Canonical Allele Identifier: CA1327076547

Gene: BARD1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214792129_214792131delinsTAG , CM000664.2:g.214792129_214792131delinsTAG	GRCh38
NC_000002.11:g.215656853_215656855delinsTAG , CM000664.1:g.215656853_215656855delinsTAG	GRCh37
NC_000002.10:g.215365098_215365100delinsTAG	NCBI36
NG_012047.2:g.22574_22576delinsCTA
NG_012047.3:g.22581_22583delinsCTA

Transcript Alleles

HGVS	Amino-acid change
ENST00000260947.9:c.364+166_364+168delinsCTA MANE Select	ENSP00000260947.4:n.364+166_364+168delins...
ENST00000421162.2:c.215+4930_215+4932delinsCTA	ENSP00000392245.2:n.215+4930_215+4932deli...
ENST00000613192.2:c.158+17281_158+17283delinsCTA	ENSP00000483275.2:n.158+17281_158+17283de...
ENST00000613374.5:c.158+17281_158+17283delinsCTA	ENSP00000484464.1:n.158+17281_158+17283de...
ENST00000613706.5:c.364+166_364+168delinsCTA	ENSP00000484976.2:n.364+166_364+168delins...
ENST00000617164.5:c.307+166_307+168delinsCTA	ENSP00000480470.1:n.307+166_307+168delins...
ENST00000619009.5:c.364+166_364+168delinsCTA	ENSP00000482293.1:n.364+166_364+168delins...
ENST00000650978.1:c.206+166_206+168delinsCTA
ENST00000260947.8:c.364+166_364+168delinsCTA	ENSP00000260947.4:n.364+166_364+168delins...
ENST00000421162.1:c.215+4930_215+4932delinsCTA	ENSP00000392245.1:n.215+4930_215+4932deli...
ENST00000455743.5:c.215+4930_215+4932delinsCTA	ENSP00000412186.1:n.215+4930_215+4932deli...
ENST00000471787.1:n.260-10622_260-10620delinsCTA
ENST00000613192.1:c.73+17281_73+17283delinsCTA	ENSP00000483275.1:n.73+17281_73+17283deli...
ENST00000613374.4:c.158+17281_158+17283delinsCTA	ENSP00000484464.1:n.158+17281_158+17283de...
ENST00000613706.4:c.215+4930_215+4932delinsCTA	ENSP00000484976.1:n.215+4930_215+4932deli...
ENST00000617164.4:c.307+166_307+168delinsCTA	ENSP00000480470.1:n.307+166_307+168delins...
ENST00000619009.4:c.364+166_364+168delinsCTA	ENSP00000482293.1:n.364+166_364+168delins...
ENST00000620057.4:c.364+166_364+168delinsCTA	ENSP00000481988.1:n.364+166_364+168delins...
NM_000465.3:c.364+166_364+168delinsCTA	NP_000456.2:n.364+166_364+168delinsCTA
NM_001282543.1:c.307+166_307+168delinsCTA	NP_001269472.1:n.307+166_307+168delinsCTA...
NM_001282545.1:c.215+4930_215+4932delinsCTA	NP_001269474.1:n.215+4930_215+4932delinsC...
NM_001282548.1:c.158+17281_158+17283delinsCTA	NP_001269477.1:n.158+17281_158+17283delin...
NM_001282549.1:c.364+166_364+168delinsCTA	NP_001269478.1:n.364+166_364+168delinsCTA...
NR_104212.1:n.357+4930_357+4932delinsCTA
NR_104215.1:n.301-10622_301-10620delinsCTA
NR_104216.1:n.506+166_506+168delinsCTA
XM_011511567.1:c.310+166_310+168delinsCTA	XP_011509869.1:n.310+166_310+168delinsCTA...
XM_011511568.1:c.364+166_364+168delinsCTA	XP_011509870.1:n.364+166_364+168delinsCTA...
XM_017004613.1:c.463+166_463+168delinsCTA	XP_016860102.1:n.463+166_463+168delinsCTA...
XM_017004614.1:c.463+166_463+168delinsCTA	XP_016860103.1:n.463+166_463+168delinsCTA...
XR_002959322.1:n.554+166_554+168delinsCTA
NM_000465.4:c.364+166_364+168delinsCTA MANE Select	NP_000456.2:n.364+166_364+168delinsCTA
NM_001282543.2:c.307+166_307+168delinsCTA	NP_001269472.1:n.307+166_307+168delinsCTA...
NM_001282545.2:c.215+4930_215+4932delinsCTA	NP_001269474.1:n.215+4930_215+4932delinsC...
NM_001282548.2:c.158+17281_158+17283delinsCTA	NP_001269477.1:n.158+17281_158+17283delin...
NM_001282549.2:c.364+166_364+168delinsCTA	NP_001269478.1:n.364+166_364+168delinsCTA...
NR_104212.2:n.329+4930_329+4932delinsCTA
NR_104215.2:n.273-10622_273-10620delinsCTA
NR_104216.2:n.478+166_478+168delinsCTA