Canonical Allele Identifier: CA350455173

Gene: BARD1

Linked Data

• ClinVar Variation Id: 863046
• ClinVar RCV Id: RCV001069913
• dbSNP Id: rs1449269582
• MyVariant Identifiers: chr2:g.215645722C>G (hg19) ; chr2:g.214780998C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214780998C>G , CM000664.2:g.214780998C>G	GRCh38
NC_000002.11:g.215645722C>G , CM000664.1:g.215645722C>G	GRCh37
NC_000002.10:g.215353967C>G	NCBI36
NG_012047.2:g.33707G>C
NG_012047.3:g.33714G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.876G>C MANE Select	ENSP00000260947.4:p.Lys292Asn
ENST00000421162.2:c.215+16063G>C	ENSP00000392245.2:n.215+16063G>C
ENST00000613192.2:c.158+28414G>C	ENSP00000483275.2:n.158+28414G>C
ENST00000613374.5:c.158+28414G>C	ENSP00000484464.1:n.158+28414G>C
ENST00000613706.5:c.876G>C	ENSP00000484976.2:p.Lys292Asn
ENST00000617164.5:c.819G>C	ENSP00000480470.1:p.Lys273Asn
ENST00000619009.5:c.364+11299G>C	ENSP00000482293.1:n.364+11299G>C
ENST00000650978.1:c.718G>C
ENST00000260947.8:c.876G>C	ENSP00000260947.4:p.Lys292Asn
ENST00000421162.1:c.215+16063G>C	ENSP00000392245.1:n.215+16063G>C
ENST00000455743.5:c.*496G>C	ENSP00000412186.1:n.*496G>C
ENST00000471787.1:n.771G>C
ENST00000613192.1:c.73+28414G>C	ENSP00000483275.1:n.73+28414G>C
ENST00000613374.4:c.158+28414G>C	ENSP00000484464.1:n.158+28414G>C
ENST00000613706.4:c.215+16063G>C	ENSP00000484976.1:n.215+16063G>C
ENST00000617164.4:c.819G>C	ENSP00000480470.1:p.Lys273Asn
ENST00000619009.4:c.364+11299G>C	ENSP00000482293.1:n.364+11299G>C
ENST00000620057.4:c.364+11299G>C	ENSP00000481988.1:n.364+11299G>C
NM_000465.3:c.876G>C	NP_000456.2:p.Lys292Asn
NM_001282543.1:c.819G>C	NP_001269472.1:p.Lys273Asn
NM_001282545.1:c.215+16063G>C	NP_001269474.1:n.215+16063G>C
NM_001282548.1:c.158+28414G>C	NP_001269477.1:n.158+28414G>C
NM_001282549.1:c.364+11299G>C	NP_001269478.1:n.364+11299G>C
NR_104212.1:n.869G>C
NR_104215.1:n.812G>C
NR_104216.1:n.506+11299G>C
XM_011511567.1:c.822G>C	XP_011509869.1:p.Lys274Asn
XM_011511568.1:c.876G>C	XP_011509870.1:p.Lys292Asn
XM_017004613.1:c.975G>C	XP_016860102.1:p.Lys325Asn
XM_017004614.1:c.975G>C	XP_016860103.1:p.Lys325Asn
XR_002959322.1:n.1066G>C
NM_000465.4:c.876G>C MANE Select	NP_000456.2:p.Lys292Asn
NM_001282543.2:c.819G>C	NP_001269472.1:p.Lys273Asn
NM_001282545.2:c.215+16063G>C	NP_001269474.1:n.215+16063G>C
NM_001282548.2:c.158+28414G>C	NP_001269477.1:n.158+28414G>C
NM_001282549.2:c.364+11299G>C	NP_001269478.1:n.364+11299G>C
NR_104212.2:n.841G>C
NR_104215.2:n.784G>C
NR_104216.2:n.478+11299G>C