Canonical Allele Identifier: CA2540879609

Gene: BARD1

Linked Data

• gnomAD v4: 2-214728527-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214728529del , CM000664.2:g.214728529del	GRCh38
NC_000002.11:g.215593253del , CM000664.1:g.215593253del	GRCh37
NC_000002.10:g.215301498del	NCBI36
NG_012047.2:g.86177del
NG_012047.3:g.86184del

Transcript Alleles

HGVS	Amino-acid change
ENST00000260947.9:c.*148del MANE Select	ENSP00000260947.4:n.*148del
ENST00000260947.8:c.*148del	ENSP00000260947.4:n.*148del
ENST00000471590.5:n.817del
ENST00000613374.4:c.*148del	ENSP00000484464.1:n.*148del
ENST00000613706.4:c.*148del	ENSP00000484976.1:n.*148del
ENST00000617164.4:c.*148del	ENSP00000480470.1:n.*148del
ENST00000619009.4:c.*148del	ENSP00000482293.1:n.*148del
NM_000465.3:c.*148del	NP_000456.2:n.*148del
NM_001282543.1:c.*148del	NP_001269472.1:n.*148del
NM_001282545.1:c.*148del	NP_001269474.1:n.*148del
NM_001282548.1:c.*148del	NP_001269477.1:n.*148del
NM_001282549.1:c.*148del	NP_001269478.1:n.*148del
NR_104212.1:n.2475del
NR_104215.1:n.2418del
NR_104216.1:n.1674del
XM_011511567.1:c.*148del	XP_011509869.1:n.*148del
XM_017004613.1:c.*148del	XP_016860102.1:n.*148del
NM_000465.4:c.*148del MANE Select	NP_000456.2:n.*148del
NM_001282543.2:c.*148del	NP_001269472.1:n.*148del
NM_001282545.2:c.*148del	NP_001269474.1:n.*148del
NM_001282548.2:c.*148del	NP_001269477.1:n.*148del
NM_001282549.2:c.*148del	NP_001269478.1:n.*148del
NR_104212.2:n.2447del
NR_104215.2:n.2390del
NR_104216.2:n.1646del