Canonical Allele Identifier: CA1327070981
Gene: BARD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214780676_214780687delinsTTAATGTAGAAG , CM000664.2:g.214780676_214780687delinsTTAATGTAGAAG GRCh38
NC_000002.11:g.215645400_215645411delinsTTAATGTAGAAG , CM000664.1:g.215645400_215645411delinsTTAATGTAGAAG GRCh37
NC_000002.10:g.215353645_215353656delinsTTAATGTAGAAG NCBI36
NG_012047.2:g.34018_34029delinsCTTCTACATTAA
NG_012047.3:g.34025_34036delinsCTTCTACATTAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000260947.9:c.1187_1198delinsCTTCTACATTAA MANE Select ENSP00000260947.4:p.Pro396=
ENST00000421162.2:c.215+16374_215+16385delinsCTTCTACATTAA ENSP00000392245.2:n.215+16374_215+16385delinsCTTCTACATTAA
ENST00000613192.2:c.158+28725_158+28736delinsCTTCTACATTAA ENSP00000483275.2:n.158+28725_158+28736delinsCTTCTACATTAA
ENST00000613374.5:c.159-28132_159-28121delinsCTTCTACATTAA ENSP00000484464.1:n.159-28132_159-28121delinsCTTCTACATTAA
ENST00000613706.5:c.906+281_906+292delinsCTTCTACATTAA ENSP00000484976.2:n.906+281_906+292delinsCTTCTACATTAA
ENST00000617164.5:c.1130_1141delinsCTTCTACATTAA ENSP00000480470.1:p.Pro377=
ENST00000619009.5:c.364+11610_364+11621delinsCTTCTACATTAA ENSP00000482293.1:n.364+11610_364+11621delinsCTTCTACATTAA
ENST00000650978.1:c.1029_1040delinsCTTCTACATTAA
ENST00000260947.8:c.1187_1198delinsCTTCTACATTAA ENSP00000260947.4:p.Pro396=
ENST00000421162.1:c.215+16374_215+16385delinsCTTCTACATTAA ENSP00000392245.1:n.215+16374_215+16385delinsCTTCTACATTAA
ENST00000455743.5:c.*807_*818delinsCTTCTACATTAA ENSP00000412186.1:n.*807_*818delinsCTTCTACATTAA
ENST00000613192.1:c.73+28725_73+28736delinsCTTCTACATTAA ENSP00000483275.1:n.73+28725_73+28736delinsCTTCTACATTAA
ENST00000613374.4:c.159-28132_159-28121delinsCTTCTACATTAA ENSP00000484464.1:n.159-28132_159-28121delinsCTTCTACATTAA
ENST00000613706.4:c.215+16374_215+16385delinsCTTCTACATTAA ENSP00000484976.1:n.215+16374_215+16385delinsCTTCTACATTAA
ENST00000617164.4:c.1130_1141delinsCTTCTACATTAA ENSP00000480470.1:p.Pro377=
ENST00000619009.4:c.364+11610_364+11621delinsCTTCTACATTAA ENSP00000482293.1:n.364+11610_364+11621delinsCTTCTACATTAA
ENST00000620057.4:c.365-11375_365-11364delinsCTTCTACATTAA ENSP00000481988.1:n.365-11375_365-11364delinsCTTCTACATTAA
NM_000465.3:c.1187_1198delinsCTTCTACATTAA NP_000456.2:p.Pro396=
NM_001282543.1:c.1130_1141delinsCTTCTACATTAA NP_001269472.1:p.Pro377=
NM_001282545.1:c.215+16374_215+16385delinsCTTCTACATTAA NP_001269474.1:n.215+16374_215+16385delinsCTTCTACATTAA
NM_001282548.1:c.159-28132_159-28121delinsCTTCTACATTAA NP_001269477.1:n.159-28132_159-28121delinsCTTCTACATTAA
NM_001282549.1:c.364+11610_364+11621delinsCTTCTACATTAA NP_001269478.1:n.364+11610_364+11621delinsCTTCTACATTAA
NR_104212.1:n.1180_1191delinsCTTCTACATTAA
NR_104215.1:n.1123_1134delinsCTTCTACATTAA
NR_104216.1:n.507-11375_507-11364delinsCTTCTACATTAA
XM_011511567.1:c.1133_1144delinsCTTCTACATTAA XP_011509869.1:p.Pro378=
XM_011511568.1:c.1187_1198delinsCTTCTACATTAA XP_011509870.1:p.Pro396=
XM_017004613.1:c.1286_1297delinsCTTCTACATTAA XP_016860102.1:p.Pro429=
XM_017004614.1:c.1286_1297delinsCTTCTACATTAA XP_016860103.1:p.Pro429=
XR_002959322.1:n.1377_1388delinsCTTCTACATTAA
NM_000465.4:c.1187_1198delinsCTTCTACATTAA MANE Select NP_000456.2:p.Pro396=
NM_001282543.2:c.1130_1141delinsCTTCTACATTAA NP_001269472.1:p.Pro377=
NM_001282545.2:c.215+16374_215+16385delinsCTTCTACATTAA NP_001269474.1:n.215+16374_215+16385delinsCTTCTACATTAA
NM_001282548.2:c.159-28132_159-28121delinsCTTCTACATTAA NP_001269477.1:n.159-28132_159-28121delinsCTTCTACATTAA
NM_001282549.2:c.364+11610_364+11621delinsCTTCTACATTAA NP_001269478.1:n.364+11610_364+11621delinsCTTCTACATTAA
NR_104212.2:n.1152_1163delinsCTTCTACATTAA
NR_104215.2:n.1095_1106delinsCTTCTACATTAA
NR_104216.2:n.479-11375_479-11364delinsCTTCTACATTAA