Canonical Allele Identifier: CA2662969806
Gene: BARD1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214728568A>G , CM000664.2:g.214728568A>G GRCh38
NC_000002.11:g.215593292A>G , CM000664.1:g.215593292A>G GRCh37
NC_000002.10:g.215301537A>G NCBI36
NG_012047.2:g.86137T>C
NG_012047.3:g.86144T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000260947.9:c.*108T>C MANE Select ENSP00000260947.4:n.*108T>C
ENST00000613374.5:c.*108T>C ENSP00000484464.1:n.*108T>C
ENST00000617164.5:c.*108T>C ENSP00000480470.1:n.*108T>C
ENST00000619009.5:c.*108T>C ENSP00000482293.1:n.*108T>C
ENST00000260947.8:c.*108T>C ENSP00000260947.4:n.*108T>C
ENST00000432456.5:c.585T>C
ENST00000471590.5:n.777T>C
ENST00000613374.4:c.*108T>C ENSP00000484464.1:n.*108T>C
ENST00000613706.4:c.*108T>C ENSP00000484976.1:n.*108T>C
ENST00000617164.4:c.*108T>C ENSP00000480470.1:n.*108T>C
ENST00000619009.4:c.*108T>C ENSP00000482293.1:n.*108T>C
NM_000465.3:c.*108T>C NP_000456.2:n.*108T>C
NM_001282543.1:c.*108T>C NP_001269472.1:n.*108T>C
NM_001282545.1:c.*108T>C NP_001269474.1:n.*108T>C
NM_001282548.1:c.*108T>C NP_001269477.1:n.*108T>C
NM_001282549.1:c.*108T>C NP_001269478.1:n.*108T>C
NR_104212.1:n.2435T>C
NR_104215.1:n.2378T>C
NR_104216.1:n.1634T>C
XM_011511567.1:c.*108T>C XP_011509869.1:n.*108T>C
XM_017004613.1:c.*108T>C XP_016860102.1:n.*108T>C
XR_002959322.1:n.2808T>C
NM_000465.4:c.*108T>C MANE Select NP_000456.2:n.*108T>C
NM_001282543.2:c.*108T>C NP_001269472.1:n.*108T>C
NM_001282545.2:c.*108T>C NP_001269474.1:n.*108T>C
NM_001282548.2:c.*108T>C NP_001269477.1:n.*108T>C
NM_001282549.2:c.*108T>C NP_001269478.1:n.*108T>C
NR_104212.2:n.2407T>C
NR_104215.2:n.2350T>C
NR_104216.2:n.1606T>C