Canonical Allele Identifier: CA1327071582

Gene: BARD1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214781526_214781530delinsAAAAG , CM000664.2:g.214781526_214781530delinsAAAAG	GRCh38
NC_000002.11:g.215646250_215646254delinsAAAAG , CM000664.1:g.215646250_215646254delinsAAAAG	GRCh37
NC_000002.10:g.215354495_215354499delinsAAAAG	NCBI36
NG_012047.2:g.33175_33179delinsCTTTT
NG_012047.3:g.33182_33186delinsCTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.365-21_365-17delinsCTTTT MANE Select	ENSP00000260947.4:n.365-21_365-17delinsCTTTT
ENST00000421162.2:c.215+15531_215+15535delinsCTTTT	ENSP00000392245.2:n.215+15531_215+15535delinsCTTTT
ENST00000613192.2:c.158+27882_158+27886delinsCTTTT	ENSP00000483275.2:n.158+27882_158+27886delinsCTTTT
ENST00000613374.5:c.158+27882_158+27886delinsCTTTT	ENSP00000484464.1:n.158+27882_158+27886delinsCTTTT
ENST00000613706.5:c.365-21_365-17delinsCTTTT	ENSP00000484976.2:n.365-21_365-17delinsCTTTT
ENST00000617164.5:c.308-21_308-17delinsCTTTT	ENSP00000480470.1:n.308-21_308-17delinsCTTTT
ENST00000619009.5:c.364+10767_364+10771delinsCTTTT	ENSP00000482293.1:n.364+10767_364+10771delinsCTTTT
ENST00000650978.1:c.207-21_207-17delinsCTTTT
ENST00000260947.8:c.365-21_365-17delinsCTTTT	ENSP00000260947.4:n.365-21_365-17delinsCTTTT
ENST00000421162.1:c.215+15531_215+15535delinsCTTTT	ENSP00000392245.1:n.215+15531_215+15535delinsCTTTT
ENST00000455743.5:c.216-21_216-17delinsCTTTT	ENSP00000412186.1:n.216-21_216-17delinsCTTTT
ENST00000471787.1:n.260-21_260-17delinsCTTTT
ENST00000613192.1:c.73+27882_73+27886delinsCTTTT	ENSP00000483275.1:n.73+27882_73+27886delinsCTTTT
ENST00000613374.4:c.158+27882_158+27886delinsCTTTT	ENSP00000484464.1:n.158+27882_158+27886delinsCTTTT
ENST00000613706.4:c.215+15531_215+15535delinsCTTTT	ENSP00000484976.1:n.215+15531_215+15535delinsCTTTT
ENST00000617164.4:c.308-21_308-17delinsCTTTT	ENSP00000480470.1:n.308-21_308-17delinsCTTTT
ENST00000619009.4:c.364+10767_364+10771delinsCTTTT	ENSP00000482293.1:n.364+10767_364+10771delinsCTTTT
ENST00000620057.4:c.364+10767_364+10771delinsCTTTT	ENSP00000481988.1:n.364+10767_364+10771delinsCTTTT
NM_000465.3:c.365-21_365-17delinsCTTTT	NP_000456.2:n.365-21_365-17delinsCTTTT
NM_001282543.1:c.308-21_308-17delinsCTTTT	NP_001269472.1:n.308-21_308-17delinsCTTTT
NM_001282545.1:c.215+15531_215+15535delinsCTTTT	NP_001269474.1:n.215+15531_215+15535delinsCTTTT
NM_001282548.1:c.158+27882_158+27886delinsCTTTT	NP_001269477.1:n.158+27882_158+27886delinsCTTTT
NM_001282549.1:c.364+10767_364+10771delinsCTTTT	NP_001269478.1:n.364+10767_364+10771delinsCTTTT
NR_104212.1:n.358-21_358-17delinsCTTTT
NR_104215.1:n.301-21_301-17delinsCTTTT
NR_104216.1:n.506+10767_506+10771delinsCTTTT
XM_011511567.1:c.311-21_311-17delinsCTTTT	XP_011509869.1:n.311-21_311-17delinsCTTTT
XM_011511568.1:c.365-21_365-17delinsCTTTT	XP_011509870.1:n.365-21_365-17delinsCTTTT
XM_017004613.1:c.464-21_464-17delinsCTTTT	XP_016860102.1:n.464-21_464-17delinsCTTTT
XM_017004614.1:c.464-21_464-17delinsCTTTT	XP_016860103.1:n.464-21_464-17delinsCTTTT
XR_002959322.1:n.555-21_555-17delinsCTTTT
NM_000465.4:c.365-21_365-17delinsCTTTT MANE Select	NP_000456.2:n.365-21_365-17delinsCTTTT
NM_001282543.2:c.308-21_308-17delinsCTTTT	NP_001269472.1:n.308-21_308-17delinsCTTTT
NM_001282545.2:c.215+15531_215+15535delinsCTTTT	NP_001269474.1:n.215+15531_215+15535delinsCTTTT
NM_001282548.2:c.158+27882_158+27886delinsCTTTT	NP_001269477.1:n.158+27882_158+27886delinsCTTTT
NM_001282549.2:c.364+10767_364+10771delinsCTTTT	NP_001269478.1:n.364+10767_364+10771delinsCTTTT
NR_104212.2:n.330-21_330-17delinsCTTTT
NR_104215.2:n.273-21_273-17delinsCTTTT
NR_104216.2:n.478+10767_478+10771delinsCTTTT