Canonical Allele Identifier: CA1327045409
Gene: BARD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214728637C= , CM000664.2:g.214728637C= GRCh38
NC_000002.11:g.215593361C= , CM000664.1:g.215593361C= GRCh37
NC_000002.10:g.215301606C= NCBI36
NG_012047.2:g.86068G=
NG_012047.3:g.86075G=

Transcript Alleles

HGVS Amino-acid change
ENST00000260947.9:c.*39G= MANE Select ENSP00000260947.4:n.*39G=
ENST00000613374.5:c.*39G= ENSP00000484464.1:n.*39G=
ENST00000613706.5:c.*39G= ENSP00000484976.2:n.*39G=
ENST00000617164.5:c.*39G= ENSP00000480470.1:n.*39G=
ENST00000619009.5:c.*39G= ENSP00000482293.1:n.*39G=
ENST00000650978.1:c.3748G=
ENST00000260947.8:c.*39G= ENSP00000260947.4:n.*39G=
ENST00000432456.5:c.516G=
ENST00000471590.5:n.708G=
ENST00000613374.4:c.*39G= ENSP00000484464.1:n.*39G=
ENST00000613706.4:c.*39G= ENSP00000484976.1:n.*39G=
ENST00000617164.4:c.*39G= ENSP00000480470.1:n.*39G=
ENST00000619009.4:c.*39G= ENSP00000482293.1:n.*39G=
NM_000465.3:c.*39G= NP_000456.2:n.*39G=
NM_001282543.1:c.*39G= NP_001269472.1:n.*39G=
NM_001282545.1:c.*39G= NP_001269474.1:n.*39G=
NM_001282548.1:c.*39G= NP_001269477.1:n.*39G=
NM_001282549.1:c.*39G= NP_001269478.1:n.*39G=
NR_104212.1:n.2366G=
NR_104215.1:n.2309G=
NR_104216.1:n.1565G=
XM_011511567.1:c.*39G= XP_011509869.1:n.*39G=
XM_017004613.1:c.*39G= XP_016860102.1:n.*39G=
XR_002959322.1:n.2739G=
NM_000465.4:c.*39G= MANE Select NP_000456.2:n.*39G=
NM_001282543.2:c.*39G= NP_001269472.1:n.*39G=
NM_001282545.2:c.*39G= NP_001269474.1:n.*39G=
NM_001282548.2:c.*39G= NP_001269477.1:n.*39G=
NM_001282549.2:c.*39G= NP_001269478.1:n.*39G=
NR_104212.2:n.2338G=
NR_104215.2:n.2281G=
NR_104216.2:n.1537G=