Canonical Allele Identifier: CA1327071013

Gene: BARD1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214780713_214780714delinsGA , CM000664.2:g.214780713_214780714delinsGA	GRCh38
NC_000002.11:g.215645437_215645438delinsGA , CM000664.1:g.215645437_215645438delinsGA	GRCh37
NC_000002.10:g.215353682_215353683delinsGA	NCBI36
NG_012047.2:g.33991_33992delinsTC
NG_012047.3:g.33998_33999delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.1160_1161delinsTC MANE Select	ENSP00000260947.4:p.Phe387=
ENST00000421162.2:c.215+16347_215+16348delinsTC	ENSP00000392245.2:n.215+16347_215+16348delinsTC
ENST00000613192.2:c.158+28698_158+28699delinsTC	ENSP00000483275.2:n.158+28698_158+28699delinsTC
ENST00000613374.5:c.159-28159_159-28158delinsTC	ENSP00000484464.1:n.159-28159_159-28158delinsTC
ENST00000613706.5:c.906+254_906+255delinsTC	ENSP00000484976.2:n.906+254_906+255delinsTC
ENST00000617164.5:c.1103_1104delinsTC	ENSP00000480470.1:p.Phe368=
ENST00000619009.5:c.364+11583_364+11584delinsTC	ENSP00000482293.1:n.364+11583_364+11584delinsTC
ENST00000650978.1:c.1002_1003delinsTC
ENST00000260947.8:c.1160_1161delinsTC	ENSP00000260947.4:p.Phe387=
ENST00000421162.1:c.215+16347_215+16348delinsTC	ENSP00000392245.1:n.215+16347_215+16348delinsTC
ENST00000455743.5:c.*780_*781delinsTC	ENSP00000412186.1:n.*780_*781delinsTC
ENST00000613192.1:c.73+28698_73+28699delinsTC	ENSP00000483275.1:n.73+28698_73+28699delinsTC
ENST00000613374.4:c.159-28159_159-28158delinsTC	ENSP00000484464.1:n.159-28159_159-28158delinsTC
ENST00000613706.4:c.215+16347_215+16348delinsTC	ENSP00000484976.1:n.215+16347_215+16348delinsTC
ENST00000617164.4:c.1103_1104delinsTC	ENSP00000480470.1:p.Phe368=
ENST00000619009.4:c.364+11583_364+11584delinsTC	ENSP00000482293.1:n.364+11583_364+11584delinsTC
ENST00000620057.4:c.365-11402_365-11401delinsTC	ENSP00000481988.1:n.365-11402_365-11401delinsTC
NM_000465.3:c.1160_1161delinsTC	NP_000456.2:p.Phe387=
NM_001282543.1:c.1103_1104delinsTC	NP_001269472.1:p.Phe368=
NM_001282545.1:c.215+16347_215+16348delinsTC	NP_001269474.1:n.215+16347_215+16348delinsTC
NM_001282548.1:c.159-28159_159-28158delinsTC	NP_001269477.1:n.159-28159_159-28158delinsTC
NM_001282549.1:c.364+11583_364+11584delinsTC	NP_001269478.1:n.364+11583_364+11584delinsTC
NR_104212.1:n.1153_1154delinsTC
NR_104215.1:n.1096_1097delinsTC
NR_104216.1:n.507-11402_507-11401delinsTC
XM_011511567.1:c.1106_1107delinsTC	XP_011509869.1:p.Phe369=
XM_011511568.1:c.1160_1161delinsTC	XP_011509870.1:p.Phe387=
XM_017004613.1:c.1259_1260delinsTC	XP_016860102.1:p.Phe420=
XM_017004614.1:c.1259_1260delinsTC	XP_016860103.1:p.Phe420=
XR_002959322.1:n.1350_1351delinsTC
NM_000465.4:c.1160_1161delinsTC MANE Select	NP_000456.2:p.Phe387=
NM_001282543.2:c.1103_1104delinsTC	NP_001269472.1:p.Phe368=
NM_001282545.2:c.215+16347_215+16348delinsTC	NP_001269474.1:n.215+16347_215+16348delinsTC
NM_001282548.2:c.159-28159_159-28158delinsTC	NP_001269477.1:n.159-28159_159-28158delinsTC
NM_001282549.2:c.364+11583_364+11584delinsTC	NP_001269478.1:n.364+11583_364+11584delinsTC
NR_104212.2:n.1125_1126delinsTC
NR_104215.2:n.1068_1069delinsTC
NR_104216.2:n.479-11402_479-11401delinsTC