Canonical Allele Identifier: CA1327071459

Gene: BARD1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214781337_214781339delinsTGA , CM000664.2:g.214781337_214781339delinsTGA	GRCh38
NC_000002.11:g.215646061_215646063delinsTGA , CM000664.1:g.215646061_215646063delinsTGA	GRCh37
NC_000002.10:g.215354306_215354308delinsTGA	NCBI36
NG_012047.2:g.33366_33368delinsTCA
NG_012047.3:g.33373_33375delinsTCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.535_537delinsTCA MANE Select	ENSP00000260947.4:p.Ser179=
ENST00000421162.2:c.215+15722_215+15724delinsTCA	ENSP00000392245.2:n.215+15722_215+15724delinsTCA
ENST00000613192.2:c.158+28073_158+28075delinsTCA	ENSP00000483275.2:n.158+28073_158+28075delinsTCA
ENST00000613374.5:c.158+28073_158+28075delinsTCA	ENSP00000484464.1:n.158+28073_158+28075delinsTCA
ENST00000613706.5:c.535_537delinsTCA	ENSP00000484976.2:p.Ser179=
ENST00000617164.5:c.478_480delinsTCA	ENSP00000480470.1:p.Ser160=
ENST00000619009.5:c.364+10958_364+10960delinsTCA	ENSP00000482293.1:n.364+10958_364+10960delinsTCA
ENST00000650978.1:c.377_379delinsTCA
ENST00000260947.8:c.535_537delinsTCA	ENSP00000260947.4:p.Ser179=
ENST00000421162.1:c.215+15722_215+15724delinsTCA	ENSP00000392245.1:n.215+15722_215+15724delinsTCA
ENST00000455743.5:c.*155_*157delinsTCA	ENSP00000412186.1:n.*155_*157delinsTCA
ENST00000471787.1:n.430_432delinsTCA
ENST00000613192.1:c.73+28073_73+28075delinsTCA	ENSP00000483275.1:n.73+28073_73+28075delinsTCA
ENST00000613374.4:c.158+28073_158+28075delinsTCA	ENSP00000484464.1:n.158+28073_158+28075delinsTCA
ENST00000613706.4:c.215+15722_215+15724delinsTCA	ENSP00000484976.1:n.215+15722_215+15724delinsTCA
ENST00000617164.4:c.478_480delinsTCA	ENSP00000480470.1:p.Ser160=
ENST00000619009.4:c.364+10958_364+10960delinsTCA	ENSP00000482293.1:n.364+10958_364+10960delinsTCA
ENST00000620057.4:c.364+10958_364+10960delinsTCA	ENSP00000481988.1:n.364+10958_364+10960delinsTCA
NM_000465.3:c.535_537delinsTCA	NP_000456.2:p.Ser179=
NM_001282543.1:c.478_480delinsTCA	NP_001269472.1:p.Ser160=
NM_001282545.1:c.215+15722_215+15724delinsTCA	NP_001269474.1:n.215+15722_215+15724delinsTCA
NM_001282548.1:c.158+28073_158+28075delinsTCA	NP_001269477.1:n.158+28073_158+28075delinsTCA
NM_001282549.1:c.364+10958_364+10960delinsTCA	NP_001269478.1:n.364+10958_364+10960delinsTCA
NR_104212.1:n.528_530delinsTCA
NR_104215.1:n.471_473delinsTCA
NR_104216.1:n.506+10958_506+10960delinsTCA
XM_011511567.1:c.481_483delinsTCA	XP_011509869.1:p.Ser161=
XM_011511568.1:c.535_537delinsTCA	XP_011509870.1:p.Ser179=
XM_017004613.1:c.634_636delinsTCA	XP_016860102.1:p.Ser212=
XM_017004614.1:c.634_636delinsTCA	XP_016860103.1:p.Ser212=
XR_002959322.1:n.725_727delinsTCA
NM_000465.4:c.535_537delinsTCA MANE Select	NP_000456.2:p.Ser179=
NM_001282543.2:c.478_480delinsTCA	NP_001269472.1:p.Ser160=
NM_001282545.2:c.215+15722_215+15724delinsTCA	NP_001269474.1:n.215+15722_215+15724delinsTCA
NM_001282548.2:c.158+28073_158+28075delinsTCA	NP_001269477.1:n.158+28073_158+28075delinsTCA
NM_001282549.2:c.364+10958_364+10960delinsTCA	NP_001269478.1:n.364+10958_364+10960delinsTCA
NR_104212.2:n.500_502delinsTCA
NR_104215.2:n.443_445delinsTCA
NR_104216.2:n.478+10958_478+10960delinsTCA