Canonical Allele Identifier: CA1327071497

Gene: BARD1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214781403_214781412delinsAACATATCTG , CM000664.2:g.214781403_214781412delinsAACATATCTG	GRCh38
NC_000002.11:g.215646127_215646136delinsAACATATCTG , CM000664.1:g.215646127_215646136delinsAACATATCTG	GRCh37
NC_000002.10:g.215354372_215354381delinsAACATATCTG	NCBI36
NG_012047.2:g.33293_33302delinsCAGATATGTT
NG_012047.3:g.33300_33309delinsCAGATATGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.462_471delinsCAGATATGTT MANE Select	ENSP00000260947.4:p.Val154=
ENST00000421162.2:c.215+15649_215+15658delinsCAGATATGTT	ENSP00000392245.2:n.215+15649_215+15658delinsCAGATATGTT
ENST00000613192.2:c.158+28000_158+28009delinsCAGATATGTT	ENSP00000483275.2:n.158+28000_158+28009delinsCAGATATGTT
ENST00000613374.5:c.158+28000_158+28009delinsCAGATATGTT	ENSP00000484464.1:n.158+28000_158+28009delinsCAGATATGTT
ENST00000613706.5:c.462_471delinsCAGATATGTT	ENSP00000484976.2:p.Val154=
ENST00000617164.5:c.405_414delinsCAGATATGTT	ENSP00000480470.1:p.Val135=
ENST00000619009.5:c.364+10885_364+10894delinsCAGATATGTT	ENSP00000482293.1:n.364+10885_364+10894delinsCAGATATGTT
ENST00000650978.1:c.304_313delinsCAGATATGTT
ENST00000260947.8:c.462_471delinsCAGATATGTT	ENSP00000260947.4:p.Val154=
ENST00000421162.1:c.215+15649_215+15658delinsCAGATATGTT	ENSP00000392245.1:n.215+15649_215+15658delinsCAGATATGTT
ENST00000455743.5:c.*82_*91delinsCAGATATGTT	ENSP00000412186.1:n.*82_*91delinsCAGATATGTT
ENST00000471787.1:n.357_366delinsCAGATATGTT
ENST00000613192.1:c.73+28000_73+28009delinsCAGATATGTT	ENSP00000483275.1:n.73+28000_73+28009delinsCAGATATGTT
ENST00000613374.4:c.158+28000_158+28009delinsCAGATATGTT	ENSP00000484464.1:n.158+28000_158+28009delinsCAGATATGTT
ENST00000613706.4:c.215+15649_215+15658delinsCAGATATGTT	ENSP00000484976.1:n.215+15649_215+15658delinsCAGATATGTT
ENST00000617164.4:c.405_414delinsCAGATATGTT	ENSP00000480470.1:p.Val135=
ENST00000619009.4:c.364+10885_364+10894delinsCAGATATGTT	ENSP00000482293.1:n.364+10885_364+10894delinsCAGATATGTT
ENST00000620057.4:c.364+10885_364+10894delinsCAGATATGTT	ENSP00000481988.1:n.364+10885_364+10894delinsCAGATATGTT
NM_000465.3:c.462_471delinsCAGATATGTT	NP_000456.2:p.Val154=
NM_001282543.1:c.405_414delinsCAGATATGTT	NP_001269472.1:p.Val135=
NM_001282545.1:c.215+15649_215+15658delinsCAGATATGTT	NP_001269474.1:n.215+15649_215+15658delinsCAGATATGTT
NM_001282548.1:c.158+28000_158+28009delinsCAGATATGTT	NP_001269477.1:n.158+28000_158+28009delinsCAGATATGTT
NM_001282549.1:c.364+10885_364+10894delinsCAGATATGTT	NP_001269478.1:n.364+10885_364+10894delinsCAGATATGTT
NR_104212.1:n.455_464delinsCAGATATGTT
NR_104215.1:n.398_407delinsCAGATATGTT
NR_104216.1:n.506+10885_506+10894delinsCAGATATGTT
XM_011511567.1:c.408_417delinsCAGATATGTT	XP_011509869.1:p.Val136=
XM_011511568.1:c.462_471delinsCAGATATGTT	XP_011509870.1:p.Val154=
XM_017004613.1:c.561_570delinsCAGATATGTT	XP_016860102.1:p.Val187=
XM_017004614.1:c.561_570delinsCAGATATGTT	XP_016860103.1:p.Val187=
XR_002959322.1:n.652_661delinsCAGATATGTT
NM_000465.4:c.462_471delinsCAGATATGTT MANE Select	NP_000456.2:p.Val154=
NM_001282543.2:c.405_414delinsCAGATATGTT	NP_001269472.1:p.Val135=
NM_001282545.2:c.215+15649_215+15658delinsCAGATATGTT	NP_001269474.1:n.215+15649_215+15658delinsCAGATATGTT
NM_001282548.2:c.158+28000_158+28009delinsCAGATATGTT	NP_001269477.1:n.158+28000_158+28009delinsCAGATATGTT
NM_001282549.2:c.364+10885_364+10894delinsCAGATATGTT	NP_001269478.1:n.364+10885_364+10894delinsCAGATATGTT
NR_104212.2:n.427_436delinsCAGATATGTT
NR_104215.2:n.370_379delinsCAGATATGTT
NR_104216.2:n.478+10885_478+10894delinsCAGATATGTT