Canonical Allele Identifier: CA1327053334

Gene: BARD1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214745097_214745098delinsGA , CM000664.2:g.214745097_214745098delinsGA	GRCh38
NC_000002.11:g.215609821_215609822delinsGA , CM000664.1:g.215609821_215609822delinsGA	GRCh37
NC_000002.10:g.215318066_215318067delinsGA	NCBI36
NG_012047.2:g.69607_69608delinsTC
NG_012047.3:g.69614_69615delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.1872_1873delinsTC MANE Select	ENSP00000260947.4:p.Ile624=
ENST00000421162.2:c.519_520delinsTC	ENSP00000392245.2:p.Ile173=
ENST00000613192.2:c.159-14590_159-14589delinsTC	ENSP00000483275.2:n.159-14590_159-14589delinsTC
ENST00000613374.5:c.462_463delinsTC	ENSP00000484464.1:p.Ile154=
ENST00000613706.5:c.1464_1465delinsTC	ENSP00000484976.2:p.Ile488=
ENST00000617164.5:c.1815_1816delinsTC	ENSP00000480470.1:p.Ile605=
ENST00000619009.5:c.365-14590_365-14589delinsTC	ENSP00000482293.1:n.365-14590_365-14589delinsTC
ENST00000650978.1:c.3247_3248delinsTC
ENST00000260947.8:c.1872_1873delinsTC	ENSP00000260947.4:p.Ile624=
ENST00000421162.1:c.519_520delinsTC	ENSP00000392245.1:p.Ile173=
ENST00000455743.5:c.*1492_*1493delinsTC	ENSP00000412186.1:n.*1492_*1493delinsTC
ENST00000613192.1:c.74-14590_74-14589delinsTC	ENSP00000483275.1:n.74-14590_74-14589delinsTC
ENST00000613374.4:c.462_463delinsTC	ENSP00000484464.1:p.Ile154=
ENST00000613706.4:c.519_520delinsTC	ENSP00000484976.1:p.Ile173=
ENST00000617164.4:c.1815_1816delinsTC	ENSP00000480470.1:p.Ile605=
ENST00000619009.4:c.365-14590_365-14589delinsTC	ENSP00000482293.1:n.365-14590_365-14589delinsTC
ENST00000620057.4:c.*538_*539delinsTC	ENSP00000481988.1:n.*538_*539delinsTC
NM_000465.3:c.1872_1873delinsTC	NP_000456.2:p.Ile624=
NM_001282543.1:c.1815_1816delinsTC	NP_001269472.1:p.Ile605=
NM_001282545.1:c.519_520delinsTC	NP_001269474.1:p.Ile173=
NM_001282548.1:c.462_463delinsTC	NP_001269477.1:p.Ile154=
NM_001282549.1:c.365-14590_365-14589delinsTC	NP_001269478.1:n.365-14590_365-14589delinsTC
NR_104212.1:n.1865_1866delinsTC
NR_104215.1:n.1808_1809delinsTC
NR_104216.1:n.1064_1065delinsTC
XM_011511567.1:c.1818_1819delinsTC	XP_011509869.1:p.Ile606=
XM_011511568.1:c.1872_1873delinsTC	XP_011509870.1:p.Ile624=
XM_017004613.1:c.1971_1972delinsTC	XP_016860102.1:p.Ile657=
XM_017004614.1:c.1971_1972delinsTC	XP_016860103.1:p.Ile657=
XR_002959322.1:n.2062_2063delinsTC
NM_000465.4:c.1872_1873delinsTC MANE Select	NP_000456.2:p.Ile624=
NM_001282543.2:c.1815_1816delinsTC	NP_001269472.1:p.Ile605=
NM_001282545.2:c.519_520delinsTC	NP_001269474.1:p.Ile173=
NM_001282548.2:c.462_463delinsTC	NP_001269477.1:p.Ile154=
NM_001282549.2:c.365-14590_365-14589delinsTC	NP_001269478.1:n.365-14590_365-14589delinsTC
NR_104212.2:n.1837_1838delinsTC
NR_104215.2:n.1780_1781delinsTC
NR_104216.2:n.1036_1037delinsTC