Canonical Allele Identifier: CA1327076608
Gene: BARD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214792228_214792229delinsCT , CM000664.2:g.214792228_214792229delinsCT GRCh38
NC_000002.11:g.215656952_215656953delinsCT , CM000664.1:g.215656952_215656953delinsCT GRCh37
NC_000002.10:g.215365197_215365198delinsCT NCBI36
NG_012047.2:g.22476_22477delinsAG
NG_012047.3:g.22483_22484delinsAG

Transcript Alleles

HGVS Amino-acid change
ENST00000260947.9:c.364+68_364+69delinsAG MANE Select ENSP00000260947.4:n.364+68_364+69delinsAG...
ENST00000421162.2:c.215+4832_215+4833delinsAG ENSP00000392245.2:n.215+4832_215+4833deli...
ENST00000613192.2:c.158+17183_158+17184delinsAG ENSP00000483275.2:n.158+17183_158+17184de...
ENST00000613374.5:c.158+17183_158+17184delinsAG ENSP00000484464.1:n.158+17183_158+17184de...
ENST00000613706.5:c.364+68_364+69delinsAG ENSP00000484976.2:n.364+68_364+69delinsAG...
ENST00000617164.5:c.307+68_307+69delinsAG ENSP00000480470.1:n.307+68_307+69delinsAG...
ENST00000619009.5:c.364+68_364+69delinsAG ENSP00000482293.1:n.364+68_364+69delinsAG...
ENST00000650978.1:c.206+68_206+69delinsAG
ENST00000260947.8:c.364+68_364+69delinsAG ENSP00000260947.4:n.364+68_364+69delinsAG...
ENST00000421162.1:c.215+4832_215+4833delinsAG ENSP00000392245.1:n.215+4832_215+4833deli...
ENST00000455743.5:c.215+4832_215+4833delinsAG ENSP00000412186.1:n.215+4832_215+4833deli...
ENST00000471787.1:n.260-10720_260-10719delinsAG
ENST00000613192.1:c.73+17183_73+17184delinsAG ENSP00000483275.1:n.73+17183_73+17184deli...
ENST00000613374.4:c.158+17183_158+17184delinsAG ENSP00000484464.1:n.158+17183_158+17184de...
ENST00000613706.4:c.215+4832_215+4833delinsAG ENSP00000484976.1:n.215+4832_215+4833deli...
ENST00000617164.4:c.307+68_307+69delinsAG ENSP00000480470.1:n.307+68_307+69delinsAG...
ENST00000619009.4:c.364+68_364+69delinsAG ENSP00000482293.1:n.364+68_364+69delinsAG...
ENST00000620057.4:c.364+68_364+69delinsAG ENSP00000481988.1:n.364+68_364+69delinsAG...
NM_000465.3:c.364+68_364+69delinsAG NP_000456.2:n.364+68_364+69delinsAG
NM_001282543.1:c.307+68_307+69delinsAG NP_001269472.1:n.307+68_307+69delinsAG
NM_001282545.1:c.215+4832_215+4833delinsAG NP_001269474.1:n.215+4832_215+4833delinsA...
NM_001282548.1:c.158+17183_158+17184delinsAG NP_001269477.1:n.158+17183_158+17184delin...
NM_001282549.1:c.364+68_364+69delinsAG NP_001269478.1:n.364+68_364+69delinsAG
NR_104212.1:n.357+4832_357+4833delinsAG
NR_104215.1:n.301-10720_301-10719delinsAG
NR_104216.1:n.506+68_506+69delinsAG
XM_011511567.1:c.310+68_310+69delinsAG XP_011509869.1:n.310+68_310+69delinsAG
XM_011511568.1:c.364+68_364+69delinsAG XP_011509870.1:n.364+68_364+69delinsAG
XM_017004613.1:c.463+68_463+69delinsAG XP_016860102.1:n.463+68_463+69delinsAG
XM_017004614.1:c.463+68_463+69delinsAG XP_016860103.1:n.463+68_463+69delinsAG
XR_002959322.1:n.554+68_554+69delinsAG
NM_000465.4:c.364+68_364+69delinsAG MANE Select NP_000456.2:n.364+68_364+69delinsAG
NM_001282543.2:c.307+68_307+69delinsAG NP_001269472.1:n.307+68_307+69delinsAG
NM_001282545.2:c.215+4832_215+4833delinsAG NP_001269474.1:n.215+4832_215+4833delinsA...
NM_001282548.2:c.158+17183_158+17184delinsAG NP_001269477.1:n.158+17183_158+17184delin...
NM_001282549.2:c.364+68_364+69delinsAG NP_001269478.1:n.364+68_364+69delinsAG
NR_104212.2:n.329+4832_329+4833delinsAG
NR_104215.2:n.273-10720_273-10719delinsAG
NR_104216.2:n.478+68_478+69delinsAG