Canonical Allele Identifier: CA333190

Gene: BARD1

Linked Data

• ClinVar Variation Id: 141051
• ClinVar RCV Id: RCV000129387 ; RCV000203936 ; RCV000378845 ; RCV001356926
• dbSNP Id: rs587781456
• gnomAD v2: 2-215645763-A-G
• gnomAD v3: 2-214781039-A-G
• gnomAD v4: 2-214781039-A-G
• MyVariant Identifiers: chr2:g.215645763A>G (hg19) ; chr2:g.214781039A>G (hg38)
• PubMed: PMID:26350354

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214781039A>G , CM000664.2:g.214781039A>G	GRCh38
NC_000002.11:g.215645763A>G , CM000664.1:g.215645763A>G	GRCh37
NC_000002.10:g.215354008A>G	NCBI36
NG_012047.2:g.33666T>C
NG_012047.3:g.33673T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.835T>C MANE Select	ENSP00000260947.4:p.Ser279Pro
ENST00000421162.2:c.215+16022T>C	ENSP00000392245.2:n.215+16022T>C
ENST00000613192.2:c.158+28373T>C	ENSP00000483275.2:n.158+28373T>C
ENST00000613374.5:c.158+28373T>C	ENSP00000484464.1:n.158+28373T>C
ENST00000613706.5:c.835T>C	ENSP00000484976.2:p.Ser279Pro
ENST00000617164.5:c.778T>C	ENSP00000480470.1:p.Ser260Pro
ENST00000619009.5:c.364+11258T>C	ENSP00000482293.1:n.364+11258T>C
ENST00000650978.1:c.677T>C
ENST00000260947.8:c.835T>C	ENSP00000260947.4:p.Ser279Pro
ENST00000421162.1:c.215+16022T>C	ENSP00000392245.1:n.215+16022T>C
ENST00000455743.5:c.*455T>C	ENSP00000412186.1:n.*455T>C
ENST00000471787.1:n.730T>C
ENST00000613192.1:c.73+28373T>C	ENSP00000483275.1:n.73+28373T>C
ENST00000613374.4:c.158+28373T>C	ENSP00000484464.1:n.158+28373T>C
ENST00000613706.4:c.215+16022T>C	ENSP00000484976.1:n.215+16022T>C
ENST00000617164.4:c.778T>C	ENSP00000480470.1:p.Ser260Pro
ENST00000619009.4:c.364+11258T>C	ENSP00000482293.1:n.364+11258T>C
ENST00000620057.4:c.364+11258T>C	ENSP00000481988.1:n.364+11258T>C
NM_000465.3:c.835T>C	NP_000456.2:p.Ser279Pro
NM_001282543.1:c.778T>C	NP_001269472.1:p.Ser260Pro
NM_001282545.1:c.215+16022T>C	NP_001269474.1:n.215+16022T>C
NM_001282548.1:c.158+28373T>C	NP_001269477.1:n.158+28373T>C
NM_001282549.1:c.364+11258T>C	NP_001269478.1:n.364+11258T>C
NR_104212.1:n.828T>C
NR_104215.1:n.771T>C
NR_104216.1:n.506+11258T>C
XM_011511567.1:c.781T>C	XP_011509869.1:p.Ser261Pro
XM_011511568.1:c.835T>C	XP_011509870.1:p.Ser279Pro
XM_017004613.1:c.934T>C	XP_016860102.1:p.Ser312Pro
XM_017004614.1:c.934T>C	XP_016860103.1:p.Ser312Pro
XR_002959322.1:n.1025T>C
NM_000465.4:c.835T>C MANE Select	NP_000456.2:p.Ser279Pro
NM_001282543.2:c.778T>C	NP_001269472.1:p.Ser260Pro
NM_001282545.2:c.215+16022T>C	NP_001269474.1:n.215+16022T>C
NM_001282548.2:c.158+28373T>C	NP_001269477.1:n.158+28373T>C
NM_001282549.2:c.364+11258T>C	NP_001269478.1:n.364+11258T>C
NR_104212.2:n.800T>C
NR_104215.2:n.743T>C
NR_104216.2:n.478+11258T>C