Canonical Allele Identifier: CA1327076625
Gene: BARD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214792272_214792276delinsTAAGA , CM000664.2:g.214792272_214792276delinsTAAGA GRCh38
NC_000002.11:g.215656996_215657000delinsTAAGA , CM000664.1:g.215656996_215657000delinsTAAGA GRCh37
NC_000002.10:g.215365241_215365245delinsTAAGA NCBI36
NG_012047.2:g.22429_22433delinsTCTTA
NG_012047.3:g.22436_22440delinsTCTTA

Transcript Alleles

HGVS Amino-acid change
ENST00000260947.9:c.364+21_364+25delinsTCTTA MANE Select ENSP00000260947.4:n.364+21_364+25delinsTC...
ENST00000421162.2:c.215+4785_215+4789delinsTCTTA ENSP00000392245.2:n.215+4785_215+4789deli...
ENST00000613192.2:c.158+17136_158+17140delinsTCTTA ENSP00000483275.2:n.158+17136_158+17140de...
ENST00000613374.5:c.158+17136_158+17140delinsTCTTA ENSP00000484464.1:n.158+17136_158+17140de...
ENST00000613706.5:c.364+21_364+25delinsTCTTA ENSP00000484976.2:n.364+21_364+25delinsTC...
ENST00000617164.5:c.307+21_307+25delinsTCTTA ENSP00000480470.1:n.307+21_307+25delinsTC...
ENST00000619009.5:c.364+21_364+25delinsTCTTA ENSP00000482293.1:n.364+21_364+25delinsTC...
ENST00000650978.1:c.206+21_206+25delinsTCTTA
ENST00000260947.8:c.364+21_364+25delinsTCTTA ENSP00000260947.4:n.364+21_364+25delinsTC...
ENST00000421162.1:c.215+4785_215+4789delinsTCTTA ENSP00000392245.1:n.215+4785_215+4789deli...
ENST00000455743.5:c.215+4785_215+4789delinsTCTTA ENSP00000412186.1:n.215+4785_215+4789deli...
ENST00000471787.1:n.260-10767_260-10763delinsTCTTA
ENST00000613192.1:c.73+17136_73+17140delinsTCTTA ENSP00000483275.1:n.73+17136_73+17140deli...
ENST00000613374.4:c.158+17136_158+17140delinsTCTTA ENSP00000484464.1:n.158+17136_158+17140de...
ENST00000613706.4:c.215+4785_215+4789delinsTCTTA ENSP00000484976.1:n.215+4785_215+4789deli...
ENST00000617164.4:c.307+21_307+25delinsTCTTA ENSP00000480470.1:n.307+21_307+25delinsTC...
ENST00000619009.4:c.364+21_364+25delinsTCTTA ENSP00000482293.1:n.364+21_364+25delinsTC...
ENST00000620057.4:c.364+21_364+25delinsTCTTA ENSP00000481988.1:n.364+21_364+25delinsTC...
NM_000465.3:c.364+21_364+25delinsTCTTA NP_000456.2:n.364+21_364+25delinsTCTTA
NM_001282543.1:c.307+21_307+25delinsTCTTA NP_001269472.1:n.307+21_307+25delinsTCTTA...
NM_001282545.1:c.215+4785_215+4789delinsTCTTA NP_001269474.1:n.215+4785_215+4789delinsT...
NM_001282548.1:c.158+17136_158+17140delinsTCTTA NP_001269477.1:n.158+17136_158+17140delin...
NM_001282549.1:c.364+21_364+25delinsTCTTA NP_001269478.1:n.364+21_364+25delinsTCTTA...
NR_104212.1:n.357+4785_357+4789delinsTCTTA
NR_104215.1:n.301-10767_301-10763delinsTCTTA
NR_104216.1:n.506+21_506+25delinsTCTTA
XM_011511567.1:c.310+21_310+25delinsTCTTA XP_011509869.1:n.310+21_310+25delinsTCTTA...
XM_011511568.1:c.364+21_364+25delinsTCTTA XP_011509870.1:n.364+21_364+25delinsTCTTA...
XM_017004613.1:c.463+21_463+25delinsTCTTA XP_016860102.1:n.463+21_463+25delinsTCTTA...
XM_017004614.1:c.463+21_463+25delinsTCTTA XP_016860103.1:n.463+21_463+25delinsTCTTA...
XR_002959322.1:n.554+21_554+25delinsTCTTA
NM_000465.4:c.364+21_364+25delinsTCTTA MANE Select NP_000456.2:n.364+21_364+25delinsTCTTA
NM_001282543.2:c.307+21_307+25delinsTCTTA NP_001269472.1:n.307+21_307+25delinsTCTTA...
NM_001282545.2:c.215+4785_215+4789delinsTCTTA NP_001269474.1:n.215+4785_215+4789delinsT...
NM_001282548.2:c.158+17136_158+17140delinsTCTTA NP_001269477.1:n.158+17136_158+17140delin...
NM_001282549.2:c.364+21_364+25delinsTCTTA NP_001269478.1:n.364+21_364+25delinsTCTTA...
NR_104212.2:n.329+4785_329+4789delinsTCTTA
NR_104215.2:n.273-10767_273-10763delinsTCTTA
NR_104216.2:n.478+21_478+25delinsTCTTA