Canonical Allele Identifier: CA350452178

Gene: BARD1

Linked Data

• ClinVar Variation Id: 479116
• ClinVar RCV Id: RCV000573834 ; RCV000792709
• dbSNP Id: rs786203673
• MyVariant Identifiers: chr2:g.215609836A>C (hg19) ; chr2:g.214745112A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214745112A>C , CM000664.2:g.214745112A>C	GRCh38
NC_000002.11:g.215609836A>C , CM000664.1:g.215609836A>C	GRCh37
NC_000002.10:g.215318081A>C	NCBI36
NG_012047.2:g.69593T>G
NG_012047.3:g.69600T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000260947.9:c.1858T>G MANE Select	ENSP00000260947.4:p.Cys620Gly
ENST00000421162.2:c.505T>G	ENSP00000392245.2:p.Cys169Gly
ENST00000613192.2:c.159-14604T>G	ENSP00000483275.2:n.159-14604T>G
ENST00000613374.5:c.448T>G	ENSP00000484464.1:p.Cys150Gly
ENST00000613706.5:c.1450T>G	ENSP00000484976.2:p.Cys484Gly
ENST00000617164.5:c.1801T>G	ENSP00000480470.1:p.Cys601Gly
ENST00000619009.5:c.365-14604T>G	ENSP00000482293.1:n.365-14604T>G
ENST00000650978.1:c.3233T>G
ENST00000260947.8:c.1858T>G	ENSP00000260947.4:p.Cys620Gly
ENST00000421162.1:c.505T>G	ENSP00000392245.1:p.Cys169Gly
ENST00000455743.5:c.*1478T>G	ENSP00000412186.1:n.*1478T>G
ENST00000613192.1:c.74-14604T>G	ENSP00000483275.1:n.74-14604T>G
ENST00000613374.4:c.448T>G	ENSP00000484464.1:p.Cys150Gly
ENST00000613706.4:c.505T>G	ENSP00000484976.1:p.Cys169Gly
ENST00000617164.4:c.1801T>G	ENSP00000480470.1:p.Cys601Gly
ENST00000619009.4:c.365-14604T>G	ENSP00000482293.1:n.365-14604T>G
ENST00000620057.4:c.*524T>G	ENSP00000481988.1:n.*524T>G
NM_000465.3:c.1858T>G	NP_000456.2:p.Cys620Gly
NM_001282543.1:c.1801T>G	NP_001269472.1:p.Cys601Gly
NM_001282545.1:c.505T>G	NP_001269474.1:p.Cys169Gly
NM_001282548.1:c.448T>G	NP_001269477.1:p.Cys150Gly
NM_001282549.1:c.365-14604T>G	NP_001269478.1:n.365-14604T>G
NR_104212.1:n.1851T>G
NR_104215.1:n.1794T>G
NR_104216.1:n.1050T>G
XM_011511567.1:c.1804T>G	XP_011509869.1:p.Cys602Gly
XM_011511568.1:c.1858T>G	XP_011509870.1:p.Cys620Gly
XM_017004613.1:c.1957T>G	XP_016860102.1:p.Cys653Gly
XM_017004614.1:c.1957T>G	XP_016860103.1:p.Cys653Gly
XR_002959322.1:n.2048T>G
NM_000465.4:c.1858T>G MANE Select	NP_000456.2:p.Cys620Gly
NM_001282543.2:c.1801T>G	NP_001269472.1:p.Cys601Gly
NM_001282545.2:c.505T>G	NP_001269474.1:p.Cys169Gly
NM_001282548.2:c.448T>G	NP_001269477.1:p.Cys150Gly
NM_001282549.2:c.365-14604T>G	NP_001269478.1:n.365-14604T>G
NR_104212.2:n.1823T>G
NR_104215.2:n.1766T>G
NR_104216.2:n.1022T>G