Canonical Allele Identifier: CA1327053303
Gene: BARD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214745051_214745052delinsCA , CM000664.2:g.214745051_214745052delinsCA GRCh38
NC_000002.11:g.215609775_215609776delinsCA , CM000664.1:g.215609775_215609776delinsCA GRCh37
NC_000002.10:g.215318020_215318021delinsCA NCBI36
NG_012047.2:g.69653_69654delinsTG
NG_012047.3:g.69660_69661delinsTG

Transcript Alleles

HGVS Amino-acid change
ENST00000260947.9:c.1903+15_1903+16delinsTG MANE Select ENSP00000260947.4:n.1903+15_1903+16delins...
ENST00000421162.2:c.550+15_550+16delinsTG ENSP00000392245.2:n.550+15_550+16delinsTG...
ENST00000613192.2:c.159-14544_159-14543delinsTG ENSP00000483275.2:n.159-14544_159-14543de...
ENST00000613374.5:c.493+15_493+16delinsTG ENSP00000484464.1:n.493+15_493+16delinsTG...
ENST00000613706.5:c.1495+15_1495+16delinsTG ENSP00000484976.2:n.1495+15_1495+16delins...
ENST00000617164.5:c.1846+15_1846+16delinsTG ENSP00000480470.1:n.1846+15_1846+16delins...
ENST00000619009.5:c.365-14544_365-14543delinsTG ENSP00000482293.1:n.365-14544_365-14543de...
ENST00000650978.1:c.3278+15_3278+16delinsTG
ENST00000260947.8:c.1903+15_1903+16delinsTG ENSP00000260947.4:n.1903+15_1903+16delins...
ENST00000421162.1:c.550+15_550+16delinsTG ENSP00000392245.1:n.550+15_550+16delinsTG...
ENST00000455743.5:c.*1523+15_*1523+16delinsTG ENSP00000412186.1:n.*1523+15_*1523+16deli...
ENST00000613192.1:c.74-14544_74-14543delinsTG ENSP00000483275.1:n.74-14544_74-14543deli...
ENST00000613374.4:c.493+15_493+16delinsTG ENSP00000484464.1:n.493+15_493+16delinsTG...
ENST00000613706.4:c.550+15_550+16delinsTG ENSP00000484976.1:n.550+15_550+16delinsTG...
ENST00000617164.4:c.1846+15_1846+16delinsTG ENSP00000480470.1:n.1846+15_1846+16delins...
ENST00000619009.4:c.365-14544_365-14543delinsTG ENSP00000482293.1:n.365-14544_365-14543de...
ENST00000620057.4:c.*569+15_*569+16delinsTG ENSP00000481988.1:n.*569+15_*569+16delins...
NM_000465.3:c.1903+15_1903+16delinsTG NP_000456.2:n.1903+15_1903+16delinsTG
NM_001282543.1:c.1846+15_1846+16delinsTG NP_001269472.1:n.1846+15_1846+16delinsTG
NM_001282545.1:c.550+15_550+16delinsTG NP_001269474.1:n.550+15_550+16delinsTG
NM_001282548.1:c.493+15_493+16delinsTG NP_001269477.1:n.493+15_493+16delinsTG
NM_001282549.1:c.365-14544_365-14543delinsTG NP_001269478.1:n.365-14544_365-14543delin...
NR_104212.1:n.1896+15_1896+16delinsTG
NR_104215.1:n.1839+15_1839+16delinsTG
NR_104216.1:n.1095+15_1095+16delinsTG
XM_011511567.1:c.1849+15_1849+16delinsTG XP_011509869.1:n.1849+15_1849+16delinsTG
XM_011511568.1:c.1903+15_1903+16delinsTG XP_011509870.1:n.1903+15_1903+16delinsTG
XM_017004613.1:c.2002+15_2002+16delinsTG XP_016860102.1:n.2002+15_2002+16delinsTG
XM_017004614.1:c.2002+15_2002+16delinsTG XP_016860103.1:n.2002+15_2002+16delinsTG
XR_002959322.1:n.2093+15_2093+16delinsTG
NM_000465.4:c.1903+15_1903+16delinsTG MANE Select NP_000456.2:n.1903+15_1903+16delinsTG
NM_001282543.2:c.1846+15_1846+16delinsTG NP_001269472.1:n.1846+15_1846+16delinsTG
NM_001282545.2:c.550+15_550+16delinsTG NP_001269474.1:n.550+15_550+16delinsTG
NM_001282548.2:c.493+15_493+16delinsTG NP_001269477.1:n.493+15_493+16delinsTG
NM_001282549.2:c.365-14544_365-14543delinsTG NP_001269478.1:n.365-14544_365-14543delin...
NR_104212.2:n.1868+15_1868+16delinsTG
NR_104215.2:n.1811+15_1811+16delinsTG
NR_104216.2:n.1067+15_1067+16delinsTG