Canonical Allele Identifier: CA1327076685
Gene: BARD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214792365_214792369delinsCTATT , CM000664.2:g.214792365_214792369delinsCTATT GRCh38
NC_000002.11:g.215657089_215657093delinsCTATT , CM000664.1:g.215657089_215657093delinsCTATT GRCh37
NC_000002.10:g.215365334_215365338delinsCTATT NCBI36
NG_012047.2:g.22336_22340delinsAATAG
NG_012047.3:g.22343_22347delinsAATAG

Transcript Alleles

HGVS Amino-acid change
ENST00000260947.9:c.292_296delinsAATAG MANE Select ENSP00000260947.4:p.Asn98=
ENST00000421162.2:c.215+4692_215+4696delinsAATAG ENSP00000392245.2:n.215+4692_215+4696deli...
ENST00000613192.2:c.158+17043_158+17047delinsAATAG ENSP00000483275.2:n.158+17043_158+17047de...
ENST00000613374.5:c.158+17043_158+17047delinsAATAG ENSP00000484464.1:n.158+17043_158+17047de...
ENST00000613706.5:c.292_296delinsAATAG ENSP00000484976.2:p.Asn98=
ENST00000617164.5:c.235_239delinsAATAG ENSP00000480470.1:p.Asn79=
ENST00000619009.5:c.292_296delinsAATAG ENSP00000482293.1:p.Asn98=
ENST00000650978.1:c.134_138delinsAATAG
ENST00000260947.8:c.292_296delinsAATAG ENSP00000260947.4:p.Asn98=
ENST00000421162.1:c.215+4692_215+4696delinsAATAG ENSP00000392245.1:n.215+4692_215+4696deli...
ENST00000455743.5:c.215+4692_215+4696delinsAATAG ENSP00000412186.1:n.215+4692_215+4696deli...
ENST00000471787.1:n.260-10860_260-10856delinsAATAG
ENST00000613192.1:c.73+17043_73+17047delinsAATAG ENSP00000483275.1:n.73+17043_73+17047deli...
ENST00000613374.4:c.158+17043_158+17047delinsAATAG ENSP00000484464.1:n.158+17043_158+17047de...
ENST00000613706.4:c.215+4692_215+4696delinsAATAG ENSP00000484976.1:n.215+4692_215+4696deli...
ENST00000617164.4:c.235_239delinsAATAG ENSP00000480470.1:p.Asn79=
ENST00000619009.4:c.292_296delinsAATAG ENSP00000482293.1:p.Asn98=
ENST00000620057.4:c.292_296delinsAATAG ENSP00000481988.1:p.Asn98=
NM_000465.3:c.292_296delinsAATAG NP_000456.2:p.Asn98=
NM_001282543.1:c.235_239delinsAATAG NP_001269472.1:p.Asn79=
NM_001282545.1:c.215+4692_215+4696delinsAATAG NP_001269474.1:n.215+4692_215+4696delinsA...
NM_001282548.1:c.158+17043_158+17047delinsAATAG NP_001269477.1:n.158+17043_158+17047delin...
NM_001282549.1:c.292_296delinsAATAG NP_001269478.1:p.Asn98=
NR_104212.1:n.357+4692_357+4696delinsAATAG
NR_104215.1:n.301-10860_301-10856delinsAATAG
NR_104216.1:n.434_438delinsAATAG
XM_011511567.1:c.238_242delinsAATAG XP_011509869.1:p.Asn80=
XM_011511568.1:c.292_296delinsAATAG XP_011509870.1:p.Asn98=
XM_017004613.1:c.391_395delinsAATAG XP_016860102.1:p.Asn131=
XM_017004614.1:c.391_395delinsAATAG XP_016860103.1:p.Asn131=
XR_002959322.1:n.482_486delinsAATAG
NM_000465.4:c.292_296delinsAATAG MANE Select NP_000456.2:p.Asn98=
NM_001282543.2:c.235_239delinsAATAG NP_001269472.1:p.Asn79=
NM_001282545.2:c.215+4692_215+4696delinsAATAG NP_001269474.1:n.215+4692_215+4696delinsA...
NM_001282548.2:c.158+17043_158+17047delinsAATAG NP_001269477.1:n.158+17043_158+17047delin...
NM_001282549.2:c.292_296delinsAATAG NP_001269478.1:p.Asn98=
NR_104212.2:n.329+4692_329+4696delinsAATAG
NR_104215.2:n.273-10860_273-10856delinsAATAG
NR_104216.2:n.406_410delinsAATAG