Canonical Allele Identifier: CA1327078908
Gene: BARD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214797032A= , CM000664.2:g.214797032A= GRCh38
NC_000002.11:g.215661756A= , CM000664.1:g.215661756A= GRCh37
NC_000002.10:g.215370001A= NCBI36
NG_012047.2:g.17673T=
NG_012047.3:g.17680T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000260947.9:c.215+29T= MANE Select ENSP00000260947.4:n.215+29T=
ENST00000421162.2:c.215+29T= ENSP00000392245.2:n.215+29T=
ENST00000613192.2:c.158+12380T= ENSP00000483275.2:n.158+12380T=
ENST00000613374.5:c.158+12380T= ENSP00000484464.1:n.158+12380T=
ENST00000613706.5:c.215+29T= ENSP00000484976.2:n.215+29T=
ENST00000617164.5:c.159-4587T= ENSP00000480470.1:n.159-4587T=
ENST00000619009.5:c.215+29T= ENSP00000482293.1:n.215+29T=
ENST00000650978.1:c.57+29T=
ENST00000260947.8:c.215+29T= ENSP00000260947.4:n.215+29T=
ENST00000421162.1:c.215+29T= ENSP00000392245.1:n.215+29T=
ENST00000455743.5:c.215+29T= ENSP00000412186.1:n.215+29T=
ENST00000471787.1:n.259+12380T=
ENST00000479904.1:n.335T=
ENST00000613192.1:c.73+12380T= ENSP00000483275.1:n.73+12380T=
ENST00000613374.4:c.158+12380T= ENSP00000484464.1:n.158+12380T=
ENST00000613706.4:c.215+29T= ENSP00000484976.1:n.215+29T=
ENST00000617164.4:c.159-4587T= ENSP00000480470.1:n.159-4587T=
ENST00000619009.4:c.215+29T= ENSP00000482293.1:n.215+29T=
ENST00000620057.4:c.215+29T= ENSP00000481988.1:n.215+29T=
NM_000465.3:c.215+29T= NP_000456.2:n.215+29T=
NM_001282543.1:c.159-4587T= NP_001269472.1:n.159-4587T=
NM_001282545.1:c.215+29T= NP_001269474.1:n.215+29T=
NM_001282548.1:c.158+12380T= NP_001269477.1:n.158+12380T=
NM_001282549.1:c.215+29T= NP_001269478.1:n.215+29T=
NR_104212.1:n.357+29T=
NR_104215.1:n.300+12380T=
NR_104216.1:n.357+29T=
XM_011511567.1:c.161+29T= XP_011509869.1:n.161+29T=
XM_011511568.1:c.215+29T= XP_011509870.1:n.215+29T=
XM_017004613.1:c.215+29T= XP_016860102.1:n.215+29T=
XM_017004614.1:c.215+29T= XP_016860103.1:n.215+29T=
XR_002959322.1:n.306+29T=
NM_000465.4:c.215+29T= MANE Select NP_000456.2:n.215+29T=
NM_001282543.2:c.159-4587T= NP_001269472.1:n.159-4587T=
NM_001282545.2:c.215+29T= NP_001269474.1:n.215+29T=
NM_001282548.2:c.158+12380T= NP_001269477.1:n.158+12380T=
NM_001282549.2:c.215+29T= NP_001269478.1:n.215+29T=
NR_104212.2:n.329+29T=
NR_104215.2:n.272+12380T=
NR_104216.2:n.329+29T=