Canonical Allele Identifier: CA350461030

Gene: BARD1

Linked Data

• ClinVar Variation Id: 2450474
• ClinVar RCV Id: RCV003176968
• MyVariant Identifiers: chr2:g.215657093T>A (hg19) ; chr2:g.214792369T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214792369T>A , CM000664.2:g.214792369T>A	GRCh38
NC_000002.11:g.215657093T>A , CM000664.1:g.215657093T>A	GRCh37
NC_000002.10:g.215365338T>A	NCBI36
NG_012047.2:g.22336A>T
NG_012047.3:g.22343A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.292A>T MANE Select	ENSP00000260947.4:p.Asn98Tyr
ENST00000421162.2:c.215+4692A>T	ENSP00000392245.2:n.215+4692A>T
ENST00000613192.2:c.158+17043A>T	ENSP00000483275.2:n.158+17043A>T
ENST00000613374.5:c.158+17043A>T	ENSP00000484464.1:n.158+17043A>T
ENST00000613706.5:c.292A>T	ENSP00000484976.2:p.Asn98Tyr
ENST00000617164.5:c.235A>T	ENSP00000480470.1:p.Asn79Tyr
ENST00000619009.5:c.292A>T	ENSP00000482293.1:p.Asn98Tyr
ENST00000650978.1:c.134A>T
ENST00000260947.8:c.292A>T	ENSP00000260947.4:p.Asn98Tyr
ENST00000421162.1:c.215+4692A>T	ENSP00000392245.1:n.215+4692A>T
ENST00000455743.5:c.215+4692A>T	ENSP00000412186.1:n.215+4692A>T
ENST00000471787.1:n.260-10860A>T
ENST00000613192.1:c.73+17043A>T	ENSP00000483275.1:n.73+17043A>T
ENST00000613374.4:c.158+17043A>T	ENSP00000484464.1:n.158+17043A>T
ENST00000613706.4:c.215+4692A>T	ENSP00000484976.1:n.215+4692A>T
ENST00000617164.4:c.235A>T	ENSP00000480470.1:p.Asn79Tyr
ENST00000619009.4:c.292A>T	ENSP00000482293.1:p.Asn98Tyr
ENST00000620057.4:c.292A>T	ENSP00000481988.1:p.Asn98Tyr
NM_000465.3:c.292A>T	NP_000456.2:p.Asn98Tyr
NM_001282543.1:c.235A>T	NP_001269472.1:p.Asn79Tyr
NM_001282545.1:c.215+4692A>T	NP_001269474.1:n.215+4692A>T
NM_001282548.1:c.158+17043A>T	NP_001269477.1:n.158+17043A>T
NM_001282549.1:c.292A>T	NP_001269478.1:p.Asn98Tyr
NR_104212.1:n.357+4692A>T
NR_104215.1:n.301-10860A>T
NR_104216.1:n.434A>T
XM_011511567.1:c.238A>T	XP_011509869.1:p.Asn80Tyr
XM_011511568.1:c.292A>T	XP_011509870.1:p.Asn98Tyr
XM_017004613.1:c.391A>T	XP_016860102.1:p.Asn131Tyr
XM_017004614.1:c.391A>T	XP_016860103.1:p.Asn131Tyr
XR_002959322.1:n.482A>T
NM_000465.4:c.292A>T MANE Select	NP_000456.2:p.Asn98Tyr
NM_001282543.2:c.235A>T	NP_001269472.1:p.Asn79Tyr
NM_001282545.2:c.215+4692A>T	NP_001269474.1:n.215+4692A>T
NM_001282548.2:c.158+17043A>T	NP_001269477.1:n.158+17043A>T
NM_001282549.2:c.292A>T	NP_001269478.1:p.Asn98Tyr
NR_104212.2:n.329+4692A>T
NR_104215.2:n.273-10860A>T
NR_104216.2:n.406A>T