA ENSP00000484464.1:n.159-28305_159-28304delinsCA
ENST00000613706.5:c.906+108_906+109delinsCA ENSP00000484976.2:n.906+108_906+109delinsCA
ENST00000617164.5:c.957_958delinsCA ENSP00000480470.1:p.Thr319=
ENST00000619009.5:c.364+11437_364+11438delinsCA ENSP00000482293.1:n.364+11437_364+11438delinsCA
ENST00000650978.1:c.856_857delinsCA
ENST00000260947.8:c.1014_1015delinsCA ENSP00000260947.4:p.Thr338=
ENST00000421162.1:c.215+16201_215+16202delinsCA ENSP00000392245.1:n.215+16201_215+16202delinsCA
ENST00000455743.5:c.*634_*635delinsCA ENSP00000412186.1:n.*634_*635delinsCA
ENST00000613192.1:c.73+28552_73+28553delinsCA ENSP00000483275.1:n.73+28552_73+28553delinsCA
ENST00000613374.4:c.159-28305_159-28304delinsCA ENSP00000484464.1:n.159-28305_159-28304delinsCA
ENST00000613706.4:c.215+16201_215+16202delinsCA ENSP00000484976.1:n.215+16201_215+16202delinsCA
ENST00000617164.4:c.957_958delinsCA ENSP00000480470.1:p.Thr319=
ENST00000619009.4:c.364+11437_364+11438delinsCA ENSP00000482293.1:n.364+11437_364+11438delinsCA
ENST00000620057.4:c.364+11437_364+11438delinsCA ENSP00000481988.1:n.364+11437_364+11438delinsCA
NM_000465.3:c.1014_1015delinsCA NP_000456.2:p.Thr338=
NM_001282543.1:c.957_958delinsCA NP_001269472.1:p.Thr319=
NM_001282545.1:c.215+16201_215+16202delinsCA NP_001269474.1:n.215+16201_215+16202delinsCA
NM_001282548.1:c.159-28305_159-28304delinsCA NP_001269477.1:n.159-28305_159-28304delinsCA
NM_001282549.1:c.364+11437_364+11438delinsCA NP_001269478.1:n.364+11437_364+11438delinsCA
NR_104212.1:n.1007_1008delinsCA
NR_104215.1:n.950_951delinsCA
NR_104216.1:n.506+11437_506+11438delinsCA
XM_011511567.1:c.960_961delinsCA XP_011509869.1:p.Thr320=
XM_011511568.1:c.1014_1015delinsCA XP_011509870.1:p.Thr338=
XM_017004613.1:c.1113_1114delinsCA XP_016860102.1:p.Thr371=
XM_017004614.1:c.1113_1114delinsCA XP_016860103.1:p.Thr371=
XR_002959322.1:n.1204_1205delinsCA
NM_000465.4:c.1014_1015delinsCA MANE Select NP_000456.2:p.Thr338=
NM_001282543.2:c.957_958delinsCA NP_001269472.1:p.Thr319=
NM_001282545.2:c.215+16201_215+16202delinsCA NP_001269474.1:n.215+16201_215+16202delinsCA
NM_001282548.2:c.159-28305_159-28304delinsCA NP_001269477.1:n.159-28305_159-28304delinsCA
NM_001282549.2:c.364+11437_364+11438delinsCA NP_001269478.1:n.364+11437_364+11438delinsCA
NR_104212.2:n.979_980delinsCA
NR_104215.2:n.922_923delinsCA
NR_104216.2:n.478+11437_478+11438delinsCA