Canonical Allele Identifier: CA1327070904
Gene: BARD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214780589_214780590delinsCT , CM000664.2:g.214780589_214780590delinsCT GRCh38
NC_000002.11:g.215645313_215645314delinsCT , CM000664.1:g.215645313_215645314delinsCT GRCh37
NC_000002.10:g.215353558_215353559delinsCT NCBI36
NG_012047.2:g.34115_34116delinsAG
NG_012047.3:g.34122_34123delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000260947.9:c.1284_1285delinsAG MANE Select ENSP00000260947.4:p.Gly428=
ENST00000421162.2:c.215+16471_215+16472delinsAG ENSP00000392245.2:n.215+16471_215+16472delinsAG
ENST00000613192.2:c.158+28822_158+28823delinsAG ENSP00000483275.2:n.158+28822_158+28823delinsAG
ENST00000613374.5:c.159-28035_159-28034delinsAG ENSP00000484464.1:n.159-28035_159-28034delinsAG
ENST00000613706.5:c.906+378_906+379delinsAG ENSP00000484976.2:n.906+378_906+379delinsAG
ENST00000617164.5:c.1227_1228delinsAG ENSP00000480470.1:p.Gly409=
ENST00000619009.5:c.364+11707_364+11708delinsAG ENSP00000482293.1:n.364+11707_364+11708delinsAG
ENST00000650978.1:c.1126_1127delinsAG
ENST00000260947.8:c.1284_1285delinsAG ENSP00000260947.4:p.Gly428=
ENST00000421162.1:c.215+16471_215+16472delinsAG ENSP00000392245.1:n.215+16471_215+16472delinsAG
ENST00000455743.5:c.*904_*905delinsAG ENSP00000412186.1:n.*904_*905delinsAG
ENST00000613192.1:c.73+28822_73+28823delinsAG ENSP00000483275.1:n.73+28822_73+28823delinsAG
ENST00000613374.4:c.159-28035_159-28034delinsAG ENSP00000484464.1:n.159-28035_159-28034delinsAG
ENST00000613706.4:c.215+16471_215+16472delinsAG ENSP00000484976.1:n.215+16471_215+16472delinsAG
ENST00000617164.4:c.1227_1228delinsAG ENSP00000480470.1:p.Gly409=
ENST00000619009.4:c.364+11707_364+11708delinsAG ENSP00000482293.1:n.364+11707_364+11708delinsAG
ENST00000620057.4:c.365-11278_365-11277delinsAG ENSP00000481988.1:n.365-11278_365-11277delinsAG
NM_000465.3:c.1284_1285delinsAG NP_000456.2:p.Gly428=
NM_001282543.1:c.1227_1228delinsAG NP_001269472.1:p.Gly409=
NM_001282545.1:c.215+16471_215+16472delinsAG NP_001269474.1:n.215+16471_215+16472delinsAG
NM_001282548.1:c.159-28035_159-28034delinsAG NP_001269477.1:n.159-28035_159-28034delinsAG
NM_001282549.1:c.364+11707_364+11708delinsAG NP_001269478.1:n.364+11707_364+11708delinsAG
NR_104212.1:n.1277_1278delinsAG
NR_104215.1:n.1220_1221delinsAG
NR_104216.1:n.507-11278_507-11277delinsAG
XM_011511567.1:c.1230_1231delinsAG XP_011509869.1:p.Gly410=
XM_011511568.1:c.1284_1285delinsAG XP_011509870.1:p.Gly428=
XM_017004613.1:c.1383_1384delinsAG XP_016860102.1:p.Gly461=
XM_017004614.1:c.1383_1384delinsAG XP_016860103.1:p.Gly461=
XR_002959322.1:n.1474_1475delinsAG
NM_000465.4:c.1284_1285delinsAG MANE Select NP_000456.2:p.Gly428=
NM_001282543.2:c.1227_1228delinsAG NP_001269472.1:p.Gly409=
NM_001282545.2:c.215+16471_215+16472delinsAG NP_001269474.1:n.215+16471_215+16472delinsAG
NM_001282548.2:c.159-28035_159-28034delinsAG NP_001269477.1:n.159-28035_159-28034delinsAG
NM_001282549.2:c.364+11707_364+11708delinsAG NP_001269478.1:n.364+11707_364+11708delinsAG
NR_104212.2:n.1249_1250delinsAG
NR_104215.2:n.1192_1193delinsAG
NR_104216.2:n.479-11278_479-11277delinsAG