Canonical Allele Identifier: CA1327066274
Gene: BARD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214771056_214771059delinsGGAA , CM000664.2:g.214771056_214771059delinsGGAA GRCh38
NC_000002.11:g.215635780_215635783delinsGGAA , CM000664.1:g.215635780_215635783delinsGGAA GRCh37
NC_000002.10:g.215344025_215344028delinsGGAA NCBI36
NG_012047.2:g.43646_43649delinsTTCC
NG_012047.3:g.43653_43656delinsTTCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000260947.9:c.1315-1747_1315-1744delinsTTCC MANE Select ENSP00000260947.4:n.1315-1747_1315-1744delinsTTCC
ENST00000421162.2:c.216-18504_216-18501delinsTTCC ENSP00000392245.2:n.216-18504_216-18501delinsTTCC
ENST00000613192.2:c.158+38353_158+38356delinsTTCC ENSP00000483275.2:n.158+38353_158+38356delinsTTCC
ENST00000613374.5:c.159-18504_159-18501delinsTTCC ENSP00000484464.1:n.159-18504_159-18501delinsTTCC
ENST00000613706.5:c.907-1747_907-1744delinsTTCC ENSP00000484976.2:n.907-1747_907-1744delinsTTCC
ENST00000617164.5:c.1258-1747_1258-1744delinsTTCC ENSP00000480470.1:n.1258-1747_1258-1744delinsTTCC
ENST00000619009.5:c.364+21238_364+21241delinsTTCC ENSP00000482293.1:n.364+21238_364+21241delinsTTCC
ENST00000650978.1:c.1157-214_1157-211delinsTTCC
ENST00000260947.8:c.1315-1747_1315-1744delinsTTCC ENSP00000260947.4:n.1315-1747_1315-1744delinsTTCC
ENST00000421162.1:c.216-18504_216-18501delinsTTCC ENSP00000392245.1:n.216-18504_216-18501delinsTTCC
ENST00000455743.5:c.*935-1747_*935-1744delinsTTCC ENSP00000412186.1:n.*935-1747_*935-1744delinsTTCC
ENST00000613192.1:c.73+38353_73+38356delinsTTCC ENSP00000483275.1:n.73+38353_73+38356delinsTTCC
ENST00000613374.4:c.159-18504_159-18501delinsTTCC ENSP00000484464.1:n.159-18504_159-18501delinsTTCC
ENST00000613706.4:c.216-18504_216-18501delinsTTCC ENSP00000484976.1:n.216-18504_216-18501delinsTTCC
ENST00000617164.4:c.1258-1747_1258-1744delinsTTCC ENSP00000480470.1:n.1258-1747_1258-1744delinsTTCC
ENST00000619009.4:c.364+21238_364+21241delinsTTCC ENSP00000482293.1:n.364+21238_364+21241delinsTTCC
ENST00000620057.4:c.365-1747_365-1744delinsTTCC ENSP00000481988.1:n.365-1747_365-1744delinsTTCC
NM_000465.3:c.1315-1747_1315-1744delinsTTCC NP_000456.2:n.1315-1747_1315-1744delinsTTCC
NM_001282543.1:c.1258-1747_1258-1744delinsTTCC NP_001269472.1:n.1258-1747_1258-1744delinsTTCC
NM_001282545.1:c.216-18504_216-18501delinsTTCC NP_001269474.1:n.216-18504_216-18501delinsTTCC
NM_001282548.1:c.159-18504_159-18501delinsTTCC NP_001269477.1:n.159-18504_159-18501delinsTTCC
NM_001282549.1:c.364+21238_364+21241delinsTTCC NP_001269478.1:n.364+21238_364+21241delinsTTCC
NR_104212.1:n.1308-1747_1308-1744delinsTTCC
NR_104215.1:n.1251-1747_1251-1744delinsTTCC
NR_104216.1:n.507-1747_507-1744delinsTTCC
XM_011511567.1:c.1261-1747_1261-1744delinsTTCC XP_011509869.1:n.1261-1747_1261-1744delinsTTCC
XM_011511568.1:c.1315-1747_1315-1744delinsTTCC XP_011509870.1:n.1315-1747_1315-1744delinsTTCC
XM_017004613.1:c.1414-1747_1414-1744delinsTTCC XP_016860102.1:n.1414-1747_1414-1744delinsTTCC
XM_017004614.1:c.1414-1747_1414-1744delinsTTCC XP_016860103.1:n.1414-1747_1414-1744delinsTTCC
XR_002959322.1:n.1505-1747_1505-1744delinsTTCC
NM_000465.4:c.1315-1747_1315-1744delinsTTCC MANE Select NP_000456.2:n.1315-1747_1315-1744delinsTTCC
NM_001282543.2:c.1258-1747_1258-1744delinsTTCC NP_001269472.1:n.1258-1747_1258-1744delinsTTCC
NM_001282545.2:c.216-18504_216-18501delinsTTCC NP_001269474.1:n.216-18504_216-18501delinsTTCC
NM_001282548.2:c.159-18504_159-18501delinsTTCC NP_001269477.1:n.159-18504_159-18501delinsTTCC
NM_001282549.2:c.364+21238_364+21241delinsTTCC NP_001269478.1:n.364+21238_364+21241delinsTTCC
NR_104212.2:n.1280-1747_1280-1744delinsTTCC
NR_104215.2:n.1223-1747_1223-1744delinsTTCC
NR_104216.2:n.479-1747_479-1744delinsTTCC