Canonical Allele Identifier: CA1327085151

Gene: BARD1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214809453_214809455delinsGGC , CM000664.2:g.214809453_214809455delinsGGC	GRCh38
NC_000002.11:g.215674177_215674179delinsGGC , CM000664.1:g.215674177_215674179delinsGGC	GRCh37
NC_000002.10:g.215382422_215382424delinsGGC	NCBI36
NG_012047.2:g.5250_5252delinsGCC
NG_012047.3:g.5257_5259delinsGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.115_117delinsGCC MANE Select	ENSP00000260947.4:p.Ala39=
ENST00000421162.2:c.115_117delinsGCC	ENSP00000392245.2:p.Ala39=
ENST00000613192.2:c.115_117delinsGCC	ENSP00000483275.2:p.Ala39=
ENST00000613374.5:c.115_117delinsGCC	ENSP00000484464.1:p.Ala39=
ENST00000613706.5:c.115_117delinsGCC	ENSP00000484976.2:p.Ala39=
ENST00000617164.5:c.115_117delinsGCC	ENSP00000480470.1:p.Ala39=
ENST00000619009.5:c.115_117delinsGCC	ENSP00000482293.1:p.Ala39=
ENST00000260947.8:c.115_117delinsGCC	ENSP00000260947.4:p.Ala39=
ENST00000421162.1:c.115_117delinsGCC	ENSP00000392245.1:p.Ala39=
ENST00000455743.5:c.115_117delinsGCC	ENSP00000412186.1:p.Ala39=
ENST00000471787.1:n.216_218delinsGCC
ENST00000479904.1:n.206_208delinsGCC
ENST00000613192.1:c.30_32delinsGCC	ENSP00000483275.1:p.Ala10=
ENST00000613374.4:c.115_117delinsGCC	ENSP00000484464.1:p.Ala39=
ENST00000613706.4:c.115_117delinsGCC	ENSP00000484976.1:p.Ala39=
ENST00000617164.4:c.115_117delinsGCC	ENSP00000480470.1:p.Ala39=
ENST00000619009.4:c.115_117delinsGCC	ENSP00000482293.1:p.Ala39=
ENST00000620057.4:c.115_117delinsGCC	ENSP00000481988.1:p.Ala39=
NM_000465.3:c.115_117delinsGCC	NP_000456.2:p.Ala39=
NM_001282543.1:c.115_117delinsGCC	NP_001269472.1:p.Ala39=
NM_001282545.1:c.115_117delinsGCC	NP_001269474.1:p.Ala39=
NM_001282548.1:c.115_117delinsGCC	NP_001269477.1:p.Ala39=
NM_001282549.1:c.115_117delinsGCC	NP_001269478.1:p.Ala39=
NR_104212.1:n.257_259delinsGCC
NR_104215.1:n.257_259delinsGCC
NR_104216.1:n.257_259delinsGCC
XM_011511568.1:c.115_117delinsGCC	XP_011509870.1:p.Ala39=
XM_017004613.1:c.115_117delinsGCC	XP_016860102.1:p.Ala39=
XM_017004614.1:c.115_117delinsGCC	XP_016860103.1:p.Ala39=
XR_002959322.1:n.206_208delinsGCC
NM_000465.4:c.115_117delinsGCC MANE Select	NP_000456.2:p.Ala39=
NM_001282543.2:c.115_117delinsGCC	NP_001269472.1:p.Ala39=
NM_001282545.2:c.115_117delinsGCC	NP_001269474.1:p.Ala39=
NM_001282548.2:c.115_117delinsGCC	NP_001269477.1:p.Ala39=
NM_001282549.2:c.115_117delinsGCC	NP_001269478.1:p.Ala39=
NR_104212.2:n.229_231delinsGCC
NR_104215.2:n.229_231delinsGCC
NR_104216.2:n.229_231delinsGCC