Canonical Allele Identifier: CA1327071179

Gene: BARD1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214780952_214780954delinsGAT , CM000664.2:g.214780952_214780954delinsGAT	GRCh38
NC_000002.11:g.215645676_215645678delinsGAT , CM000664.1:g.215645676_215645678delinsGAT	GRCh37
NC_000002.10:g.215353921_215353923delinsGAT	NCBI36
NG_012047.2:g.33751_33753delinsATC
NG_012047.3:g.33758_33760delinsATC

Transcript Alleles

HGVS	Amino-acid change
ENST00000260947.9:c.920_922delinsATC MANE Select	ENSP00000260947.4:p.Tyr307=
ENST00000421162.2:c.215+16107_215+16109delinsATC	ENSP00000392245.2:n.215+16107_215+16109delinsATC
ENST00000613192.2:c.158+28458_158+28460delinsATC	ENSP00000483275.2:n.158+28458_158+28460delinsATC
ENST00000613374.5:c.159-28399_159-28397delinsATC	ENSP00000484464.1:n.159-28399_159-28397delinsATC
ENST00000613706.5:c.906+14_906+16delinsATC	ENSP00000484976.2:n.906+14_906+16delinsATC
ENST00000617164.5:c.863_865delinsATC	ENSP00000480470.1:p.Tyr288=
ENST00000619009.5:c.364+11343_364+11345delinsATC	ENSP00000482293.1:n.364+11343_364+11345delinsATC
ENST00000650978.1:c.762_764delinsATC
ENST00000260947.8:c.920_922delinsATC	ENSP00000260947.4:p.Tyr307=
ENST00000421162.1:c.215+16107_215+16109delinsATC	ENSP00000392245.1:n.215+16107_215+16109delinsATC
ENST00000455743.5:c.*540_*542delinsATC	ENSP00000412186.1:n.*540_*542delinsATC
ENST00000471787.1:n.815_817delinsATC
ENST00000613192.1:c.73+28458_73+28460delinsATC	ENSP00000483275.1:n.73+28458_73+28460delinsATC
ENST00000613374.4:c.159-28399_159-28397delinsATC	ENSP00000484464.1:n.159-28399_159-28397delinsATC
ENST00000613706.4:c.215+16107_215+16109delinsATC	ENSP00000484976.1:n.215+16107_215+16109delinsATC
ENST00000617164.4:c.863_865delinsATC	ENSP00000480470.1:p.Tyr288=
ENST00000619009.4:c.364+11343_364+11345delinsATC	ENSP00000482293.1:n.364+11343_364+11345delinsATC
ENST00000620057.4:c.364+11343_364+11345delinsATC	ENSP00000481988.1:n.364+11343_364+11345delinsATC
NM_000465.3:c.920_922delinsATC	NP_000456.2:p.Tyr307=
NM_001282543.1:c.863_865delinsATC	NP_001269472.1:p.Tyr288=
NM_001282545.1:c.215+16107_215+16109delinsATC	NP_001269474.1:n.215+16107_215+16109delinsATC
NM_001282548.1:c.159-28399_159-28397delinsATC	NP_001269477.1:n.159-28399_159-28397delinsATC
NM_001282549.1:c.364+11343_364+11345delinsATC	NP_001269478.1:n.364+11343_364+11345delinsATC
NR_104212.1:n.913_915delinsATC
NR_104215.1:n.856_858delinsATC
NR_104216.1:n.506+11343_506+11345delinsATC
XM_011511567.1:c.866_868delinsATC	XP_011509869.1:p.Tyr289=
XM_011511568.1:c.920_922delinsATC	XP_011509870.1:p.Tyr307=
XM_017004613.1:c.1019_1021delinsATC	XP_016860102.1:p.Tyr340=
XM_017004614.1:c.1019_1021delinsATC	XP_016860103.1:p.Tyr340=
XR_002959322.1:n.1110_1112delinsATC
NM_000465.4:c.920_922delinsATC MANE Select	NP_000456.2:p.Tyr307=
NM_001282543.2:c.863_865delinsATC	NP_001269472.1:p.Tyr288=
NM_001282545.2:c.215+16107_215+16109delinsATC	NP_001269474.1:n.215+16107_215+16109delinsATC
NM_001282548.2:c.159-28399_159-28397delinsATC	NP_001269477.1:n.159-28399_159-28397delinsATC
NM_001282549.2:c.364+11343_364+11345delinsATC	NP_001269478.1:n.364+11343_364+11345delinsATC
NR_104212.2:n.885_887delinsATC
NR_104215.2:n.828_830delinsATC
NR_104216.2:n.478+11343_478+11345delinsATC