Canonical Allele Identifier: CA1327045448

Gene: BARD1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214728702_214728703delinsAG , CM000664.2:g.214728702_214728703delinsAG	GRCh38
NC_000002.11:g.215593426_215593427delinsAG , CM000664.1:g.215593426_215593427delinsAG	GRCh37
NC_000002.10:g.215301671_215301672delinsAG	NCBI36
NG_012047.2:g.86002_86003delinsCT
NG_012047.3:g.86009_86010delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.2307_2308delinsCT MANE Select	ENSP00000260947.4:p.Ser769=
ENST00000421162.2:c.954_955delinsCT	ENSP00000392245.2:p.Ser318=
ENST00000613192.2:c.*370_*371delinsCT	ENSP00000483275.2:n.*370_*371delinsCT
ENST00000613374.5:c.897_898delinsCT	ENSP00000484464.1:p.Ser299=
ENST00000613706.5:c.1899_1900delinsCT	ENSP00000484976.2:p.Ser633=
ENST00000617164.5:c.2250_2251delinsCT	ENSP00000480470.1:p.Ser750=
ENST00000619009.5:c.768_769delinsCT	ENSP00000482293.1:p.Ser256=
ENST00000650978.1:c.3682_3683delinsCT
ENST00000260947.8:c.2307_2308delinsCT	ENSP00000260947.4:p.Ser769=
ENST00000432456.5:c.450_451delinsCT
ENST00000471590.5:n.642_643delinsCT
ENST00000613192.1:c.477_478delinsCT	ENSP00000483275.1:p.Ser159=
ENST00000613374.4:c.897_898delinsCT	ENSP00000484464.1:p.Ser299=
ENST00000613706.4:c.954_955delinsCT	ENSP00000484976.1:p.Ser318=
ENST00000617164.4:c.2250_2251delinsCT	ENSP00000480470.1:p.Ser750=
ENST00000619009.4:c.768_769delinsCT	ENSP00000482293.1:p.Ser256=
ENST00000620057.4:c.*973_*974delinsCT	ENSP00000481988.1:n.*973_*974delinsCT
NM_000465.3:c.2307_2308delinsCT	NP_000456.2:p.Ser769=
NM_001282543.1:c.2250_2251delinsCT	NP_001269472.1:p.Ser750=
NM_001282545.1:c.954_955delinsCT	NP_001269474.1:p.Ser318=
NM_001282548.1:c.897_898delinsCT	NP_001269477.1:p.Ser299=
NM_001282549.1:c.768_769delinsCT	NP_001269478.1:p.Ser256=
NR_104212.1:n.2300_2301delinsCT
NR_104215.1:n.2243_2244delinsCT
NR_104216.1:n.1499_1500delinsCT
XM_011511567.1:c.2253_2254delinsCT	XP_011509869.1:p.Ser751=
XM_017004613.1:c.2406_2407delinsCT	XP_016860102.1:p.Ser802=
XR_002959322.1:n.2673_2674delinsCT
NM_000465.4:c.2307_2308delinsCT MANE Select	NP_000456.2:p.Ser769=
NM_001282543.2:c.2250_2251delinsCT	NP_001269472.1:p.Ser750=
NM_001282545.2:c.954_955delinsCT	NP_001269474.1:p.Ser318=
NM_001282548.2:c.897_898delinsCT	NP_001269477.1:p.Ser299=
NM_001282549.2:c.768_769delinsCT	NP_001269478.1:p.Ser256=
NR_104212.2:n.2272_2273delinsCT
NR_104215.2:n.2215_2216delinsCT
NR_104216.2:n.1471_1472delinsCT