Canonical Allele Identifier: CA1327066312
Gene: BARD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214771142A= , CM000664.2:g.214771142A= GRCh38
NC_000002.11:g.215635866A= , CM000664.1:g.215635866A= GRCh37
NC_000002.10:g.215344111A= NCBI36
NG_012047.2:g.43563T=
NG_012047.3:g.43570T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000260947.9:c.1315-1830T= MANE Select ENSP00000260947.4:n.1315-1830T=
ENST00000421162.2:c.216-18587T= ENSP00000392245.2:n.216-18587T=
ENST00000613192.2:c.158+38270T= ENSP00000483275.2:n.158+38270T=
ENST00000613374.5:c.159-18587T= ENSP00000484464.1:n.159-18587T=
ENST00000613706.5:c.907-1830T= ENSP00000484976.2:n.907-1830T=
ENST00000617164.5:c.1258-1830T= ENSP00000480470.1:n.1258-1830T=
ENST00000619009.5:c.364+21155T= ENSP00000482293.1:n.364+21155T=
ENST00000650978.1:c.1157-297T=
ENST00000260947.8:c.1315-1830T= ENSP00000260947.4:n.1315-1830T=
ENST00000421162.1:c.216-18587T= ENSP00000392245.1:n.216-18587T=
ENST00000455743.5:c.*935-1830T= ENSP00000412186.1:n.*935-1830T=
ENST00000613192.1:c.73+38270T= ENSP00000483275.1:n.73+38270T=
ENST00000613374.4:c.159-18587T= ENSP00000484464.1:n.159-18587T=
ENST00000613706.4:c.216-18587T= ENSP00000484976.1:n.216-18587T=
ENST00000617164.4:c.1258-1830T= ENSP00000480470.1:n.1258-1830T=
ENST00000619009.4:c.364+21155T= ENSP00000482293.1:n.364+21155T=
ENST00000620057.4:c.365-1830T= ENSP00000481988.1:n.365-1830T=
NM_000465.3:c.1315-1830T= NP_000456.2:n.1315-1830T=
NM_001282543.1:c.1258-1830T= NP_001269472.1:n.1258-1830T=
NM_001282545.1:c.216-18587T= NP_001269474.1:n.216-18587T=
NM_001282548.1:c.159-18587T= NP_001269477.1:n.159-18587T=
NM_001282549.1:c.364+21155T= NP_001269478.1:n.364+21155T=
NR_104212.1:n.1308-1830T=
NR_104215.1:n.1251-1830T=
NR_104216.1:n.507-1830T=
XM_011511567.1:c.1261-1830T= XP_011509869.1:n.1261-1830T=
XM_011511568.1:c.1315-1830T= XP_011509870.1:n.1315-1830T=
XM_017004613.1:c.1414-1830T= XP_016860102.1:n.1414-1830T=
XM_017004614.1:c.1414-1830T= XP_016860103.1:n.1414-1830T=
XR_002959322.1:n.1505-1830T=
NM_000465.4:c.1315-1830T= MANE Select NP_000456.2:n.1315-1830T=
NM_001282543.2:c.1258-1830T= NP_001269472.1:n.1258-1830T=
NM_001282545.2:c.216-18587T= NP_001269474.1:n.216-18587T=
NM_001282548.2:c.159-18587T= NP_001269477.1:n.159-18587T=
NM_001282549.2:c.364+21155T= NP_001269478.1:n.364+21155T=
NR_104212.2:n.1280-1830T=
NR_104215.2:n.1223-1830T=
NR_104216.2:n.479-1830T=