Canonical Allele Identifier: CA1327053266

Gene: BARD1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214744963_214744964delinsAG , CM000664.2:g.214744963_214744964delinsAG	GRCh38
NC_000002.11:g.215609687_215609688delinsAG , CM000664.1:g.215609687_215609688delinsAG	GRCh37
NC_000002.10:g.215317932_215317933delinsAG	NCBI36
NG_012047.2:g.69741_69742delinsCT
NG_012047.3:g.69748_69749delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000260947.9:c.1903+103_1903+104delinsCT MANE Select	ENSP00000260947.4:n.1903+103_1903+104deli...
ENST00000421162.2:c.550+103_550+104delinsCT	ENSP00000392245.2:n.550+103_550+104delins...
ENST00000613192.2:c.159-14456_159-14455delinsCT	ENSP00000483275.2:n.159-14456_159-14455de...
ENST00000613374.5:c.493+103_493+104delinsCT	ENSP00000484464.1:n.493+103_493+104delins...
ENST00000613706.5:c.1495+103_1495+104delinsCT	ENSP00000484976.2:n.1495+103_1495+104deli...
ENST00000617164.5:c.1846+103_1846+104delinsCT	ENSP00000480470.1:n.1846+103_1846+104deli...
ENST00000619009.5:c.365-14456_365-14455delinsCT	ENSP00000482293.1:n.365-14456_365-14455de...
ENST00000650978.1:c.3278+103_3278+104delinsCT
ENST00000260947.8:c.1903+103_1903+104delinsCT	ENSP00000260947.4:n.1903+103_1903+104deli...
ENST00000421162.1:c.550+103_550+104delinsCT	ENSP00000392245.1:n.550+103_550+104delins...
ENST00000455743.5:c.*1523+103_*1523+104delinsCT	ENSP00000412186.1:n.*1523+103_*1523+104de...
ENST00000613192.1:c.74-14456_74-14455delinsCT	ENSP00000483275.1:n.74-14456_74-14455deli...
ENST00000613374.4:c.493+103_493+104delinsCT	ENSP00000484464.1:n.493+103_493+104delins...
ENST00000613706.4:c.550+103_550+104delinsCT	ENSP00000484976.1:n.550+103_550+104delins...
ENST00000617164.4:c.1846+103_1846+104delinsCT	ENSP00000480470.1:n.1846+103_1846+104deli...
ENST00000619009.4:c.365-14456_365-14455delinsCT	ENSP00000482293.1:n.365-14456_365-14455de...
ENST00000620057.4:c.*569+103_*569+104delinsCT	ENSP00000481988.1:n.*569+103_*569+104deli...
NM_000465.3:c.1903+103_1903+104delinsCT	NP_000456.2:n.1903+103_1903+104delinsCT
NM_001282543.1:c.1846+103_1846+104delinsCT	NP_001269472.1:n.1846+103_1846+104delinsC...
NM_001282545.1:c.550+103_550+104delinsCT	NP_001269474.1:n.550+103_550+104delinsCT
NM_001282548.1:c.493+103_493+104delinsCT	NP_001269477.1:n.493+103_493+104delinsCT
NM_001282549.1:c.365-14456_365-14455delinsCT	NP_001269478.1:n.365-14456_365-14455delin...
NR_104212.1:n.1896+103_1896+104delinsCT
NR_104215.1:n.1839+103_1839+104delinsCT
NR_104216.1:n.1095+103_1095+104delinsCT
XM_011511567.1:c.1849+103_1849+104delinsCT	XP_011509869.1:n.1849+103_1849+104delinsC...
XM_011511568.1:c.1903+103_1903+104delinsCT	XP_011509870.1:n.1903+103_1903+104delinsC...
XM_017004613.1:c.2002+103_2002+104delinsCT	XP_016860102.1:n.2002+103_2002+104delinsC...
XM_017004614.1:c.2002+103_2002+104delinsCT	XP_016860103.1:n.2002+103_2002+104delinsC...
XR_002959322.1:n.2093+103_2093+104delinsCT
NM_000465.4:c.1903+103_1903+104delinsCT MANE Select	NP_000456.2:n.1903+103_1903+104delinsCT
NM_001282543.2:c.1846+103_1846+104delinsCT	NP_001269472.1:n.1846+103_1846+104delinsC...
NM_001282545.2:c.550+103_550+104delinsCT	NP_001269474.1:n.550+103_550+104delinsCT
NM_001282548.2:c.493+103_493+104delinsCT	NP_001269477.1:n.493+103_493+104delinsCT
NM_001282549.2:c.365-14456_365-14455delinsCT	NP_001269478.1:n.365-14456_365-14455delin...
NR_104212.2:n.1868+103_1868+104delinsCT
NR_104215.2:n.1811+103_1811+104delinsCT
NR_104216.2:n.1067+103_1067+104delinsCT