Canonical Allele Identifier: CA1327046433

Gene: BARD1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214730517_214730519delinsAAC , CM000664.2:g.214730517_214730519delinsAAC	GRCh38
NC_000002.11:g.215595241_215595243delinsAAC , CM000664.1:g.215595241_215595243delinsAAC	GRCh37
NC_000002.10:g.215303486_215303488delinsAAC	NCBI36
NG_012047.2:g.84186_84188delinsGTT
NG_012047.3:g.84193_84195delinsGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.1904-11_1904-9delinsGTT MANE Select	ENSP00000260947.4:n.1904-11_1904-9delinsGTT
ENST00000421162.2:c.551-11_551-9delinsGTT	ENSP00000392245.2:n.551-11_551-9delinsGTT
ENST00000613192.2:c.159-11_159-9delinsGTT	ENSP00000483275.2:n.159-11_159-9delinsGTT
ENST00000613374.5:c.494-11_494-9delinsGTT	ENSP00000484464.1:n.494-11_494-9delinsGTT
ENST00000613706.5:c.1496-11_1496-9delinsGTT	ENSP00000484976.2:n.1496-11_1496-9delinsGTT
ENST00000617164.5:c.1847-11_1847-9delinsGTT	ENSP00000480470.1:n.1847-11_1847-9delinsGTT
ENST00000619009.5:c.365-11_365-9delinsGTT	ENSP00000482293.1:n.365-11_365-9delinsGTT
ENST00000650978.1:c.3279-11_3279-9delinsGTT
ENST00000260947.8:c.1904-11_1904-9delinsGTT	ENSP00000260947.4:n.1904-11_1904-9delinsGTT
ENST00000421162.1:c.551-11_551-9delinsGTT	ENSP00000392245.1:n.551-11_551-9delinsGTT
ENST00000455743.5:c.*1524-11_*1524-9delinsGTT	ENSP00000412186.1:n.*1524-11_*1524-9delinsGTT
ENST00000471590.5:n.239-11_239-9delinsGTT
ENST00000613192.1:c.74-11_74-9delinsGTT	ENSP00000483275.1:n.74-11_74-9delinsGTT
ENST00000613374.4:c.494-11_494-9delinsGTT	ENSP00000484464.1:n.494-11_494-9delinsGTT
ENST00000613706.4:c.551-11_551-9delinsGTT	ENSP00000484976.1:n.551-11_551-9delinsGTT
ENST00000617164.4:c.1847-11_1847-9delinsGTT	ENSP00000480470.1:n.1847-11_1847-9delinsGTT
ENST00000619009.4:c.365-11_365-9delinsGTT	ENSP00000482293.1:n.365-11_365-9delinsGTT
ENST00000620057.4:c.*570-11_*570-9delinsGTT	ENSP00000481988.1:n.*570-11_*570-9delinsGTT
NM_000465.3:c.1904-11_1904-9delinsGTT	NP_000456.2:n.1904-11_1904-9delinsGTT
NM_001282543.1:c.1847-11_1847-9delinsGTT	NP_001269472.1:n.1847-11_1847-9delinsGTT
NM_001282545.1:c.551-11_551-9delinsGTT	NP_001269474.1:n.551-11_551-9delinsGTT
NM_001282548.1:c.494-11_494-9delinsGTT	NP_001269477.1:n.494-11_494-9delinsGTT
NM_001282549.1:c.365-11_365-9delinsGTT	NP_001269478.1:n.365-11_365-9delinsGTT
NR_104212.1:n.1897-11_1897-9delinsGTT
NR_104215.1:n.1840-11_1840-9delinsGTT
NR_104216.1:n.1096-11_1096-9delinsGTT
XM_011511567.1:c.1850-11_1850-9delinsGTT	XP_011509869.1:n.1850-11_1850-9delinsGTT
XM_017004613.1:c.2003-11_2003-9delinsGTT	XP_016860102.1:n.2003-11_2003-9delinsGTT
XR_002959322.1:n.2094-11_2094-9delinsGTT
NM_000465.4:c.1904-11_1904-9delinsGTT MANE Select	NP_000456.2:n.1904-11_1904-9delinsGTT
NM_001282543.2:c.1847-11_1847-9delinsGTT	NP_001269472.1:n.1847-11_1847-9delinsGTT
NM_001282545.2:c.551-11_551-9delinsGTT	NP_001269474.1:n.551-11_551-9delinsGTT
NM_001282548.2:c.494-11_494-9delinsGTT	NP_001269477.1:n.494-11_494-9delinsGTT
NM_001282549.2:c.365-11_365-9delinsGTT	NP_001269478.1:n.365-11_365-9delinsGTT
NR_104212.2:n.1869-11_1869-9delinsGTT
NR_104215.2:n.1812-11_1812-9delinsGTT
NR_104216.2:n.1068-11_1068-9delinsGTT