Canonical Allele Identifier: CA1327076630
Gene: BARD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214792278_214792284delinsAGATAGG , CM000664.2:g.214792278_214792284delinsAGATAGG GRCh38
NC_000002.11:g.215657002_215657008delinsAGATAGG , CM000664.1:g.215657002_215657008delinsAGATAGG GRCh37
NC_000002.10:g.215365247_215365253delinsAGATAGG NCBI36
NG_012047.2:g.22421_22427delinsCCTATCT
NG_012047.3:g.22428_22434delinsCCTATCT

Transcript Alleles

HGVS Amino-acid change
ENST00000260947.9:c.364+13_364+19delinsCCTATCT MANE Select ENSP00000260947.4:n.364+13_364+19delinsCC...
ENST00000421162.2:c.215+4777_215+4783delinsCCTATCT ENSP00000392245.2:n.215+4777_215+4783deli...
ENST00000613192.2:c.158+17128_158+17134delinsCCTATCT ENSP00000483275.2:n.158+17128_158+17134de...
ENST00000613374.5:c.158+17128_158+17134delinsCCTATCT ENSP00000484464.1:n.158+17128_158+17134de...
ENST00000613706.5:c.364+13_364+19delinsCCTATCT ENSP00000484976.2:n.364+13_364+19delinsCC...
ENST00000617164.5:c.307+13_307+19delinsCCTATCT ENSP00000480470.1:n.307+13_307+19delinsCC...
ENST00000619009.5:c.364+13_364+19delinsCCTATCT ENSP00000482293.1:n.364+13_364+19delinsCC...
ENST00000650978.1:c.206+13_206+19delinsCCTATCT
ENST00000260947.8:c.364+13_364+19delinsCCTATCT ENSP00000260947.4:n.364+13_364+19delinsCC...
ENST00000421162.1:c.215+4777_215+4783delinsCCTATCT ENSP00000392245.1:n.215+4777_215+4783deli...
ENST00000455743.5:c.215+4777_215+4783delinsCCTATCT ENSP00000412186.1:n.215+4777_215+4783deli...
ENST00000471787.1:n.260-10775_260-10769delinsCCTATCT
ENST00000613192.1:c.73+17128_73+17134delinsCCTATCT ENSP00000483275.1:n.73+17128_73+17134deli...
ENST00000613374.4:c.158+17128_158+17134delinsCCTATCT ENSP00000484464.1:n.158+17128_158+17134de...
ENST00000613706.4:c.215+4777_215+4783delinsCCTATCT ENSP00000484976.1:n.215+4777_215+4783deli...
ENST00000617164.4:c.307+13_307+19delinsCCTATCT ENSP00000480470.1:n.307+13_307+19delinsCC...
ENST00000619009.4:c.364+13_364+19delinsCCTATCT ENSP00000482293.1:n.364+13_364+19delinsCC...
ENST00000620057.4:c.364+13_364+19delinsCCTATCT ENSP00000481988.1:n.364+13_364+19delinsCC...
NM_000465.3:c.364+13_364+19delinsCCTATCT NP_000456.2:n.364+13_364+19delinsCCTATCT
NM_001282543.1:c.307+13_307+19delinsCCTATCT NP_001269472.1:n.307+13_307+19delinsCCTAT...
NM_001282545.1:c.215+4777_215+4783delinsCCTATCT NP_001269474.1:n.215+4777_215+4783delinsC...
NM_001282548.1:c.158+17128_158+17134delinsCCTATCT NP_001269477.1:n.158+17128_158+17134delin...
NM_001282549.1:c.364+13_364+19delinsCCTATCT NP_001269478.1:n.364+13_364+19delinsCCTAT...
NR_104212.1:n.357+4777_357+4783delinsCCTATCT
NR_104215.1:n.301-10775_301-10769delinsCCTATCT
NR_104216.1:n.506+13_506+19delinsCCTATCT
XM_011511567.1:c.310+13_310+19delinsCCTATCT XP_011509869.1:n.310+13_310+19delinsCCTAT...
XM_011511568.1:c.364+13_364+19delinsCCTATCT XP_011509870.1:n.364+13_364+19delinsCCTAT...
XM_017004613.1:c.463+13_463+19delinsCCTATCT XP_016860102.1:n.463+13_463+19delinsCCTAT...
XM_017004614.1:c.463+13_463+19delinsCCTATCT XP_016860103.1:n.463+13_463+19delinsCCTAT...
XR_002959322.1:n.554+13_554+19delinsCCTATCT
NM_000465.4:c.364+13_364+19delinsCCTATCT MANE Select NP_000456.2:n.364+13_364+19delinsCCTATCT
NM_001282543.2:c.307+13_307+19delinsCCTATCT NP_001269472.1:n.307+13_307+19delinsCCTAT...
NM_001282545.2:c.215+4777_215+4783delinsCCTATCT NP_001269474.1:n.215+4777_215+4783delinsC...
NM_001282548.2:c.158+17128_158+17134delinsCCTATCT NP_001269477.1:n.158+17128_158+17134delin...
NM_001282549.2:c.364+13_364+19delinsCCTATCT NP_001269478.1:n.364+13_364+19delinsCCTAT...
NR_104212.2:n.329+4777_329+4783delinsCCTATCT
NR_104215.2:n.273-10775_273-10769delinsCCTATCT
NR_104216.2:n.478+13_478+19delinsCCTATCT