Canonical Allele Identifier: CA1139655679
Gene: BARD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 971610
ClinVar RCV Id: RCV001247428
dbSNP Id: rs1695560646

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214792370_214792378del , CM000664.2:g.214792370_214792378del GRCh38
NC_000002.11:g.215657094_215657102del , CM000664.1:g.215657094_215657102del GRCh37
NC_000002.10:g.215365339_215365347del NCBI36
NG_012047.2:g.22327_22335del
NG_012047.3:g.22334_22342del

Transcript Alleles

HGVS Amino-acid change
ENST00000260947.9:c.283_291del MANE Select ENSP00000260947.4:p.Leu95_Ile97del
ENST00000421162.2:c.215+4683_215+4691del ENSP00000392245.2:n.215+4683_215+4691del
ENST00000613192.2:c.158+17034_158+17042del ENSP00000483275.2:n.158+17034_158+17042de...
ENST00000613374.5:c.158+17034_158+17042del ENSP00000484464.1:n.158+17034_158+17042de...
ENST00000613706.5:c.283_291del ENSP00000484976.2:p.Leu95_Ile97del
ENST00000617164.5:c.226_234del ENSP00000480470.1:p.Leu76_Ile78del
ENST00000619009.5:c.283_291del ENSP00000482293.1:p.Leu95_Ile97del
ENST00000650978.1:c.125_133del
ENST00000260947.8:c.283_291del ENSP00000260947.4:p.Leu95_Ile97del
ENST00000421162.1:c.215+4683_215+4691del ENSP00000392245.1:n.215+4683_215+4691del
ENST00000455743.5:c.215+4683_215+4691del ENSP00000412186.1:n.215+4683_215+4691del
ENST00000471787.1:n.260-10869_260-10861del
ENST00000613192.1:c.73+17034_73+17042del ENSP00000483275.1:n.73+17034_73+17042del
ENST00000613374.4:c.158+17034_158+17042del ENSP00000484464.1:n.158+17034_158+17042de...
ENST00000613706.4:c.215+4683_215+4691del ENSP00000484976.1:n.215+4683_215+4691del
ENST00000617164.4:c.226_234del ENSP00000480470.1:p.Leu76_Ile78del
ENST00000619009.4:c.283_291del ENSP00000482293.1:p.Leu95_Ile97del
ENST00000620057.4:c.283_291del ENSP00000481988.1:p.Leu95_Ile97del
NM_000465.3:c.283_291del NP_000456.2:p.Leu95_Ile97del
NM_001282543.1:c.226_234del NP_001269472.1:p.Leu76_Ile78del
NM_001282545.1:c.215+4683_215+4691del NP_001269474.1:n.215+4683_215+4691del
NM_001282548.1:c.158+17034_158+17042del NP_001269477.1:n.158+17034_158+17042del
NM_001282549.1:c.283_291del NP_001269478.1:p.Leu95_Ile97del
NR_104212.1:n.357+4683_357+4691del
NR_104215.1:n.301-10869_301-10861del
NR_104216.1:n.425_433del
XM_011511567.1:c.229_237del XP_011509869.1:p.Leu77_Ile79del
XM_011511568.1:c.283_291del XP_011509870.1:p.Leu95_Ile97del
XM_017004613.1:c.382_390del XP_016860102.1:p.Leu128_Ile130del
XM_017004614.1:c.382_390del XP_016860103.1:p.Leu128_Ile130del
XR_002959322.1:n.473_481del
NM_000465.4:c.283_291del MANE Select NP_000456.2:p.Leu95_Ile97del
NM_001282543.2:c.226_234del NP_001269472.1:p.Leu76_Ile78del
NM_001282545.2:c.215+4683_215+4691del NP_001269474.1:n.215+4683_215+4691del
NM_001282548.2:c.158+17034_158+17042del NP_001269477.1:n.158+17034_158+17042del
NM_001282549.2:c.283_291del NP_001269478.1:p.Leu95_Ile97del
NR_104212.2:n.329+4683_329+4691del
NR_104215.2:n.273-10869_273-10861del
NR_104216.2:n.397_405del