Canonical Allele Identifier: CA188538

Gene: BARD1

Linked Data

• ClinVar Variation Id: 184301
• ClinVar RCV Id: RCV000163529 ; RCV000237014 ; RCV000461423 ; RCV000781938
• dbSNP Id: rs774929973
• ExAC: 2:215645954 T / C
• gnomAD v2: 2-215645954-T-C
• gnomAD v3: 2-214781230-T-C
• gnomAD v4: 2-214781230-T-C
• MyVariant Identifiers: chr2:g.215645954T>C (hg19) ; chr2:g.214781230T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214781230T>C , CM000664.2:g.214781230T>C	GRCh38
NC_000002.11:g.215645954T>C , CM000664.1:g.215645954T>C	GRCh37
NC_000002.10:g.215354199T>C	NCBI36
NG_012047.2:g.33475A>G
NG_012047.3:g.33482A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.644A>G MANE Select	ENSP00000260947.4:p.Asn215Ser
ENST00000421162.2:c.215+15831A>G	ENSP00000392245.2:n.215+15831A>G
ENST00000613192.2:c.158+28182A>G	ENSP00000483275.2:n.158+28182A>G
ENST00000613374.5:c.158+28182A>G	ENSP00000484464.1:n.158+28182A>G
ENST00000613706.5:c.644A>G	ENSP00000484976.2:p.Asn215Ser
ENST00000617164.5:c.587A>G	ENSP00000480470.1:p.Asn196Ser
ENST00000619009.5:c.364+11067A>G	ENSP00000482293.1:n.364+11067A>G
ENST00000650978.1:c.486A>G
ENST00000260947.8:c.644A>G	ENSP00000260947.4:p.Asn215Ser
ENST00000421162.1:c.215+15831A>G	ENSP00000392245.1:n.215+15831A>G
ENST00000455743.5:c.*264A>G	ENSP00000412186.1:n.*264A>G
ENST00000471787.1:n.539A>G
ENST00000613192.1:c.73+28182A>G	ENSP00000483275.1:n.73+28182A>G
ENST00000613374.4:c.158+28182A>G	ENSP00000484464.1:n.158+28182A>G
ENST00000613706.4:c.215+15831A>G	ENSP00000484976.1:n.215+15831A>G
ENST00000617164.4:c.587A>G	ENSP00000480470.1:p.Asn196Ser
ENST00000619009.4:c.364+11067A>G	ENSP00000482293.1:n.364+11067A>G
ENST00000620057.4:c.364+11067A>G	ENSP00000481988.1:n.364+11067A>G
NM_000465.3:c.644A>G	NP_000456.2:p.Asn215Ser
NM_001282543.1:c.587A>G	NP_001269472.1:p.Asn196Ser
NM_001282545.1:c.215+15831A>G	NP_001269474.1:n.215+15831A>G
NM_001282548.1:c.158+28182A>G	NP_001269477.1:n.158+28182A>G
NM_001282549.1:c.364+11067A>G	NP_001269478.1:n.364+11067A>G
NR_104212.1:n.637A>G
NR_104215.1:n.580A>G
NR_104216.1:n.506+11067A>G
XM_011511567.1:c.590A>G	XP_011509869.1:p.Asn197Ser
XM_011511568.1:c.644A>G	XP_011509870.1:p.Asn215Ser
XM_017004613.1:c.743A>G	XP_016860102.1:p.Asn248Ser
XM_017004614.1:c.743A>G	XP_016860103.1:p.Asn248Ser
XR_002959322.1:n.834A>G
NM_000465.4:c.644A>G MANE Select	NP_000456.2:p.Asn215Ser
NM_001282543.2:c.587A>G	NP_001269472.1:p.Asn196Ser
NM_001282545.2:c.215+15831A>G	NP_001269474.1:n.215+15831A>G
NM_001282548.2:c.158+28182A>G	NP_001269477.1:n.158+28182A>G
NM_001282549.2:c.364+11067A>G	NP_001269478.1:n.364+11067A>G
NR_104212.2:n.609A>G
NR_104215.2:n.552A>G
NR_104216.2:n.478+11067A>G