Canonical Allele Identifier: CA2701492846

Gene: BARD1

Linked Data

• dbSNP Id: rs2106018369

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214744963_214744964del , CM000664.2:g.214744963_214744964del	GRCh38
NC_000002.11:g.215609687_215609688del , CM000664.1:g.215609687_215609688del	GRCh37
NC_000002.10:g.215317932_215317933del	NCBI36
NG_012047.2:g.69743_69744del
NG_012047.3:g.69750_69751del

Transcript Alleles

HGVS	Amino-acid change
ENST00000260947.9:c.1903+105_1903+106del MANE Select	ENSP00000260947.4:n.1903+105_1903+106del
ENST00000421162.2:c.550+105_550+106del	ENSP00000392245.2:n.550+105_550+106del
ENST00000613192.2:c.159-14454_159-14453del	ENSP00000483275.2:n.159-14454_159-14453de...
ENST00000613374.5:c.493+105_493+106del	ENSP00000484464.1:n.493+105_493+106del
ENST00000613706.5:c.1495+105_1495+106del	ENSP00000484976.2:n.1495+105_1495+106del
ENST00000617164.5:c.1846+105_1846+106del	ENSP00000480470.1:n.1846+105_1846+106del
ENST00000619009.5:c.365-14454_365-14453del	ENSP00000482293.1:n.365-14454_365-14453de...
ENST00000650978.1:c.3278+105_3278+106del
ENST00000260947.8:c.1903+105_1903+106del	ENSP00000260947.4:n.1903+105_1903+106del
ENST00000421162.1:c.550+105_550+106del	ENSP00000392245.1:n.550+105_550+106del
ENST00000455743.5:c.*1523+105_*1523+106del	ENSP00000412186.1:n.*1523+105_*1523+106de...
ENST00000613192.1:c.74-14454_74-14453del	ENSP00000483275.1:n.74-14454_74-14453del
ENST00000613374.4:c.493+105_493+106del	ENSP00000484464.1:n.493+105_493+106del
ENST00000613706.4:c.550+105_550+106del	ENSP00000484976.1:n.550+105_550+106del
ENST00000617164.4:c.1846+105_1846+106del	ENSP00000480470.1:n.1846+105_1846+106del
ENST00000619009.4:c.365-14454_365-14453del	ENSP00000482293.1:n.365-14454_365-14453de...
ENST00000620057.4:c.*569+105_*569+106del	ENSP00000481988.1:n.*569+105_*569+106del
NM_000465.3:c.1903+105_1903+106del	NP_000456.2:n.1903+105_1903+106del
NM_001282543.1:c.1846+105_1846+106del	NP_001269472.1:n.1846+105_1846+106del
NM_001282545.1:c.550+105_550+106del	NP_001269474.1:n.550+105_550+106del
NM_001282548.1:c.493+105_493+106del	NP_001269477.1:n.493+105_493+106del
NM_001282549.1:c.365-14454_365-14453del	NP_001269478.1:n.365-14454_365-14453del
NR_104212.1:n.1896+105_1896+106del
NR_104215.1:n.1839+105_1839+106del
NR_104216.1:n.1095+105_1095+106del
XM_011511567.1:c.1849+105_1849+106del	XP_011509869.1:n.1849+105_1849+106del
XM_011511568.1:c.1903+105_1903+106del	XP_011509870.1:n.1903+105_1903+106del
XM_017004613.1:c.2002+105_2002+106del	XP_016860102.1:n.2002+105_2002+106del
XM_017004614.1:c.2002+105_2002+106del	XP_016860103.1:n.2002+105_2002+106del
XR_002959322.1:n.2093+105_2093+106del
NM_000465.4:c.1903+105_1903+106del MANE Select	NP_000456.2:n.1903+105_1903+106del
NM_001282543.2:c.1846+105_1846+106del	NP_001269472.1:n.1846+105_1846+106del
NM_001282545.2:c.550+105_550+106del	NP_001269474.1:n.550+105_550+106del
NM_001282548.2:c.493+105_493+106del	NP_001269477.1:n.493+105_493+106del
NM_001282549.2:c.365-14454_365-14453del	NP_001269478.1:n.365-14454_365-14453del
NR_104212.2:n.1868+105_1868+106del
NR_104215.2:n.1811+105_1811+106del
NR_104216.2:n.1067+105_1067+106del