Canonical Allele Identifier: CA1327071530

Gene: BARD1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214781457_214781459delinsCTT , CM000664.2:g.214781457_214781459delinsCTT	GRCh38
NC_000002.11:g.215646181_215646183delinsCTT , CM000664.1:g.215646181_215646183delinsCTT	GRCh37
NC_000002.10:g.215354426_215354428delinsCTT	NCBI36
NG_012047.2:g.33246_33248delinsAAG
NG_012047.3:g.33253_33255delinsAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.415_417delinsAAG MANE Select	ENSP00000260947.4:p.Lys139=
ENST00000421162.2:c.215+15602_215+15604delinsAAG	ENSP00000392245.2:n.215+15602_215+15604delinsAAG
ENST00000613192.2:c.158+27953_158+27955delinsAAG	ENSP00000483275.2:n.158+27953_158+27955delinsAAG
ENST00000613374.5:c.158+27953_158+27955delinsAAG	ENSP00000484464.1:n.158+27953_158+27955delinsAAG
ENST00000613706.5:c.415_417delinsAAG	ENSP00000484976.2:p.Lys139=
ENST00000617164.5:c.358_360delinsAAG	ENSP00000480470.1:p.Lys120=
ENST00000619009.5:c.364+10838_364+10840delinsAAG	ENSP00000482293.1:n.364+10838_364+10840delinsAAG
ENST00000650978.1:c.257_259delinsAAG
ENST00000260947.8:c.415_417delinsAAG	ENSP00000260947.4:p.Lys139=
ENST00000421162.1:c.215+15602_215+15604delinsAAG	ENSP00000392245.1:n.215+15602_215+15604delinsAAG
ENST00000455743.5:c.*35_*37delinsAAG	ENSP00000412186.1:n.*35_*37delinsAAG
ENST00000471787.1:n.310_312delinsAAG
ENST00000613192.1:c.73+27953_73+27955delinsAAG	ENSP00000483275.1:n.73+27953_73+27955delinsAAG
ENST00000613374.4:c.158+27953_158+27955delinsAAG	ENSP00000484464.1:n.158+27953_158+27955delinsAAG
ENST00000613706.4:c.215+15602_215+15604delinsAAG	ENSP00000484976.1:n.215+15602_215+15604delinsAAG
ENST00000617164.4:c.358_360delinsAAG	ENSP00000480470.1:p.Lys120=
ENST00000619009.4:c.364+10838_364+10840delinsAAG	ENSP00000482293.1:n.364+10838_364+10840delinsAAG
ENST00000620057.4:c.364+10838_364+10840delinsAAG	ENSP00000481988.1:n.364+10838_364+10840delinsAAG
NM_000465.3:c.415_417delinsAAG	NP_000456.2:p.Lys139=
NM_001282543.1:c.358_360delinsAAG	NP_001269472.1:p.Lys120=
NM_001282545.1:c.215+15602_215+15604delinsAAG	NP_001269474.1:n.215+15602_215+15604delinsAAG
NM_001282548.1:c.158+27953_158+27955delinsAAG	NP_001269477.1:n.158+27953_158+27955delinsAAG
NM_001282549.1:c.364+10838_364+10840delinsAAG	NP_001269478.1:n.364+10838_364+10840delinsAAG
NR_104212.1:n.408_410delinsAAG
NR_104215.1:n.351_353delinsAAG
NR_104216.1:n.506+10838_506+10840delinsAAG
XM_011511567.1:c.361_363delinsAAG	XP_011509869.1:p.Lys121=
XM_011511568.1:c.415_417delinsAAG	XP_011509870.1:p.Lys139=
XM_017004613.1:c.514_516delinsAAG	XP_016860102.1:p.Lys172=
XM_017004614.1:c.514_516delinsAAG	XP_016860103.1:p.Lys172=
XR_002959322.1:n.605_607delinsAAG
NM_000465.4:c.415_417delinsAAG MANE Select	NP_000456.2:p.Lys139=
NM_001282543.2:c.358_360delinsAAG	NP_001269472.1:p.Lys120=
NM_001282545.2:c.215+15602_215+15604delinsAAG	NP_001269474.1:n.215+15602_215+15604delinsAAG
NM_001282548.2:c.158+27953_158+27955delinsAAG	NP_001269477.1:n.158+27953_158+27955delinsAAG
NM_001282549.2:c.364+10838_364+10840delinsAAG	NP_001269478.1:n.364+10838_364+10840delinsAAG
NR_104212.2:n.380_382delinsAAG
NR_104215.2:n.323_325delinsAAG
NR_104216.2:n.478+10838_478+10840delinsAAG