Canonical Allele Identifier: CA1327070876

Gene: BARD1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214780554_214780555delinsTC , CM000664.2:g.214780554_214780555delinsTC	GRCh38
NC_000002.11:g.215645278_215645279delinsTC , CM000664.1:g.215645278_215645279delinsTC	GRCh37
NC_000002.10:g.215353523_215353524delinsTC	NCBI36
NG_012047.2:g.34150_34151delinsGA
NG_012047.3:g.34157_34158delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.1314+5_1314+6delinsGA MANE Select	ENSP00000260947.4:n.1314+5_1314+6delinsGA
ENST00000421162.2:c.215+16506_215+16507delinsGA	ENSP00000392245.2:n.215+16506_215+16507delinsGA
ENST00000613192.2:c.158+28857_158+28858delinsGA	ENSP00000483275.2:n.158+28857_158+28858delinsGA
ENST00000613374.5:c.159-28000_159-27999delinsGA	ENSP00000484464.1:n.159-28000_159-27999delinsGA
ENST00000613706.5:c.906+413_906+414delinsGA	ENSP00000484976.2:n.906+413_906+414delinsGA
ENST00000617164.5:c.1257+5_1257+6delinsGA	ENSP00000480470.1:n.1257+5_1257+6delinsGA
ENST00000619009.5:c.364+11742_364+11743delinsGA	ENSP00000482293.1:n.364+11742_364+11743delinsGA
ENST00000650978.1:c.1156+5_1156+6delinsGA
ENST00000260947.8:c.1314+5_1314+6delinsGA	ENSP00000260947.4:n.1314+5_1314+6delinsGA
ENST00000421162.1:c.215+16506_215+16507delinsGA	ENSP00000392245.1:n.215+16506_215+16507delinsGA
ENST00000455743.5:c.*934+5_*934+6delinsGA	ENSP00000412186.1:n.*934+5_*934+6delinsGA
ENST00000613192.1:c.73+28857_73+28858delinsGA	ENSP00000483275.1:n.73+28857_73+28858delinsGA
ENST00000613374.4:c.159-28000_159-27999delinsGA	ENSP00000484464.1:n.159-28000_159-27999delinsGA
ENST00000613706.4:c.215+16506_215+16507delinsGA	ENSP00000484976.1:n.215+16506_215+16507delinsGA
ENST00000617164.4:c.1257+5_1257+6delinsGA	ENSP00000480470.1:n.1257+5_1257+6delinsGA
ENST00000619009.4:c.364+11742_364+11743delinsGA	ENSP00000482293.1:n.364+11742_364+11743delinsGA
ENST00000620057.4:c.365-11243_365-11242delinsGA	ENSP00000481988.1:n.365-11243_365-11242delinsGA
NM_000465.3:c.1314+5_1314+6delinsGA	NP_000456.2:n.1314+5_1314+6delinsGA
NM_001282543.1:c.1257+5_1257+6delinsGA	NP_001269472.1:n.1257+5_1257+6delinsGA
NM_001282545.1:c.215+16506_215+16507delinsGA	NP_001269474.1:n.215+16506_215+16507delinsGA
NM_001282548.1:c.159-28000_159-27999delinsGA	NP_001269477.1:n.159-28000_159-27999delinsGA
NM_001282549.1:c.364+11742_364+11743delinsGA	NP_001269478.1:n.364+11742_364+11743delinsGA
NR_104212.1:n.1307+5_1307+6delinsGA
NR_104215.1:n.1250+5_1250+6delinsGA
NR_104216.1:n.507-11243_507-11242delinsGA
XM_011511567.1:c.1260+5_1260+6delinsGA	XP_011509869.1:n.1260+5_1260+6delinsGA
XM_011511568.1:c.1314+5_1314+6delinsGA	XP_011509870.1:n.1314+5_1314+6delinsGA
XM_017004613.1:c.1413+5_1413+6delinsGA	XP_016860102.1:n.1413+5_1413+6delinsGA
XM_017004614.1:c.1413+5_1413+6delinsGA	XP_016860103.1:n.1413+5_1413+6delinsGA
XR_002959322.1:n.1504+5_1504+6delinsGA
NM_000465.4:c.1314+5_1314+6delinsGA MANE Select	NP_000456.2:n.1314+5_1314+6delinsGA
NM_001282543.2:c.1257+5_1257+6delinsGA	NP_001269472.1:n.1257+5_1257+6delinsGA
NM_001282545.2:c.215+16506_215+16507delinsGA	NP_001269474.1:n.215+16506_215+16507delinsGA
NM_001282548.2:c.159-28000_159-27999delinsGA	NP_001269477.1:n.159-28000_159-27999delinsGA
NM_001282549.2:c.364+11742_364+11743delinsGA	NP_001269478.1:n.364+11742_364+11743delinsGA
NR_104212.2:n.1279+5_1279+6delinsGA
NR_104215.2:n.1222+5_1222+6delinsGA
NR_104216.2:n.479-11243_479-11242delinsGA