Canonical Allele Identifier: CA2662969738

Gene: BARD1

Linked Data

• gnomAD v4: 2-214728551-T-TTTGATTTAAAGACAAATATGAA

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214728552_214728553insTGATTTAAAGACAAATATGAAT , CM000664.2:g.214728552_214728553insTGATTTAAAGACAAATATGAAT	GRCh38
NC_000002.11:g.215593276_215593277insTGATTTAAAGACAAATATGAAT , CM000664.1:g.215593276_215593277insTGATTTAAAGACAAATATGAAT	GRCh37
NC_000002.10:g.215301521_215301522insTGATTTAAAGACAAATATGAAT	NCBI36
NG_012047.2:g.86153_86154insTTCATATTTGTCTTTAAATCAA
NG_012047.3:g.86160_86161insTTCATATTTGTCTTTAAATCAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.*124_*125insTTCATATTTGTCTTTAAATCAA MANE Select	ENSP00000260947.4:n.*124_*125insTTCATATTTGTCTTTAAATCAA
ENST00000260947.8:c.*124_*125insTTCATATTTGTCTTTAAATCAA	ENSP00000260947.4:n.*124_*125insTTCATATTTGTCTTTAAATCAA
ENST00000432456.5:c.601_602insTTCATATTTGTCTTTAAATCAA
ENST00000471590.5:n.793_794insTTCATATTTGTCTTTAAATCAA
ENST00000613374.4:c.*124_*125insTTCATATTTGTCTTTAAATCAA	ENSP00000484464.1:n.*124_*125insTTCATATTTGTCTTTAAATCAA
ENST00000613706.4:c.*124_*125insTTCATATTTGTCTTTAAATCAA	ENSP00000484976.1:n.*124_*125insTTCATATTTGTCTTTAAATCAA
ENST00000617164.4:c.*124_*125insTTCATATTTGTCTTTAAATCAA	ENSP00000480470.1:n.*124_*125insTTCATATTTGTCTTTAAATCAA
ENST00000619009.4:c.*124_*125insTTCATATTTGTCTTTAAATCAA	ENSP00000482293.1:n.*124_*125insTTCATATTTGTCTTTAAATCAA
NM_000465.3:c.*124_*125insTTCATATTTGTCTTTAAATCAA	NP_000456.2:n.*124_*125insTTCATATTTGTCTTTAAATCAA
NM_001282543.1:c.*124_*125insTTCATATTTGTCTTTAAATCAA	NP_001269472.1:n.*124_*125insTTCATATTTGTCTTTAAATCAA
NM_001282545.1:c.*124_*125insTTCATATTTGTCTTTAAATCAA	NP_001269474.1:n.*124_*125insTTCATATTTGTCTTTAAATCAA
NM_001282548.1:c.*124_*125insTTCATATTTGTCTTTAAATCAA	NP_001269477.1:n.*124_*125insTTCATATTTGTCTTTAAATCAA
NM_001282549.1:c.*124_*125insTTCATATTTGTCTTTAAATCAA	NP_001269478.1:n.*124_*125insTTCATATTTGTCTTTAAATCAA
NR_104212.1:n.2451_2452insTTCATATTTGTCTTTAAATCAA
NR_104215.1:n.2394_2395insTTCATATTTGTCTTTAAATCAA
NR_104216.1:n.1650_1651insTTCATATTTGTCTTTAAATCAA
XM_011511567.1:c.*124_*125insTTCATATTTGTCTTTAAATCAA	XP_011509869.1:n.*124_*125insTTCATATTTGTCTTTAAATCAA
XM_017004613.1:c.*124_*125insTTCATATTTGTCTTTAAATCAA	XP_016860102.1:n.*124_*125insTTCATATTTGTCTTTAAATCAA
XR_002959322.1:n.2824_2825insTTCATATTTGTCTTTAAATCAA
NM_000465.4:c.*124_*125insTTCATATTTGTCTTTAAATCAA MANE Select	NP_000456.2:n.*124_*125insTTCATATTTGTCTTTAAATCAA
NM_001282543.2:c.*124_*125insTTCATATTTGTCTTTAAATCAA	NP_001269472.1:n.*124_*125insTTCATATTTGTCTTTAAATCAA
NM_001282545.2:c.*124_*125insTTCATATTTGTCTTTAAATCAA	NP_001269474.1:n.*124_*125insTTCATATTTGTCTTTAAATCAA
NM_001282548.2:c.*124_*125insTTCATATTTGTCTTTAAATCAA	NP_001269477.1:n.*124_*125insTTCATATTTGTCTTTAAATCAA
NM_001282549.2:c.*124_*125insTTCATATTTGTCTTTAAATCAA	NP_001269478.1:n.*124_*125insTTCATATTTGTCTTTAAATCAA
NR_104212.2:n.2423_2424insTTCATATTTGTCTTTAAATCAA
NR_104215.2:n.2366_2367insTTCATATTTGTCTTTAAATCAA
NR_104216.2:n.1622_1623insTTCATATTTGTCTTTAAATCAA