Canonical Allele Identifier: CA1327045565

Gene: BARD1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214728836_214728838delinsCTC , CM000664.2:g.214728836_214728838delinsCTC	GRCh38
NC_000002.11:g.215593560_215593562delinsCTC , CM000664.1:g.215593560_215593562delinsCTC	GRCh37
NC_000002.10:g.215301805_215301807delinsCTC	NCBI36
NG_012047.2:g.85867_85869delinsGAG
NG_012047.3:g.85874_85876delinsGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.2172_2174delinsGAG MANE Select	ENSP00000260947.4:p.Ala724=
ENST00000421162.2:c.819_821delinsGAG	ENSP00000392245.2:p.Ala273=
ENST00000613192.2:c.*235_*237delinsGAG	ENSP00000483275.2:n.*235_*237delinsGAG
ENST00000613374.5:c.762_764delinsGAG	ENSP00000484464.1:p.Ala254=
ENST00000613706.5:c.1764_1766delinsGAG	ENSP00000484976.2:p.Ala588=
ENST00000617164.5:c.2115_2117delinsGAG	ENSP00000480470.1:p.Ala705=
ENST00000619009.5:c.633_635delinsGAG	ENSP00000482293.1:p.Ala211=
ENST00000650978.1:c.3547_3549delinsGAG
ENST00000260947.8:c.2172_2174delinsGAG	ENSP00000260947.4:p.Ala724=
ENST00000432456.5:c.315_317delinsGAG
ENST00000455743.5:c.*1792_*1794delinsGAG	ENSP00000412186.1:n.*1792_*1794delinsGAG
ENST00000471590.5:n.507_509delinsGAG
ENST00000613192.1:c.342_344delinsGAG	ENSP00000483275.1:p.Ala114=
ENST00000613374.4:c.762_764delinsGAG	ENSP00000484464.1:p.Ala254=
ENST00000613706.4:c.819_821delinsGAG	ENSP00000484976.1:p.Ala273=
ENST00000617164.4:c.2115_2117delinsGAG	ENSP00000480470.1:p.Ala705=
ENST00000619009.4:c.633_635delinsGAG	ENSP00000482293.1:p.Ala211=
ENST00000620057.4:c.*838_*840delinsGAG	ENSP00000481988.1:n.*838_*840delinsGAG
NM_000465.3:c.2172_2174delinsGAG	NP_000456.2:p.Ala724=
NM_001282543.1:c.2115_2117delinsGAG	NP_001269472.1:p.Ala705=
NM_001282545.1:c.819_821delinsGAG	NP_001269474.1:p.Ala273=
NM_001282548.1:c.762_764delinsGAG	NP_001269477.1:p.Ala254=
NM_001282549.1:c.633_635delinsGAG	NP_001269478.1:p.Ala211=
NR_104212.1:n.2165_2167delinsGAG
NR_104215.1:n.2108_2110delinsGAG
NR_104216.1:n.1364_1366delinsGAG
XM_011511567.1:c.2118_2120delinsGAG	XP_011509869.1:p.Ala706=
XM_017004613.1:c.2271_2273delinsGAG	XP_016860102.1:p.Ala757=
XR_002959322.1:n.2538_2540delinsGAG
NM_000465.4:c.2172_2174delinsGAG MANE Select	NP_000456.2:p.Ala724=
NM_001282543.2:c.2115_2117delinsGAG	NP_001269472.1:p.Ala705=
NM_001282545.2:c.819_821delinsGAG	NP_001269474.1:p.Ala273=
NM_001282548.2:c.762_764delinsGAG	NP_001269477.1:p.Ala254=
NM_001282549.2:c.633_635delinsGAG	NP_001269478.1:p.Ala211=
NR_104212.2:n.2137_2139delinsGAG
NR_104215.2:n.2080_2082delinsGAG
NR_104216.2:n.1336_1338delinsGAG