Canonical Allele Identifier: CA1327057519

Gene: BARD1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214752804_214752806delinsATT , CM000664.2:g.214752804_214752806delinsATT	GRCh38
NC_000002.11:g.215617528_215617530delinsATT , CM000664.1:g.215617528_215617530delinsATT	GRCh37
NC_000002.10:g.215325773_215325775delinsATT	NCBI36
NG_012047.2:g.61899_61901delinsAAT
NG_012047.3:g.61906_61908delinsAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.1569-251_1569-249delinsAAT MANE Select	ENSP00000260947.4:n.1569-251_1569-249delinsAAT
ENST00000421162.2:c.216-251_216-249delinsAAT	ENSP00000392245.2:n.216-251_216-249delinsAAT
ENST00000613192.2:c.159-22298_159-22296delinsAAT	ENSP00000483275.2:n.159-22298_159-22296delinsAAT
ENST00000613374.5:c.159-251_159-249delinsAAT	ENSP00000484464.1:n.159-251_159-249delinsAAT
ENST00000613706.5:c.1161-251_1161-249delinsAAT	ENSP00000484976.2:n.1161-251_1161-249delinsAAT
ENST00000617164.5:c.1512-251_1512-249delinsAAT	ENSP00000480470.1:n.1512-251_1512-249delinsAAT
ENST00000619009.5:c.365-22298_365-22296delinsAAT	ENSP00000482293.1:n.365-22298_365-22296delinsAAT
ENST00000650978.1:c.2944-251_2944-249delinsAAT
ENST00000260947.8:c.1569-251_1569-249delinsAAT	ENSP00000260947.4:n.1569-251_1569-249delinsAAT
ENST00000421162.1:c.216-251_216-249delinsAAT	ENSP00000392245.1:n.216-251_216-249delinsAAT
ENST00000455743.5:c.*1189-251_*1189-249delinsAAT	ENSP00000412186.1:n.*1189-251_*1189-249delinsAAT
ENST00000613192.1:c.74-22298_74-22296delinsAAT	ENSP00000483275.1:n.74-22298_74-22296delinsAAT
ENST00000613374.4:c.159-251_159-249delinsAAT	ENSP00000484464.1:n.159-251_159-249delinsAAT
ENST00000613706.4:c.216-251_216-249delinsAAT	ENSP00000484976.1:n.216-251_216-249delinsAAT
ENST00000617164.4:c.1512-251_1512-249delinsAAT	ENSP00000480470.1:n.1512-251_1512-249delinsAAT
ENST00000619009.4:c.365-22298_365-22296delinsAAT	ENSP00000482293.1:n.365-22298_365-22296delinsAAT
ENST00000620057.4:c.*235-251_*235-249delinsAAT	ENSP00000481988.1:n.*235-251_*235-249delinsAAT
NM_000465.3:c.1569-251_1569-249delinsAAT	NP_000456.2:n.1569-251_1569-249delinsAAT
NM_001282543.1:c.1512-251_1512-249delinsAAT	NP_001269472.1:n.1512-251_1512-249delinsAAT
NM_001282545.1:c.216-251_216-249delinsAAT	NP_001269474.1:n.216-251_216-249delinsAAT
NM_001282548.1:c.159-251_159-249delinsAAT	NP_001269477.1:n.159-251_159-249delinsAAT
NM_001282549.1:c.365-22298_365-22296delinsAAT	NP_001269478.1:n.365-22298_365-22296delinsAAT
NR_104212.1:n.1562-251_1562-249delinsAAT
NR_104215.1:n.1505-251_1505-249delinsAAT
NR_104216.1:n.761-251_761-249delinsAAT
XM_011511567.1:c.1515-251_1515-249delinsAAT	XP_011509869.1:n.1515-251_1515-249delinsAAT
XM_011511568.1:c.1569-251_1569-249delinsAAT	XP_011509870.1:n.1569-251_1569-249delinsAAT
XM_017004613.1:c.1668-251_1668-249delinsAAT	XP_016860102.1:n.1668-251_1668-249delinsAAT
XM_017004614.1:c.1668-251_1668-249delinsAAT	XP_016860103.1:n.1668-251_1668-249delinsAAT
XR_002959322.1:n.1759-251_1759-249delinsAAT
NM_000465.4:c.1569-251_1569-249delinsAAT MANE Select	NP_000456.2:n.1569-251_1569-249delinsAAT
NM_001282543.2:c.1512-251_1512-249delinsAAT	NP_001269472.1:n.1512-251_1512-249delinsAAT
NM_001282545.2:c.216-251_216-249delinsAAT	NP_001269474.1:n.216-251_216-249delinsAAT
NM_001282548.2:c.159-251_159-249delinsAAT	NP_001269477.1:n.159-251_159-249delinsAAT
NM_001282549.2:c.365-22298_365-22296delinsAAT	NP_001269478.1:n.365-22298_365-22296delinsAAT
NR_104212.2:n.1534-251_1534-249delinsAAT
NR_104215.2:n.1477-251_1477-249delinsAAT
NR_104216.2:n.733-251_733-249delinsAAT