Canonical Allele Identifier: CA1327053669

Gene: BARD1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214745770_214745774delinsGCTCA , CM000664.2:g.214745770_214745774delinsGCTCA	GRCh38
NC_000002.11:g.215610494_215610498delinsGCTCA , CM000664.1:g.215610494_215610498delinsGCTCA	GRCh37
NC_000002.10:g.215318739_215318743delinsGCTCA	NCBI36
NG_012047.2:g.68931_68935delinsTGAGC
NG_012047.3:g.68938_68942delinsTGAGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.1758_1762delinsTGAGC MANE Select	ENSP00000260947.4:p.Ser586=
ENST00000421162.2:c.405_409delinsTGAGC	ENSP00000392245.2:p.Ser135=
ENST00000613192.2:c.159-15266_159-15262delinsTGAGC	ENSP00000483275.2:n.159-15266_159-15262delinsTGAGC
ENST00000613374.5:c.348_352delinsTGAGC	ENSP00000484464.1:p.Ser116=
ENST00000613706.5:c.1350_1354delinsTGAGC	ENSP00000484976.2:p.Ser450=
ENST00000617164.5:c.1701_1705delinsTGAGC	ENSP00000480470.1:p.Ser567=
ENST00000619009.5:c.365-15266_365-15262delinsTGAGC	ENSP00000482293.1:n.365-15266_365-15262delinsTGAGC
ENST00000650978.1:c.3133_3137delinsTGAGC
ENST00000260947.8:c.1758_1762delinsTGAGC	ENSP00000260947.4:p.Ser586=
ENST00000421162.1:c.405_409delinsTGAGC	ENSP00000392245.1:p.Ser135=
ENST00000455743.5:c.*1378_*1382delinsTGAGC	ENSP00000412186.1:n.*1378_*1382delinsTGAGC
ENST00000465841.1:n.113_117delinsTGAGC
ENST00000613192.1:c.74-15266_74-15262delinsTGAGC	ENSP00000483275.1:n.74-15266_74-15262delinsTGAGC
ENST00000613374.4:c.348_352delinsTGAGC	ENSP00000484464.1:p.Ser116=
ENST00000613706.4:c.405_409delinsTGAGC	ENSP00000484976.1:p.Ser135=
ENST00000617164.4:c.1701_1705delinsTGAGC	ENSP00000480470.1:p.Ser567=
ENST00000619009.4:c.365-15266_365-15262delinsTGAGC	ENSP00000482293.1:n.365-15266_365-15262delinsTGAGC
ENST00000620057.4:c.*424_*428delinsTGAGC	ENSP00000481988.1:n.*424_*428delinsTGAGC
NM_000465.3:c.1758_1762delinsTGAGC	NP_000456.2:p.Ser586=
NM_001282543.1:c.1701_1705delinsTGAGC	NP_001269472.1:p.Ser567=
NM_001282545.1:c.405_409delinsTGAGC	NP_001269474.1:p.Ser135=
NM_001282548.1:c.348_352delinsTGAGC	NP_001269477.1:p.Ser116=
NM_001282549.1:c.365-15266_365-15262delinsTGAGC	NP_001269478.1:n.365-15266_365-15262delinsTGAGC
NR_104212.1:n.1751_1755delinsTGAGC
NR_104215.1:n.1694_1698delinsTGAGC
NR_104216.1:n.950_954delinsTGAGC
XM_011511567.1:c.1704_1708delinsTGAGC	XP_011509869.1:p.Ser568=
XM_011511568.1:c.1758_1762delinsTGAGC	XP_011509870.1:p.Ser586=
XM_017004613.1:c.1857_1861delinsTGAGC	XP_016860102.1:p.Ser619=
XM_017004614.1:c.1857_1861delinsTGAGC	XP_016860103.1:p.Ser619=
XR_002959322.1:n.1948_1952delinsTGAGC
NM_000465.4:c.1758_1762delinsTGAGC MANE Select	NP_000456.2:p.Ser586=
NM_001282543.2:c.1701_1705delinsTGAGC	NP_001269472.1:p.Ser567=
NM_001282545.2:c.405_409delinsTGAGC	NP_001269474.1:p.Ser135=
NM_001282548.2:c.348_352delinsTGAGC	NP_001269477.1:p.Ser116=
NM_001282549.2:c.365-15266_365-15262delinsTGAGC	NP_001269478.1:n.365-15266_365-15262delinsTGAGC
NR_104212.2:n.1723_1727delinsTGAGC
NR_104215.2:n.1666_1670delinsTGAGC
NR_104216.2:n.922_926delinsTGAGC