Canonical Allele Identifier: CA2662971095

Gene: BARD1

Linked Data

• gnomAD v4: 2-214730521-CAAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214730524_214730526del , CM000664.2:g.214730524_214730526del	GRCh38
NC_000002.11:g.215595248_215595250del , CM000664.1:g.215595248_215595250del	GRCh37
NC_000002.10:g.215303493_215303495del	NCBI36
NG_012047.2:g.84181_84183del
NG_012047.3:g.84188_84190del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.1904-16_1904-14del MANE Select	ENSP00000260947.4:n.1904-16_1904-14del
ENST00000421162.2:c.551-16_551-14del	ENSP00000392245.2:n.551-16_551-14del
ENST00000613192.2:c.159-16_159-14del	ENSP00000483275.2:n.159-16_159-14del
ENST00000613374.5:c.494-16_494-14del	ENSP00000484464.1:n.494-16_494-14del
ENST00000613706.5:c.1496-16_1496-14del	ENSP00000484976.2:n.1496-16_1496-14del
ENST00000617164.5:c.1847-16_1847-14del	ENSP00000480470.1:n.1847-16_1847-14del
ENST00000619009.5:c.365-16_365-14del	ENSP00000482293.1:n.365-16_365-14del
ENST00000650978.1:c.3279-16_3279-14del
ENST00000260947.8:c.1904-16_1904-14del	ENSP00000260947.4:n.1904-16_1904-14del
ENST00000421162.1:c.551-16_551-14del	ENSP00000392245.1:n.551-16_551-14del
ENST00000455743.5:c.*1524-16_*1524-14del	ENSP00000412186.1:n.*1524-16_*1524-14del
ENST00000471590.5:n.239-16_239-14del
ENST00000613192.1:c.74-16_74-14del	ENSP00000483275.1:n.74-16_74-14del
ENST00000613374.4:c.494-16_494-14del	ENSP00000484464.1:n.494-16_494-14del
ENST00000613706.4:c.551-16_551-14del	ENSP00000484976.1:n.551-16_551-14del
ENST00000617164.4:c.1847-16_1847-14del	ENSP00000480470.1:n.1847-16_1847-14del
ENST00000619009.4:c.365-16_365-14del	ENSP00000482293.1:n.365-16_365-14del
ENST00000620057.4:c.*570-16_*570-14del	ENSP00000481988.1:n.*570-16_*570-14del
NM_000465.3:c.1904-16_1904-14del	NP_000456.2:n.1904-16_1904-14del
NM_001282543.1:c.1847-16_1847-14del	NP_001269472.1:n.1847-16_1847-14del
NM_001282545.1:c.551-16_551-14del	NP_001269474.1:n.551-16_551-14del
NM_001282548.1:c.494-16_494-14del	NP_001269477.1:n.494-16_494-14del
NM_001282549.1:c.365-16_365-14del	NP_001269478.1:n.365-16_365-14del
NR_104212.1:n.1897-16_1897-14del
NR_104215.1:n.1840-16_1840-14del
NR_104216.1:n.1096-16_1096-14del
XM_011511567.1:c.1850-16_1850-14del	XP_011509869.1:n.1850-16_1850-14del
XM_017004613.1:c.2003-16_2003-14del	XP_016860102.1:n.2003-16_2003-14del
XR_002959322.1:n.2094-16_2094-14del
NM_000465.4:c.1904-16_1904-14del MANE Select	NP_000456.2:n.1904-16_1904-14del
NM_001282543.2:c.1847-16_1847-14del	NP_001269472.1:n.1847-16_1847-14del
NM_001282545.2:c.551-16_551-14del	NP_001269474.1:n.551-16_551-14del
NM_001282548.2:c.494-16_494-14del	NP_001269477.1:n.494-16_494-14del
NM_001282549.2:c.365-16_365-14del	NP_001269478.1:n.365-16_365-14del
NR_104212.2:n.1869-16_1869-14del
NR_104215.2:n.1812-16_1812-14del
NR_104216.2:n.1068-16_1068-14del