Canonical Allele Identifier: CA2662971137

Gene: BARD1

Linked Data

• gnomAD v4: 2-214730642-CAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214730644_214730645del , CM000664.2:g.214730644_214730645del	GRCh38
NC_000002.11:g.215595368_215595369del , CM000664.1:g.215595368_215595369del	GRCh37
NC_000002.10:g.215303613_215303614del	NCBI36
NG_012047.2:g.84061_84062del
NG_012047.3:g.84068_84069del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.1904-136_1904-135del MANE Select	ENSP00000260947.4:n.1904-136_1904-135del
ENST00000421162.2:c.551-136_551-135del	ENSP00000392245.2:n.551-136_551-135del
ENST00000613192.2:c.159-136_159-135del	ENSP00000483275.2:n.159-136_159-135del
ENST00000613374.5:c.494-136_494-135del	ENSP00000484464.1:n.494-136_494-135del
ENST00000613706.5:c.1496-136_1496-135del	ENSP00000484976.2:n.1496-136_1496-135del
ENST00000617164.5:c.1847-136_1847-135del	ENSP00000480470.1:n.1847-136_1847-135del
ENST00000619009.5:c.365-136_365-135del	ENSP00000482293.1:n.365-136_365-135del
ENST00000650978.1:c.3279-136_3279-135del
ENST00000260947.8:c.1904-136_1904-135del	ENSP00000260947.4:n.1904-136_1904-135del
ENST00000421162.1:c.551-136_551-135del	ENSP00000392245.1:n.551-136_551-135del
ENST00000455743.5:c.*1524-136_*1524-135del	ENSP00000412186.1:n.*1524-136_*1524-135del
ENST00000471590.5:n.239-136_239-135del
ENST00000613192.1:c.74-136_74-135del	ENSP00000483275.1:n.74-136_74-135del
ENST00000613374.4:c.494-136_494-135del	ENSP00000484464.1:n.494-136_494-135del
ENST00000613706.4:c.551-136_551-135del	ENSP00000484976.1:n.551-136_551-135del
ENST00000617164.4:c.1847-136_1847-135del	ENSP00000480470.1:n.1847-136_1847-135del
ENST00000619009.4:c.365-136_365-135del	ENSP00000482293.1:n.365-136_365-135del
ENST00000620057.4:c.*570-136_*570-135del	ENSP00000481988.1:n.*570-136_*570-135del
NM_000465.3:c.1904-136_1904-135del	NP_000456.2:n.1904-136_1904-135del
NM_001282543.1:c.1847-136_1847-135del	NP_001269472.1:n.1847-136_1847-135del
NM_001282545.1:c.551-136_551-135del	NP_001269474.1:n.551-136_551-135del
NM_001282548.1:c.494-136_494-135del	NP_001269477.1:n.494-136_494-135del
NM_001282549.1:c.365-136_365-135del	NP_001269478.1:n.365-136_365-135del
NR_104212.1:n.1897-136_1897-135del
NR_104215.1:n.1840-136_1840-135del
NR_104216.1:n.1096-136_1096-135del
XM_011511567.1:c.1850-136_1850-135del	XP_011509869.1:n.1850-136_1850-135del
XM_017004613.1:c.2003-136_2003-135del	XP_016860102.1:n.2003-136_2003-135del
XR_002959322.1:n.2094-136_2094-135del
NM_000465.4:c.1904-136_1904-135del MANE Select	NP_000456.2:n.1904-136_1904-135del
NM_001282543.2:c.1847-136_1847-135del	NP_001269472.1:n.1847-136_1847-135del
NM_001282545.2:c.551-136_551-135del	NP_001269474.1:n.551-136_551-135del
NM_001282548.2:c.494-136_494-135del	NP_001269477.1:n.494-136_494-135del
NM_001282549.2:c.365-136_365-135del	NP_001269478.1:n.365-136_365-135del
NR_104212.2:n.1869-136_1869-135del
NR_104215.2:n.1812-136_1812-135del
NR_104216.2:n.1068-136_1068-135del