Canonical Allele Identifier: CA1327053250

Gene: BARD1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214744921_214744922delinsAC , CM000664.2:g.214744921_214744922delinsAC	GRCh38
NC_000002.11:g.215609645_215609646delinsAC , CM000664.1:g.215609645_215609646delinsAC	GRCh37
NC_000002.10:g.215317890_215317891delinsAC	NCBI36
NG_012047.2:g.69783_69784delinsGT
NG_012047.3:g.69790_69791delinsGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000260947.9:c.1903+145_1903+146delinsGT MANE Select	ENSP00000260947.4:n.1903+145_1903+146deli...
ENST00000421162.2:c.550+145_550+146delinsGT	ENSP00000392245.2:n.550+145_550+146delins...
ENST00000613192.2:c.159-14414_159-14413delinsGT	ENSP00000483275.2:n.159-14414_159-14413de...
ENST00000613374.5:c.493+145_493+146delinsGT	ENSP00000484464.1:n.493+145_493+146delins...
ENST00000613706.5:c.1495+145_1495+146delinsGT	ENSP00000484976.2:n.1495+145_1495+146deli...
ENST00000617164.5:c.1846+145_1846+146delinsGT	ENSP00000480470.1:n.1846+145_1846+146deli...
ENST00000619009.5:c.365-14414_365-14413delinsGT	ENSP00000482293.1:n.365-14414_365-14413de...
ENST00000650978.1:c.3278+145_3278+146delinsGT
ENST00000260947.8:c.1903+145_1903+146delinsGT	ENSP00000260947.4:n.1903+145_1903+146deli...
ENST00000421162.1:c.550+145_550+146delinsGT	ENSP00000392245.1:n.550+145_550+146delins...
ENST00000455743.5:c.*1523+145_*1523+146delinsGT	ENSP00000412186.1:n.*1523+145_*1523+146de...
ENST00000613192.1:c.74-14414_74-14413delinsGT	ENSP00000483275.1:n.74-14414_74-14413deli...
ENST00000613374.4:c.493+145_493+146delinsGT	ENSP00000484464.1:n.493+145_493+146delins...
ENST00000613706.4:c.550+145_550+146delinsGT	ENSP00000484976.1:n.550+145_550+146delins...
ENST00000617164.4:c.1846+145_1846+146delinsGT	ENSP00000480470.1:n.1846+145_1846+146deli...
ENST00000619009.4:c.365-14414_365-14413delinsGT	ENSP00000482293.1:n.365-14414_365-14413de...
ENST00000620057.4:c.*569+145_*569+146delinsGT	ENSP00000481988.1:n.*569+145_*569+146deli...
NM_000465.3:c.1903+145_1903+146delinsGT	NP_000456.2:n.1903+145_1903+146delinsGT
NM_001282543.1:c.1846+145_1846+146delinsGT	NP_001269472.1:n.1846+145_1846+146delinsG...
NM_001282545.1:c.550+145_550+146delinsGT	NP_001269474.1:n.550+145_550+146delinsGT
NM_001282548.1:c.493+145_493+146delinsGT	NP_001269477.1:n.493+145_493+146delinsGT
NM_001282549.1:c.365-14414_365-14413delinsGT	NP_001269478.1:n.365-14414_365-14413delin...
NR_104212.1:n.1896+145_1896+146delinsGT
NR_104215.1:n.1839+145_1839+146delinsGT
NR_104216.1:n.1095+145_1095+146delinsGT
XM_011511567.1:c.1849+145_1849+146delinsGT	XP_011509869.1:n.1849+145_1849+146delinsG...
XM_011511568.1:c.1903+145_1903+146delinsGT	XP_011509870.1:n.1903+145_1903+146delinsG...
XM_017004613.1:c.2002+145_2002+146delinsGT	XP_016860102.1:n.2002+145_2002+146delinsG...
XM_017004614.1:c.2002+145_2002+146delinsGT	XP_016860103.1:n.2002+145_2002+146delinsG...
XR_002959322.1:n.2093+145_2093+146delinsGT
NM_000465.4:c.1903+145_1903+146delinsGT MANE Select	NP_000456.2:n.1903+145_1903+146delinsGT
NM_001282543.2:c.1846+145_1846+146delinsGT	NP_001269472.1:n.1846+145_1846+146delinsG...
NM_001282545.2:c.550+145_550+146delinsGT	NP_001269474.1:n.550+145_550+146delinsGT
NM_001282548.2:c.493+145_493+146delinsGT	NP_001269477.1:n.493+145_493+146delinsGT
NM_001282549.2:c.365-14414_365-14413delinsGT	NP_001269478.1:n.365-14414_365-14413delin...
NR_104212.2:n.1868+145_1868+146delinsGT
NR_104215.2:n.1811+145_1811+146delinsGT
NR_104216.2:n.1067+145_1067+146delinsGT