Canonical Allele Identifier: CA647580017
Gene: BARD1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214728553_214728554insT , CM000664.2:g.214728553_214728554insT GRCh38
NC_000002.11:g.215593277_215593278insT , CM000664.1:g.215593277_215593278insT GRCh37
NC_000002.10:g.215301522_215301523insT NCBI36
NG_012047.2:g.86151_86152insA
NG_012047.3:g.86158_86159insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000260947.9:c.*122_*123insA MANE Select ENSP00000260947.4:n.*122_*123insA
ENST00000617164.5:c.*122_*123insA ENSP00000480470.1:n.*122_*123insA
ENST00000619009.5:c.*122_*123insA ENSP00000482293.1:n.*122_*123insA
ENST00000260947.8:c.*122_*123insA ENSP00000260947.4:n.*122_*123insA
ENST00000432456.5:c.599_600insA
ENST00000471590.5:n.791_792insA
ENST00000613374.4:c.*122_*123insA ENSP00000484464.1:n.*122_*123insA
ENST00000613706.4:c.*122_*123insA ENSP00000484976.1:n.*122_*123insA
ENST00000617164.4:c.*122_*123insA ENSP00000480470.1:n.*122_*123insA
ENST00000619009.4:c.*122_*123insA ENSP00000482293.1:n.*122_*123insA
NM_000465.3:c.*122_*123insA NP_000456.2:n.*122_*123insA
NM_001282543.1:c.*122_*123insA NP_001269472.1:n.*122_*123insA
NM_001282545.1:c.*122_*123insA NP_001269474.1:n.*122_*123insA
NM_001282548.1:c.*122_*123insA NP_001269477.1:n.*122_*123insA
NM_001282549.1:c.*122_*123insA NP_001269478.1:n.*122_*123insA
NR_104212.1:n.2449_2450insA
NR_104215.1:n.2392_2393insA
NR_104216.1:n.1648_1649insA
XM_011511567.1:c.*122_*123insA XP_011509869.1:n.*122_*123insA
XM_017004613.1:c.*122_*123insA XP_016860102.1:n.*122_*123insA
XR_002959322.1:n.2822_2823insA
NM_000465.4:c.*122_*123insA MANE Select NP_000456.2:n.*122_*123insA
NM_001282543.2:c.*122_*123insA NP_001269472.1:n.*122_*123insA
NM_001282545.2:c.*122_*123insA NP_001269474.1:n.*122_*123insA
NM_001282548.2:c.*122_*123insA NP_001269477.1:n.*122_*123insA
NM_001282549.2:c.*122_*123insA NP_001269478.1:n.*122_*123insA
NR_104212.2:n.2421_2422insA
NR_104215.2:n.2364_2365insA
NR_104216.2:n.1620_1621insA