Canonical Allele Identifier: CA2559471339

Gene: BARD1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214792290_214792291insATT , CM000664.2:g.214792290_214792291insATT	GRCh38
NC_000002.11:g.215657014_215657015insATT , CM000664.1:g.215657014_215657015insATT	GRCh37
NC_000002.10:g.215365259_215365260insATT	NCBI36
NG_012047.2:g.22415_22416insATA
NG_012047.3:g.22422_22423insATA

Transcript Alleles

HGVS	Amino-acid change
ENST00000260947.9:c.364+7_364+8insATA MANE Select	ENSP00000260947.4:n.364+7_364+8insATA
ENST00000421162.2:c.215+4771_215+4772insATA	ENSP00000392245.2:n.215+4771_215+4772insA...
ENST00000613192.2:c.158+17122_158+17123insATA	ENSP00000483275.2:n.158+17122_158+17123in...
ENST00000613374.5:c.158+17122_158+17123insATA	ENSP00000484464.1:n.158+17122_158+17123in...
ENST00000613706.5:c.364+7_364+8insATA	ENSP00000484976.2:n.364+7_364+8insATA
ENST00000617164.5:c.307+7_307+8insATA	ENSP00000480470.1:n.307+7_307+8insATA
ENST00000619009.5:c.364+7_364+8insATA	ENSP00000482293.1:n.364+7_364+8insATA
ENST00000650978.1:c.206+7_206+8insATA
ENST00000260947.8:c.364+7_364+8insATA	ENSP00000260947.4:n.364+7_364+8insATA
ENST00000421162.1:c.215+4771_215+4772insATA	ENSP00000392245.1:n.215+4771_215+4772insA...
ENST00000455743.5:c.215+4771_215+4772insATA	ENSP00000412186.1:n.215+4771_215+4772insA...
ENST00000471787.1:n.260-10781_260-10780insATA
ENST00000613192.1:c.73+17122_73+17123insATA	ENSP00000483275.1:n.73+17122_73+17123insA...
ENST00000613374.4:c.158+17122_158+17123insATA	ENSP00000484464.1:n.158+17122_158+17123in...
ENST00000613706.4:c.215+4771_215+4772insATA	ENSP00000484976.1:n.215+4771_215+4772insA...
ENST00000617164.4:c.307+7_307+8insATA	ENSP00000480470.1:n.307+7_307+8insATA
ENST00000619009.4:c.364+7_364+8insATA	ENSP00000482293.1:n.364+7_364+8insATA
ENST00000620057.4:c.364+7_364+8insATA	ENSP00000481988.1:n.364+7_364+8insATA
NM_000465.3:c.364+7_364+8insATA	NP_000456.2:n.364+7_364+8insATA
NM_001282543.1:c.307+7_307+8insATA	NP_001269472.1:n.307+7_307+8insATA
NM_001282545.1:c.215+4771_215+4772insATA	NP_001269474.1:n.215+4771_215+4772insATA
NM_001282548.1:c.158+17122_158+17123insATA	NP_001269477.1:n.158+17122_158+17123insAT...
NM_001282549.1:c.364+7_364+8insATA	NP_001269478.1:n.364+7_364+8insATA
NR_104212.1:n.357+4771_357+4772insATA
NR_104215.1:n.301-10781_301-10780insATA
NR_104216.1:n.506+7_506+8insATA
XM_011511567.1:c.310+7_310+8insATA	XP_011509869.1:n.310+7_310+8insATA
XM_011511568.1:c.364+7_364+8insATA	XP_011509870.1:n.364+7_364+8insATA
XM_017004613.1:c.463+7_463+8insATA	XP_016860102.1:n.463+7_463+8insATA
XM_017004614.1:c.463+7_463+8insATA	XP_016860103.1:n.463+7_463+8insATA
XR_002959322.1:n.554+7_554+8insATA
NM_000465.4:c.364+7_364+8insATA MANE Select	NP_000456.2:n.364+7_364+8insATA
NM_001282543.2:c.307+7_307+8insATA	NP_001269472.1:n.307+7_307+8insATA
NM_001282545.2:c.215+4771_215+4772insATA	NP_001269474.1:n.215+4771_215+4772insATA
NM_001282548.2:c.158+17122_158+17123insATA	NP_001269477.1:n.158+17122_158+17123insAT...
NM_001282549.2:c.364+7_364+8insATA	NP_001269478.1:n.364+7_364+8insATA
NR_104212.2:n.329+4771_329+4772insATA
NR_104215.2:n.273-10781_273-10780insATA
NR_104216.2:n.478+7_478+8insATA