Canonical Allele Identifier: CA2090460

Gene: BARD1

Linked Data

• ClinVar Variation Id: 371950
• ClinVar RCV Id: RCV000412075 ; RCV000564100 ; RCV001030674
• dbSNP Id: rs199780731
• ExAC: 2:215657152 C / T
• gnomAD v2: 2-215657152-C-T
• gnomAD v3: 2-214792428-C-T
• gnomAD v4: 2-214792428-C-T
• MyVariant Identifiers: chr2:g.215657152C>T (hg19) ; chr2:g.214792428C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214792428C>T , CM000664.2:g.214792428C>T	GRCh38
NC_000002.11:g.215657152C>T , CM000664.1:g.215657152C>T	GRCh37
NC_000002.10:g.215365397C>T	NCBI36
NG_012047.2:g.22277G>A
NG_012047.3:g.22284G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000260947.9:c.233G>A MANE Select	ENSP00000260947.4:p.Cys78Tyr
ENST00000421162.2:c.215+4633G>A	ENSP00000392245.2:n.215+4633G>A
ENST00000613192.2:c.158+16984G>A	ENSP00000483275.2:n.158+16984G>A
ENST00000613374.5:c.158+16984G>A	ENSP00000484464.1:n.158+16984G>A
ENST00000613706.5:c.233G>A	ENSP00000484976.2:p.Cys78Tyr
ENST00000617164.5:c.176G>A	ENSP00000480470.1:p.Cys59Tyr
ENST00000619009.5:c.233G>A	ENSP00000482293.1:p.Cys78Tyr
ENST00000650978.1:c.75G>A
ENST00000260947.8:c.233G>A	ENSP00000260947.4:p.Cys78Tyr
ENST00000421162.1:c.215+4633G>A	ENSP00000392245.1:n.215+4633G>A
ENST00000455743.5:c.215+4633G>A	ENSP00000412186.1:n.215+4633G>A
ENST00000471787.1:n.260-10919G>A
ENST00000613192.1:c.73+16984G>A	ENSP00000483275.1:n.73+16984G>A
ENST00000613374.4:c.158+16984G>A	ENSP00000484464.1:n.158+16984G>A
ENST00000613706.4:c.215+4633G>A	ENSP00000484976.1:n.215+4633G>A
ENST00000617164.4:c.176G>A	ENSP00000480470.1:p.Cys59Tyr
ENST00000619009.4:c.233G>A	ENSP00000482293.1:p.Cys78Tyr
ENST00000620057.4:c.233G>A	ENSP00000481988.1:p.Cys78Tyr
NM_000465.3:c.233G>A	NP_000456.2:p.Cys78Tyr
NM_001282543.1:c.176G>A	NP_001269472.1:p.Cys59Tyr
NM_001282545.1:c.215+4633G>A	NP_001269474.1:n.215+4633G>A
NM_001282548.1:c.158+16984G>A	NP_001269477.1:n.158+16984G>A
NM_001282549.1:c.233G>A	NP_001269478.1:p.Cys78Tyr
NR_104212.1:n.357+4633G>A
NR_104215.1:n.301-10919G>A
NR_104216.1:n.375G>A
XM_011511567.1:c.179G>A	XP_011509869.1:p.Cys60Tyr
XM_011511568.1:c.233G>A	XP_011509870.1:p.Cys78Tyr
XM_017004613.1:c.332G>A	XP_016860102.1:p.Cys111Tyr
XM_017004614.1:c.332G>A	XP_016860103.1:p.Cys111Tyr
XR_002959322.1:n.423G>A
NM_000465.4:c.233G>A MANE Select	NP_000456.2:p.Cys78Tyr
NM_001282543.2:c.176G>A	NP_001269472.1:p.Cys59Tyr
NM_001282545.2:c.215+4633G>A	NP_001269474.1:n.215+4633G>A
NM_001282548.2:c.158+16984G>A	NP_001269477.1:n.158+16984G>A
NM_001282549.2:c.233G>A	NP_001269478.1:p.Cys78Tyr
NR_104212.2:n.329+4633G>A
NR_104215.2:n.273-10919G>A
NR_104216.2:n.347G>A