Canonical Allele Identifier: CA193178

Gene: BARD1

Linked Data

• ClinVar Variation Id: 185858
• ClinVar RCV Id: RCV000165356
• dbSNP Id: rs786202512
• MyVariant Identifiers: chr2:g.215609877T>G (hg19) ; chr2:g.214745153T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214745153T>G , CM000664.2:g.214745153T>G	GRCh38
NC_000002.11:g.215609877T>G , CM000664.1:g.215609877T>G	GRCh37
NC_000002.10:g.215318122T>G	NCBI36
NG_012047.2:g.69552A>C
NG_012047.3:g.69559A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.1817A>C MANE Select	ENSP00000260947.4:p.His606Pro
ENST00000421162.2:c.464A>C	ENSP00000392245.2:p.His155Pro
ENST00000613192.2:c.159-14645A>C	ENSP00000483275.2:n.159-14645A>C
ENST00000613374.5:c.407A>C	ENSP00000484464.1:p.His136Pro
ENST00000613706.5:c.1409A>C	ENSP00000484976.2:p.His470Pro
ENST00000617164.5:c.1760A>C	ENSP00000480470.1:p.His587Pro
ENST00000619009.5:c.365-14645A>C	ENSP00000482293.1:n.365-14645A>C
ENST00000650978.1:c.3192A>C
ENST00000260947.8:c.1817A>C	ENSP00000260947.4:p.His606Pro
ENST00000421162.1:c.464A>C	ENSP00000392245.1:p.His155Pro
ENST00000455743.5:c.*1437A>C	ENSP00000412186.1:n.*1437A>C
ENST00000613192.1:c.74-14645A>C	ENSP00000483275.1:n.74-14645A>C
ENST00000613374.4:c.407A>C	ENSP00000484464.1:p.His136Pro
ENST00000613706.4:c.464A>C	ENSP00000484976.1:p.His155Pro
ENST00000617164.4:c.1760A>C	ENSP00000480470.1:p.His587Pro
ENST00000619009.4:c.365-14645A>C	ENSP00000482293.1:n.365-14645A>C
ENST00000620057.4:c.*483A>C	ENSP00000481988.1:n.*483A>C
NM_000465.3:c.1817A>C	NP_000456.2:p.His606Pro
NM_001282543.1:c.1760A>C	NP_001269472.1:p.His587Pro
NM_001282545.1:c.464A>C	NP_001269474.1:p.His155Pro
NM_001282548.1:c.407A>C	NP_001269477.1:p.His136Pro
NM_001282549.1:c.365-14645A>C	NP_001269478.1:n.365-14645A>C
NR_104212.1:n.1810A>C
NR_104215.1:n.1753A>C
NR_104216.1:n.1009A>C
XM_011511567.1:c.1763A>C	XP_011509869.1:p.His588Pro
XM_011511568.1:c.1817A>C	XP_011509870.1:p.His606Pro
XM_017004613.1:c.1916A>C	XP_016860102.1:p.His639Pro
XM_017004614.1:c.1916A>C	XP_016860103.1:p.His639Pro
XR_002959322.1:n.2007A>C
NM_000465.4:c.1817A>C MANE Select	NP_000456.2:p.His606Pro
NM_001282543.2:c.1760A>C	NP_001269472.1:p.His587Pro
NM_001282545.2:c.464A>C	NP_001269474.1:p.His155Pro
NM_001282548.2:c.407A>C	NP_001269477.1:p.His136Pro
NM_001282549.2:c.365-14645A>C	NP_001269478.1:n.365-14645A>C
NR_104212.2:n.1782A>C
NR_104215.2:n.1725A>C
NR_104216.2:n.981A>C