Canonical Allele Identifier: CA1327071575

Gene: BARD1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214781516_214781517delinsGA , CM000664.2:g.214781516_214781517delinsGA	GRCh38
NC_000002.11:g.215646240_215646241delinsGA , CM000664.1:g.215646240_215646241delinsGA	GRCh37
NC_000002.10:g.215354485_215354486delinsGA	NCBI36
NG_012047.2:g.33188_33189delinsTC
NG_012047.3:g.33195_33196delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.365-8_365-7delinsTC MANE Select	ENSP00000260947.4:n.365-8_365-7delinsTC
ENST00000421162.2:c.215+15544_215+15545delinsTC	ENSP00000392245.2:n.215+15544_215+15545delinsTC
ENST00000613192.2:c.158+27895_158+27896delinsTC	ENSP00000483275.2:n.158+27895_158+27896delinsTC
ENST00000613374.5:c.158+27895_158+27896delinsTC	ENSP00000484464.1:n.158+27895_158+27896delinsTC
ENST00000613706.5:c.365-8_365-7delinsTC	ENSP00000484976.2:n.365-8_365-7delinsTC
ENST00000617164.5:c.308-8_308-7delinsTC	ENSP00000480470.1:n.308-8_308-7delinsTC
ENST00000619009.5:c.364+10780_364+10781delinsTC	ENSP00000482293.1:n.364+10780_364+10781delinsTC
ENST00000650978.1:c.207-8_207-7delinsTC
ENST00000260947.8:c.365-8_365-7delinsTC	ENSP00000260947.4:n.365-8_365-7delinsTC
ENST00000421162.1:c.215+15544_215+15545delinsTC	ENSP00000392245.1:n.215+15544_215+15545delinsTC
ENST00000455743.5:c.216-8_216-7delinsTC	ENSP00000412186.1:n.216-8_216-7delinsTC
ENST00000471787.1:n.260-8_260-7delinsTC
ENST00000613192.1:c.73+27895_73+27896delinsTC	ENSP00000483275.1:n.73+27895_73+27896delinsTC
ENST00000613374.4:c.158+27895_158+27896delinsTC	ENSP00000484464.1:n.158+27895_158+27896delinsTC
ENST00000613706.4:c.215+15544_215+15545delinsTC	ENSP00000484976.1:n.215+15544_215+15545delinsTC
ENST00000617164.4:c.308-8_308-7delinsTC	ENSP00000480470.1:n.308-8_308-7delinsTC
ENST00000619009.4:c.364+10780_364+10781delinsTC	ENSP00000482293.1:n.364+10780_364+10781delinsTC
ENST00000620057.4:c.364+10780_364+10781delinsTC	ENSP00000481988.1:n.364+10780_364+10781delinsTC
NM_000465.3:c.365-8_365-7delinsTC	NP_000456.2:n.365-8_365-7delinsTC
NM_001282543.1:c.308-8_308-7delinsTC	NP_001269472.1:n.308-8_308-7delinsTC
NM_001282545.1:c.215+15544_215+15545delinsTC	NP_001269474.1:n.215+15544_215+15545delinsTC
NM_001282548.1:c.158+27895_158+27896delinsTC	NP_001269477.1:n.158+27895_158+27896delinsTC
NM_001282549.1:c.364+10780_364+10781delinsTC	NP_001269478.1:n.364+10780_364+10781delinsTC
NR_104212.1:n.358-8_358-7delinsTC
NR_104215.1:n.301-8_301-7delinsTC
NR_104216.1:n.506+10780_506+10781delinsTC
XM_011511567.1:c.311-8_311-7delinsTC	XP_011509869.1:n.311-8_311-7delinsTC
XM_011511568.1:c.365-8_365-7delinsTC	XP_011509870.1:n.365-8_365-7delinsTC
XM_017004613.1:c.464-8_464-7delinsTC	XP_016860102.1:n.464-8_464-7delinsTC
XM_017004614.1:c.464-8_464-7delinsTC	XP_016860103.1:n.464-8_464-7delinsTC
XR_002959322.1:n.555-8_555-7delinsTC
NM_000465.4:c.365-8_365-7delinsTC MANE Select	NP_000456.2:n.365-8_365-7delinsTC
NM_001282543.2:c.308-8_308-7delinsTC	NP_001269472.1:n.308-8_308-7delinsTC
NM_001282545.2:c.215+15544_215+15545delinsTC	NP_001269474.1:n.215+15544_215+15545delinsTC
NM_001282548.2:c.158+27895_158+27896delinsTC	NP_001269477.1:n.158+27895_158+27896delinsTC
NM_001282549.2:c.364+10780_364+10781delinsTC	NP_001269478.1:n.364+10780_364+10781delinsTC
NR_104212.2:n.330-8_330-7delinsTC
NR_104215.2:n.273-8_273-7delinsTC
NR_104216.2:n.478+10780_478+10781delinsTC