Canonical Allele Identifier: CA2503877737

Gene: BARD1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214792058_214792059insTTTGAAA , CM000664.2:g.214792058_214792059insTTTGAAA	GRCh38
NC_000002.11:g.215656782_215656783insTTTGAAA , CM000664.1:g.215656782_215656783insTTTGAAA	GRCh37
NC_000002.10:g.215365027_215365028insTTTGAAA	NCBI36
NG_012047.2:g.22646_22647insTTTCAAA
NG_012047.3:g.22653_22654insTTTCAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.364+238_364+239insTTTCAAA MANE Select	ENSP00000260947.4:n.364+238_364+239insTTTCAAA
ENST00000421162.2:c.215+5002_215+5003insTTTCAAA	ENSP00000392245.2:n.215+5002_215+5003insTTTCAAA
ENST00000613192.2:c.158+17353_158+17354insTTTCAAA	ENSP00000483275.2:n.158+17353_158+17354insTTTCAAA
ENST00000613374.5:c.158+17353_158+17354insTTTCAAA	ENSP00000484464.1:n.158+17353_158+17354insTTTCAAA
ENST00000613706.5:c.364+238_364+239insTTTCAAA	ENSP00000484976.2:n.364+238_364+239insTTTCAAA
ENST00000617164.5:c.307+238_307+239insTTTCAAA	ENSP00000480470.1:n.307+238_307+239insTTTCAAA
ENST00000619009.5:c.364+238_364+239insTTTCAAA	ENSP00000482293.1:n.364+238_364+239insTTTCAAA
ENST00000650978.1:c.206+238_206+239insTTTCAAA
ENST00000260947.8:c.364+238_364+239insTTTCAAA	ENSP00000260947.4:n.364+238_364+239insTTTCAAA
ENST00000421162.1:c.215+5002_215+5003insTTTCAAA	ENSP00000392245.1:n.215+5002_215+5003insTTTCAAA
ENST00000455743.5:c.215+5002_215+5003insTTTCAAA	ENSP00000412186.1:n.215+5002_215+5003insTTTCAAA
ENST00000471787.1:n.260-10550_260-10549insTTTCAAA
ENST00000613192.1:c.73+17353_73+17354insTTTCAAA	ENSP00000483275.1:n.73+17353_73+17354insTTTCAAA
ENST00000613374.4:c.158+17353_158+17354insTTTCAAA	ENSP00000484464.1:n.158+17353_158+17354insTTTCAAA
ENST00000613706.4:c.215+5002_215+5003insTTTCAAA	ENSP00000484976.1:n.215+5002_215+5003insTTTCAAA
ENST00000617164.4:c.307+238_307+239insTTTCAAA	ENSP00000480470.1:n.307+238_307+239insTTTCAAA
ENST00000619009.4:c.364+238_364+239insTTTCAAA	ENSP00000482293.1:n.364+238_364+239insTTTCAAA
ENST00000620057.4:c.364+238_364+239insTTTCAAA	ENSP00000481988.1:n.364+238_364+239insTTTCAAA
NM_000465.3:c.364+238_364+239insTTTCAAA	NP_000456.2:n.364+238_364+239insTTTCAAA
NM_001282543.1:c.307+238_307+239insTTTCAAA	NP_001269472.1:n.307+238_307+239insTTTCAAA
NM_001282545.1:c.215+5002_215+5003insTTTCAAA	NP_001269474.1:n.215+5002_215+5003insTTTCAAA
NM_001282548.1:c.158+17353_158+17354insTTTCAAA	NP_001269477.1:n.158+17353_158+17354insTTTCAAA
NM_001282549.1:c.364+238_364+239insTTTCAAA	NP_001269478.1:n.364+238_364+239insTTTCAAA
NR_104212.1:n.357+5002_357+5003insTTTCAAA
NR_104215.1:n.301-10550_301-10549insTTTCAAA
NR_104216.1:n.506+238_506+239insTTTCAAA
XM_011511567.1:c.310+238_310+239insTTTCAAA	XP_011509869.1:n.310+238_310+239insTTTCAAA
XM_011511568.1:c.364+238_364+239insTTTCAAA	XP_011509870.1:n.364+238_364+239insTTTCAAA
XM_017004613.1:c.463+238_463+239insTTTCAAA	XP_016860102.1:n.463+238_463+239insTTTCAAA
XM_017004614.1:c.463+238_463+239insTTTCAAA	XP_016860103.1:n.463+238_463+239insTTTCAAA
XR_002959322.1:n.554+238_554+239insTTTCAAA
NM_000465.4:c.364+238_364+239insTTTCAAA MANE Select	NP_000456.2:n.364+238_364+239insTTTCAAA
NM_001282543.2:c.307+238_307+239insTTTCAAA	NP_001269472.1:n.307+238_307+239insTTTCAAA
NM_001282545.2:c.215+5002_215+5003insTTTCAAA	NP_001269474.1:n.215+5002_215+5003insTTTCAAA
NM_001282548.2:c.158+17353_158+17354insTTTCAAA	NP_001269477.1:n.158+17353_158+17354insTTTCAAA
NM_001282549.2:c.364+238_364+239insTTTCAAA	NP_001269478.1:n.364+238_364+239insTTTCAAA
NR_104212.2:n.329+5002_329+5003insTTTCAAA
NR_104215.2:n.273-10550_273-10549insTTTCAAA
NR_104216.2:n.478+238_478+239insTTTCAAA