Canonical Allele Identifier: CA539837271
Gene: BARD1 HGNC NCBI

Linked Data

dbSNP Id: rs773111818

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214728663T>C , CM000664.2:g.214728663T>C GRCh38
NC_000002.11:g.215593387T>C , CM000664.1:g.215593387T>C GRCh37
NC_000002.10:g.215301632T>C NCBI36
NG_012047.2:g.86042A>G
NG_012047.3:g.86049A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000260947.9:c.*13A>G MANE Select ENSP00000260947.4:n.*13A>G
ENST00000613374.5:c.*13A>G ENSP00000484464.1:n.*13A>G
ENST00000613706.5:c.*13A>G ENSP00000484976.2:n.*13A>G
ENST00000617164.5:c.*13A>G ENSP00000480470.1:n.*13A>G
ENST00000619009.5:c.*13A>G ENSP00000482293.1:n.*13A>G
ENST00000650978.1:c.3722A>G
ENST00000260947.8:c.*13A>G ENSP00000260947.4:n.*13A>G
ENST00000432456.5:c.490A>G
ENST00000471590.5:n.682A>G
ENST00000613374.4:c.*13A>G ENSP00000484464.1:n.*13A>G
ENST00000613706.4:c.*13A>G ENSP00000484976.1:n.*13A>G
ENST00000617164.4:c.*13A>G ENSP00000480470.1:n.*13A>G
ENST00000619009.4:c.*13A>G ENSP00000482293.1:n.*13A>G
NM_000465.3:c.*13A>G NP_000456.2:n.*13A>G
NM_001282543.1:c.*13A>G NP_001269472.1:n.*13A>G
NM_001282545.1:c.*13A>G NP_001269474.1:n.*13A>G
NM_001282548.1:c.*13A>G NP_001269477.1:n.*13A>G
NM_001282549.1:c.*13A>G NP_001269478.1:n.*13A>G
NR_104212.1:n.2340A>G
NR_104215.1:n.2283A>G
NR_104216.1:n.1539A>G
XM_011511567.1:c.*13A>G XP_011509869.1:n.*13A>G
XM_017004613.1:c.*13A>G XP_016860102.1:n.*13A>G
XR_002959322.1:n.2713A>G
NM_000465.4:c.*13A>G MANE Select NP_000456.2:n.*13A>G
NM_001282543.2:c.*13A>G NP_001269472.1:n.*13A>G
NM_001282545.2:c.*13A>G NP_001269474.1:n.*13A>G
NM_001282548.2:c.*13A>G NP_001269477.1:n.*13A>G
NM_001282549.2:c.*13A>G NP_001269478.1:n.*13A>G
NR_104212.2:n.2312A>G
NR_104215.2:n.2255A>G
NR_104216.2:n.1511A>G