Canonical Allele Identifier: CA1327066257

Gene: BARD1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214771022_214771025delinsATAC , CM000664.2:g.214771022_214771025delinsATAC	GRCh38
NC_000002.11:g.215635746_215635749delinsATAC , CM000664.1:g.215635746_215635749delinsATAC	GRCh37
NC_000002.10:g.215343991_215343994delinsATAC	NCBI36
NG_012047.2:g.43680_43683delinsGTAT
NG_012047.3:g.43687_43690delinsGTAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.1315-1713_1315-1710delinsGTAT MANE Select	ENSP00000260947.4:n.1315-1713_1315-1710delinsGTAT
ENST00000421162.2:c.216-18470_216-18467delinsGTAT	ENSP00000392245.2:n.216-18470_216-18467delinsGTAT
ENST00000613192.2:c.158+38387_158+38390delinsGTAT	ENSP00000483275.2:n.158+38387_158+38390delinsGTAT
ENST00000613374.5:c.159-18470_159-18467delinsGTAT	ENSP00000484464.1:n.159-18470_159-18467delinsGTAT
ENST00000613706.5:c.907-1713_907-1710delinsGTAT	ENSP00000484976.2:n.907-1713_907-1710delinsGTAT
ENST00000617164.5:c.1258-1713_1258-1710delinsGTAT	ENSP00000480470.1:n.1258-1713_1258-1710delinsGTAT
ENST00000619009.5:c.364+21272_364+21275delinsGTAT	ENSP00000482293.1:n.364+21272_364+21275delinsGTAT
ENST00000650978.1:c.1157-180_1157-177delinsGTAT
ENST00000260947.8:c.1315-1713_1315-1710delinsGTAT	ENSP00000260947.4:n.1315-1713_1315-1710delinsGTAT
ENST00000421162.1:c.216-18470_216-18467delinsGTAT	ENSP00000392245.1:n.216-18470_216-18467delinsGTAT
ENST00000455743.5:c.*935-1713_*935-1710delinsGTAT	ENSP00000412186.1:n.*935-1713_*935-1710delinsGTAT
ENST00000613192.1:c.73+38387_73+38390delinsGTAT	ENSP00000483275.1:n.73+38387_73+38390delinsGTAT
ENST00000613374.4:c.159-18470_159-18467delinsGTAT	ENSP00000484464.1:n.159-18470_159-18467delinsGTAT
ENST00000613706.4:c.216-18470_216-18467delinsGTAT	ENSP00000484976.1:n.216-18470_216-18467delinsGTAT
ENST00000617164.4:c.1258-1713_1258-1710delinsGTAT	ENSP00000480470.1:n.1258-1713_1258-1710delinsGTAT
ENST00000619009.4:c.364+21272_364+21275delinsGTAT	ENSP00000482293.1:n.364+21272_364+21275delinsGTAT
ENST00000620057.4:c.365-1713_365-1710delinsGTAT	ENSP00000481988.1:n.365-1713_365-1710delinsGTAT
NM_000465.3:c.1315-1713_1315-1710delinsGTAT	NP_000456.2:n.1315-1713_1315-1710delinsGTAT
NM_001282543.1:c.1258-1713_1258-1710delinsGTAT	NP_001269472.1:n.1258-1713_1258-1710delinsGTAT
NM_001282545.1:c.216-18470_216-18467delinsGTAT	NP_001269474.1:n.216-18470_216-18467delinsGTAT
NM_001282548.1:c.159-18470_159-18467delinsGTAT	NP_001269477.1:n.159-18470_159-18467delinsGTAT
NM_001282549.1:c.364+21272_364+21275delinsGTAT	NP_001269478.1:n.364+21272_364+21275delinsGTAT
NR_104212.1:n.1308-1713_1308-1710delinsGTAT
NR_104215.1:n.1251-1713_1251-1710delinsGTAT
NR_104216.1:n.507-1713_507-1710delinsGTAT
XM_011511567.1:c.1261-1713_1261-1710delinsGTAT	XP_011509869.1:n.1261-1713_1261-1710delinsGTAT
XM_011511568.1:c.1315-1713_1315-1710delinsGTAT	XP_011509870.1:n.1315-1713_1315-1710delinsGTAT
XM_017004613.1:c.1414-1713_1414-1710delinsGTAT	XP_016860102.1:n.1414-1713_1414-1710delinsGTAT
XM_017004614.1:c.1414-1713_1414-1710delinsGTAT	XP_016860103.1:n.1414-1713_1414-1710delinsGTAT
XR_002959322.1:n.1505-1713_1505-1710delinsGTAT
NM_000465.4:c.1315-1713_1315-1710delinsGTAT MANE Select	NP_000456.2:n.1315-1713_1315-1710delinsGTAT
NM_001282543.2:c.1258-1713_1258-1710delinsGTAT	NP_001269472.1:n.1258-1713_1258-1710delinsGTAT
NM_001282545.2:c.216-18470_216-18467delinsGTAT	NP_001269474.1:n.216-18470_216-18467delinsGTAT
NM_001282548.2:c.159-18470_159-18467delinsGTAT	NP_001269477.1:n.159-18470_159-18467delinsGTAT
NM_001282549.2:c.364+21272_364+21275delinsGTAT	NP_001269478.1:n.364+21272_364+21275delinsGTAT
NR_104212.2:n.1280-1713_1280-1710delinsGTAT
NR_104215.2:n.1223-1713_1223-1710delinsGTAT
NR_104216.2:n.479-1713_479-1710delinsGTAT