Canonical Allele Identifier: CA1327053328
Gene: BARD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214745090_214745094delinsCCATT , CM000664.2:g.214745090_214745094delinsCCATT GRCh38
NC_000002.11:g.215609814_215609818delinsCCATT , CM000664.1:g.215609814_215609818delinsCCATT GRCh37
NC_000002.10:g.215318059_215318063delinsCCATT NCBI36
NG_012047.2:g.69611_69615delinsAATGG
NG_012047.3:g.69618_69622delinsAATGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000260947.9:c.1876_1880delinsAATGG MANE Select ENSP00000260947.4:p.Asn626=
ENST00000421162.2:c.523_527delinsAATGG ENSP00000392245.2:p.Asn175=
ENST00000613192.2:c.159-14586_159-14582delinsAATGG ENSP00000483275.2:n.159-14586_159-14582delinsAATGG
ENST00000613374.5:c.466_470delinsAATGG ENSP00000484464.1:p.Asn156=
ENST00000613706.5:c.1468_1472delinsAATGG ENSP00000484976.2:p.Asn490=
ENST00000617164.5:c.1819_1823delinsAATGG ENSP00000480470.1:p.Asn607=
ENST00000619009.5:c.365-14586_365-14582delinsAATGG ENSP00000482293.1:n.365-14586_365-14582delinsAATGG
ENST00000650978.1:c.3251_3255delinsAATGG
ENST00000260947.8:c.1876_1880delinsAATGG ENSP00000260947.4:p.Asn626=
ENST00000421162.1:c.523_527delinsAATGG ENSP00000392245.1:p.Asn175=
ENST00000455743.5:c.*1496_*1500delinsAATGG ENSP00000412186.1:n.*1496_*1500delinsAATGG
ENST00000613192.1:c.74-14586_74-14582delinsAATGG ENSP00000483275.1:n.74-14586_74-14582delinsAATGG
ENST00000613374.4:c.466_470delinsAATGG ENSP00000484464.1:p.Asn156=
ENST00000613706.4:c.523_527delinsAATGG ENSP00000484976.1:p.Asn175=
ENST00000617164.4:c.1819_1823delinsAATGG ENSP00000480470.1:p.Asn607=
ENST00000619009.4:c.365-14586_365-14582delinsAATGG ENSP00000482293.1:n.365-14586_365-14582delinsAATGG
ENST00000620057.4:c.*542_*546delinsAATGG ENSP00000481988.1:n.*542_*546delinsAATGG
NM_000465.3:c.1876_1880delinsAATGG NP_000456.2:p.Asn626=
NM_001282543.1:c.1819_1823delinsAATGG NP_001269472.1:p.Asn607=
NM_001282545.1:c.523_527delinsAATGG NP_001269474.1:p.Asn175=
NM_001282548.1:c.466_470delinsAATGG NP_001269477.1:p.Asn156=
NM_001282549.1:c.365-14586_365-14582delinsAATGG NP_001269478.1:n.365-14586_365-14582delinsAATGG
NR_104212.1:n.1869_1873delinsAATGG
NR_104215.1:n.1812_1816delinsAATGG
NR_104216.1:n.1068_1072delinsAATGG
XM_011511567.1:c.1822_1826delinsAATGG XP_011509869.1:p.Asn608=
XM_011511568.1:c.1876_1880delinsAATGG XP_011509870.1:p.Asn626=
XM_017004613.1:c.1975_1979delinsAATGG XP_016860102.1:p.Asn659=
XM_017004614.1:c.1975_1979delinsAATGG XP_016860103.1:p.Asn659=
XR_002959322.1:n.2066_2070delinsAATGG
NM_000465.4:c.1876_1880delinsAATGG MANE Select NP_000456.2:p.Asn626=
NM_001282543.2:c.1819_1823delinsAATGG NP_001269472.1:p.Asn607=
NM_001282545.2:c.523_527delinsAATGG NP_001269474.1:p.Asn175=
NM_001282548.2:c.466_470delinsAATGG NP_001269477.1:p.Asn156=
NM_001282549.2:c.365-14586_365-14582delinsAATGG NP_001269478.1:n.365-14586_365-14582delinsAATGG
NR_104212.2:n.1841_1845delinsAATGG
NR_104215.2:n.1784_1788delinsAATGG
NR_104216.2:n.1040_1044delinsAATGG