Canonical Allele Identifier: CA1327053371

Gene: BARD1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214745151_214745153delinsCAT , CM000664.2:g.214745151_214745153delinsCAT	GRCh38
NC_000002.11:g.215609875_215609877delinsCAT , CM000664.1:g.215609875_215609877delinsCAT	GRCh37
NC_000002.10:g.215318120_215318122delinsCAT	NCBI36
NG_012047.2:g.69552_69554delinsATG
NG_012047.3:g.69559_69561delinsATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.1817_1819delinsATG MANE Select	ENSP00000260947.4:p.His606=
ENST00000421162.2:c.464_466delinsATG	ENSP00000392245.2:p.His155=
ENST00000613192.2:c.159-14645_159-14643delinsATG	ENSP00000483275.2:n.159-14645_159-14643delinsATG
ENST00000613374.5:c.407_409delinsATG	ENSP00000484464.1:p.His136=
ENST00000613706.5:c.1409_1411delinsATG	ENSP00000484976.2:p.His470=
ENST00000617164.5:c.1760_1762delinsATG	ENSP00000480470.1:p.His587=
ENST00000619009.5:c.365-14645_365-14643delinsATG	ENSP00000482293.1:n.365-14645_365-14643delinsATG
ENST00000650978.1:c.3192_3194delinsATG
ENST00000260947.8:c.1817_1819delinsATG	ENSP00000260947.4:p.His606=
ENST00000421162.1:c.464_466delinsATG	ENSP00000392245.1:p.His155=
ENST00000455743.5:c.*1437_*1439delinsATG	ENSP00000412186.1:n.*1437_*1439delinsATG
ENST00000613192.1:c.74-14645_74-14643delinsATG	ENSP00000483275.1:n.74-14645_74-14643delinsATG
ENST00000613374.4:c.407_409delinsATG	ENSP00000484464.1:p.His136=
ENST00000613706.4:c.464_466delinsATG	ENSP00000484976.1:p.His155=
ENST00000617164.4:c.1760_1762delinsATG	ENSP00000480470.1:p.His587=
ENST00000619009.4:c.365-14645_365-14643delinsATG	ENSP00000482293.1:n.365-14645_365-14643delinsATG
ENST00000620057.4:c.*483_*485delinsATG	ENSP00000481988.1:n.*483_*485delinsATG
NM_000465.3:c.1817_1819delinsATG	NP_000456.2:p.His606=
NM_001282543.1:c.1760_1762delinsATG	NP_001269472.1:p.His587=
NM_001282545.1:c.464_466delinsATG	NP_001269474.1:p.His155=
NM_001282548.1:c.407_409delinsATG	NP_001269477.1:p.His136=
NM_001282549.1:c.365-14645_365-14643delinsATG	NP_001269478.1:n.365-14645_365-14643delinsATG
NR_104212.1:n.1810_1812delinsATG
NR_104215.1:n.1753_1755delinsATG
NR_104216.1:n.1009_1011delinsATG
XM_011511567.1:c.1763_1765delinsATG	XP_011509869.1:p.His588=
XM_011511568.1:c.1817_1819delinsATG	XP_011509870.1:p.His606=
XM_017004613.1:c.1916_1918delinsATG	XP_016860102.1:p.His639=
XM_017004614.1:c.1916_1918delinsATG	XP_016860103.1:p.His639=
XR_002959322.1:n.2007_2009delinsATG
NM_000465.4:c.1817_1819delinsATG MANE Select	NP_000456.2:p.His606=
NM_001282543.2:c.1760_1762delinsATG	NP_001269472.1:p.His587=
NM_001282545.2:c.464_466delinsATG	NP_001269474.1:p.His155=
NM_001282548.2:c.407_409delinsATG	NP_001269477.1:p.His136=
NM_001282549.2:c.365-14645_365-14643delinsATG	NP_001269478.1:n.365-14645_365-14643delinsATG
NR_104212.2:n.1782_1784delinsATG
NR_104215.2:n.1725_1727delinsATG
NR_104216.2:n.981_983delinsATG