Canonical Allele Identifier: CA2662960665

Gene: BARD1

Linked Data

• gnomAD v4: 2-214780444-C-CAT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214780445_214780446dup , CM000664.2:g.214780445_214780446dup	GRCh38
NC_000002.11:g.215645169_215645170dup , CM000664.1:g.215645169_215645170dup	GRCh37
NC_000002.10:g.215353414_215353415dup	NCBI36
NG_012047.2:g.34259_34260dup
NG_012047.3:g.34266_34267dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.1314+114_1314+115dup MANE Select	ENSP00000260947.4:n.1314+114_1314+115dup
ENST00000421162.2:c.215+16615_215+16616dup	ENSP00000392245.2:n.215+16615_215+16616dup
ENST00000613192.2:c.158+28966_158+28967dup	ENSP00000483275.2:n.158+28966_158+28967dup
ENST00000613374.5:c.159-27891_159-27890dup	ENSP00000484464.1:n.159-27891_159-27890dup
ENST00000613706.5:c.906+522_906+523dup	ENSP00000484976.2:n.906+522_906+523dup
ENST00000617164.5:c.1257+114_1257+115dup	ENSP00000480470.1:n.1257+114_1257+115dup
ENST00000619009.5:c.364+11851_364+11852dup	ENSP00000482293.1:n.364+11851_364+11852dup
ENST00000650978.1:c.1156+114_1156+115dup
ENST00000260947.8:c.1314+114_1314+115dup	ENSP00000260947.4:n.1314+114_1314+115dup
ENST00000421162.1:c.215+16615_215+16616dup	ENSP00000392245.1:n.215+16615_215+16616dup
ENST00000455743.5:c.*934+114_*934+115dup	ENSP00000412186.1:n.*934+114_*934+115dup
ENST00000613192.1:c.73+28966_73+28967dup	ENSP00000483275.1:n.73+28966_73+28967dup
ENST00000613374.4:c.159-27891_159-27890dup	ENSP00000484464.1:n.159-27891_159-27890dup
ENST00000613706.4:c.215+16615_215+16616dup	ENSP00000484976.1:n.215+16615_215+16616dup
ENST00000617164.4:c.1257+114_1257+115dup	ENSP00000480470.1:n.1257+114_1257+115dup
ENST00000619009.4:c.364+11851_364+11852dup	ENSP00000482293.1:n.364+11851_364+11852dup
ENST00000620057.4:c.365-11134_365-11133dup	ENSP00000481988.1:n.365-11134_365-11133dup
NM_000465.3:c.1314+114_1314+115dup	NP_000456.2:n.1314+114_1314+115dup
NM_001282543.1:c.1257+114_1257+115dup	NP_001269472.1:n.1257+114_1257+115dup
NM_001282545.1:c.215+16615_215+16616dup	NP_001269474.1:n.215+16615_215+16616dup
NM_001282548.1:c.159-27891_159-27890dup	NP_001269477.1:n.159-27891_159-27890dup
NM_001282549.1:c.364+11851_364+11852dup	NP_001269478.1:n.364+11851_364+11852dup
NR_104212.1:n.1307+114_1307+115dup
NR_104215.1:n.1250+114_1250+115dup
NR_104216.1:n.507-11134_507-11133dup
XM_011511567.1:c.1260+114_1260+115dup	XP_011509869.1:n.1260+114_1260+115dup
XM_011511568.1:c.1314+114_1314+115dup	XP_011509870.1:n.1314+114_1314+115dup
XM_017004613.1:c.1413+114_1413+115dup	XP_016860102.1:n.1413+114_1413+115dup
XM_017004614.1:c.1413+114_1413+115dup	XP_016860103.1:n.1413+114_1413+115dup
XR_002959322.1:n.1504+114_1504+115dup
NM_000465.4:c.1314+114_1314+115dup MANE Select	NP_000456.2:n.1314+114_1314+115dup
NM_001282543.2:c.1257+114_1257+115dup	NP_001269472.1:n.1257+114_1257+115dup
NM_001282545.2:c.215+16615_215+16616dup	NP_001269474.1:n.215+16615_215+16616dup
NM_001282548.2:c.159-27891_159-27890dup	NP_001269477.1:n.159-27891_159-27890dup
NM_001282549.2:c.364+11851_364+11852dup	NP_001269478.1:n.364+11851_364+11852dup
NR_104212.2:n.1279+114_1279+115dup
NR_104215.2:n.1222+114_1222+115dup
NR_104216.2:n.479-11134_479-11133dup