Canonical Allele Identifier: CA1327066297

Gene: BARD1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214771110_214771113delinsCATT , CM000664.2:g.214771110_214771113delinsCATT	GRCh38
NC_000002.11:g.215635834_215635837delinsCATT , CM000664.1:g.215635834_215635837delinsCATT	GRCh37
NC_000002.10:g.215344079_215344082delinsCATT	NCBI36
NG_012047.2:g.43592_43595delinsAATG
NG_012047.3:g.43599_43602delinsAATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.1315-1801_1315-1798delinsAATG MANE Select	ENSP00000260947.4:n.1315-1801_1315-1798delinsAATG
ENST00000421162.2:c.216-18558_216-18555delinsAATG	ENSP00000392245.2:n.216-18558_216-18555delinsAATG
ENST00000613192.2:c.158+38299_158+38302delinsAATG	ENSP00000483275.2:n.158+38299_158+38302delinsAATG
ENST00000613374.5:c.159-18558_159-18555delinsAATG	ENSP00000484464.1:n.159-18558_159-18555delinsAATG
ENST00000613706.5:c.907-1801_907-1798delinsAATG	ENSP00000484976.2:n.907-1801_907-1798delinsAATG
ENST00000617164.5:c.1258-1801_1258-1798delinsAATG	ENSP00000480470.1:n.1258-1801_1258-1798delinsAATG
ENST00000619009.5:c.364+21184_364+21187delinsAATG	ENSP00000482293.1:n.364+21184_364+21187delinsAATG
ENST00000650978.1:c.1157-268_1157-265delinsAATG
ENST00000260947.8:c.1315-1801_1315-1798delinsAATG	ENSP00000260947.4:n.1315-1801_1315-1798delinsAATG
ENST00000421162.1:c.216-18558_216-18555delinsAATG	ENSP00000392245.1:n.216-18558_216-18555delinsAATG
ENST00000455743.5:c.*935-1801_*935-1798delinsAATG	ENSP00000412186.1:n.*935-1801_*935-1798delinsAATG
ENST00000613192.1:c.73+38299_73+38302delinsAATG	ENSP00000483275.1:n.73+38299_73+38302delinsAATG
ENST00000613374.4:c.159-18558_159-18555delinsAATG	ENSP00000484464.1:n.159-18558_159-18555delinsAATG
ENST00000613706.4:c.216-18558_216-18555delinsAATG	ENSP00000484976.1:n.216-18558_216-18555delinsAATG
ENST00000617164.4:c.1258-1801_1258-1798delinsAATG	ENSP00000480470.1:n.1258-1801_1258-1798delinsAATG
ENST00000619009.4:c.364+21184_364+21187delinsAATG	ENSP00000482293.1:n.364+21184_364+21187delinsAATG
ENST00000620057.4:c.365-1801_365-1798delinsAATG	ENSP00000481988.1:n.365-1801_365-1798delinsAATG
NM_000465.3:c.1315-1801_1315-1798delinsAATG	NP_000456.2:n.1315-1801_1315-1798delinsAATG
NM_001282543.1:c.1258-1801_1258-1798delinsAATG	NP_001269472.1:n.1258-1801_1258-1798delinsAATG
NM_001282545.1:c.216-18558_216-18555delinsAATG	NP_001269474.1:n.216-18558_216-18555delinsAATG
NM_001282548.1:c.159-18558_159-18555delinsAATG	NP_001269477.1:n.159-18558_159-18555delinsAATG
NM_001282549.1:c.364+21184_364+21187delinsAATG	NP_001269478.1:n.364+21184_364+21187delinsAATG
NR_104212.1:n.1308-1801_1308-1798delinsAATG
NR_104215.1:n.1251-1801_1251-1798delinsAATG
NR_104216.1:n.507-1801_507-1798delinsAATG
XM_011511567.1:c.1261-1801_1261-1798delinsAATG	XP_011509869.1:n.1261-1801_1261-1798delinsAATG
XM_011511568.1:c.1315-1801_1315-1798delinsAATG	XP_011509870.1:n.1315-1801_1315-1798delinsAATG
XM_017004613.1:c.1414-1801_1414-1798delinsAATG	XP_016860102.1:n.1414-1801_1414-1798delinsAATG
XM_017004614.1:c.1414-1801_1414-1798delinsAATG	XP_016860103.1:n.1414-1801_1414-1798delinsAATG
XR_002959322.1:n.1505-1801_1505-1798delinsAATG
NM_000465.4:c.1315-1801_1315-1798delinsAATG MANE Select	NP_000456.2:n.1315-1801_1315-1798delinsAATG
NM_001282543.2:c.1258-1801_1258-1798delinsAATG	NP_001269472.1:n.1258-1801_1258-1798delinsAATG
NM_001282545.2:c.216-18558_216-18555delinsAATG	NP_001269474.1:n.216-18558_216-18555delinsAATG
NM_001282548.2:c.159-18558_159-18555delinsAATG	NP_001269477.1:n.159-18558_159-18555delinsAATG
NM_001282549.2:c.364+21184_364+21187delinsAATG	NP_001269478.1:n.364+21184_364+21187delinsAATG
NR_104212.2:n.1280-1801_1280-1798delinsAATG
NR_104215.2:n.1223-1801_1223-1798delinsAATG
NR_104216.2:n.479-1801_479-1798delinsAATG