Canonical Allele Identifier: CA431391278

Gene: BARD1

Linked Data

• ClinVar Variation Id: 1759607
• ClinVar RCV Id: RCV002394107
• gnomAD v4: 2-214780628-G-A
• MyVariant Identifiers: chr2:g.215645352G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214780628G>A , CM000664.2:g.214780628G>A	GRCh38
NC_000002.11:g.215645352G>A , CM000664.1:g.215645352G>A	GRCh37
NC_000002.10:g.215353597G>A	NCBI36
NG_012047.2:g.34077C>T
NG_012047.3:g.34084C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.1246C>T MANE Select	ENSP00000260947.4:p.Leu416=
ENST00000421162.2:c.215+16433C>T	ENSP00000392245.2:n.215+16433C>T
ENST00000613192.2:c.158+28784C>T	ENSP00000483275.2:n.158+28784C>T
ENST00000613374.5:c.159-28073C>T	ENSP00000484464.1:n.159-28073C>T
ENST00000613706.5:c.906+340C>T	ENSP00000484976.2:n.906+340C>T
ENST00000617164.5:c.1189C>T	ENSP00000480470.1:p.Leu397=
ENST00000619009.5:c.364+11669C>T	ENSP00000482293.1:n.364+11669C>T
ENST00000650978.1:c.1088C>T
ENST00000260947.8:c.1246C>T	ENSP00000260947.4:p.Leu416=
ENST00000421162.1:c.215+16433C>T	ENSP00000392245.1:n.215+16433C>T
ENST00000455743.5:c.*866C>T	ENSP00000412186.1:n.*866C>T
ENST00000613192.1:c.73+28784C>T	ENSP00000483275.1:n.73+28784C>T
ENST00000613374.4:c.159-28073C>T	ENSP00000484464.1:n.159-28073C>T
ENST00000613706.4:c.215+16433C>T	ENSP00000484976.1:n.215+16433C>T
ENST00000617164.4:c.1189C>T	ENSP00000480470.1:p.Leu397=
ENST00000619009.4:c.364+11669C>T	ENSP00000482293.1:n.364+11669C>T
ENST00000620057.4:c.365-11316C>T	ENSP00000481988.1:n.365-11316C>T
NM_000465.3:c.1246C>T	NP_000456.2:p.Leu416=
NM_001282543.1:c.1189C>T	NP_001269472.1:p.Leu397=
NM_001282545.1:c.215+16433C>T	NP_001269474.1:n.215+16433C>T
NM_001282548.1:c.159-28073C>T	NP_001269477.1:n.159-28073C>T
NM_001282549.1:c.364+11669C>T	NP_001269478.1:n.364+11669C>T
NR_104212.1:n.1239C>T
NR_104215.1:n.1182C>T
NR_104216.1:n.507-11316C>T
XM_011511567.1:c.1192C>T	XP_011509869.1:p.Leu398=
XM_011511568.1:c.1246C>T	XP_011509870.1:p.Leu416=
XM_017004613.1:c.1345C>T	XP_016860102.1:p.Leu449=
XM_017004614.1:c.1345C>T	XP_016860103.1:p.Leu449=
XR_002959322.1:n.1436C>T
NM_000465.4:c.1246C>T MANE Select	NP_000456.2:p.Leu416=
NM_001282543.2:c.1189C>T	NP_001269472.1:p.Leu397=
NM_001282545.2:c.215+16433C>T	NP_001269474.1:n.215+16433C>T
NM_001282548.2:c.159-28073C>T	NP_001269477.1:n.159-28073C>T
NM_001282549.2:c.364+11669C>T	NP_001269478.1:n.364+11669C>T
NR_104212.2:n.1211C>T
NR_104215.2:n.1154C>T
NR_104216.2:n.479-11316C>T