Canonical Allele Identifier: CA2662971064
Gene: BARD1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214752659C>A , CM000664.2:g.214752659C>A GRCh38
NC_000002.11:g.215617383C>A , CM000664.1:g.215617383C>A GRCh37
NC_000002.10:g.215325628C>A NCBI36
NG_012047.2:g.62046G>T
NG_012047.3:g.62053G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000260947.9:c.1569-104G>T MANE Select ENSP00000260947.4:n.1569-104G>T
ENST00000421162.2:c.216-104G>T ENSP00000392245.2:n.216-104G>T
ENST00000613192.2:c.159-22151G>T ENSP00000483275.2:n.159-22151G>T
ENST00000613374.5:c.159-104G>T ENSP00000484464.1:n.159-104G>T
ENST00000613706.5:c.1161-104G>T ENSP00000484976.2:n.1161-104G>T
ENST00000617164.5:c.1512-104G>T ENSP00000480470.1:n.1512-104G>T
ENST00000619009.5:c.365-22151G>T ENSP00000482293.1:n.365-22151G>T
ENST00000650978.1:c.2944-104G>T
ENST00000260947.8:c.1569-104G>T ENSP00000260947.4:n.1569-104G>T
ENST00000421162.1:c.216-104G>T ENSP00000392245.1:n.216-104G>T
ENST00000455743.5:c.*1189-104G>T ENSP00000412186.1:n.*1189-104G>T
ENST00000613192.1:c.74-22151G>T ENSP00000483275.1:n.74-22151G>T
ENST00000613374.4:c.159-104G>T ENSP00000484464.1:n.159-104G>T
ENST00000613706.4:c.216-104G>T ENSP00000484976.1:n.216-104G>T
ENST00000617164.4:c.1512-104G>T ENSP00000480470.1:n.1512-104G>T
ENST00000619009.4:c.365-22151G>T ENSP00000482293.1:n.365-22151G>T
ENST00000620057.4:c.*235-104G>T ENSP00000481988.1:n.*235-104G>T
NM_000465.3:c.1569-104G>T NP_000456.2:n.1569-104G>T
NM_001282543.1:c.1512-104G>T NP_001269472.1:n.1512-104G>T
NM_001282545.1:c.216-104G>T NP_001269474.1:n.216-104G>T
NM_001282548.1:c.159-104G>T NP_001269477.1:n.159-104G>T
NM_001282549.1:c.365-22151G>T NP_001269478.1:n.365-22151G>T
NR_104212.1:n.1562-104G>T
NR_104215.1:n.1505-104G>T
NR_104216.1:n.761-104G>T
XM_011511567.1:c.1515-104G>T XP_011509869.1:n.1515-104G>T
XM_011511568.1:c.1569-104G>T XP_011509870.1:n.1569-104G>T
XM_017004613.1:c.1668-104G>T XP_016860102.1:n.1668-104G>T
XM_017004614.1:c.1668-104G>T XP_016860103.1:n.1668-104G>T
XR_002959322.1:n.1759-104G>T
NM_000465.4:c.1569-104G>T MANE Select NP_000456.2:n.1569-104G>T
NM_001282543.2:c.1512-104G>T NP_001269472.1:n.1512-104G>T
NM_001282545.2:c.216-104G>T NP_001269474.1:n.216-104G>T
NM_001282548.2:c.159-104G>T NP_001269477.1:n.159-104G>T
NM_001282549.2:c.365-22151G>T NP_001269478.1:n.365-22151G>T
NR_104212.2:n.1534-104G>T
NR_104215.2:n.1477-104G>T
NR_104216.2:n.733-104G>T