Canonical Allele Identifier: CA2662960686

Gene: BARD1

Linked Data

• gnomAD v4: 2-214780475-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214780477del , CM000664.2:g.214780477del	GRCh38
NC_000002.11:g.215645201del , CM000664.1:g.215645201del	GRCh37
NC_000002.10:g.215353446del	NCBI36
NG_012047.2:g.34229del
NG_012047.3:g.34236del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.1314+84del MANE Select	ENSP00000260947.4:n.1314+84del
ENST00000421162.2:c.215+16585del	ENSP00000392245.2:n.215+16585del
ENST00000613192.2:c.158+28936del	ENSP00000483275.2:n.158+28936del
ENST00000613374.5:c.159-27921del	ENSP00000484464.1:n.159-27921del
ENST00000613706.5:c.906+492del	ENSP00000484976.2:n.906+492del
ENST00000617164.5:c.1257+84del	ENSP00000480470.1:n.1257+84del
ENST00000619009.5:c.364+11821del	ENSP00000482293.1:n.364+11821del
ENST00000650978.1:c.1156+84del
ENST00000260947.8:c.1314+84del	ENSP00000260947.4:n.1314+84del
ENST00000421162.1:c.215+16585del	ENSP00000392245.1:n.215+16585del
ENST00000455743.5:c.*934+84del	ENSP00000412186.1:n.*934+84del
ENST00000613192.1:c.73+28936del	ENSP00000483275.1:n.73+28936del
ENST00000613374.4:c.159-27921del	ENSP00000484464.1:n.159-27921del
ENST00000613706.4:c.215+16585del	ENSP00000484976.1:n.215+16585del
ENST00000617164.4:c.1257+84del	ENSP00000480470.1:n.1257+84del
ENST00000619009.4:c.364+11821del	ENSP00000482293.1:n.364+11821del
ENST00000620057.4:c.365-11164del	ENSP00000481988.1:n.365-11164del
NM_000465.3:c.1314+84del	NP_000456.2:n.1314+84del
NM_001282543.1:c.1257+84del	NP_001269472.1:n.1257+84del
NM_001282545.1:c.215+16585del	NP_001269474.1:n.215+16585del
NM_001282548.1:c.159-27921del	NP_001269477.1:n.159-27921del
NM_001282549.1:c.364+11821del	NP_001269478.1:n.364+11821del
NR_104212.1:n.1307+84del
NR_104215.1:n.1250+84del
NR_104216.1:n.507-11164del
XM_011511567.1:c.1260+84del	XP_011509869.1:n.1260+84del
XM_011511568.1:c.1314+84del	XP_011509870.1:n.1314+84del
XM_017004613.1:c.1413+84del	XP_016860102.1:n.1413+84del
XM_017004614.1:c.1413+84del	XP_016860103.1:n.1413+84del
XR_002959322.1:n.1504+84del
NM_000465.4:c.1314+84del MANE Select	NP_000456.2:n.1314+84del
NM_001282543.2:c.1257+84del	NP_001269472.1:n.1257+84del
NM_001282545.2:c.215+16585del	NP_001269474.1:n.215+16585del
NM_001282548.2:c.159-27921del	NP_001269477.1:n.159-27921del
NM_001282549.2:c.364+11821del	NP_001269478.1:n.364+11821del
NR_104212.2:n.1279+84del
NR_104215.2:n.1222+84del
NR_104216.2:n.479-11164del