Canonical Allele Identifier: CA1327076693
Gene: BARD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214792371_214792374delinsATCT , CM000664.2:g.214792371_214792374delinsATCT GRCh38
NC_000002.11:g.215657095_215657098delinsATCT , CM000664.1:g.215657095_215657098delinsATCT GRCh37
NC_000002.10:g.215365340_215365343delinsATCT NCBI36
NG_012047.2:g.22331_22334delinsAGAT
NG_012047.3:g.22338_22341delinsAGAT

Transcript Alleles

HGVS Amino-acid change
ENST00000260947.9:c.287_290delinsAGAT MANE Select ENSP00000260947.4:p.Lys96=
ENST00000421162.2:c.215+4687_215+4690delinsAGAT ENSP00000392245.2:n.215+4687_215+4690deli...
ENST00000613192.2:c.158+17038_158+17041delinsAGAT ENSP00000483275.2:n.158+17038_158+17041de...
ENST00000613374.5:c.158+17038_158+17041delinsAGAT ENSP00000484464.1:n.158+17038_158+17041de...
ENST00000613706.5:c.287_290delinsAGAT ENSP00000484976.2:p.Lys96=
ENST00000617164.5:c.230_233delinsAGAT ENSP00000480470.1:p.Lys77=
ENST00000619009.5:c.287_290delinsAGAT ENSP00000482293.1:p.Lys96=
ENST00000650978.1:c.129_132delinsAGAT
ENST00000260947.8:c.287_290delinsAGAT ENSP00000260947.4:p.Lys96=
ENST00000421162.1:c.215+4687_215+4690delinsAGAT ENSP00000392245.1:n.215+4687_215+4690deli...
ENST00000455743.5:c.215+4687_215+4690delinsAGAT ENSP00000412186.1:n.215+4687_215+4690deli...
ENST00000471787.1:n.260-10865_260-10862delinsAGAT
ENST00000613192.1:c.73+17038_73+17041delinsAGAT ENSP00000483275.1:n.73+17038_73+17041deli...
ENST00000613374.4:c.158+17038_158+17041delinsAGAT ENSP00000484464.1:n.158+17038_158+17041de...
ENST00000613706.4:c.215+4687_215+4690delinsAGAT ENSP00000484976.1:n.215+4687_215+4690deli...
ENST00000617164.4:c.230_233delinsAGAT ENSP00000480470.1:p.Lys77=
ENST00000619009.4:c.287_290delinsAGAT ENSP00000482293.1:p.Lys96=
ENST00000620057.4:c.287_290delinsAGAT ENSP00000481988.1:p.Lys96=
NM_000465.3:c.287_290delinsAGAT NP_000456.2:p.Lys96=
NM_001282543.1:c.230_233delinsAGAT NP_001269472.1:p.Lys77=
NM_001282545.1:c.215+4687_215+4690delinsAGAT NP_001269474.1:n.215+4687_215+4690delinsA...
NM_001282548.1:c.158+17038_158+17041delinsAGAT NP_001269477.1:n.158+17038_158+17041delin...
NM_001282549.1:c.287_290delinsAGAT NP_001269478.1:p.Lys96=
NR_104212.1:n.357+4687_357+4690delinsAGAT
NR_104215.1:n.301-10865_301-10862delinsAGAT
NR_104216.1:n.429_432delinsAGAT
XM_011511567.1:c.233_236delinsAGAT XP_011509869.1:p.Lys78=
XM_011511568.1:c.287_290delinsAGAT XP_011509870.1:p.Lys96=
XM_017004613.1:c.386_389delinsAGAT XP_016860102.1:p.Lys129=
XM_017004614.1:c.386_389delinsAGAT XP_016860103.1:p.Lys129=
XR_002959322.1:n.477_480delinsAGAT
NM_000465.4:c.287_290delinsAGAT MANE Select NP_000456.2:p.Lys96=
NM_001282543.2:c.230_233delinsAGAT NP_001269472.1:p.Lys77=
NM_001282545.2:c.215+4687_215+4690delinsAGAT NP_001269474.1:n.215+4687_215+4690delinsA...
NM_001282548.2:c.158+17038_158+17041delinsAGAT NP_001269477.1:n.158+17038_158+17041delin...
NM_001282549.2:c.287_290delinsAGAT NP_001269478.1:p.Lys96=
NR_104212.2:n.329+4687_329+4690delinsAGAT
NR_104215.2:n.273-10865_273-10862delinsAGAT
NR_104216.2:n.401_404delinsAGAT