Canonical Allele Identifier: CA1327076497

Gene: BARD1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214792021_214792022delinsCA , CM000664.2:g.214792021_214792022delinsCA	GRCh38
NC_000002.11:g.215656745_215656746delinsCA , CM000664.1:g.215656745_215656746delinsCA	GRCh37
NC_000002.10:g.215364990_215364991delinsCA	NCBI36
NG_012047.2:g.22683_22684delinsTG
NG_012047.3:g.22690_22691delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.364+275_364+276delinsTG MANE Select	ENSP00000260947.4:n.364+275_364+276delinsTG
ENST00000421162.2:c.215+5039_215+5040delinsTG	ENSP00000392245.2:n.215+5039_215+5040delinsTG
ENST00000613192.2:c.158+17390_158+17391delinsTG	ENSP00000483275.2:n.158+17390_158+17391delinsTG
ENST00000613374.5:c.158+17390_158+17391delinsTG	ENSP00000484464.1:n.158+17390_158+17391delinsTG
ENST00000613706.5:c.364+275_364+276delinsTG	ENSP00000484976.2:n.364+275_364+276delinsTG
ENST00000617164.5:c.307+275_307+276delinsTG	ENSP00000480470.1:n.307+275_307+276delinsTG
ENST00000619009.5:c.364+275_364+276delinsTG	ENSP00000482293.1:n.364+275_364+276delinsTG
ENST00000650978.1:c.206+275_206+276delinsTG
ENST00000260947.8:c.364+275_364+276delinsTG	ENSP00000260947.4:n.364+275_364+276delinsTG
ENST00000421162.1:c.215+5039_215+5040delinsTG	ENSP00000392245.1:n.215+5039_215+5040delinsTG
ENST00000455743.5:c.215+5039_215+5040delinsTG	ENSP00000412186.1:n.215+5039_215+5040delinsTG
ENST00000471787.1:n.260-10513_260-10512delinsTG
ENST00000613192.1:c.73+17390_73+17391delinsTG	ENSP00000483275.1:n.73+17390_73+17391delinsTG
ENST00000613374.4:c.158+17390_158+17391delinsTG	ENSP00000484464.1:n.158+17390_158+17391delinsTG
ENST00000613706.4:c.215+5039_215+5040delinsTG	ENSP00000484976.1:n.215+5039_215+5040delinsTG
ENST00000617164.4:c.307+275_307+276delinsTG	ENSP00000480470.1:n.307+275_307+276delinsTG
ENST00000619009.4:c.364+275_364+276delinsTG	ENSP00000482293.1:n.364+275_364+276delinsTG
ENST00000620057.4:c.364+275_364+276delinsTG	ENSP00000481988.1:n.364+275_364+276delinsTG
NM_000465.3:c.364+275_364+276delinsTG	NP_000456.2:n.364+275_364+276delinsTG
NM_001282543.1:c.307+275_307+276delinsTG	NP_001269472.1:n.307+275_307+276delinsTG
NM_001282545.1:c.215+5039_215+5040delinsTG	NP_001269474.1:n.215+5039_215+5040delinsTG
NM_001282548.1:c.158+17390_158+17391delinsTG	NP_001269477.1:n.158+17390_158+17391delinsTG
NM_001282549.1:c.364+275_364+276delinsTG	NP_001269478.1:n.364+275_364+276delinsTG
NR_104212.1:n.357+5039_357+5040delinsTG
NR_104215.1:n.301-10513_301-10512delinsTG
NR_104216.1:n.506+275_506+276delinsTG
XM_011511567.1:c.310+275_310+276delinsTG	XP_011509869.1:n.310+275_310+276delinsTG
XM_011511568.1:c.364+275_364+276delinsTG	XP_011509870.1:n.364+275_364+276delinsTG
XM_017004613.1:c.463+275_463+276delinsTG	XP_016860102.1:n.463+275_463+276delinsTG
XM_017004614.1:c.463+275_463+276delinsTG	XP_016860103.1:n.463+275_463+276delinsTG
XR_002959322.1:n.554+275_554+276delinsTG
NM_000465.4:c.364+275_364+276delinsTG MANE Select	NP_000456.2:n.364+275_364+276delinsTG
NM_001282543.2:c.307+275_307+276delinsTG	NP_001269472.1:n.307+275_307+276delinsTG
NM_001282545.2:c.215+5039_215+5040delinsTG	NP_001269474.1:n.215+5039_215+5040delinsTG
NM_001282548.2:c.158+17390_158+17391delinsTG	NP_001269477.1:n.158+17390_158+17391delinsTG
NM_001282549.2:c.364+275_364+276delinsTG	NP_001269478.1:n.364+275_364+276delinsTG
NR_104212.2:n.329+5039_329+5040delinsTG
NR_104215.2:n.273-10513_273-10512delinsTG
NR_104216.2:n.478+275_478+276delinsTG