Canonical Allele Identifier: CA1327070956
Gene: BARD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214780646_214780650delinsTAGAC , CM000664.2:g.214780646_214780650delinsTAGAC GRCh38
NC_000002.11:g.215645370_215645374delinsTAGAC , CM000664.1:g.215645370_215645374delinsTAGAC GRCh37
NC_000002.10:g.215353615_215353619delinsTAGAC NCBI36
NG_012047.2:g.34055_34059delinsGTCTA
NG_012047.3:g.34062_34066delinsGTCTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000260947.9:c.1224_1228delinsGTCTA MANE Select ENSP00000260947.4:p.Met408=
ENST00000421162.2:c.215+16411_215+16415delinsGTCTA ENSP00000392245.2:n.215+16411_215+16415delinsGTCTA
ENST00000613192.2:c.158+28762_158+28766delinsGTCTA ENSP00000483275.2:n.158+28762_158+28766delinsGTCTA
ENST00000613374.5:c.159-28095_159-28091delinsGTCTA ENSP00000484464.1:n.159-28095_159-28091delinsGTCTA
ENST00000613706.5:c.906+318_906+322delinsGTCTA ENSP00000484976.2:n.906+318_906+322delinsGTCTA
ENST00000617164.5:c.1167_1171delinsGTCTA ENSP00000480470.1:p.Met389=
ENST00000619009.5:c.364+11647_364+11651delinsGTCTA ENSP00000482293.1:n.364+11647_364+11651delinsGTCTA
ENST00000650978.1:c.1066_1070delinsGTCTA
ENST00000260947.8:c.1224_1228delinsGTCTA ENSP00000260947.4:p.Met408=
ENST00000421162.1:c.215+16411_215+16415delinsGTCTA ENSP00000392245.1:n.215+16411_215+16415delinsGTCTA
ENST00000455743.5:c.*844_*848delinsGTCTA ENSP00000412186.1:n.*844_*848delinsGTCTA
ENST00000613192.1:c.73+28762_73+28766delinsGTCTA ENSP00000483275.1:n.73+28762_73+28766delinsGTCTA
ENST00000613374.4:c.159-28095_159-28091delinsGTCTA ENSP00000484464.1:n.159-28095_159-28091delinsGTCTA
ENST00000613706.4:c.215+16411_215+16415delinsGTCTA ENSP00000484976.1:n.215+16411_215+16415delinsGTCTA
ENST00000617164.4:c.1167_1171delinsGTCTA ENSP00000480470.1:p.Met389=
ENST00000619009.4:c.364+11647_364+11651delinsGTCTA ENSP00000482293.1:n.364+11647_364+11651delinsGTCTA
ENST00000620057.4:c.365-11338_365-11334delinsGTCTA ENSP00000481988.1:n.365-11338_365-11334delinsGTCTA
NM_000465.3:c.1224_1228delinsGTCTA NP_000456.2:p.Met408=
NM_001282543.1:c.1167_1171delinsGTCTA NP_001269472.1:p.Met389=
NM_001282545.1:c.215+16411_215+16415delinsGTCTA NP_001269474.1:n.215+16411_215+16415delinsGTCTA
NM_001282548.1:c.159-28095_159-28091delinsGTCTA NP_001269477.1:n.159-28095_159-28091delinsGTCTA
NM_001282549.1:c.364+11647_364+11651delinsGTCTA NP_001269478.1:n.364+11647_364+11651delinsGTCTA
NR_104212.1:n.1217_1221delinsGTCTA
NR_104215.1:n.1160_1164delinsGTCTA
NR_104216.1:n.507-11338_507-11334delinsGTCTA
XM_011511567.1:c.1170_1174delinsGTCTA XP_011509869.1:p.Met390=
XM_011511568.1:c.1224_1228delinsGTCTA XP_011509870.1:p.Met408=
XM_017004613.1:c.1323_1327delinsGTCTA XP_016860102.1:p.Met441=
XM_017004614.1:c.1323_1327delinsGTCTA XP_016860103.1:p.Met441=
XR_002959322.1:n.1414_1418delinsGTCTA
NM_000465.4:c.1224_1228delinsGTCTA MANE Select NP_000456.2:p.Met408=
NM_001282543.2:c.1167_1171delinsGTCTA NP_001269472.1:p.Met389=
NM_001282545.2:c.215+16411_215+16415delinsGTCTA NP_001269474.1:n.215+16411_215+16415delinsGTCTA
NM_001282548.2:c.159-28095_159-28091delinsGTCTA NP_001269477.1:n.159-28095_159-28091delinsGTCTA
NM_001282549.2:c.364+11647_364+11651delinsGTCTA NP_001269478.1:n.364+11647_364+11651delinsGTCTA
NR_104212.2:n.1189_1193delinsGTCTA
NR_104215.2:n.1132_1136delinsGTCTA
NR_104216.2:n.479-11338_479-11334delinsGTCTA