Canonical Allele Identifier: CA1327053287

Gene: BARD1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214745019_214745020delinsCA , CM000664.2:g.214745019_214745020delinsCA	GRCh38
NC_000002.11:g.215609743_215609744delinsCA , CM000664.1:g.215609743_215609744delinsCA	GRCh37
NC_000002.10:g.215317988_215317989delinsCA	NCBI36
NG_012047.2:g.69685_69686delinsTG
NG_012047.3:g.69692_69693delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.1903+47_1903+48delinsTG MANE Select	ENSP00000260947.4:n.1903+47_1903+48delinsTG
ENST00000421162.2:c.550+47_550+48delinsTG	ENSP00000392245.2:n.550+47_550+48delinsTG
ENST00000613192.2:c.159-14512_159-14511delinsTG	ENSP00000483275.2:n.159-14512_159-14511delinsTG
ENST00000613374.5:c.493+47_493+48delinsTG	ENSP00000484464.1:n.493+47_493+48delinsTG
ENST00000613706.5:c.1495+47_1495+48delinsTG	ENSP00000484976.2:n.1495+47_1495+48delinsTG
ENST00000617164.5:c.1846+47_1846+48delinsTG	ENSP00000480470.1:n.1846+47_1846+48delinsTG
ENST00000619009.5:c.365-14512_365-14511delinsTG	ENSP00000482293.1:n.365-14512_365-14511delinsTG
ENST00000650978.1:c.3278+47_3278+48delinsTG
ENST00000260947.8:c.1903+47_1903+48delinsTG	ENSP00000260947.4:n.1903+47_1903+48delinsTG
ENST00000421162.1:c.550+47_550+48delinsTG	ENSP00000392245.1:n.550+47_550+48delinsTG
ENST00000455743.5:c.*1523+47_*1523+48delinsTG	ENSP00000412186.1:n.*1523+47_*1523+48delinsTG
ENST00000613192.1:c.74-14512_74-14511delinsTG	ENSP00000483275.1:n.74-14512_74-14511delinsTG
ENST00000613374.4:c.493+47_493+48delinsTG	ENSP00000484464.1:n.493+47_493+48delinsTG
ENST00000613706.4:c.550+47_550+48delinsTG	ENSP00000484976.1:n.550+47_550+48delinsTG
ENST00000617164.4:c.1846+47_1846+48delinsTG	ENSP00000480470.1:n.1846+47_1846+48delinsTG
ENST00000619009.4:c.365-14512_365-14511delinsTG	ENSP00000482293.1:n.365-14512_365-14511delinsTG
ENST00000620057.4:c.*569+47_*569+48delinsTG	ENSP00000481988.1:n.*569+47_*569+48delinsTG
NM_000465.3:c.1903+47_1903+48delinsTG	NP_000456.2:n.1903+47_1903+48delinsTG
NM_001282543.1:c.1846+47_1846+48delinsTG	NP_001269472.1:n.1846+47_1846+48delinsTG
NM_001282545.1:c.550+47_550+48delinsTG	NP_001269474.1:n.550+47_550+48delinsTG
NM_001282548.1:c.493+47_493+48delinsTG	NP_001269477.1:n.493+47_493+48delinsTG
NM_001282549.1:c.365-14512_365-14511delinsTG	NP_001269478.1:n.365-14512_365-14511delinsTG
NR_104212.1:n.1896+47_1896+48delinsTG
NR_104215.1:n.1839+47_1839+48delinsTG
NR_104216.1:n.1095+47_1095+48delinsTG
XM_011511567.1:c.1849+47_1849+48delinsTG	XP_011509869.1:n.1849+47_1849+48delinsTG
XM_011511568.1:c.1903+47_1903+48delinsTG	XP_011509870.1:n.1903+47_1903+48delinsTG
XM_017004613.1:c.2002+47_2002+48delinsTG	XP_016860102.1:n.2002+47_2002+48delinsTG
XM_017004614.1:c.2002+47_2002+48delinsTG	XP_016860103.1:n.2002+47_2002+48delinsTG
XR_002959322.1:n.2093+47_2093+48delinsTG
NM_000465.4:c.1903+47_1903+48delinsTG MANE Select	NP_000456.2:n.1903+47_1903+48delinsTG
NM_001282543.2:c.1846+47_1846+48delinsTG	NP_001269472.1:n.1846+47_1846+48delinsTG
NM_001282545.2:c.550+47_550+48delinsTG	NP_001269474.1:n.550+47_550+48delinsTG
NM_001282548.2:c.493+47_493+48delinsTG	NP_001269477.1:n.493+47_493+48delinsTG
NM_001282549.2:c.365-14512_365-14511delinsTG	NP_001269478.1:n.365-14512_365-14511delinsTG
NR_104212.2:n.1868+47_1868+48delinsTG
NR_104215.2:n.1811+47_1811+48delinsTG
NR_104216.2:n.1067+47_1067+48delinsTG