Canonical Allele Identifier: CA1327076628
Gene: BARD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214792273_214792277delinsAAGAG , CM000664.2:g.214792273_214792277delinsAAGAG GRCh38
NC_000002.11:g.215656997_215657001delinsAAGAG , CM000664.1:g.215656997_215657001delinsAAGAG GRCh37
NC_000002.10:g.215365242_215365246delinsAAGAG NCBI36
NG_012047.2:g.22428_22432delinsCTCTT
NG_012047.3:g.22435_22439delinsCTCTT

Transcript Alleles

HGVS Amino-acid change
ENST00000260947.9:c.364+20_364+24delinsCTCTT MANE Select ENSP00000260947.4:n.364+20_364+24delinsCT...
ENST00000421162.2:c.215+4784_215+4788delinsCTCTT ENSP00000392245.2:n.215+4784_215+4788deli...
ENST00000613192.2:c.158+17135_158+17139delinsCTCTT ENSP00000483275.2:n.158+17135_158+17139de...
ENST00000613374.5:c.158+17135_158+17139delinsCTCTT ENSP00000484464.1:n.158+17135_158+17139de...
ENST00000613706.5:c.364+20_364+24delinsCTCTT ENSP00000484976.2:n.364+20_364+24delinsCT...
ENST00000617164.5:c.307+20_307+24delinsCTCTT ENSP00000480470.1:n.307+20_307+24delinsCT...
ENST00000619009.5:c.364+20_364+24delinsCTCTT ENSP00000482293.1:n.364+20_364+24delinsCT...
ENST00000650978.1:c.206+20_206+24delinsCTCTT
ENST00000260947.8:c.364+20_364+24delinsCTCTT ENSP00000260947.4:n.364+20_364+24delinsCT...
ENST00000421162.1:c.215+4784_215+4788delinsCTCTT ENSP00000392245.1:n.215+4784_215+4788deli...
ENST00000455743.5:c.215+4784_215+4788delinsCTCTT ENSP00000412186.1:n.215+4784_215+4788deli...
ENST00000471787.1:n.260-10768_260-10764delinsCTCTT
ENST00000613192.1:c.73+17135_73+17139delinsCTCTT ENSP00000483275.1:n.73+17135_73+17139deli...
ENST00000613374.4:c.158+17135_158+17139delinsCTCTT ENSP00000484464.1:n.158+17135_158+17139de...
ENST00000613706.4:c.215+4784_215+4788delinsCTCTT ENSP00000484976.1:n.215+4784_215+4788deli...
ENST00000617164.4:c.307+20_307+24delinsCTCTT ENSP00000480470.1:n.307+20_307+24delinsCT...
ENST00000619009.4:c.364+20_364+24delinsCTCTT ENSP00000482293.1:n.364+20_364+24delinsCT...
ENST00000620057.4:c.364+20_364+24delinsCTCTT ENSP00000481988.1:n.364+20_364+24delinsCT...
NM_000465.3:c.364+20_364+24delinsCTCTT NP_000456.2:n.364+20_364+24delinsCTCTT
NM_001282543.1:c.307+20_307+24delinsCTCTT NP_001269472.1:n.307+20_307+24delinsCTCTT...
NM_001282545.1:c.215+4784_215+4788delinsCTCTT NP_001269474.1:n.215+4784_215+4788delinsC...
NM_001282548.1:c.158+17135_158+17139delinsCTCTT NP_001269477.1:n.158+17135_158+17139delin...
NM_001282549.1:c.364+20_364+24delinsCTCTT NP_001269478.1:n.364+20_364+24delinsCTCTT...
NR_104212.1:n.357+4784_357+4788delinsCTCTT
NR_104215.1:n.301-10768_301-10764delinsCTCTT
NR_104216.1:n.506+20_506+24delinsCTCTT
XM_011511567.1:c.310+20_310+24delinsCTCTT XP_011509869.1:n.310+20_310+24delinsCTCTT...
XM_011511568.1:c.364+20_364+24delinsCTCTT XP_011509870.1:n.364+20_364+24delinsCTCTT...
XM_017004613.1:c.463+20_463+24delinsCTCTT XP_016860102.1:n.463+20_463+24delinsCTCTT...
XM_017004614.1:c.463+20_463+24delinsCTCTT XP_016860103.1:n.463+20_463+24delinsCTCTT...
XR_002959322.1:n.554+20_554+24delinsCTCTT
NM_000465.4:c.364+20_364+24delinsCTCTT MANE Select NP_000456.2:n.364+20_364+24delinsCTCTT
NM_001282543.2:c.307+20_307+24delinsCTCTT NP_001269472.1:n.307+20_307+24delinsCTCTT...
NM_001282545.2:c.215+4784_215+4788delinsCTCTT NP_001269474.1:n.215+4784_215+4788delinsC...
NM_001282548.2:c.158+17135_158+17139delinsCTCTT NP_001269477.1:n.158+17135_158+17139delin...
NM_001282549.2:c.364+20_364+24delinsCTCTT NP_001269478.1:n.364+20_364+24delinsCTCTT...
NR_104212.2:n.329+4784_329+4788delinsCTCTT
NR_104215.2:n.273-10768_273-10764delinsCTCTT
NR_104216.2:n.478+20_478+24delinsCTCTT