Canonical Allele Identifier: CA1327053308
Gene: BARD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214745059_214745060delinsAC , CM000664.2:g.214745059_214745060delinsAC GRCh38
NC_000002.11:g.215609783_215609784delinsAC , CM000664.1:g.215609783_215609784delinsAC GRCh37
NC_000002.10:g.215318028_215318029delinsAC NCBI36
NG_012047.2:g.69645_69646delinsGT
NG_012047.3:g.69652_69653delinsGT

Transcript Alleles

HGVS Amino-acid change
ENST00000260947.9:c.1903+7_1903+8delinsGT MANE Select ENSP00000260947.4:n.1903+7_1903+8delinsGT...
ENST00000421162.2:c.550+7_550+8delinsGT ENSP00000392245.2:n.550+7_550+8delinsGT
ENST00000613192.2:c.159-14552_159-14551delinsGT ENSP00000483275.2:n.159-14552_159-14551de...
ENST00000613374.5:c.493+7_493+8delinsGT ENSP00000484464.1:n.493+7_493+8delinsGT
ENST00000613706.5:c.1495+7_1495+8delinsGT ENSP00000484976.2:n.1495+7_1495+8delinsGT...
ENST00000617164.5:c.1846+7_1846+8delinsGT ENSP00000480470.1:n.1846+7_1846+8delinsGT...
ENST00000619009.5:c.365-14552_365-14551delinsGT ENSP00000482293.1:n.365-14552_365-14551de...
ENST00000650978.1:c.3278+7_3278+8delinsGT
ENST00000260947.8:c.1903+7_1903+8delinsGT ENSP00000260947.4:n.1903+7_1903+8delinsGT...
ENST00000421162.1:c.550+7_550+8delinsGT ENSP00000392245.1:n.550+7_550+8delinsGT
ENST00000455743.5:c.*1523+7_*1523+8delinsGT ENSP00000412186.1:n.*1523+7_*1523+8delins...
ENST00000613192.1:c.74-14552_74-14551delinsGT ENSP00000483275.1:n.74-14552_74-14551deli...
ENST00000613374.4:c.493+7_493+8delinsGT ENSP00000484464.1:n.493+7_493+8delinsGT
ENST00000613706.4:c.550+7_550+8delinsGT ENSP00000484976.1:n.550+7_550+8delinsGT
ENST00000617164.4:c.1846+7_1846+8delinsGT ENSP00000480470.1:n.1846+7_1846+8delinsGT...
ENST00000619009.4:c.365-14552_365-14551delinsGT ENSP00000482293.1:n.365-14552_365-14551de...
ENST00000620057.4:c.*569+7_*569+8delinsGT ENSP00000481988.1:n.*569+7_*569+8delinsGT...
NM_000465.3:c.1903+7_1903+8delinsGT NP_000456.2:n.1903+7_1903+8delinsGT
NM_001282543.1:c.1846+7_1846+8delinsGT NP_001269472.1:n.1846+7_1846+8delinsGT
NM_001282545.1:c.550+7_550+8delinsGT NP_001269474.1:n.550+7_550+8delinsGT
NM_001282548.1:c.493+7_493+8delinsGT NP_001269477.1:n.493+7_493+8delinsGT
NM_001282549.1:c.365-14552_365-14551delinsGT NP_001269478.1:n.365-14552_365-14551delin...
NR_104212.1:n.1896+7_1896+8delinsGT
NR_104215.1:n.1839+7_1839+8delinsGT
NR_104216.1:n.1095+7_1095+8delinsGT
XM_011511567.1:c.1849+7_1849+8delinsGT XP_011509869.1:n.1849+7_1849+8delinsGT
XM_011511568.1:c.1903+7_1903+8delinsGT XP_011509870.1:n.1903+7_1903+8delinsGT
XM_017004613.1:c.2002+7_2002+8delinsGT XP_016860102.1:n.2002+7_2002+8delinsGT
XM_017004614.1:c.2002+7_2002+8delinsGT XP_016860103.1:n.2002+7_2002+8delinsGT
XR_002959322.1:n.2093+7_2093+8delinsGT
NM_000465.4:c.1903+7_1903+8delinsGT MANE Select NP_000456.2:n.1903+7_1903+8delinsGT
NM_001282543.2:c.1846+7_1846+8delinsGT NP_001269472.1:n.1846+7_1846+8delinsGT
NM_001282545.2:c.550+7_550+8delinsGT NP_001269474.1:n.550+7_550+8delinsGT
NM_001282548.2:c.493+7_493+8delinsGT NP_001269477.1:n.493+7_493+8delinsGT
NM_001282549.2:c.365-14552_365-14551delinsGT NP_001269478.1:n.365-14552_365-14551delin...
NR_104212.2:n.1868+7_1868+8delinsGT
NR_104215.2:n.1811+7_1811+8delinsGT
NR_104216.2:n.1067+7_1067+8delinsGT